Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Lizelotte J M T, Parren"'
Publikováno v:
Archives of Dermatological Research, 310(7), 599-606. Springer
Mutations in the tumor suppressor gene CYLD underlie phenotypically heterogeneous hereditary tumor disorders of the skin appendages. These diseases are inherited autosomal dominantly and include Brooke-Spiegler syndrome (BSS; OMIM 605041), familial c
Autor:
M. van Geel, Jorge Frank, Yvonne Marquardt, P.M. Steijlen, Sylvia Joussen, Lizelotte J. M. T. Parren, Sandra Hanneken, Jens M. Baron, M.A.M. van Steensel
Publikováno v:
Journal of the European Academy of Dermatology and Venereology, 32(8), E331-E333. Wiley
Autor:
Jorge Frank, Lizelotte J. M. T. Parren, M.A.M. van Steensel, Véronique Winnepenninckx, K. Munte, M. van Geel, P.M. Steijlen
Publikováno v:
Clinical and Experimental Dermatology, 41(6), 682-684. Wiley-Blackwell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ae9d95e4eb91fc70b23ba8e3dee950b
https://cris.maastrichtuniversity.nl/en/publications/1f9b6d0e-b403-4167-835c-7a7dd1b6af3f
https://cris.maastrichtuniversity.nl/en/publications/1f9b6d0e-b403-4167-835c-7a7dd1b6af3f
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 26:117-121
Background Bazex–Dupre–Christol syndrome (BDCS) is an X-linked dominantly inherited disorder affecting hair follicle structures. Currently, hypotrichosis, follicular atrophoderma and basal cell carcinomas are considered frequent symptoms of the d
Autor:
Jorge Frank, Peter M. Steijlen, T. Wagenvoort, Lizelotte J M T Parren, F. Abuzahra, M. van Geel, F. Koene, M.A.M. van Steensel
Publikováno v:
British Journal of Dermatology. 165:201-203
Autor:
Ruud G. L. Nellen, Lizelotte J M T Parren, Pamela Poblete-Gutiérrez, Jorge Frank, Arienne M. W. Van Marion, C. Henquet
Publikováno v:
International Journal of Dermatology. 47:7-9
Pyoderma gangrenosum is an ulcerative skin disease with variable clinical outcomes. The diagnosis is based on clinical features and exclusion of other ulcerative diseases. To date, a specific treatment is not known. Since the disease can be destructi
Autor:
Patrick I. Ferdinandus, Lizelotte J. M. T. Parren, René R. W. J. van der Hulst, Jorge Frank, Stefania Tuinder
Publikováno v:
International Journal of Dermatology, 53(2), 246-249. Wiley-Blackwell
Background Brooke–Spiegler syndrome is a hereditary tumor predisposition disorder characterized by the development of cylindromas, trichoepitheliomas, and spiradenomas. Predilection sites of the disease are hair follicles and sweat glands of the he
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 154
A 17-year-old boy presented with small papules on his right shoulder and was diagnosed with syringocystadenoma papilliferum.
Publikováno v:
International journal of dermatology. 47
Brooke-Spiegler syndrome is an autosomal dominant tumor predisposition disorder. The disease is characterized by the occurrence of multiple skin appendage tumors, including cylindroma, trichoepithelioma, and spiradenoma. In some patients, tumors cove
Autor:
Arienne M. W. Van Marion, Lizelotte J M T Parren, Nicole W.J. Kelleners-Smeets, Jorge Frank, Anja Sommer, Aimee H.M.M. Arits
Publikováno v:
International journal of dermatology. 47
Difficulty in differentiation between a solitary basal cell carcinoma, which is known as a malign skin lesion and a benign trichoepithelioma, is a frequent problem in all day dermatologic practice. Clinically as well as histopathologically there are