Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | Date | No Grouping
Number of items: 21.

Journal Article

Basmanav, F. Buket, Cesarato, Nicole, Kumar, Sheetal ORCID: 0000-0002-5240-079X, Borisov, Oleg, Kokordelis, Pavlos, Ralser, Damian J., Wehner, Maria, Axt, Daisy, Xiong, Xing ORCID: 0000-0001-5728-150X, Thiele, Holger, Dolgin, Vadim, Gossmann, Yasmina, Fricker, Nadine, Dewenter, Malin Katharina, Weller, Karsten, Suri, Mohnish ORCID: 0000-0001-9037-701X, Reichenbach, Herbert, Oji, Vinzenz, Addor, Marie-Claude, Ramirez, Karla, Stewart, Helen, Bartels, Natalie Garcia, Weibel, Lisa, Wagner, Nicola, George, Susannah, Kilic, Arzu, Tantcheva-Poor, Iliana, Stewart, Alison, Dikow, Nicola, Blaumeiser, Bettina ORCID: 0000-0001-9993-7319, Medvecz, Marta, Blume-Peytavi, Ulrike, Farrant, Paul, Grimalt, Ramon, Bertok, Sara, Bradley, Lisa, Eskin-Schwartz, Marina, Birk, Ohad Samuel, Bygum, Anette ORCID: 0000-0002-3004-0180, Simon, Michel ORCID: 0000-0003-3655-6329, Krawitz, Peter, Fischer, Christine, Hamm, Henning, Fritz, Gunter and Betz, Regina C. (2022). Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals. JAMA Dermatol., 158 (11). S. 1245 - 1254. CHICAGO: AMER MEDICAL ASSOC. ISSN 2168-6084

Felcht, Moritz, Klemke, Claus-Detlev, Nicolay, Jan Peter, Weiss, Christel, Assaf, Chalid, Wobser, Marion, Schlaak, Max, Hillen, Uwe, Moritz, Rose, Tantcheva-Poor, Iliana, Nashan, Dorothee, Beyer, Marc, Dippel, Edgar, Mueller, Cornelia Sigrid Lissi, Sachse, Michael Max, Meiss, Frank, Geraud, Cyrill ORCID: 0000-0001-9432-6869, Marx, Alexander, Goerdt, Sergij, Geissinger, Eva and Kempf, Werner (2019). Primary cutaneous diffuse large B-cell lymphoma, NOS and leg type: Clinical, morphologic and prognostic differences. J. Dtsch. Dermatol. Ges., 17 (3). S. 275 - 286. HOBOKEN: WILEY. ISSN 1610-0387

Fischer, Bjoern, Dimopoulou, Aikaterini, Egerer, Johannes, Gardeitchik, Thatjana, Kidd, Alexa, Jost, Dominik, Kayserili, Hulya ORCID: 0000-0003-0376-499X, Alanay, Yasemin ORCID: 0000-0003-0683-9731, Tantcheva-Poor, Iliana, Mangold, Elisabeth, Daumer-Haas, Cornelia, Phadke, Shubha ORCID: 0000-0002-6624-082X, Peirano, Reto I., Heusel, Julia, Desphande, Charu, Gupta, Neerja, Nanda, Arti ORCID: 0000-0002-1223-3181, Felix, Emma, Berry-Kravis, Elisabeth, Kabra, Madhulika, Wevers, Ron A. ORCID: 0000-0003-2278-9746, van Maldergem, Lionel, Mundlos, Stefan, Morava, Eva and Kornak, Uwe (2012). Further characterization of ATP6V0A2-related autosomal recessive cutis laxa. Hum. Genet., 131 (11). S. 1761 - 1774. NEW YORK: SPRINGER. ISSN 0340-6717

Fromme, Julia E., Tantcheva-Poor, Iliana and Foelster-Holst, Regina (2022). Viral exanthems in children. Hautarzt, 73 (6). S. 452 - 461. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1432-1173

Ghouse, Shanawaz Mohammed, Polikarpova, Anastasia ORCID: 0000-0002-9788-5057, Muhandes, Lina, Dudeck, Jan, Tantcheva-Poor, Iliana, Hartmann, Karin ORCID: 0000-0002-4595-8226, Lesche, Matthias, Dahl, Andreas ORCID: 0000-0002-2668-8371, Eming, Sabine, Mueller, Werner, Behrendt, Rayk ORCID: 0000-0002-1091-2877 and Roers, Axel (2018). Although Abundant in Tumor Tissue, Mast Cells Have No Effect on Immunological Micro-milieu or Growth of HPV-Induced or Transplanted Tumors. Cell Reports, 22 (1). S. 27 - 36. CAMBRIDGE: CELL PRESS. ISSN 2211-1247

Has, Cristina ORCID: 0000-0001-6066-507X, Hess, Moritz, Anemueller, Waltraud, Blume-Peytavi, Ulrike, Emmert, Steffen, Foelster-Holst, Regina, Frank, Jorge, Giehl, Kathrin, Guenther, Claudia, Hammersen, Johanna ORCID: 0000-0001-8821-5775, Hillmann, Kathrin, Hoeflein, Bettina, Hoeger, Peter H., Hotz, Alrun, Oji, Vinzenz, Schneider, Holm, Suessmuth, Kira, Tantcheva-Poor, Iliana, Thielking, Frederieke, Zirn, Birgit, Fischer, Judith and Reimer-Taschenbrecker, Antonia . Epidemiology of inherited epidermolysis bullosa in Germany. J. Eur. Acad. Dermatol. Venereol.. HOBOKEN: WILEY. ISSN 1468-3083

Has, Cristina ORCID: 0000-0001-6066-507X, Kiritsi, Dimitra ORCID: 0000-0002-2331-8981, Mellerio, Jemima E., Franzke, Claus-Werner, Wedgeworth, Emma, Tantcheva-Poor, Iliana, Kernland-Lang, Kristin, Itin, Peter, Simpson, Michael A., Dopping-Hepenstal, Patricia J., Fujimoto, Wataru, McGrath, John A. and Bruckner-Tuderman, Leena (2014). The Missense Mutation p.R1303Q in Type XVII Collagen Underlies Junctional Epidermolysis Bullosa Resembling Kindler Syndrome. J. Invest. Dermatol., 134 (3). S. 845 - 850. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1523-1747

Hayashi, Shujiro, Kaminaga, Tomoko, Tantcheva-Poor, Iliana, Hamasaki, Yoichiro and Hatamochi, Atsushi (2016). Patient with extensive Mongolian spots, nevus flammeus and nevus vascularis mixtus: A novel case of phacomatosis pigmentovascularis. J. Dermatol., 43 (2). S. 225 - 227. HOBOKEN: WILEY-BLACKWELL. ISSN 1346-8138

Helbig, Doris, Ihle, Michaela Angelika, Puetz, Katharina, Tantcheva-Poor, Iliana, Mauch, Cornelia, Buettner, Reinhard and Quaas, Alexander (2016). Oncogene and therapeutic target analyses in Atypical fibroxanthomas and pleomorphic dermal sarcomas. Oncotarget, 7 (16). S. 21763 - 21775. ORCHARD PARK: IMPACT JOURNALS LLC. ISSN 1949-2553

Hotz, Alrun ORCID: 0000-0003-2560-3951, Kopp, Julia, Bourrat, Emmanuelle, Oji, Vinzenz, Komlosi, Katalin, Giehl, Kathrin, Bouadjar, Bakar, Bygum, Anette ORCID: 0000-0002-3004-0180, Tantcheva-Poor, Iliana, Hellstrom Pigg, Maritta, Has, Cristina ORCID: 0000-0001-6066-507X, Yang, Zhou, Irvine, Alan D., Betz, Regina C., Zambruno, Giovanna, Tadini, Gianluca, Suessmuth, Kira, Gruber, Robert, Schmuth, Matthias, Mazereeuw-Hautier, Juliette, Jonca, Natalie, Guez, Sophie, Brena, Michela, Hernandez-Martin, Angela, van den Akker, Peter ORCID: 0000-0002-3734-753X, Bolling, Maria C., Hannula-Jouppi, Katariina, Zimmer, Andreas D., Alter, Svenja, Vahlquist, Anders and Fischer, Judith ORCID: 0000-0002-8580-8118 (2021). Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients. Genes, 12 (1). BASEL: MDPI. ISSN 2073-4425

Kempf, Werner ORCID: 0000-0002-6552-8629, Kazakov, Dmitry V., Scheidegger, Paul E., Schlaak, Max and Tantcheva-Poor, Iliana (2014). Two Cases of Primary Cutaneous Lymphoma With a gamma/delta plus Phenotype and an Indolent Course: Further Evidence of Heterogeneity of Cutaneous gamma/delta plus T-Cell Lymphomas. Am. J. Dermatopathol., 36 (7). S. 570 - 578. PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS. ISSN 1533-0311

Knuever, Jana and Tantcheva-Poor, Iliana (2017). Generalized pustular psoriasis: A possible association with severe hypocalcaemia due to primary hypoparathyroidism. J. Dermatol., 44 (12). S. 1416 - 1418. HOBOKEN: WILEY. ISSN 1346-8138

Lazova, Rossitza ORCID: 0000-0002-0796-692X, Smoot, Katy, Anderson, Heather, Powell, Matthew J., Rosenberg, Arlene S., Rongioletti, Franco, Pilloni, Luca, D'Hallewin, Sara, Gueorguieva, Ralitza, Tantcheva-Poor, Iliana, Obadofin, Omobolade, Camacho, Christine, Hsi, Andy, Kluger, Harriet H., Fadare, Oluwole and Seeley, Erin H. (2020). Histopathology - guided mass spectrometry differentiates benign nevi from malignant melanoma. J. Cutan. Pathol., 47 (3). S. 226 - 241. HOBOKEN: WILEY. ISSN 1600-0560

Lazova, Rossitza, Tantcheva-Poor, Iliana and Sigal, Alicia C. (2010). P75 nerve growth factor receptor staining is superior to S100 in identifying spindle cell and desmoplastic melanoma. J. Am. Acad. Dermatol., 63 (5). S. 852 - 859. NEW YORK: MOSBY-ELSEVIER. ISSN 0190-9622

Lehr, Saskia, Felber, Felicitas, Tantcheva-Poor, Iliana, Kessler, Christina, Eming, Ruediger, Nystroem, Alexander, Rizzi, Marta and Kiritsi, Dimitra (2022). Occurrence of autoantibodies against skin proteins in patients with hereditary epidermolysis bullosa predisposes to development of autoimmune blistering disease. Front. Immunol., 13. LAUSANNE: FRONTIERS MEDIA SA. ISSN 1664-3224

Moeckel, Maureen, de la Cruz, Nydia C., Ruebsam, Matthias, Wirtz, Lisa, Tantcheva-Poor, Iliana, Malter, Wolfram, Zinser, Max, Bieber, Thomas and Knebel-Moersdorf, Dagmar (2022). Herpes Simplex Virus 1 Can Bypass Impaired Epidermal Barriers upon Ex Vivo Infection of Skin from Atopic Dermatitis Patients. J. Virol., 96 (17). WASHINGTON: AMER SOC MICROBIOLOGY. ISSN 1098-5514

Persa, Oana-Diana, Fischer, Judith ORCID: 0000-0002-8580-8118 and Tantcheva-Poor, Iliana (2016). Linear Scars in a 4-Week-Old Girl. JAMA Dermatol., 152 (2). S. 209 - 211. CHICAGO: AMER MEDICAL ASSOC. ISSN 2168-6084

Peters, Franziska ORCID: 0000-0002-3250-3740, Fiebig, Britta, Lundberg, Pontus, Jaspers, Natalie-Isabel, Holzapfel, Bianca, Ghadimi, Markus P. H., Drebber, Uta, Tuchscherer, Armin, Ullrich, Roland, Hartmann, Karin ORCID: 0000-0002-4595-8226 and Tantcheva-Poor, Iliana (2021). Detection of the germline KIT S476I mutation in a kindred with familial mastocytosis associated with gastrointestinal stromal tumors. J. Allergy Clin. Immunol.-Pract., 9 (5). S. 2123 - 2127. AMSTERDAM: ELSEVIER. ISSN 2213-2201

Tantcheva-Poor, Iliana and Has, Cristina ORCID: 0000-0001-6066-507X (2019). Neonate female with Blister Formation shortly after Birth Preparation for the Specialist Examination: Part 34. Hautarzt, 70. S. 31 - 34. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1432-1173

Tantcheva-Poor, Iliana, Oji, Vinzenz ORCID: 0000-0003-1380-4828 and Has, Cristina ORCID: 0000-0001-6066-507X (2016). A multistep approach to the diagnosis of rare genodermatoses. J. Dtsch. Dermatol. Ges., 14 (10). S. 969 - 986. HOBOKEN: WILEY-BLACKWELL. ISSN 1610-0387

Tantcheva-Poor, Iliana, Vanecek, Tomas, Lurati, Massimo C. R., Rychly, Boris, Kempf, Werner ORCID: 0000-0002-6552-8629, Michal, Michal and Kazakov, Dmitry V. (2016). Report of Three Novel Germline CYLD Mutations in Unrelated Patients with Brooke-Spiegler Syndrome, Including Classic Phenotype, Multiple Familial Trichoepitheliomas and Malignant Transformation. Dermatology, 232 (1). S. 30 - 38. BASEL: KARGER. ISSN 1421-9832

This list was generated on Thu Apr 25 14:08:50 2024 CEST.