Zobrazeno 1 - 10
of 33
pro vyhledávání: '"M E Rick"'
Autor:
Cynthia E. Dunbar, D Follman, John F. Tisdale, Elizabeth M. Kang, G N Schwartz, M E Rick, S Kim, Neelam Giri, Neal S. Young, Margarita Rivera
Publikováno v:
British Journal of Haematology. 108:167-175
Diamond-Blackfan anaemia (DBA) is a constitutional pure red cell aplasia presenting in early childhood. In some patients, neutropenia and/or thrombocytopenia have also been observed during the course of the disease. We have followed 28 patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::622fbec693b43507e43f6447cc492de8
https://doi.org/10.1046/j.1365-2141.2000.01796.x
https://doi.org/10.1046/j.1365-2141.2000.01796.x
Autor:
J. P. Girma, Armando Tripodi, M. E. Rick, Ulrich Budde, Kenneth D. Friedman, Martina Böhm, Veena Chantarangkul, Peter Turecek, Joel F. Moake, Miriam Galbusera, Jing-fei Dong, P. M. Mannucci, Jan-Dirk Studt
Publikováno v:
Journal of thrombosis and haemostasis : JTH. 2(9)
Summary. Background: ADAMTS-13 is a von Willebrand factor (VFW)-cleaving protease. Its congenital or acquired deficiency is associated with thrombotic thrombocytopenic purpura (TTP) and more rarely with the hemolytic uremic syndrome. We report on a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8abad181a3e0d65e029dfc4ab2806800
https://pubmed.ncbi.nlm.nih.gov/15333037
https://pubmed.ncbi.nlm.nih.gov/15333037
Publikováno v:
Vox sanguinis. 85(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce52896dd896cd5e5c8a8f145a2b8628
https://pubmed.ncbi.nlm.nih.gov/12925168
https://pubmed.ncbi.nlm.nih.gov/12925168
Publikováno v:
The Journal of urology. 165(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b5a484020416cd32498434fe42daceb4
https://pubmed.ncbi.nlm.nih.gov/11342931
https://pubmed.ncbi.nlm.nih.gov/11342931
Autor:
D M, Kirzek, M E, Rick
Publikováno v:
Electrophoresis. 22(5)
A method for evaluating the activity of the von Willebrand factor (vWF) protease is described, and a clinical application is illustrated. The procedure utilizes gel electrophoresis, Western blotting, and luminographic detection methods to evaluate th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e145071bb5b15cce25dc367ee0c26600
https://pubmed.ncbi.nlm.nih.gov/11332762
https://pubmed.ncbi.nlm.nih.gov/11332762
Publikováno v:
Thrombosis and haemostasis. 85(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::497122fd725c30393a1995f77bec6018
https://pubmed.ncbi.nlm.nih.gov/11204576
https://pubmed.ncbi.nlm.nih.gov/11204576
Publikováno v:
British journal of haematology. 112(1)
We describe a new mutation in glycoprotein IX (GPIX) in a patient with Bernard-Soulier syndrome (BSS). Sequencing of GPIX revealed a homozygous (T--C) transition at nucleotide 1717 (GenBank/HUMGPIX/M80478), resulting in a Cys(8) (TGT)--Arg (CGT) repl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b14df1a461a7bc5bbc27dc3dc979c06
https://pubmed.ncbi.nlm.nih.gov/11167791
https://pubmed.ncbi.nlm.nih.gov/11167791
Publikováno v:
American journal of hematology. 64(3)
The occurrence of factor VIII inhibitors in non-hemophilic patients is a rare event with a potentially lethal outcome. Despite its infrequent occurrence, the association of this inhibitor with multiple autoimmune diseases is well recognized. We repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dc4dcde345b1caec643608e8d1ffe04c
https://pubmed.ncbi.nlm.nih.gov/10861820
https://pubmed.ncbi.nlm.nih.gov/10861820
Autor:
N, Giri, E, Kang, J F, Tisdale, D, Follman, M, Rivera, G N, Schwartz, S, Kim, N S, Young, M E, Rick, C E, Dunbar
Publikováno v:
British journal of haematology. 108(1)
Diamond-Blackfan anaemia (DBA) is a constitutional pure red cell aplasia presenting in early childhood. In some patients, neutropenia and/or thrombocytopenia have also been observed during the course of the disease. We have followed 28 patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a3afef3c18fb9cf42137f0a9e9b3a30
https://pubmed.ncbi.nlm.nih.gov/10651740
https://pubmed.ncbi.nlm.nih.gov/10651740
Autor:
L P, McKeown, K E, Hansmann, O, Wilson, W, Gahl, H R, Gralnick, K E, Rosenfeld, S J, Rosenfeld, M K, Horne, M E, Rick
Publikováno v:
American journal of hematology. 59(2)
The Hermansky-Pudlak Syndrome (HPS) is an autosomal recessive inherited disorder characterized by oculocutaneous albinism, tissue accumulation of ceroid pigment, and a mild to moderate bleeding diathesis attributed to storage-pool deficient (SPD) pla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::50e3c5a3b4888ceb13d603abada54c58
https://pubmed.ncbi.nlm.nih.gov/9766795
https://pubmed.ncbi.nlm.nih.gov/9766795