Items where Author is "Itin, Peter H."

2020

Burger, Bettina and Ghosh, A. and Ng, Choon Khong and Piscuoglio, Salvatore and Spoerri, Iris and Itin, Peter H. and Greer, K. and Elbaum, David. (2020) Discovery of heterozygous KRT10 alterations in MAUIE cases underlines the importance of regular skin cancer screening in ichthyosis with confetti. British Journal of Dermatology, 183 (5). pp. 954-955.

Imahorn, Elias and Aushev, Magomet and Herms, Stefan and Hoffmann, Per and Cichon, Sven and Reichelt, Julia and Itin, Peter H. and Burger, Bettina. (2020) Gene expression is stable in a complete CIB1 knockout keratinocyte model. Scientific reports, 10 (1). p. 14952.

Mueller, Simon M. and Carruthers, Helen R. and Navarini, Alexander A. and Goldust, Mohamad and Gysin, Stefan and Itin, Peter H.. (2020) Pruritic and antipruritic colors: An exploratory pilot study. Dermatologic Therapy, 33 (3). e13447.

Mueller, Simon M. and Itin, Peter H. and Navarini, Alexander A. and Goldust, Mohamad and Brandt, Oliver and Griffiths, Christopher E. M. and Kleyn, Christine E.. (2020) The relationship between PASI and DLQI with itch, stress, and depression: Do we need additional decision-making tools in psoriasis? Dermatologic Therapy, 33 (3). e13276.

2019

Renz, Patricia and Imahorn, Elias and Spoerri, Iris and Aushev, Magomet and March, Oliver P. and Wariwoda, Hedwig and Von Arb, Sarah and Volz, Andreas and Itin, Peter H. and Reichelt, Julia and Burger, Bettina. (2019) Arginine- but not alanine-rich carboxy-termini trigger nuclear translocation of mutant keratin 10 in ichthyosis with confetti. Journal of cellular and molecular medicine, 23 (12). pp. 8442-8452.

Burger, Bettina and Spoerri, Iris and Imahorn, Elias and Wariwoda, Hedwig and Leeb, T. and Itin, Peter H.. (2019) Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: intrafamilial overlap of phenotypes in patients with the same KRT14 frameshift variant. British Journal of Dermatology, 181 (4). pp. 864-866.

Anzengruber, Florian and Augustin, Matthias and Radtke, Marc A. and Thaci, Diamant and Yawalkar, Nikhil and Streit, Markus and Reich, Kristian and Drach, Mathias and Sorbe, Christina and French, Lars E. and Mrowietz, Ulrich and Maul, Julia-Tatjana and Itin, Peter H. and Navarini, Alexander A.. (2019) Smoking does not Alter the Therapy Response to Systemic Anti-psoriatic Therapies: A Two-country, Multi-centre, Prospective, Non-interventional Study. Acta Dermato-Venereologica, 99 (10). pp. 871-877.

2018

Spoerri, Iris and Herms, Stefan and Eytan, O. and Sarig, Ofer and Heinimann, Karl and Sprecher, E. and Itin, Peter H. and Burger, Bettina. (2018) Immune-regulatory genes as possible modifiers of familial pityriasis rubra pilaris - Lessons from a family with PRP and psoriasis. Journal of the European Academy of Dermatology and Venereology : JEADV, 32 (10). e389-e392.

2015

Burger, Bettina and Spörri, Iris and Stegmann, Danielle A. and De Mesmaker, Julie and Schaub, Stefan and Itin, Peter H. and Steiger, Jürg and Arnold, Andreas W.. (2015) Risk of Cutaneous Squamous Cell Carcinoma Development in Renal Transplant Recipients Is Independent of TMC/EVER Alterations. Dermatology, 231 (3). pp. 245-252.

Spoerri, Iris and Brena, Michela and De Mesmaeker, Julie and Schlipf, Nina and Fischer, Judith and Tadini, Gianluca and Itin, Peter H. and Burger, Bettina. (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.

2014

Eytan, O. and Qiaoli, L. and Nousbeck, Janna and van Steensel, Maurice and Burger, Bettina and Hohl, Daniel and Taieb, A. and Prey, S. and Bachmann, Daniel and Avitan-Hersh, Emily and Jin Chung, H. and Shemer, Avner and Trau, Henri and Bergman, R. and Fuchs-Telem, D. and Warshauer, E. and Israeli, S. and Itin, Peter H. and Sarig, Ofer and Uitto, Jouni and Sprecher, E.. (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. 1196-1198.

2013

Itin, Peter H.. (2013) Ectodermal dysplasia: thoughts and practical concepts concerning disease classification - the role of functional pathways in the molecular genetic diagnosis. Dermatology, Vol. 226 (2). pp. 111-114.

Bruegger, Christelle and Kempf, Werner and Spoerri, Iris and Arnold, Andreas W. and Itin, Peter H. and Burger, Bettina. (2013) MicroRNA expression differs in cutaneous squamous cell carcinomas and healthy skin of immunocompetent individuals. Experimental dermatology, 22 (6). pp. 426-428.

2012

Arnold, Andreas W. and Kiritsi, Dimitra and Happle, Rudolf and Kohlhase, Jürgen and Hausser, Ingrid and Bruckner-Tuderman, Leena and Has, Cristina and Itin, Peter H.. (2012) Type 1 segmental Galli-Galli disease resulting from a previously unreported keratin 5 mutation. Journal of investigative dermatology, Vol. 132, H. 8. pp. 2100-2103.

2011

Arnold, Andreas W. and Burger, Bettina and Kump, Erwin and Rufle, Alexander and Tyring, Stephen K. and Kempf, Werner and Häusermann, Peter and Itin, Peter H.. (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 (1). pp. 81-86.

2010

Burger, Bettina and Hershkovitz, Dov and Indelman, Margarita and Kovac, Michal and Galambos, Jörg and Haeusermann, Peter and Sprecher, Eli and Itin, Peter H.. (2010) Buschke-Ollendorff syndrome in a three-generation family: influence of a novel LEMD3 mutation to tropoelastin expression. European journal of dermatology : EJD, 20 (6). pp. 693-697.

Burger, Bettina and Kind, Fabiola and Spoerri, Iris and Rütten, Arno and Battegay, Manuel and Häusermann, Peter and Itin, Peter H. and Arnold, Andreas W.. (2010) HIV-positive child with epidermodysplasia verruciformis-like lesions and homozygous mutation in TMC6. AIDS, 24 (17). pp. 2758-2760.

Itin, Peter H. and Heinimann, Karl and Attenhofer, Michèle and Boesch, Nemya and De Lorenzo, Rosaria and Trüb, Swantje and Burger, Bettina. (2010) Precalcaneal congenital fibrolipomatous hamartomas: is there a pathogenetic relationship with Gardner Syndrome? European journal of dermatology : EJD, 20 (2). pp. 246-247.

Itin, Peter H. and Burger, Bettina. (2010) Spontaneous fading of reticular pigmentation in Naegeli-Franceschetti-Jadassohn syndrome. Dermatology, 221 (2). pp. 135-136.

Itin, Peter H. and Burger, Bettina. (2010) [Genodermatoses for practitioners--principles and concepts]. Therapeutische Umschau. Revue thérapeutique, 67 (9). pp. 483-485.

2009

Itin, Peter H. and Hengge, Ulrich R. and Battegay, Manuel. (2009) [The skin, an interdisciplinary organ]. Der Internist, 50 (2). pp. 135-136.