Zobrazeno 1 - 10
of 15
pro vyhledávání: '"D P, Lillicrap"'
Publikováno v:
Blood. 77:1476-1483
Recent reports of the mutations resulting in von Willebrand disease (vWD) have indicated that some cases of type IIA vWD are caused by single nucleotide substitutions in the gene encoding von Willebrand factor (vWF). However, the molecular pathogenes
Publikováno v:
Stroke. 21:66-71
Lupus anticoagulant and antiphospholipid antibodies are associated with thromboembolic phenomena in individuals both with and without systemic lupus erythematosus. A 32-year-old woman (the index case) with lupus anticoagulant, multiple cerebrovascula
Publikováno v:
American journal of hematology. 62(1)
Two patients developed catastrophic multicentric skin necrosis while receiving warfarin to treat venous thromboembolism complicated by immune-mediated heparin-induced thrombocytopenia (HIT). Patient 1 developed skin necrosis involving the breasts, th
Publikováno v:
Blood. 92(4)
AIMS--To evaluate the rapid detection of various forms of monoclonal B cell proliferations by using the polymerase chain reaction (PCR) to identify clonal immunoglobulin heavy chain genomic rearrangements. METHODS--Thirty four B cell lymphomas define
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82534427f17dc22cb5aa2f4d335f19d8
https://europepmc.org/articles/PMC501390/
https://europepmc.org/articles/PMC501390/
Publikováno v:
Thrombosis and haemostasis. 67(1)
Christmas disease was first reported as a distinct clinical entity in two manuscripts published in 1952. The eponym associated with this disorder, is the surname of the first patient examined in detail and reported by Biggs and colleagues in a paper
Publikováno v:
American journal of human genetics. 47(2)
Spontaneous mutation provides the substrate for evolution on one hand and for genetic susceptibility to disease on the other hand. X-linked diseases such as hemophilia B offer an opportunity to examine recent germ-line mutations in humans. By utilizi
Autor:
F. Giannelli, P. M. Green, K. A. High, J. N. Lozier, D. P. Lillicrap, M. Ludwig, K. Olek, P. H. Reitsma, M. Goossens, A. Yoshioka, S. Sommer, G. G. Brownlee
Publikováno v:
Nucleic acids research. 18(14)
Publikováno v:
Progress in clinical and biological research. 324
Publikováno v:
British Journal of Haematology. 62:557-565
Summary. Carrier detection in haemophilia B has previously involved pedigree analysis and assessment of the coagulation phenotype. At best using these methods, carrier evaluation may be made with about 80% certainty (Orstavik et al, 1981). With isola