Items where contributor is "Itin, Peter"

2017

Ruf, Marie-Thérèse and Andreoli, Arianna and Vujic, Gabriel and Itin, Peter and Pluschke, Gerd and Schmid, Peter. (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.

2014

Has, Cristina and Kiritsi, Dimitra and Mellerio, Jemima E. and Franzke, Claus-Werner and Wedgeworth, Emma and Tantcheva-Poor, Iliana and Kernland-Lang, Kristin and Itin, Peter and Simpson, Michael A. and Dopping-Hepenstal, Patricia J. and Fujimoto, Wataru and McGrath, John A. and Bruckner-Tuderman, Leena. (2014) The Missense Mutation p.R1303Q in Type XVII Collagen Underlies Junctional Epidermolysis Bullosa Resembling Kindler Syndrome. Journal of investigative dermatology, Vol. 134, H. 3. pp. 845-849.

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.

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.

Burger, B. and Spoerri, I. and Schubert, M. and Has, C. and Itin, P. H.. (2012) Description of the natural course and clinical manifestations of ichthyosis with confetti caused by a novel KRT10 mutation. British journal of dermatology, Vol. 166, H. 2. pp. 434-439.

2011

Burger, B. and Cattani, N. and Trueb, S. and de Lorenzo, R. and Albertini, M. and Bontognali, E. and Itin, C. and Schaub, N. and Itin, P. H. and Heinimann, K.. (2011) Prevalence of skin lesions in familial adenomatous polyposis : a marker for presymptomatic diagnosis? The Oncologist, 16 (12). pp. 1698-1705.

Mertz, K. D. and Schmid, M. and Burger, B. and Itin, P. and Palmedo, G. and Schärer, L. and Kutzner, H. and Fernández Figueras, M. T. and Cribier, B. and Pfaltz, M. and Kempf, W.. (2011) Detection of Merkel cell polyomavirus in epidermodysplasia-verruciformis-associated skin neoplasms. Dermatology, 222 (1). pp. 87-92.

Nousbeck, Janna and Burger, Bettina and Fuchs-Telem, Dana and Pavlovsky, Mor and Fenig, Shlomit and Sarig, Ofer and Itin, Peter and Sprecher, Eli. (2011) A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia. American journal of human genetics, Vol. 89, H. 2. pp. 302-307.

Burger, Bettina and Fuchs, Dana and Sprecher, Eli and Itin, Peter. (2011) The immigration delay disease : adermatoglyphia-inherited absence of epidermal ridges. Journal of the American Academy of Dermatology, Vol. 64, H. 5. pp. 974-980.

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.

2008

Lugassy, Jennie and McGrath, John A. and Itin, Peter and Shemer, Revital and Verbov, Julian and Murphy, Helen R. and Ishida-Yamamoto, Akemi and Digiovanna, John J. and Bercovich, Dani and Karin, Nathan and Vitenshtein, Alon and Uitto, Jouni and Bergman, Reuven and Richard, Gabriele and Sprecher, Eli. (2008) KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome. Journal of investigative dermatology, Vol. 128, no. 6. pp. 1517-1524.

Sumila, Marcin and Notter, Markus and Itin, Peter and Bodis, Stephan and Gruber, Guenther. (2008) Long-term results of radiotherapy in patients with chronic palmo-plantar eczema or psoriasis. Strahlentherapie und Onkologie, 184 (4). pp. 218-223.

Burger, B. and Itin, P.. (2008) Hereditäre Hauttumoren speziell bei der Frau. Schweizer Zeitschrift für Onkologie, 2008, H. 2. pp. 20-24.

Fisch, A. and Itin, P. and 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.

Kägi, M. K. and Bindschedler, M. and Itin, P.. (2008) Orales Isotretinoin zur Behandlung schwerer Akne vulgaris. Information und Empfehlungen. Schweizerisches Medizin-Forum, 8 (6). pp. 98-99.

Itin, P.. (2008) Hautveränderungen bei Essstörungen. Schweizer Zeitschrift für Ernährungsmedizin, 2008 (3). pp. 30-32.

Burger, Bettina and Itin, Peter. (2008) Muir-Torre syndrome. Dermatology, 217 (1). pp. 56-57.

Beltraminelli, Helmut and Itin, Peter. (2008) Skin and psyche--from the surface to the depth of the inner world. Journal der Deutschen Dermatologischen Gesellschaft, Vol. 6, no. 1. pp. 8-14.

Häusermann, Peter and Walter, Roland B. and Halter, Jörg and Biedermann, Barbara C. and Tichelli, André and Itin, Peter and Gratwohl, Alois. (2008) Cutaneous graft-versus-host disease : a guide for the dermatologist. Dermatology, 216 (4). pp. 287-304.