Zobrazeno 1 - 8
of 8
pro vyhledávání: '"E. C. Sattler"'
Autor:
E. C. Sattler, O. K. Steinlein
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-4 (2018)
Abstract Background Birt-Hogg-Dubé syndrome is a genetic syndrome caused by mutations in the FLCN gene. The main symptoms are lung bullae and pneumothorax, benign and malignant kidney tumors, and facial fibrofolliculoma. The risk of pneumothorax is
Externí odkaz:
https://doaj.org/article/f1f96095173a4ed8966a166ea4acd687
Publikováno v:
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte GebieteLiteratur. 72(4)
Hereditary tumor syndromes are characterized by a familial occurrence of tumors/cancer. A hereditary tumor syndrome should be suspected if a familial occurrence of cancer is seen and/or persons at younger age are affected. Some of the currently known
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::af985fc74540ba96d5189aa2f83a99e1
https://pubmed.ncbi.nlm.nih.gov/33661338
https://pubmed.ncbi.nlm.nih.gov/33661338
Autor:
E. C. Sattler, Ortrud K. Steinlein
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-4 (2018)
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-4 (2018)
Background Birt-Hogg-Dubé syndrome is a genetic syndrome caused by mutations in the FLCN gene. The main symptoms are lung bullae and pneumothorax, benign and malignant kidney tumors, and facial fibrofolliculoma. The risk of pneumothorax is considera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0de91a8754b33fd3967563432f124f7
https://pubmed.ncbi.nlm.nih.gov/29548312
https://pubmed.ncbi.nlm.nih.gov/29548312
Autor:
J. Holmes, Giovanni Pellacani, S. Ciardo, Richard Whitehead, R. Kaestle, Julia Welzel, Lotte Themstrup, E. C Sattler, N. Kindermann, Gregor B.E. Jemec, Martina Ulrich
Publikováno v:
Microvascular research. 107
Dynamic optical coherence tomography (D-OCT) is an angiographic variation of OCT that non-invasively provides images of the in vivo microvasculature of the skin by combining conventional OCT images with flow data. The objective of this study was to i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29a037787c0b76736269f21b9bc4c36c
https://pubmed.ncbi.nlm.nih.gov/27235002
https://pubmed.ncbi.nlm.nih.gov/27235002
Publikováno v:
The British journal of dermatology. 167(5)
In many Demodex-associated skin diseases Demodex mites are present in abundance and seem to be at least partially pathogenic. So far all diagnostic approaches such as scraping or standardized superficial skin biopsy are (semi-)invasive and may cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::88c02dbb8329bb1a12601f6546c4d22b
https://pubmed.ncbi.nlm.nih.gov/23659565
https://pubmed.ncbi.nlm.nih.gov/23659565
Publikováno v:
Mycoses. 56(1)
Onychomycosis is common and can mimic several different nail disorders. Accurate diagnosis is essential to choose the optimum antifungal therapy. The aim of this study was to evaluate the use of confocal laser scanning microscopy (CLSM) and optical c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::49aa9af3763f81588ecebb80acb6dba0
https://pubmed.ncbi.nlm.nih.gov/22524550
https://pubmed.ncbi.nlm.nih.gov/22524550
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADV. 27(1)
The clinical diagnosis of amelanotic melanoma is often challenging, because the classical clinical and dermoscopic features of pigmented melanoma are usually missing. The reflectance confocal microscopy (RCM) offers an additional possibility of an in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::254baf011fa277bbd6978f6b5bf1c83e
https://pubmed.ncbi.nlm.nih.gov/22324783
https://pubmed.ncbi.nlm.nih.gov/22324783