Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Zieger, Barbara"'
Autor:
Kapp, Friedrich G, Schneider, Cedric, Holm, Annegret, Glonnegger, Hannah, Niemeyer, Charlotte M, Rößler, Jochen, Zieger, Barbara
Publikováno v:
Biomolecules; Volume 12; Issue 12; Pages: 1840
Kapp, Friedrich G; Schneider, Cedric; Holm, Annegret; Glonnegger, Hannah; Niemeyer, Charlotte M; Rößler, Jochen; Zieger, Barbara (2022). Comprehensive Analyses of Coagulation Parameters in Patients with Vascular Anomalies. Biomolecules, 12(12) MDPI 10.3390/biom12121840
Kapp, Friedrich G; Schneider, Cedric; Holm, Annegret; Glonnegger, Hannah; Niemeyer, Charlotte M; Rößler, Jochen; Zieger, Barbara (2022). Comprehensive Analyses of Coagulation Parameters in Patients with Vascular Anomalies. Biomolecules, 12(12) MDPI 10.3390/biom12121840
Background: Vascular anomalies comprise a diverse group of rare diseases with altered blood flow and are often associated with coagulation disorders. The most common example is a localized intravascular coagulopathy in venous malformations leading to
Autor:
Ehl, Anne, Pannicke, Ulrich, Zimmermann, Stefanie-Yvonne, Lorenz, R., Neven, Benedicte, Fuchs, Ilka, Salzer, Ulrich, Speckmann, Carsten, Strauss, Anne, Maass, E., Collet, Benedicte, Enders, Anselm, Favier, Remi, Alessi, Marie-Christine, Rieux-Laucat, Frederic, Zieger, Barbara, Schwarz, Klaus, Ehl, Stephan, Lorenz, Myriam Ricarda, Maaβ, Eberhard
Publikováno v:
Blood
Blood, American Society of Hematology, 2015, 126 (16), pp.1967-9
Blood, American Society of Hematology, 2015, 126 (16), pp.1967-9
To the editor: The combination of splenomegaly and autoimmune cytopenia is frequently associated with primary immunodeficiencies. The most frequent disease is autoimmune lymphoproliferative syndrome (ALPS), caused by autosomal dominant germline or so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e873672035c83259837b22f411e53b22
https://hal.archives-ouvertes.fr/hal-01478138
https://hal.archives-ouvertes.fr/hal-01478138
Publikováno v:
PLoS ONE; 1/3/2019, Vol. 14 Issue 01, p1-9, 9p
Autor:
Susan Halimeh, Verena Wiegering, Lars Fischer, Karin Kurnik, Kirstin Sandrock-Lang, Dimitrios A. Tsakiris, Zieger Barbara, Brigit Brand, Michael Sigl-Kraetzig, Johannes Oldenburg, Katharina Kraetzer, Eileen Busse, Sentot Santoso, Niklas Deeg
Publikováno v:
Blood. 124:1460-1460
Background: Glanzmann thrombasthenia (GT) is an autosomal recessive bleeding disorder. Platelets from patients with GT show quantitative and/or qualitative defects of the platelet membrane glycoprotein (GP) IIb/IIIa complex, also called integrin αII
Autor:
Mostowy, Serge, Bi, Erfei, Füchtbauer, Ernst-Martin, Goryachev, Andrew B., Montagna, Cristina, Nagata, Koh-ichi, Trimble, William S., Werner, Hauke B., Yao, Xuebiao, Zieger, Barbara, Spiliotis, Elias T.
Publikováno v:
Biological Chemistry; Feb2014, Vol. 395 Issue 2, p119-121, 3p