Publications
Mueller, S. et al. (2018) “Good vibrations: Itch induction by whole body vibration exercise without the need of a pruritogen”, Experimental dermatology, 28(12), pp. 1390–1396. Available at: 10.1111/exd.13776. edoc
Mueller, S. et al. (2017) “Functional magnetic resonance imaging in dermatology: The skin, the brain and the invisible”, Experimental Dermatology, 26(10), pp. 845–853. Available at: 10.1111/exd.13305.
Conti, C.J. et al. (2017) “A study of non-melanoma skin cancer in a series of well-characterized patients with Kindler Syndrome (KS)”. ELSEVIER SCIENCE INC. Available at: 10.26226/morressier.595a9c59d462b80296ca01f3.
Imahorn, E. et al. (2017) “Epidermodysplasia verruciformis: Clinical, viral, and histopathological phenotype in patients with EVER3 mutation”. ELSEVIER SCIENCE INC. Available at: 10.1016/j.jid.2017.07.201.
Maul, J. et al. (2017) “Safety of systemic psoriasis treatments evaluated in the Swiss Dermatology Network for Targeted Therapies (SDNTT)”. ELSEVIER SCIENCE INC. Available at: 10.1016/j.jid.2017.07.133.
Burger, B. et al. (2017) “Early frameshift mutation in KRT14 cause a heterogeneous phenotype in a family with Naegeli-Franceschetti-Jadassohn syndrome”. ELSEVIER SCIENCE INC. Available at: 10.1016/j.jid.2017.07.227.
Mueller, S.M. et al. (2017) “Topical corticosteroid concerns from the clinicians’ perspective”, Journal of Dermatological Treatment, 28(5), pp. 464–468. Available at: 10.1080/09546634.2016.1255307.
Mueller, S.M. et al. (2017) “Assessment of ‘corticophobia’ as an indicator of non-adherence to topical corticosteroids: A pilot study”, Journal of Dermatological Treatment, 28(2), pp. 104–111. Available at: 10.1080/09546634.2016.1201189.
Zahn, C., Itin, P. (2017) Papular Epidermal Nevus with "skyline" Basal Cell Layer Syndrome-Natural Course: Case Report and Literature Review. 1, pp. 1–5. Available at: 10.1159/000454757.
Maul, J.-T. et al. (2017) “Efficacy and Survival of Systemic Psoriasis Treatments: An Analysis of the Swiss Registry SDNTT”, Dermatology, 232(6), pp. 640–647. Available at: 10.1159/000452740. edoc
Ruf, M.-T. et al. (2017) “Exudate collection using wound sponges - An easy, non-invasive and reliable method to explore protease activities in ulcers”, Wound Repair and Regeneration, 25(2), pp. 320–326. Available at: 10.1111/wrr.12517. edoc
Imahorn, E. et al. (2017) “Novel TMC8 splice site mutation in epidermodysplasia verruciformis and review of HPV infections in patients with the disease”, Journal of the European Academy of Dermatology and Venereology : JEADV, 31(10), pp. 1722–1726. Available at: 10.1111/jdv.14431. edoc | Open Access
Tercanli, S., Itin, P., Weber, P. (2016) “Neurocutaneous Melanosis Associated with Prenatally Diagnosed Arachnoid Cyst”., Ultraschall in der Medizin (Stuttgart, Germany : 1980), 37(6), pp. 551–554. Available at: 10.1055/s-0042-117156.
Mueller, S. et al. (2016) “Gender differences in central processing and perception of itch: ‘Same same but different’-Preliminary results of a study using functional MRI”. WILEY-BLACKWELL.
Müller, S.M. et al. (2016) “Topical Corticosteroid Concerns in Dermatological Outpatients: A Cross-Sectional and Interventional Study”, Dermatology, 232(4), pp. 444–452. Available at: 10.1159/000446068.
Imahorn, E. et al. (2016) “A keratinocyte culture model for epidermodysplasia verruciformis”. ELSEVIER SCIENCE INC. Available at: 10.1016/j.jid.2016.06.180.
Spoerri, I. et al. (2016) “One mutation - different phenotypes: Novel insights into the link between familial pityriasis rubra pilaris and psoriasis”. ELSEVIER SCIENCE INC. Available at: 10.1016/j.jid.2016.06.179.
Suter, A. et al. (2016) “Rothmund–thomson syndrome: Novel pathogenic mutations and frequencies of variants in the RECQL4 and USB1 (C16orf57) gene”, Molecular Genetics and Genomic Medicine, 4(3), pp. 359–366. Available at: 10.1002/mgg3.209.
Rothenbuehler, S. et al. (2016) “Subkutanes Granuloma anulare am Orbitarand kann eine Dermoidzyste imitieren”., Klinische Monatsblatter fur Augenheilkunde, 233(4), pp. 409–10. Available at: 10.1055/s-0042-102579.
Kolios, A.G.A. et al. (2016) “Swiss S1 Guidelines on the Systemic Treatment of Psoriasis Vulgaris”, Dermatology, 232(4), pp. 385–406. Available at: 10.1159/000445681. edoc
Jungo, P. et al. (2016) “Superiority in Quality of Life Improvement of Biologics over Conventional Systemic Drugs in a Swiss Real-Life Psoriasis Registry”, Dermatology, 232(6), pp. 655–663. Available at: 10.1159/000455042. edoc
Buehler, S., Itin, P. (2015) “Angiokeratomas Scroti Associated with Angiokeratomas of the Eyelids: Coincidence or One Entity? A Case Report and Review of the Literature”, Dermatology, 231(3), pp. 213–216. Available at: 10.1159/000435810.
Meester, J. et al. (2015) “Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome”, American Journal of Human Genetics, 97(3), pp. 475–482. Available at: 10.1016/j.ajhg.2015.07.015.
Gysin, S., Itin, P. (2015) Blaschko linear enamel defects - A marker for focal dermal hypoplasia: Case report of focal dermal hypoplasia. 2. S. Karger AG, pp. 90–94. Available at: 10.1159/000430781.
Huebner, S. et al. (2015) “[Use of Therapeutic Contact Lenses for the Treatment of Recurrent Corneal Erosions due to Epidermolysis Bullosa Dystrophica]”., Klinische Monatsblatter fur Augenheilkunde, 232(4), pp. 380–1. Available at: 10.1055/s-0034-1396331.
Burger, B. et al. (2015) “Risk of Cutaneous Squamous Cell Carcinoma Development in Renal Transplant Recipients Is Independent of TMC/EVER Alterations”, Dermatology, 231(3), pp. 245–52. Available at: 10.1159/000435910. edoc | Open Access
Conen, K. et al. (2015) “Vemurafenib-induced radiation recall dermatitis: case report and review of the literature”, Dermatology, 230(1), pp. 1–4. Available at: 10.1159/000365918. edoc
Manevski, N. et al. (2015) “Phase ii metabolism in human skin: Skin explants show full coverage for glucuronidation, sulfation, n -acetylation, catechol methylation, and glutathione conjugation”, Drug Metabolism and Disposition, 43(1), pp. 126–139. Available at: 10.1124/dmd.114.060350.
Andreoli, A. et al. (2015) “Phosphorylation of the ribosomal protein S6, a marker of mTOR (mammalian target of rapamycin) pathway activation, is strongly increased in hypertrophic scars and keloids”, British journal of dermatology, 172(5), pp. 1415–7. Available at: 10.1111/bjd.13523. edoc
Spoerri, I. et al. (2015) “The phenotypic and genotypic spectra of ichthyosis with confetti plus novel genetic variation in the 3’ end of KRT10: from disease to a syndrome”, JAMA dermatology, 151(1), pp. 64–69. Available at: 10.1001/jamadermatol.2014.2526. edoc | Open Access
Lemke, J. et al. (2014) “Monogenic human skin disorders”, Dermatology, 229(2), pp. 55–64. Available at: 10.1159/000362200.
Itin, P. (2014) “Etiology and pathogenesis of ectodermal dysplasias”, American Journal of Medical Genetics, Part A, 164(10), pp. 2472–2477. Available at: 10.1002/ajmg.a.36550.
Salinas, C. et al. (2014) “Second international conference on a classification of ectodermal dysplasias: Development of a multiaxis model”, American Journal of Medical Genetics, Part A, 164(10), pp. 2482–2489. Available at: 10.1002/ajmg.a.36507.
Itin, P. (2014) “[Alterations in nails and teeth as a clue for genodermatoses]”., Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 65(6), pp. 513–9. Available at: 10.1007/s00105-013-2713-z.
Müller, S., Ebnöther, M., Itin, P. (2014) “Green nail syndrome (pseudomonas aeruginosa nail infection): Two cases successfully treated with topical nadifloxacin, an acne medication”, Case Reports in Dermatology, 6(2), pp. 180–184. Available at: 10.1159/000365863.
Hofbauer, G. et al. (2014) “Swiss clinical practice guidelines on field cancerization of the skin”, Swiss Medical Weekly, 144, p. w14026. Available at: 10.4414/smw.2014.14026.
Fosse, N., Itin, P. (2014) “Pigmentary lines of the newborn: A case report and review of the literature”, Dermatology, 228(3), pp. 198–201. Available at: 10.1159/000357808.
Ruzza, N., Itin, P., Beltraminelli, H. (2014) “Urgent consultations at the Dermatology Department of Basel University Hospital, Switzerland: Characterisation of patients and setting - A 12-month study with 2,222 patients data and review of the literature”, Dermatology, 228(2), pp. 177–182. Available at: 10.1159/000357532.
Ruf, M.T. et al. (2014) “Ribosomal protein S6 is hyperactivated and differentially phosphorylated in epidermal lesions of patients with psoriasis and atopic dermatitis”, British journal of dermatology, 171(6), pp. 1533–6. Available at: 10.1111/bjd.13248. edoc
Nousbeck, J. et al. (2014) “Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes”, British Journal of Dermatology, 171(6), pp. 1521–4. Available at: 10.1111/bjd.13176. edoc
Eytan, O. et al. (2014) “Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris”, British Journal of Dermatology, 170(5), pp. 1196–8. Available at: 10.1111/bjd.12799. edoc
Has, C. et al. (2014) “The Missense Mutation p.R1303Q in Type XVII Collagen Underlies Junctional Epidermolysis Bullosa Resembling Kindler Syndrome”, Journal of investigative dermatology, 134(3), pp. 845–849. Available at: 10.1038/jid.2013.367. edoc
Hitz, L.I., Itin, P., Fistarol, S. (2014) “Dermatology of the lips: Inflammatory diseases”, Quintessence International, 45(10), pp. 875–883. Available at: 10.3290/j.qi.a32638.
Burger, B., Itin, P.H. (2014) “Epidermodysplasia verruciformis”, Current problems in dermatology, 45, pp. 123–131. Available at: 10.1159/000356068. edoc
Vuichard, D., Itin, P. (2013) “Wenn’s nicht nur juckt oder brennt: Klinik und Behandlung sexuell übertragbarer Erkrankungen (Teil 2)”, Praxis. Schweizerische Rundschau für Medizin, 102(15), pp. 905–11. Available at: 10.1024/1661-8157/a001349.
Vuichard, D., Itin, P. (2013) “Wenn’s nicht nur juckt oder brennt: Klinik und Behandlung sexuell übertragbarer Erkrankungen (Teil 1)”, Praxis. Schweizerische Rundschau für Medizin, 102(14), pp. 851–856. Available at: 10.1024/1661-8157/a001348.
Wettstein, R. et al. (2013) “Treatment of basal cell carcinoma with surgical excision and perilesional interferon-α”, Journal of Plastic, Reconstructive and Aesthetic Surgery, 66(7), pp. 912–916. Available at: 10.1016/j.bjps.2013.03.008.
Wicki, A. et al. (2013) “[Melanoma- finally good news]”., Praxis, 102(11), pp. 667–70. Available at: 10.1024/1661-8157/a001293.
Ivanova, K. et al. (2013) “Acute toxoplasmosis mimicking melanoma metastases: Review of conditions causing false-positive results on F-FDG PET/CT”, Dermatology, 225(4), pp. 349–353. Available at: 10.1159/000346333.
Fistarol, S., Itin, P. (2013) “Diagnosis and treatment of lichen sclerosus: An update”, American Journal of Clinical Dermatology, 14(1), pp. 27–47. Available at: 10.1007/s40257-012-0006-4.
Itin, P. (2013) “[Dermatology for general physicians]”., Praxis, 102(2), pp. 85–9. Available at: 10.1024/1661-8157/a001170.
Itin, P.H. (2013) “Ectodermal dysplasia: thoughts and practical concepts concerning disease classification - the role of functional pathways in the molecular genetic diagnosis”, Dermatology, 226(2), pp. 111–4. Available at: 10.1159/000346613. edoc | Open Access
Itin, P., Salgado, D. (2013) “[Important genodermatoses for the practitioner]”., Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 64(1), pp. 26–31. Available at: 10.1007/s00105-012-2409-9.
Bruegger, C. et al. (2013) “MicroRNA expression differs in cutaneous squamous cell carcinomas and healthy skin of immunocompetent individuals”, Experimental dermatology, 22(6), pp. 426–8. Available at: 10.1111/exd.12153. edoc | Open Access
Mueller, S., Itin, P., Haeusermann, P. (2013) “Muckle-Wells syndrome: Individualized, reflare-guided dosing of the orphan drug canakinumab”, SKINmed, 11(2), pp. 80–83.
Arnold, A. et al. (2012) “Acromelanosis albo-punctata: A distinct inherited dermatosis with acral spotty dyspigmentation without systemic involvement”, Dermatology, 224(4), pp. 331–339. Available at: 10.1159/000339328.
Tadini, G. et al. (2012) “PENS syndrome: A new neurocutaneous phenotype”, Dermatology, 224(1), pp. 24–30. Available at: 10.1159/000336794.
Battegay, R., Itin, C., Itin, P. (2012) “Dermatological signs and symptoms of measles: A prospective case series and comparison with the literature”, Dermatology, 224(1), pp. 1–4. Available at: 10.1159/000335091.
Ivanova, K., Itin, P., Haeusermann, P. (2012) “Pityriasis rubra pilaris: Treatment with biologics - A new promising therapy?”, Dermatology, 224(2), pp. 120–125. Available at: 10.1159/000337546.
Itin, P., Battegay, M. (2012) “Skin problems in immunodeficient patients”, Current Problems in Dermatology, 43, pp. 9–17. Available at: 10.1159/000335139.
Keller, D. et al. (2012) “De novo heterozygous desmoplakin mutations leading to Naxos-Carvajal disease”, Swiss Medical Weekly, 142, p. w13670. Available at: 10.4414/smw.2012.13670.
Burger, B. et al. (2012) “Description of the natural course and clinical manifestations of ichthyosis with confetti caused by a novel KRT10 mutation”, British journal of dermatology, 166(2), pp. 434–9. Available at: 10.1111/j.1365-2133.2011.10639.x. edoc
Arnold, A.W. et al. (2012) “Type 1 segmental Galli-Galli disease resulting from a previously unreported keratin 5 mutation”, Journal of investigative dermatology, 132(8), pp. 2100–3. Available at: 10.1038/jid.2012.72. edoc
Mueller, S., Itin, P., Haeusermann, P. (2011) “Muckle-wells syndrome effectively treated with canakinumab: Is the recommended dosing schedule mandatory?”, Dermatology, 223(2), pp. 113–118. Available at: 10.1159/000331580.
Has, C. et al. (2011) “Kindler syndrome: Extension of FERMT1 mutational spectrum and natural history”, Human Mutation, 32(11), pp. 1204–1212. Available at: 10.1002/humu.21576.
Leupin, O. et al. (2011) “Bone overgrowth-associated mutations in the LRP4 gene impair sclerostin facilitator function”, Journal of Biological Chemistry, 286(22), pp. 19489–19500. Available at: 10.1074/jbc.M110.190330.
Fistarol, S., Itin, P. (2011) “Anti-inflammatory treatment”, Current Problems in Dermatology, 40, pp. 58–70. Available at: 10.1159/000321051.
Vuichard, D. et al. (2011) “Bullous cellulitis with Cryptococcus neoformans”, Infection, 39, pp. 181–182. Available at: 10.1007/s15010-011-0082-z. edoc
Arnold, A.W. et al. (2011) “Homozygosity for the c.917A → T (p.N306l) polymorphism in the EVER2/TMC8 gene of two sisters with epidermodysplasia verruciformis Lewandowsky-Lutz originally described by Wilhelm Lutz”, Dermatology, 222, pp. 81–86. Available at: 10.1159/000322536.
Mertz, K.D. et al. (2011) “Detection of Merkel cell polyomavirus in epidermodysplasia-verruciformis-associated skin neoplasms”, Dermatology, 222(1), pp. 87–92. Available at: 10.1159/000321880. edoc | Open Access
Burger, B. et al. (2011) “The immigration delay disease : adermatoglyphia-inherited absence of epidermal ridges”, Journal of the American Academy of Dermatology, 64(5), pp. 974–980. Available at: 10.1016/j.jaad.2009.11.013. edoc
Hollbach, N. et al. (2011) “[Rare in the scarce: ocular involvement in kindler syndrome]”, Klinische Monatsblätter für Augenheilkunde, 228(4), pp. 350–1. Available at: 10.1055/s-0031-1273271. edoc
Burger, B. et al. (2011) “Prevalence of skin lesions in familial adenomatous polyposis : a marker for presymptomatic diagnosis?”, The Oncologist, 16(12), pp. 1698–705. Available at: 10.1634/theoncologist.2011-0244. edoc
de Roche, M. et al. (2011) “[Lymphogranuloma venereum. An old disease in a new dress]”, Der Internist, 52(5), pp. 584–9. Available at: 10.1007/s00108-010-2686-2. edoc | Open Access
Nousbeck, J. et al. (2011) “A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia”, American journal of human genetics, 89(2), pp. 302–307. Available at: 10.1016/j.ajhg.2011.07.004. edoc
Dettmer, M. et al. (2011) “Giant ectopic liver, hepatocellular carcinoma and pachydermia-a rare genetic syndrome?”, Diagnostic Pathology, 6(75), p. 75. Available at: 10.1186/1746-1596-6-75. edoc | Open Access
Duchini, G., Itin, P., Arnold, A. (2011) “A case of refractory pyoderma gangrenosum treated with a combination of Apligraf and systemic immunosuppressive agents”., Advances in skin & wound care, 24(5), pp. 217–220. Available at: 10.1097/01.asw.0000397898.56121.3f.
Arnold, A.W. et al. (2011) “Homozygosity for the c.917A -> T (p.N306I) polymorphism in the EVER2/TMC8 gene of two sisters with epidermodysplasia verruciformis Lewandowsky-Lutz originally described by Wilhelm Lutz”, Dermatology, 222(1), pp. 81–86. Available at: 10.1159/000322536. edoc | Open Access
Arnold, A., Itin, P.H. (2010) “Laptop computer-induced erythema ab igne in a child and review of the literature”, Pediatrics, 126(5), pp. e1227–30. Available at: 10.1542/peds.2010-1390.
Arnold, A. et al. (2010) “Poikiloderma with neutropenia: A novel C16orf57 mutation and clinical diagnostic criteria”, British Journal of Dermatology, 163(4), pp. 866–869. Available at: 10.1111/j.1365-2133.2010.09929.x.
Fistarol, S., Itin, P. (2010) “Disorders of pigmentation”., Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 8(3), pp. 187–201; quiz 201. Available at: 10.1111/j.1610-0387.2009.07137.x.
Burger, B. et al. (2010) “HIV-positive child with epidermodysplasia verruciformis-like lesions and homozygous mutation in TMC6”, AIDS, 24(17), pp. 2758–60. Available at: 10.1097/qad.0b013e32833fdfca. edoc
Itin, P.H., Burger, B. (2010) “Spontaneous fading of reticular pigmentation in Naegeli-Franceschetti-Jadassohn syndrome”, Dermatology, 221(2), pp. 135–6. Available at: 10.1159/000314693. edoc
Itin, P.H., Burger, B. (2010) “[Genodermatoses for practitioners--principles and concepts]”, Therapeutische Umschau. Revue thérapeutique, 67(9), pp. 483–5. Available at: 10.1024/0040-5930/a000081. edoc
Forno, C. et al. (2010) “The difficulty in diagnosis and treatment of leprosy”, Journal of Travel Medicine, 17(4), pp. 281–283. Available at: 10.1111/j.1708-8305.2010.00419.x. edoc
Fistarol, S., Itin, P. (2009) “[Oral manifestations of systemic diseases]”., Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 60(11), pp. 866–77. Available at: 10.1007/s00105-009-1802-5.
Itin, P. (2009) “Dermatologic consultations in the hospital ward: The skin, an interdisciplinary organ”. Available at: 10.1159/000232386.
Marazza, G. et al. (2009) “Incidence of bullous pemphigoid and pemphigus in Switzerland: A 2-year prospective study”, British Journal of Dermatology, 161(4), pp. 861–868. Available at: 10.1111/j.1365-2133.2009.09300.x.
Itin, P., Happle, R. (2009) “Non-syndromic hereditary basal cell carcinomas: A reduplicated discovery”. Available at: 10.1111/j.1468-3083.2009.03277.x.
DiGiovanna, J., Priolo, M., Itin, P. (2009) “Approach towards a new classification for ectodermal dysplasias: Integration of the clinical and molecular knowledge”, American Journal of Medical Genetics, Part A, 149(9), pp. 2068–2070. Available at: 10.1002/ajmg.a.32961.
Itin, P. (2009) “Rationale and background as basis for a new classification of the ectodermal dysplasias”, American Journal of Medical Genetics, Part A, 149(9), pp. 1973–1976. Available at: 10.1002/ajmg.a.32739.
Beltraminelli, H., Itin, P., Cerroni, L. (2009) “Intraepidermal bullous haemorrhage during anticoagulation with low-molecular-weight heparin: Two cases”. Available at: 10.1111/j.1365-2133.2009.09163.x.
Arnold, A. et al. (2009) “Cetuximab therapy of metastasizing cutaneous squamous cell carcinoma in a patient with severe recessive dystrophic epidermolysis bullosa”, Dermatology, 219(1), pp. 80–83. Available at: 10.1159/000218714.
Semadeni, B. et al. (2009) “Precalcaneal congenital fibrolipomatous hamartomas: Report of 3 additional cases and discussion of the differential diagnosis”, Dermatology, 218(3), pp. 260–264. Available at: 10.1159/000195175.
Itin, P. (2009) “Happle-Tinschert syndrome: Segmentally arranged basaloid follicular hamartomas, linear atrophoderma with hypo- and hyperpigmentation, enamel defects, ipsilateral hypertrichosis, and skeletal and cerebral anomalies”, Dermatology, 218(3), pp. 221–225. Available at: 10.1159/000174103.
Itin, P., Tomaschett, S. (2009) “[Cutaneous metastases from malignancies which do not originate from the skin. An epidemiological study]”., Der Internist, 50(2), pp. 179–86. Available at: 10.1007/s00108-008-2208-7.
Hohenstein, E. et al. (2009) “Epidermodysplasia verruciformis in a HIV-positive patient homozygous for the c917A-->T polymorphism in the TMC8/EVER2 gene”., Dermatology, 218(5), pp. 114–8.
Haeusermann, P. et al. (2009) “Partial reconstitution of cutaneous microvessels in long-term survivors after allogeneic bone marrow transplantation”, Dermatology, 219(1), pp. 32–41. Available at: 10.1159/000216934. edoc | Open Access
Beltraminelli, H., Itin, P. (2009) “Pachydermodactyly - Just a sign of emotional distress”, European Journal of Dermatology, 19(1), pp. 5–13. Available at: 10.1684/ejd.2008.0543.
Itin, P.H., Hengge, U.R., Battegay, M. (2009) “[The skin, an interdisciplinary organ]”, Der Internist, 50(2), pp. 135–136. Available at: 10.1007/s00108-008-2261-2. edoc | Open Access
Itin, P.H., Battegay, M. (2009) “[Mucocutaneous infections in immunosuppression]”, Der Internist, 50(2), p. 150-+. Available at: 10.1007/s00108-008-2207-8. edoc | Open Access
Buehlmann, M. et al. (2009) “Scabies outbreak in an intensive care unit with 1,659 exposed individuals--key factors for controlling the outbreak”, Infection Control and Hospital Epidemiology, 30(4), pp. 354–360. Available at: 10.1086/596113. edoc | Open Access
Happle, R. et al. (2009) “A non-scientific treatment for patients with psoriasis - advocated in a scientific journal”., J EUR ACAD DERMATOL (PRINT-AUSGABE), 23(2), pp. 1222–3; author reply 1223.
Itin, P., Burger, B. (2009) “Mosaic manifestations of monogenic skin diseases”, Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 7(9), pp. 744–48. Available at: 10.1111/j.1610-0387.2009.07033.x. edoc
Itin, P., Bircher, A. (2009) “[Egon Macher 1924-2008]”, Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 7(2), pp. 176–179. Available at: 10.1111/j.1610-0387.2008.07004.x. edoc
Burger, B., Itin, P. (2008) “Muir-Torre syndrome”. Available at: 10.1159/000123520.
Häusermann, P. et al. (2008) “Cutaneous graft-versus-host disease : a guide for the dermatologist”, Dermatology, 216(4), pp. 287–304. Available at: 10.1159/000113941. edoc | Open Access
Almeida, S. et al. (2008) “Five new CYLD mutations in skin appendage tumors and evidence that aspartic acid 681 in CYLD is essential for deubiquitinase activity”, Journal of Investigative Dermatology, 128(3), pp. 587–593. Available at: 10.1038/sj.jid.5701045.
Lugassy, J. et al. (2008) “KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome”, Journal of investigative dermatology, 128(6), pp. 1517–24. Available at: 10.1038/sj.jid.5701187. edoc
Sumila, M. et al. (2008) “Long-term results of radiotherapy in patients with chronic palmo-plantar eczema or psoriasis”, Strahlentherapie und Onkologie, 184(4), pp. 218–23. Available at: 10.1007/s00066-008-1788-4. edoc | Open Access
Kägi, M., Bindschedler, M., Itin, P. (2008) “Orales Isotretinoin zur Behandlung schwerer Akne vulgaris. Information und Empfehlungen”, Schweiz Med Forum, 8(2), pp. 98–99.
Fisch, A., Itin, P., Beltraminelli, H. (2008) “Therapieresistente systemische Sarkoidose mit kutaner Manifestation; erfolgreiche Behandlung mit einer Kombination von Infliximab, Azathioprin und neiderdosierten Steroiden”, Dermatologica helvetica, 5(2), pp. 17–18.
Beltraminelli, H., Itin, P. (2008) “Skin and psyche--from the surface to the depth of the inner world”, Journal der Deutschen Dermatologischen Gesellschaft, 6(1), pp. 8–14. Available at: 10.1111/j.1610-0387.2007.06406.x. edoc
Burger, B., Itin, P. (2008) “Hereditäre Hauttumoren speziell bei der Frau”, Schweiz Zeitschr Onkol, 2(4), pp. 20–24.
Itin, P. (2008) “Hautveränderungen bei Essstörungen”, Schw Zeitschr Ernährungsmedizin, 3(3), pp. 30–32.
Kägi, M.K., Bindschedler, M., Itin, P. (2008) “Orales Isotretinoin zur Behandlung schwerer Akne vulgaris. Information und Empfehlungen”, Schweizerisches Medizin-Forum, 8(6), pp. 98–99. Available at: https://medicalforum.ch/de/issue/edn/smf.2008.06/. edoc | Open Access
Fisch, A., Itin, P., Beltraminelli, H. (2008) “Therapieresistente systemische Sarkoidose mit kutaner Manifestation : erfolgreiche Behandlung mit einer Kombination von Infliximab, Azathioprin und neiderdosierten Steroiden”, Dermatologica Helvetica, 5, pp. 17–18. edoc | Open Access
Burger, B., Itin, P. (2008) “Hereditäre Hauttumoren speziell bei der Frau”, Schweizer Zeitschrift für Onkologie, 2, pp. 20–24. edoc
Itin, P. (2008) “Hautveränderungen bei Essstörungen”, Schweizer Zeitschrift für Ernährungsmedizin, 2008(3), pp. 30–32. Available at: https://www.rosenfluh.ch/ernaehrungsmedizin-2008-03. edoc | Open Access
Burger, B., Itin, P. (2008) “Muir-Torre syndrome”, Dermatology, 217(1), pp. 56–57. Available at: 10.1159/000123520. edoc | Open Access
Schütte, D. et al. (2007) “Development of highly organized lymphoid structures in Buruli ulcer lesions after treatment with rifampicin and streptomycin”, PLoS neglected tropical diseases, 1(1), p. e2. Available at: 10.1371/journal.pntd.0000002.
Itin, P. (2007) “Hautveränderungen bei Essstörungen”, in Springer Verlag, Berlin, Heidelberg, New York, pp. 238–241.
Itin, P. (2007) “Herpes zoster Neuralgie”, in Hans Huber Verlag, Bern, pp. 477–481.
Itin, P. (2007) Current Problems in Dermatology Vol 34: Skin protection. Pracitical applications in the occupational setting. (Karger-Verlag, Basel, 180).
Itin, P. (2007) Current Problems in Dermatology Vol 35: Environmental Factors in Skin Diseases. (Karger-Verlag, Basel, 191).
Orasch, C., Itin, P., Flückiger, U. (2007) “Lyme-Borreliose in der Schweiz”, 7(6), pp. 850–55.
Itin, P. (2007) “Ist die Verschreibung von Isotretinoion noch vertretbar?”, JDDG, 5(3), pp. 183–185.
Itin, P., Fistarol, S. (2007) “Clinical and morphological abnormalities of hair as a clue to the diagnosis of genetic disorders”, Int J Med Biol Front, 13(16), pp. 37–52.
Itin, P., Fistarol, S. (2004) “Ectodermal dysplasias”, American Journal of Medical Genetics - Seminars in Medical Genetics, 131 C(1), pp. 45–51. Available at: 10.1002/ajmg.c.30033.
Sendi, P., Itin, P. (2004) “[What is your diagnosis? Pseudocyanosis due to amiodarone]”., Praxis, 93(42), pp. 1725–6. Available at: 10.1024/0369-8394.93.42.1725.
Häusermann, P. et al. (2004) “Cutaneous plasmablastic lymphoma in an HIV-positive male: An unrecognized cutaneous manifestation”, Dermatology, 208(3), pp. 287–290. Available at: 10.1159/000077324.
Weder, P. et al. (2004) “Familial cutaneous mycosis fungoides: Successful treatment with a combination of gemcitabine and alemtuzumab”, Dermatology, 208(3), pp. 281–283. Available at: 10.1159/000077322.
Antic, M., Conen, D., Itin, P. (2004) “Teaching effects of dermatological consultations on nondermatologists in the field of internal medicine: A study of 1,290 inpatients”, Dermatology, 208(1), pp. 32–37. Available at: 10.1159/000075043.
Itin, P., Wernli, M. (2004) “[What is your diagnosis? Coumarin necrosis]”., Praxis, 93(4), pp. 94–5. Available at: 10.1024/0369-8394.93.4.94.
Spritz, R., Itin, P., Gutmann, D. (2004) “Piebaldism and Neurofibromatosis Type 1: Horses of Very Different Colors”, Journal of Investigative Dermatology, 122(2), p. xxxiv-xxxv. Available at: 10.1046/j.0022-202X.2004.22235.x.
Fistarol, S., Itin, P. (2003) “Acquired perforating dermatosis in a patient with Poland syndrome”, Dermatology, 207(4), pp. 390–394. Available at: 10.1159/000074121.
Wenk, C., Itin, P. (2003) “Epidemiology of Pediatric Dermatology and Allergology in the Region of Aargau, Switzerland”, Pediatric Dermatology, 20(6), pp. 482–487. Available at: 10.1111/j.1525-1470.2003.20605.x.
Schaller, J. et al. (2003) “Identification of human papillomavirus DNA in cutaneous lesions of cowden syndrome”, Dermatology, 207(2), pp. 134–140. Available at: 10.1159/000071782.
Itin, P., Fistarol, S. (2003) “[Genetic counseling and DNA testing in patients with increased risks for malignant melanoma]”., Therapeutische Umschau. Revue therapeutique, 60(8), pp. 469–72. Available at: 10.1024/0040-5930.60.8.469.
Itin, P., Moschopulos, M., Richard, G. (2003) “Reticular erythrokeratoderma: A new disorder of cornification”, American Journal of Medical Genetics, 120 A(2), pp. 237–240. Available at: 10.1002/ajmg.a.20036.
Hofer, T., Goldenberger, D., Itin, P. (2003) “Anetoderma and borreliosis: Is there a pathogenetic relationship?”, European Journal of Dermatology, 13(4), pp. 399–401.
Anliker, M., Itin, P. (2003) “[Herpetic folliculitis barbae. A rare cause of folliculitis]”., Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 54(3), pp. 265–7. Available at: 10.1007/s00105-002-0414-0.
Christen, A. et al. (2003) “[Secondary syphilis with ocular manifestations and oral ulceration]”., Praxis, 92(9), pp. 397–402. Available at: 10.1024/0369-8394.92.9.397.
Itin, P. (2003) “[What is your diagnosis? Nevoid basal cell carcinoma syndrome (basal cell nevus syndrome, Gorlin syndrome)]”., Praxis, 92(9), pp. 377–8. Available at: 10.1024/0369-8394.92.9.377.
Prins, C. et al. (2003) “Effect of high-dose intravenous immunoglobulin therapy in Stevens-Johnson syndrome: a retrospective, multicenter study”., Dermatology (Basel, Switzerland), 207(1), pp. 96–99. Available at: 10.1159/000070957.
Kroesen, S., Itin, P., Hasler, P. (2003) “Arthritis and interstitial granulomatous dermatitis (Ackerman syndrome) with pulmonary silicosis”, Seminars in Arthritis and Rheumatism, 32(5), pp. 334–340. Available at: 10.1053/sarh.2003.50016.
Itin, P., Happle, R. (2002) “Darier disease with paired segmental manifestation of either excessive or absent involvement: A further step in the concept of twin spotting”. Available at: 10.1159/000066423.
Fistarol, S., Anliker, M., Itin, P. (2002) “Cowden disease or multiple hamartoma syndrome - Cutaneous clue to internal malignancy”, European Journal of Dermatology, 12(5), pp. 411–421.
Itin, P. (2002) “[What is your diagnosis? Tuberous sclerosis (Bourneville-Pringle syndrome)]”., Praxis, 91(29-30), pp. 1195–6. Available at: 10.1024/0369-8394.91.29.1195.
Tanew, A. et al. (2002) “Hereditary, focal, transgressive palmoplantar keratoderma with associated clinical findings: A new entity?”, British Journal of Dermatology, 146(3), pp. 490–494. Available at: 10.1046/j.1365-2133.2002.04626.x.
Itin, P., Düggelin, M. (2002) “[Hair shaft abnormalities]”., Therapeutische Umschau. Revue therapeutique, 59(5), pp. 228–32. Available at: 10.1024/0040-5930.59.5.228.
Itin, P., Lautenschlager, S. (2002) “Acquired leukoderma in congenital pigmented nevus associated with vitiligo-like depigmentation”, Pediatric Dermatology, 19(1), pp. 73–75. Available at: 10.1046/j.1525-1470.2002.00028.x.
Fistarol, S., Itin, P. (2002) “Nail changes in genodermatoses”, European Journal of Dermatology, 12(2), pp. 119–128.
Itin, P., Lautenschlager, S. (2002) “Aquagenic syringeal acrokeratoderma (transient reactive papulotranslucent acrokeratoderma)”, Dermatology, 204(1), pp. 8–11. Available at: 10.1159/000051802.
Buechner, S., Itin, P. (2002) “Papular elastorrhexis. report of five cases”., Dermatology (Basel, Switzerland), 205(2), pp. 198–200. Available at: 10.1159/000063914.
Sprecher, E. et al. (2002) “Refined mapping of Naegeli-Franceschetti-Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and Investigation of candidate genes”, Journal of Investigative Dermatology, 119(3), pp. 692–698. Available at: 10.1046/j.1523-1747.2002.01855.x.
Borelli, S., Itin, P. (2002) “Hautvernderungen bei Erkrankungen des Magen-Darmtraktes”, Praxis, 91(8), pp. 1029–1036.
Trüeb, R., Itin, P., Itin, und S.A. für T. (2001) “[Photographic documentation of the effectiveness of 1 mg. oral finasteride in treatment of androgenic alopecia in the man in routine general practice in Switzerland]”., Praxis, 90(48), pp. 2087–93.
Z’Graggen, W. et al. (2001) “Primary cutaneous nocardiosis in an immune-competent patient”, European Journal of Dermatology, 11(6), pp. 569–571.
Stoll, S. et al. (2001) “[Cervical tuberculous lymphadenopathy--a rare complication of myelodysplastic syndrome]”., Praxis, 90(45), pp. 1976–9.
Hofer, T., Itin, P. (2001) “[Acne inversa: a dapsone-sensitive dermatosis]”., Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 52(10 Pt 2), pp. 989–92. Available at: 10.1007/s001050170015.
Laeng, R., Heilbrunner, J., Itin, P. (2001) “Late-onset eccrine angiomatous hamartoma: Clinical, histological and imaging findings”, Dermatology, 203(1), pp. 70–74. Available at: 10.1159/000051709.
Itin, P., Keserü, B., Hauser, V. (2001) “Syndactyly/brachyphalangy and nail dysplasias as marker lesions for sclerosteosis”, Dermatology, 202(3), pp. 259–260. Available at: 10.1159/000051649.
Itin, P., Laeng, R. (2001) “[Multiple pigmented basalioma of the scalp in a patient with Curschmann-Steinert myotonia dystrophica. Confirmation of a rare symptom constellation]”., Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 52(3), pp. 244–6. Available at: 10.1007/s001050051298.
Itin, P., Sarasin, A., Pittelkow, M. (2001) “Trichothiodystrophy: Update on the sulfur deficient brittle hair syndromes”, Journal of the American Academy of Dermatology, 44(6), pp. 891–924. Available at: 10.1067/mjd.2001.114294.
Heizmann, M. et al. (2001) “Successful treatment of paraneoplastic pemphigus in follicular NHL with rituximab: Report of a case and review of treatment for paraneoplastic pemphigus in NHL and CLL”, American Journal of Hematology, 66(2), pp. 142–144. Available at: 10.1002/1096-8652(200102)66:2<142::AID-AJH1032>3.0.CO;2-0.
Itin, P., Schaub-Heinimann, N. (2001) “K>ratodermies palmo-plantaires”, Flammarion, -(5), pp. 410–414.
Z’Graggen, W., Itin, P., Conen, D. (2000) “[Progressive, small spotted, confluent erythema with bullae formation and general symptoms. Acute Lyell syndrome]”., Praxis, 89(23), pp. 1022–4.
Heise, A., Itin, P. (2000) “[Thoracic skin basalioma of the pigmented type with superficial, flat ulceration]”., Praxis, 89(20), pp. 853–4.
Hediger, C., Rost, B., Itin, P. (2000) “Cutaneous manifestations in anorexia nervosa”, Schweizerische Medizinische Wochenschrift, 130(16), pp. 565–575.
Itin, P., Bargetzi, M. (2000) “Aplasia cutis congenita with precancerous transformation - The first case. Why do these scars never develop invasive tumors?”, European Journal of Dermatology, 10(3), pp. 181–183.
Stähelin-Massik, J., Gnehm, H., Itin, P. (2000) “Pseudomonas folliculitis in a young child”, Pediatric Infectious Disease Journal, 19(4), pp. 362–363. Available at: 10.1097/00006454-200004000-00024.
Bon, A., Happle, R., Itin, P. (2000) “Renbok phenomenon in alopecia areata”, Dermatology, 201(1), pp. 49–50. Available at: 10.1159/000018430.
Itin, P., Büchner, S., Happle, R. (2000) “Segmental manifestation of Darier disease. What is the genetic background in type 1 and type 2 mosaic phenotypes?”, Dermatology, 200(3), pp. 254–257. Available at: 10.1159/000018370.
Itin, P. (2000) “[Skin check-up--who and when?]”., Therapeutische Umschau. Revue therapeutique, 57(1), pp. 22–5. Available at: 10.1024/0040-5930.57.1.22.
Graggen W, Z., Itin, P., Conen, D. (2000) “Progredientes, kleinfleckiges, konfluierendes Erythem mit Blasenbildung und Allgemeinsymptomen”, Praxis, 89(4), pp. 995–998.
Itin, P., Rufli, T. (2000) “Haut- und Geschlechtskrankheiten”, Hans Huber Verlag, Bern, -(18), pp. 863–880.
Itin, P., Heitzmann, F., Stamm, B. (1999) “Metastasis to the nasal tip from a cervical carcinoma”, Dermatology, 199(2), pp. 171–173. Available at: 10.1159/000018231.
Itin, P., Schiller, P. (1999) “Double-lined frontoparietal scleroderma en coup de sabre”, Dermatology, 199(2), pp. 185–186. Available at: 10.1159/000018236.
Happle, R., Itin, P., Brun, A. (1999) “Type 2 segmental Darier disease”, European Journal of Dermatology, 9(6), pp. 449–451.
Ruiz-Perez, V. et al. (1999) “ATP2A2 mutations in Darier’s disease: Variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class”, Human Molecular Genetics, 8(9), pp. 1621–1630. Available at: 10.1093/hmg/8.9.1621.
Itin, P., Buechner, S. (1999) “Segmental forms of autosomal dominant skin disorders: The puzzle of mosaicism”, American Journal of Medical Genetics, 85(4), pp. 351–354. Available at: 10.1002/(SICI)1096-8628(19990806)85:4<351::AID-AJMG8>3.0.CO;2-0.
Helbling, F., Itin, P. (1999) “[Refractory inguinogenital dermatosis]”., Schweizerische medizinische Wochenschrift, 129(29-30), p. 1081.
Itin, P. (1999) “[The diabetic foot--the view of the dermatologist]”., Praxis, 88(27-28), pp. 1186–90.
Schmid, P., Itin, P., Cox, D. (1999) “Proteolytic inactivation of transforming growth factor β3 by elastase in venous leg ulcers: Implications for clinical trials using topically- applied peptide growth factors [2].”
Itin, P. (1999) “[Risk factors for the development of malignant melanomas]”., Therapeutische Umschau. Revue therapeutique, 56(6), pp. 298–301. Available at: 10.1024/0040-5930.56.6.298.
Schaub, N. et al. (1999) “Is there a relation between risk groups or initial CD4 T cell counts and prevalence of seborrheic dermatitis in HIV-infected patients?”, Dermatology, 198(2), pp. 126–129. Available at: 10.1159/000018087.
Trüeb, R., Wyss, M., Itin, P. (1999) “[Androgenetic alopecia, hirsutism and hypertrichosis]”., Therapeutische Umschau. Revue therapeutique, 56(4), pp. 219–24. Available at: 10.1024/0040-5930.56.4.219.
Trendelenburg, M. et al. (1999) “Hypocomplementemic urticarial vasculitis or systemic lupus erythematosus?”, American Journal of Kidney Diseases, 34(4), pp. 745–751. Available at: 10.1016/S0272-6386(99)70402-6.
Grob, H. et al. (1998) “[Chronic meningococcemia--a rare, but characteristic disease picture]”., Schweizerische medizinische Wochenschrift, 128(50), pp. 1988–93.
Richard, G. et al. (1998) “Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis”, Nature Genetics, 20(4), pp. 366–369. Available at: 10.1038/3840.
Itin, P., Lautenschlager, S. (1998) “Genodermatosis with reticulate, patchy and mottled pigmentation of the neck - A clue to rare dermatologic disorders”, Dermatology, 197(3), pp. 281–290. Available at: 10.1159/000018015.
Lautenschlager, S., Itin, P. (1998) “Reticulate, patchy and mottled pigmentation of the neck. Acquired forms”, Dermatology, 197(3), pp. 291–296. Available at: 10.1159/000018016.
Itin, P. et al. (1998) “[Cutaneous diphtheria in returning vacationers--mirror of inappropriate vaccination practice?]”., Praxis, 87(37), pp. 1188–90.
Itin, P., Helbling, F. (1998) “[Psoriasis therapy today]”., Therapeutische Umschau. Revue therapeutique, 55(8), pp. 484–91.
Itin, P., Lautenschlager, S. (1998) “Lower and upper extremity atrophy associated with a giant congenital melanocytic nevus”, Pediatric Dermatology, 15(4), pp. 287–289. Available at: 10.1046/j.1525-1470.1998.1998015287.x.
Schmid, P. et al. (1998) “Enhanced expression of transforming growth factor-β type I and type II receptors in wound granulation tissue and hypertrophic scar”, American Journal of Pathology, 152(2), pp. 485–493.
Courvoisier, S. et al. (1998) “Relationship between erythema of the proximal nailfold in HIV-infected patients and hepatitis C virus infection”, European Journal of Clinical Microbiology and Infectious Diseases, 17(8), pp. 596–597. Available at: 10.1007/BF01708630.
Itin, P. et al. (1998) “Cutaneous manifestations of paecilomyces lilacinus infection induced by a contaminated skin lotion in patients who are severely immunosuppressed”, Journal of the American Academy of Dermatology, 39(3), pp. 401–409. Available at: 10.1016/S0190-9622(98)70315-9.
Buechner, S. et al. (1997) “Regression of basal cell carcinoma by intralesional interferon-alpha treatment is mediated by CD95 (Apo-1/Fas)-CD95 ligand-induced suicide”, Journal of Clinical Investigation, 100(11), pp. 2691–2696. Available at: 10.1172/JCI119814.
Cathomas, G. et al. (1997) “Transplantation-associated malignancies: restriction of human herpes virus 8 to Kaposi’s sarcoma”., Transplantation, 64(1), pp. 175–8. Available at: 10.1097/00007890-199707150-00033.
Bohn, S., Büchner, S., Itin, P. (1997) “[Erythema nodosum: 112 cases. Epidemiology, clinical aspects and histopathology]”., Schweizerische medizinische Wochenschrift, 127(27-28), pp. 1168–76.
Itin, P. (1997) “[Hair shaft anomalies]”., Praxis, 86(23), pp. 982–6.
Bassetti, S., Courvoisier, S., Itin, P. (1997) “[Oral ulcers in HIV infection]”., Praxis, 86(21), pp. 912–3.
Cathomas, G. et al. (1997) “Absence of Kaposi’s sarcoma-associated human herpes virus 8 in transplantation-related tumors other than Kaposi’s sarcoma”, Transplantation Proceedings, 29(1-2), pp. 836–837. Available at: 10.1016/S0041-1345(96)00155-8.
Itin, P., Lautenschlager, S. (1997) “Viral lesions of the mouth in HIV-infected patients”, Dermatology, 194(1), pp. 1–7. Available at: 10.1159/000246047.
Itin, P. et al. (1997) “Superciliary upsweep or tented eyebrows: A distinct mendelian trait”, Journal of the American Academy of Dermatology, 37(2 II SUPPL.), pp. 295–297. Available at: 10.1016/s0190-9622(97)70008-2.
Itin, P. et al. (1997) “Cosmetically induced hair beads”, Journal of the American Academy of Dermatology, 36(2), pp. 260–261. Available at: 10.1016/S0190-9622(97)70293-7.
Richard, G. et al. (1997) “Linkage studies in erythrokeratodermias: Fine mapping, genetic heterogeneity, and analysis of candidate genes”, Journal of Investigative Dermatology, 109(5), pp. 666–671. Available at: 10.1111/1523-1747.ep12337713.
Bernauer, W., Itin, P., Kirtschig, G. (1997) “Cicatricial pemphigoid”., Developments in ophthalmology, 28, pp. 46–63. Available at: 10.1159/000060698.
Itin, P., Büchner, S., Pittelkow, M. (1997) “Mucocutaneous paraneoplastic disorders”., Developments in ophthalmology, 28, pp. 73–85. Available at: 10.1159/000060706.
Bernauer, W., Itin, P. (1997) “Immunological investigations in the evaluation of patients with cicatrising conjunctivitis”., Developments in ophthalmology, 28, pp. 102–110. Available at: 10.1159/000060708.
Bernauer, W., Itin, P. (1997) “Immunological investigations”, in Karger-Verlag, Basel, pp. 102–110.
Orth, B. et al. (1996) “Outbreak of Invasive Mycoses Caused by Paecilomyces lilacinus from a Contaminated Skin Lotion”, Annals of Internal Medicine, 125(10), pp. 799–806. Available at: 10.7326/0003-4819-125-10-199611150-00003.
Schaub, N. et al. (1996) “[Epidemiology of skin diseases in HIV-infected patients: a prospective cohort study]”., Praxis, 85(38), pp. 1162–6.
Pluschke, G. et al. (1996) “Molecular cloning of a human melanoma-associated chondroitin sulfate proteoglycan”, Proceedings of the National Academy of Sciences of the United States of America, 93(18), pp. 9710–9715. Available at: 10.1073/pnas.93.18.9710.
Itin, P. et al. (1996) “Secondary erythermalgia in an HIV-infected patient. Is there a pathogenetic relationship? [7]”. Available at: 10.2340/0001555576332333.
Itin, P. et al. (1996) “[Skin manifestations of graft-versus-host reaction following bone marrow transplantation]”., Schweizerische medizinische Wochenschrift, 126(9), pp. 339–47.
Nüesch, R. et al. (1996) “Oral manifestation of disseminated mycobacterium kansasii infection in a patient with AIDS”, Dermatology, 192(2), pp. 183–184. Available at: 10.1159/000246355.
Rubisz-Brzezinska, J., Büchner, S., Itin, P. (1996) “Vitiligo associated with lichen planus: Is there a pathogenetic relationship?”, Dermatology, 192(2), pp. 176–178. Available at: 10.1159/000246353.
Lautenschlager, S. et al. (1996) “Lichen ruber planus: Epidemiology, course and therapy in 580 patients”, Dermatology, 193(1), pp. 161–161.
Grob, H., Rufli, T., Itin, P. (1996) “Resistance to activated protein C - A major cause for venous leg ulcers in young persons”, Dermatology, 193(1), pp. 166–166.
Schiller, P., Itin, P. (1996) “Angiokeratomas: An update”, Dermatology, 193(4), pp. 282–275. Available at: 10.1159/000246270.
Itin, P. et al. (1996) “Trichorhinophalangeal syndrome type III”, Dermatology, 193(4), pp. 349–352. Available at: 10.1159/000246290.
Itin, P. et al. (1996) “Erythema of the proximal nailfold in HIV-infected patients”, Journal of the American Academy of Dermatology, 35(4), pp. 631–633. Available at: 10.1016/S0190-9622(96)90694-5.
Schmid, P., Itin, P., Rufli, T. (1996) “In situ analysis of transforming growth factors-β (TGF-β1, TGF-β2, TGF-β3) and TGF-β type II receptor expression in basal cell carcinomas”, British Journal of Dermatology, 134(6), pp. 1044–1051. Available at: 10.1111/j.1365-2133.1996.tb07940.x.
Richard, G. et al. (1996) “Evidence for genetic heterogeneity in monilethrix”, Journal of Investigative Dermatology, 107(6), pp. 812–814. Available at: 10.1111/1523-1747.ep12330568.
Cathomas, G. et al. (1996) “[Detection of herpes virus-like DNA in various forms of Kaposi’s sarcoma but not in other mesenchymal tumors or inflammatory changes in skin]”., Verhandlungen der Deutschen Gesellschaft fur Pathologie, 80, pp. 318–21.
Itin, P. (1995) “[Porokeratosis plantaris, palmaris et disseminataa with multiple filiform hyperkeratoses and nail dystrophy]”., Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 46(12), pp. 869–72. Available at: 10.1007/s001050050357.
Izakovic, J. et al. (1995) “[Hair-like hyperkeratoses in patients with kidney transplants. A new cyclosporin side-effect]”., Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 46(12), pp. 841–6. Available at: 10.1007/s001050050350.
Schmid, P., Itin, P., Rufli, T. (1995) “In situ analysis of transforming growth factor-βs (TGF-β1, TGF-β2, TGF-β3and TGF-3 type II receptor expression in malignant melanoma”, Carcinogenesis, 16(7), pp. 1499–1503. Available at: 10.1093/carcin/16.7.1499.
Aschwanden, M., Itin, P., Jäger, K. (1995) “[Multiple familial glomangiomas]”., Praxis, 84(14), pp. 412–4.
Itin, P., Rufli, T. (1995) “[Skin symptoms in gastrointestinal diseases]”., Therapeutische Umschau. Revue therapeutique, 52(4), pp. 236–42.
Bircher, A. et al. (1995) “Delayed hypersensitivity to one low-molecular-weight heparin with tolerance of other low-molecular-weight heparins”, British Journal of Dermatology, 132(3), pp. 461–463. Available at: 10.1111/j.1365-2133.1995.tb08684.x.
Itin, P., Buechner, S., Rufli, T. (1995) “Lichen planus of the eyelids”, Dermatology, 191(4), pp. 350–351. Available at: 10.1159/000246599.
Itin, P., Lautenschlager, S. (1995) “Pachydermodactyly: A psychocutaneous disorder”, Dermatology, 190(1), pp. 1–3. Available at: 10.1159/000246624.
Itin, P., Lautenschlager, S., Buechner, S. (1995) “Zosteriform metastases in melanoma”, Journal of the American Academy of Dermatology, 32(5 PART 2), pp. 854–857. Available at: 10.1016/0190-9622(95)91546-X.
Surber, C. et al. (1995) “Topical corticosteroids”, Journal of the American Academy of Dermatology, 32(6), pp. 1025–1030. Available at: 10.1016/0190-9622(95)91343-2.
Itin, P. et al. (1995) “Isolated lichen planus of the lip”, British Journal of Dermatology, 132(6), pp. 1000–1002. Available at: 10.1111/j.1365-2133.1995.tb16963.x.
Buechner, S. et al. (1995) “Lymphoproliferative Responses to Borrelia burgdorferi in Patients With Erythema Migrans, Acrodermatitis Chronica Atrophicans, Lymphadenosis Benigna Cutis, and Morphea”, Archives of Dermatology, 131(6), pp. 673–677. Available at: 10.1001/archderm.1995.01690180047008.
SCHMID, P., ITIN, P., RUFLI, T. (1995) “OVEREXPRESSION OF IL-1-BETA, IL-8, AND TGF-ALPHA IN KERATOACANTHOMA”, J Invest Dermatol, 104(1), pp. 626–626.
Itin, P., Lautenschlager, S. (1995) “Palmoplantar keratoderma and associated syndromes”, Seminars in Cutaneous Medicine and Surgery, 14(2), pp. 152–161. Available at: 10.1016/s1085-5629(05)80012-4.
Itin, P. et al. (1994) “Oral hairy leukoplakia in a child: Confirmation of the clinical diagnosis by ultrastructural examination of exfoliative cytologic specimens”, Dermatology, 189(2), pp. 167–169. Available at: 10.1159/000246824.
Müller, D. et al. (1994) “Acrodermatitis chronica atrophicans involving the face - Evidence for Borrelia burgdorferi infection confirmed by DNA amplification”, Dermatology, 189(4), pp. 430–431. Available at: 10.1159/000246901.
Lautenschlager, S., Itin, P., Rufli, T. (1994) “The petrified ear”, Dermatology, 189(4), pp. 435–436. Available at: 10.1159/000246903.
Itin, P. et al. (1994) “Recurrent pyogenic granuloma with satellitosis - A localized variant of bacillary angiomatosis?”, Dermatology, 189(4), pp. 409–412. Available at: 10.1159/000246892.
Itin, P., Gilli, L. (1994) “Molluscum contagiosum mimicking sebaceous nevus of Jadassohn, ecthyma and giant condylomata acuminata in HIV-infected patients”, Dermatology, 189(4), pp. 396–398. Available at: 10.1159/000246887.
Saurat, J., Itin, P. (1994) “Peroxisome disorders and cutaneous manifestations”. Available at: 10.1159/000247074.
Itin, P. et al. (1994) “A new clinical disorder of twisted and rolled body hairs with multiple, large knots”, Journal of the American Academy of Dermatology, 30(1), pp. 31–35. Available at: 10.1016/S0190-9622(94)70003-6.
Lautenschlager, S. et al. (1994) “Subcorneal pustular dermatosis at the injection site of recombinant human granulocyte-macrophage colony-stimulating factor in a patient with IgA myeloma”, Journal of the American Academy of Dermatology, 30(5), pp. 787–789. Available at: 10.1016/S0190-9622(08)81514-9.
Flückiger, R. et al. (1994) “Oral hairy leukoplakia in a patient with ulcerative colitis”, Gastroenterology, 106(2), pp. 506–508. Available at: 10.1016/0016-5085(94)90612-2.
Itin, P., Pittelkow, M., Kumar, R. (1994) “Effects of vitamin D metabolites on proliferation and differentiation of cultured human epidermal keratinocytes grown in serum-free or defined culture medium”, Endocrinology, 135(5), pp. 1793–1798. Available at: 10.1210/endo.135.5.7956903.
Lautenschlager, S., Itin, P., Rufli, T. (1994) “Pachydermodactyly: Reflecting Obsessive-Compulsive Behavior?”. Available at: 10.1001/archderm.1994.01690030123021.
Schmid, P. et al. (1994) “The Type I Interferon System Is Locally Activated in Psoriatic Lesions”, Journal of Interferon Research, 14(5), pp. 229–234. Available at: 10.1089/jir.1994.14.229.
Lautenschlager, S., Itin, P. (1993) “[Schnitzler syndrome]”., Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 44(12), pp. 781–4.
Schmid, P. et al. (1993) “In situ hybridization analysis of cytokine, proto-oncogene and tumour suppressor gene expression in psoriasis”, Archives of Dermatological Research, 285(6), pp. 334–340. Available at: 10.1007/BF00371833.
Flückiger, R., Itin, P., Widmer, A. (1993) “[Non-familial ulcero-mutilating acro-osteopathy of the foot (Bureau-Barrière syndrome)]”., Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis, 82(1), pp. 28–30.
Itin, P. et al. (1993) “Pili trianguli et canaliculi: A distinctive hair shaft defect leading to uncombable hair”, Dermatology, 187(4), pp. 296–298. Available at: 10.1159/000247273.
Itin, P. (1993) “Oral hairy leukoplakia - 10 years on”, Dermatology, 187(3), pp. 159–163. Available at: 10.1159/000247233.
Flückiger, R., Itin, P. (1993) “Keratosis extremitatum (Greither’s disease): Clinical features, histology, ultrastructure”, Dermatology, 187(4), pp. 309–311. Available at: 10.1159/000247278.
Itin, P. et al. (1993) “Oral manifestations in HIV-infected patients: Diagnosis and management”, Journal of the American Academy of Dermatology, 29(5), pp. 749–760. Available at: 10.1016/0190-9622(93)70241-K.
Itin, P. et al. (1993) “Natural history of the Naegeli-Franceschetti-Jadassohn syndrome and further delineation of its clinical manifestations”, Journal of the American Academy of Dermatology, 28(6), pp. 942–950. Available at: 10.1016/0190-9622(93)70135-G.
Scott, R. et al. (1993) “Xeroderma pigmentosum-Cockayne syndrome complex in two patients: Absence of slun tumors despite severe deficiency of DNA excision repair”, Journal of the American Academy of Dermatology, 29(5), pp. 883–889. Available at: 10.1016/0190-9622(93)70263-S.
Itin, P. et al. (1993) “Pseudo hairy leukoplakia [4]”. Available at: 10.1111/j.1365-2133.1993.tb00246.x.
Spritz, R. et al. (1993) “Novel mutations of the KIT (Mast/Stem cell growth factor receptor) proto-oncogene in human piebaldism”, Journal of Investigative Dermatology, 101(1), pp. 22–25. Available at: 10.1111/1523-1747.ep12358440.
Scott, R. et al. (1993) “Xeroderma pigmentosum-Cockayne syndrome complex in two patients: Absence of skin tumors despite servere deficiency of DNA excision repair”., J Amer Acad Dermatol, 29(7), pp. 883–889.
Itin, P. et al. (1992) “[Family study of erythrokeratodermia figurata variabilis]”., Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 43(8), pp. 500–4.
Itin, P. et al. (1992) “[Ross syndrome]”., Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 43(6), pp. 359–60.
Zimmerli, W., Itin, P. (1992) “[Localized bacterial skin infections and dermatologic manifestations of systemic infections]”., Therapeutische Umschau. Revue therapeutique, 49(4), pp. 250–6.
Rufli, T., von, S.A., Itin, P. (1992) “Congenital hypertrophy of the lateral nail folds of the hallux”, Dermatology, 184(4), pp. 296–297. Available at: 10.1159/000247575.
Surber, C., Itin, P., Büchner, S. (1992) “Clinical controversy on the effect of topical ciclosporin: What is the target site?”, Dermatology, 185(4), pp. 242–245. Available at: 10.1159/000247460.
Rufli, T., Itin, P., Gilli, L. (1992) “Localized unilateral hyperhidrosis”, Dermatology, 184(4), pp. 298–299. Available at: 10.1159/000247576.
Itin, P., Surber, C., Büchner, S. (1992) “Lack of effect after local treatment with a new ciclosporin formulation in recalcitrant erosive oral lichen planus”, Dermatology, 185(4), pp. 262–265. Available at: 10.1159/000247464.
Itin, P. (1992) “Classification of autosomal dominant palmoplanar keratoderma: Past - present - future”. Available at: 10.1159/000247439.
Itin, P., Hirsbrunner, P., Büchner, S. (1992) “Lichen planus: An unusual cause of phimosis”, Acta Dermato-Venereologica, 72(1), pp. 41–42. Available at: 10.2340/00015555724142.
Surber, C. et al. (1992) “Effect of a new topical cyclosporin formulation on human allergic contact dermatitis”, Contact Dermatitis, 26(2), pp. 116–119. Available at: 10.1111/j.1600-0536.1992.tb00895.x.
Itin, P. et al. (1992) “Localized trichorrhexis nodosa [2]”. Available at: 10.1111/j.1365-2133.1992.tb14884.x.
Büchner, S., Itin, P. (1992) “Focal Dermal Hypoplasia Syndrome in a Male Patient: Report of a Case and Histologic and Immunohistochemical Studies”, Archives of Dermatology, 128(8), pp. 1078–1082. Available at: 10.1001/archderm.1992.01680180072008.
Itin, P., Rufli, T. (1992) “ORAL HAIRY LEUKOPLAKIA”, International Journal of Dermatology, 31(5), pp. 301–306. Available at: 10.1111/j.1365-4362.1992.tb03942.x.
Surber, C., Itin, P., Rufli, T. (1992) “Skin pH after short exposure to model solutions”, Martin Dunitz LTD, -, p. -.
Itin, P., Braendli, B., Linder, P. (1991) “[What is your diagnosis? Furunculoid myiasis]”., Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis, 80(36), pp. 889–90.
Itin, P. et al. (1991) “[Oral hairy leukoplakia in patients with kidney transplantation]”., Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 42(8), pp. 487–91.
Itin, P. (1991) “[What is your diagnosis? Hemorrhagic hyperkeratosis. Synonyms: black heel, calcaneal petechiae, pseudochromidrosis plantaris]”., Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis, 80(14), pp. 343–4.
Itin, P. (1991) “[What is your diagnosis? Intertrigo]”., Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis, 80(11), pp. 245–6.
Itin, P. (1991) “[What is your diagnosis? Intertrigo]”., Schweizerische Rundschau fur Medizin Praxis = Revue suisse de medecine Praxis, 80(9), pp. 185–6.
Itin, P., Pittelkow, M. (1991) “Trichothiodystrophy with chronic neutropenia and mild mental retardation”, Journal of the American Academy of Dermatology, 24(2), pp. 356–358. Available at: 10.1016/0190-9622(91)70051-3.
Itin, P., Winkelmann, R. (1991) “Cutaneous manifestations in patients with essential thrombocythemia”, Journal of the American Academy of Dermatology, 24(1), pp. 59–63. Available at: 10.1016/0190-9622(91)70010-Y.
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