Items where Division is "03 Faculty of Medicine > Departement Biomedizin > Department of Biomedicine, University Hospital Basel > Dermatology (Itin)"

A

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.

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.

B

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.

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.

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.

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.

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.

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.

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

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

F

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.

H

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.

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.

I

Imahorn, E. and Yüksel, Z. and Spoerri, I. and Gürel, G. and Imhof, C. and Saraçoğlu, Z. N. and Koku Aksu, A. E. and Rady, P. L. and Tyring, S. K. and Kempf, W. and Itin, P. H. and Burger, B.. (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.

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.

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

K

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.

L

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.

M

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.

N

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.

S

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.