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

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Number of items at this level: 42.

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 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.

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.

Burger, B. and Itin, P. H.. (2014) Epidermodysplasia verruciformis. Current problems in dermatology, 45. pp. 123-131.

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.

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.

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) Hereditäre Hauttumoren speziell der Frau. Schweizer Zeitschrift für Onkologie, 2. pp. 20-24.

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

C

Conen, K. and Mosna-Firlejczyk, K. and Rochlitz, C. and Wicki, A. and Itin, P. and Arnold, A. W. and Gross, M. and Zimmermann, F. and Zippelius, A.. (2015) Vemurafenib-induced radiation recall dermatitis: case report and review of the literature. Dermatology, 230 (1). pp. 1-4.

D

de Jong, Sarah Jill and Créquer, Amandine and Matos, Irina and Hum, David and Gunasekharan, Vignesh and Lorenzo, Lazaro and Jabot-Hanin, Fabienne and Imahorn, Elias and Arias, Andres A. and Vahidnezhad, Hassan and Youssefian, Leila and Markle, Janet G. and Patin, Etienne and D'Amico, Aurelia and Wang, Claire Q. F. and Full, Florian and Ensser, Armin and Leisner, Tina M. and Parise, Leslie V. and Bouaziz, Matthieu and Maya, Nataly Portilla and Cadena, Xavier Rueda and Saka, Bayaki and Saeidian, Amir Hossein and Aghazadeh, Nessa and Zeinali, Sirous and Itin, Peter and Krueger, James G. and Laimins, Lou and Abel, Laurent and Fuchs, Elaine and Uitto, Jouni and Franco, Jose Luis and Burger, Bettina and Orth, Gérard and Jouanguy, Emmanuelle and Casanova, Jean-Laurent. (2018) The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses. Journal of experimental medicine, 215 (9). pp. 2289-2310.

de Jong, Sarah Jill and Imahorn, Elias and Itin, Peter and Uitto, Jouni and Orth, Gérard and Jouanguy, Emmanuelle and Casanova, Jean-Laurent and Burger, Bettina. (2018) Epidermodysplasia Verruciformis: Inborn Errors of Immunity to Human Beta-Papillomaviruses. Frontiers in Microbiology, 9. p. 1222.

E

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.

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.

Has, Cristina and Burger, Bettina and Volz, A. and Kohlhase, Jürgen and Bruckner-Tuderman, Leena and Itin, Peter. (2010) Mild clinical phenotype of Kindler syndrome associated with late diagnosis and skin cancer. Dermatology (Basel, Switzerland), 221 (4). pp. 309-312.

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, 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.

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, 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.

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 and Burger, Bettina. (2009) Mosaic manifestations of monogenic skin diseases. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 7 (9). pp. 744-748.

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

Moreau, Adrien and Gosselin-Badaroudine, Pascal and Mercier, Aurélie and Burger, Bettina and Keller, Dagmar I. and Chahine, Mohamed. (2018) A leaky voltage sensor domain of cardiac sodium channels causes arrhythmias associated with dilated cardiomyopathy. Scientific reports, 8 (1). p. 13804.

Moreau, Adrien and Mercier, Aurélie and Thériault, Olivier and Boutjdir, Mohamed and Burger, Bettina and Keller, Dagmar I. and Chahine, Mohamed. (2017) Biophysical, Molecular, and Pharmacological Characterization of Voltage-Dependent Sodium Channels From Induced Pluripotent Stem Cell-Derived Cardiomyocytes. Canadian Journal of Cardiology, 33 (2). pp. 269-278.

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, J. and Sarig, O. and Magal, L. and Warshauer, E. and Burger, B. and Itin, P. and Sprecher, E.. (2014) Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes. British Journal of Dermatology, 171 (6). pp. 1521-1524.

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.

R

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.

S

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.

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.

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.

This list was generated on Tue Oct 27 03:50:03 2020 CET.