Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Hanel, Daniela"'
Autor:
Busch, Albert, Hoffjan, Sabine, Bergmann, Frauke, Hartung, Birgit, Jung, Helena, Hanel, Daniela, Andeas Tzschach, Janos Kadar, Yskert Kodolitsch, Christoph-Thomas Germer, Trobisch, Heiner, Strasser, Erwin, Wildenauer, René
von Willebrand, Vitamin D and platelet diagnostics: The table shows the results for each patient, listed to patient ID according to Table 1, with unit and normal measurement range in brackets depending on the respective laboratory where the analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1504ab96ab307ce339c94b15c4529e56
Autor:
Busch, Albert, Hoffjan, Sabine, Bergmann, Frauke, Hartung, Birgit, Jung, Helena, Hanel, Daniela, Tzschach, Andeas, Kadar, Janos, von Kodolitsch, Yskert, Germer, Christoph-Thomas, Trobisch, Heiner, Strasser, Erwin, Wildenauer, René
Background The vascular type represents a very rare, yet the clinically most fatal entity of Ehlers-Danlos syndrome (EDS). Patients are often admitted due to arterial bleedings and the friable tissue and the altered coagulation contribute to the chal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::42ade0aa787e8e3461bd7baea30cff81
https://opus4.kobv.de/opus4-fau/frontdoor/index/index/docId/8092
https://opus4.kobv.de/opus4-fau/frontdoor/index/index/docId/8092
Autor:
Busch, Albert, Hoffjan, Sabine, Bergmann, Frauke, Hartung, Birgit, Jung, Helena, Hanel, Daniela, Andeas Tzschach, Janos Kadar, Yskert Kodolitsch, Christoph-Thomas Germer, Trobisch, Heiner, Strasser, Erwin, RenĂŠ Wildenauer
Blood count and plasmatic coagulation laboratory results: The table shows the results for each patient, listed to patient ID according to Table 1, with unit and normal measurement range. Bold red values show deviation from the normal range. Stroked
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6bbb639b25dbbc685d9a1495aca9754
Autor:
Busch A; Department for General, Visceral, Vascular & Paediatric Surgery, University Hospital of Würzburg - ZOM, Oberduerrbacher str 6, 97080, Würzburg, Germany. busch_a2@ukw.de., Hoffjan S; Department of Human Genetics, Ruhr-University, Bochum, Germany., Bergmann F; MVZ wagnerstibbe, amedes Gruppe, Hannover, Germany., Hartung B; Institute of Clinical Chemistry, University Hospital Würzburg, Würzburg, Germany., Jung H; Institute for medical genetics and molecular medicine, Cologne, Germany., Hanel D; synlab MVZ Stuttgart GmbH, Stuttgart, Germany., Tzschach A; Institute of Clinical Genetics, Technische Universität Dresden, Dresden, Germany.; UniversitätsCentrum für Seltene Erkrankungen, University Hospital Carl Gustav Carus, Dresden, Germany., Kadar J; Laboratory for Transfusion Medicine, Cologne, Germany., von Kodolitsch Y; Department of Cardiology, University Heart Center, University Hospital Hamburg-Eppendorf, Hamburg, Germany., Germer CT; Department for General, Visceral, Vascular & Paediatric Surgery, University Hospital of Würzburg - ZOM, Oberduerrbacher str 6, 97080, Würzburg, Germany., Trobisch H; Laboratory and Ambulance for Coagulation Disorders, Duisburg, Germany., Strasser E; Transfusion Medicine and Haemostaseology Department, University Hospital Erlangen, Erlangen, Germany., Wildenauer R; Department for General, Visceral, Vascular & Paediatric Surgery, University Hospital of Würzburg - ZOM, Oberduerrbacher str 6, 97080, Würzburg, Germany.
Publikováno v:
Orphanet journal of rare diseases [Orphanet J Rare Dis] 2016 Aug 03; Vol. 11 (1), pp. 111. Date of Electronic Publication: 2016 Aug 03.