Search Results - "Tantcheva‐Poór, Iliana"

Although Abundant in Tumor Tissue, Mast Cells Have No Effect on Immunological Micro-milieu or Growth of HPV-Induced or Transplanted Tumors by Ghouse, Shanawaz Mohammed, Polikarpova, Anastasia, Muhandes, Lina, Dudeck, Jan, Tantcheva-Poór, Iliana, Hartmann, Karin, Lesche, Matthias, Dahl, Andreas, Eming, Sabine, Müller, Werner, Behrendt, Rayk, Roers, Axel

“…High numbers of mast cells populate the stroma of many types of neoplasms, including human papilloma virus-induced benign and malignant tumors in man and…”
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Founder Variants in KRT5 and POGLUT1 Are Implicated in Dowling-Degos Disease by Kumar, Sheetal, Borisov, Oleg, Maj, Carlo, Ralser, Damian J, Humbatova, Aytaj, Hanneken, Sandra, Schmieder, Astrid, Groß, Janina, Maintz, Laura, Heineke, Andre, Knuever, Jana, Fagerberg, Christina, Parmentier, Laurent, Anemüller, Waltraud, Oji, Vinzenz, Tantcheva-Poór, Iliana, Fölster-Holst, Regina, Wenzel, Joerg, Krawitz, Peter M, Frank, Jorge, Betz, Regina C

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Epidermolytic ichthyosis: Clinical spectrum and burden of disease in a large German cohort by Frommherz, Leonie, Giehl, Kathrin, Hofmann, Josephine, Huebner, Stefanie, Kiekbusch, Kirstin, Sabkova, Teodora, Süßmuth, Kira, Alter, Svenja, Tantcheva-Poór, Iliana, Ott, Hagen, Fischer, Judith, Has, Cristina

“…Keratinopathic ichthyoses are a group of hereditary skin disorders caused by pathogenic variants in keratin genes such as KRT1, KRT2 and KRT10, resulting in…”
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Histopathology‐guided mass spectrometry differentiates benign nevi from malignant melanoma by Lazova, Rossitza, Smoot, Katy, Anderson, Heather, Powell, Matthew J., Rosenberg, Arlene S., Rongioletti, Franco, Pilloni, Luca, D'Hallewin, Sara, Gueorguieva, Ralitza, Tantcheva‐Poór, Iliana, Obadofin, Omobolade, Camacho, Christine, Hsi, Andy, Kluger, Harriet H., Fadare, Oluwole, Seeley, Erin H.

“…Purpose Distinguishing benign nevi from malignant melanoma using current histopathological criteria may be very challenging and is one the most difficult areas…”
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Epidemiology of inherited epidermolysis bullosa in Germany by Has, Cristina, Hess, Moritz, Anemüller, Waltraud, Blume‐Peytavi, Ulrike, Emmert, Steffen, Fölster‐Holst, Regina, Frank, Jorge, Giehl, Kathrin, Günther, Claudia, Hammersen, Johanna, Hillmann, Kathrin, Höflein, Bettina, Hoeger, Peter H., Hotz, Alrun, Mai, Thuy Anh, Oji, Vinzenz, Schneider, Holm, Süßmuth, Kira, Tantcheva‐Póor, Iliana, Thielking, Frederieke, Zirn, Birgit, Fischer, Judith, Reimer‐Taschenbrecker, Antonia

“…Background Epidermolysis bullosa (EB) is a rare genetic disorder manifesting with skin and mucosal membrane blistering in different degrees of severity…”
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Ein mehrstufiger Algorithmus zur Diagnose seltener Genodermatosen by Tantcheva-Poór, Iliana, Oji, Vinzenz, Has, Cristina

“…Zusammenfassung Jüngste Fortschritte der Genforschung haben ihren Weg in die klinische Dermatologie gefunden. Nahezu ein Drittel aller Erbkrankheiten zeigt…”
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A multistep approach to the diagnosis of rare genodermatoses by Tantcheva-Poór, Iliana, Oji, Vinzenz, Has, Cristina

“…Summary Recent advances in genetic technology have found their way into clinical dermatology. Approximately one third of all hereditary disorders show…”
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Altered Notch Signaling in Dowling-Degos Disease: Additional Mutations in POGLUT1 and Further Insights into Disease Pathogenesis by Ralser, Damian J., Takeuchi, Hideyuki, Fritz, Günter, Basmanav, F. Buket, Effern, Maike, Sivalingam, Sugirthan, El-Shabrawi-Caelen, Laila, Degirmentepe, Ece N., Kocatürk, Emek, Singh, Manuraj, Booken, Nina, Spierings, Natalia M.K., Schnabel, Viktor, Heineke, Andre, Knuever, Jana, Wolf, Sabrina, Wehner, Maria, Tronnier, Michael, Leverkus, Martin, Tantcheva-Poór, Iliana, Wenzel, Jörg, Oji, Vinzenz, Has, Cristina, Hölzel, Michael, Frank, Jorge, Haltiwanger, Robert S., Betz, Regina C.

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Generalized pustular psoriasis: A possible association with severe hypocalcaemia due to primary hypoparathyroidism by Knuever, Jana, Tantcheva‐Poor, Iliana

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Adult-onset Still’s disease: Switch to atypical skin manifestations under anakinra therapy by Klapproth, Henning, Stroucken, Birte, Helbig, Doris, Tantcheva-Poór, Iliana, Fabri, Mario

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Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis by Hotz, Alrun, Kopp, Julia, Bourrat, Emmanuelle, Oji, Vinzenz, Süßmuth, Kira, Komlosi, Katalin, Bouadjar, Bakar, Tantcheva-Poór, Iliana, Hellström Pigg, Maritta, Betz, Regina C, Giehl, Kathrin, Schedel, Fiona, Weibel, Lisa, Schulz, Solveig, Stölzl, Dora V, Tadini, Gianluca, Demiral, Emine, Berggard, Karin, Zimmer, Andreas D, Alter, Svenja, Fischer, Judith

“…Autosomal recessive congenital ichthyosis (ARCI) is a non-syndromic congenital disorder of cornification characterized by abnormal scaling of the skin. The…”
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Occurrence of autoantibodies against skin proteins in patients with hereditary epidermolysis bullosa predisposes to development of autoimmune blistering disease by Lehr, Saskia, Felber, Felicitas, Tantcheva-Poór, Iliana, Keßler, Christina, Eming, Rüdiger, Nyström, Alexander, Rizzi, Marta, Kiritsi, Dimitra

“…Skin blistering disorders are associated with inherited defects in proteins involved in the dermal-epidermal adhesion or autoantibodies targeting those…”
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Primary cutaneous diffuse large B‐cell lymphoma, NOS and leg type: Clinical, morphologic and prognostic differences by 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, Müller, Cornelia Sigrid Lissi, Sachse, Michael Max, Meiss, Frank, Géraud, Cyrill, Marx, Alexander, Goerdt, Sergij, Geissinger, Eva, Kempf, Werner

“…Summary Background and objectives Primary cutaneous diffuse large B‐cell lymphoma, NOS (PCLBCL/NOS) is a rare PCLBCL. Only few data are available for this…”
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Patient with extensive Mongolian spots, nevus flammeus and nevus vascularis mixtus: A novel case of phacomatosis pigmentovascularis by Hayashi, Shujiro, Kaminaga, Tomoko, Tantcheva-Poor, Iliana, Hamasaki, Yoichiro, Hatamochi, Atsushi

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Ein mehrstufiger Algorithmus zur Diagnose seltener Genodermatosen by Tantcheva-Poór, Iliana, Oji, Vinzenz, Has, Cristina

“…Jüngste Fortschritte der Genforschung haben ihren Weg in die klinische Dermatologie gefunden. Nahezu ein Drittel aller Erbkrankheiten zeigt charakteristische…”
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Linear Scars in a 4-Week-Old Girl by Persa, Oana-Diana, Fischer, Judith, Tantcheva-Poór, Iliana

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Phase II Trial of a Toll-Like Receptor 9–Activating Oligonucleotide in Patients With Metastatic Melanoma by PASHENKOV, Mikhail, GOËSS, Gerda, TANTCHEVA-POOR, Iliana, GRABBE, Stephan, LOQUAI, Carmen, ESSER, Stefan, FRANCKSON, Tom, SCHNEEBERGER, Achim, HAARMANN, Cäcilia, KRIEG, Arthur M, STINGL, Georg, WAGNER, Stephan N, WAGNER, Christine, HÖRMANN, Markus, JANDL, Tamara, MOSER, Anna, BRITTEN, Cedrik M, SMOLLE, Josef, KOLLER, Silvia, MAUCH, Cornelia

“…The recent identification of toll-like receptors (TLRs) and respective ligands allows the evaluation of novel dendritic cell (DC) -activating strategies…”
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Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients by Hotz, Alrun, Kopp, Julia, Bourrat, Emmanuelle, Oji, Vinzenz, Komlosi, Katalin, Giehl, Kathrin, Bouadjar, Bakar, Bygum, Anette, Tantcheva-Poor, Iliana, Hellström Pigg, Maritta, Has, Cristina, Yang, Zhou, Irvine, Alan D, Betz, Regina C, Zambruno, Giovanna, Tadini, Gianluca, Süßmuth, Kira, Gruber, Robert, Schmuth, Matthias, Mazereeuw-Hautier, Juliette, Jonca, Natalie, Guez, Sophie, Brena, Michela, Hernandez-Martin, Angela, van den Akker, Peter, Bolling, Maria C, Hannula-Jouppi, Katariina, Zimmer, Andreas D, Alter, Svenja, Vahlquist, Anders, Fischer, Judith

“…The autosomal recessive congenital ichthyoses (ARCI) are a nonsyndromic group of cornification disorders that includes lamellar ichthyosis, congenital…”
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P75 nerve growth factor receptor staining is superior to S100 in identifying spindle cell and desmoplastic melanoma by Lazova, Rossitza, MD, Tantcheva-Poor, Iliana, MD, Sigal, Alicia C., MD

“…Background Spindle cell melanoma (SCM) including desmoplastic melanoma (DM) is a rare variant of malignant melanoma that may present diagnostic difficulties…”
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Detection of the germline KIT S476I mutation in a kindred with familial mastocytosis associated with gastrointestinal stromal tumors by Peters, Franziska, Fiebig, Britta, Lundberg, Pontus, Jaspers, Natalie-Isabel, Holzapfel, Bianca, Ghadimi, Markus P.H., Drebber, Uta, Tuchscherer, Armin, Ullrich, Roland, Hartmann, Karin, Tantcheva-Poór, Iliana

“…To date, activating germline KIT mutations have been found in less than 40 families with variable combinations of mastocytosis, abnormal skin pigmentation,…”
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