134 related articles for article (PubMed ID: 21410641)
1. Large deletions identified in patients with von Willebrand disease using multiple ligation-dependent probe amplification.
Yadegari H; Driesen J; Hass M; Budde U; Pavlova A; Oldenburg J
J Thromb Haemost; 2011 May; 9(5):1083-6. PubMed ID: 21410641
[No Abstract] [Full Text] [Related]
2. Characterization of partial gene deletions in type III von Willebrand disease with alloantibody inhibitors.
Mancuso DJ; Tuley EA; Castillo R; de Bosch N; Mannucci PM; Sadler JE
Thromb Haemost; 1994 Aug; 72(2):180-5. PubMed ID: 7831648
[TBL] [Abstract][Full Text] [Related]
3. Molecular basis of human von Willebrand disease: analysis of platelet von Willebrand factor mRNA.
Ginsburg D; Konkle BA; Gill JC; Montgomery RR; Bockenstedt PL; Johnson TA; Yang AY
Proc Natl Acad Sci U S A; 1989 May; 86(10):3723-7. PubMed ID: 2786201
[TBL] [Abstract][Full Text] [Related]
4. Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients.
Yadegari H; Driesen J; Pavlova A; Biswas A; Hertfelder HJ; Oldenburg J
Thromb Haemost; 2012 Oct; 108(4):662-71. PubMed ID: 22871923
[TBL] [Abstract][Full Text] [Related]
5. Cosegregation of von Willebrand factor gene polymorphisms and possible germinal mosaicism in type IIB von Willebrand disease.
Murray EW; Giles AR; Bridge PJ; Peake IR; Lillicrap DP
Blood; 1991 Apr; 77(7):1476-83. PubMed ID: 2009368
[TBL] [Abstract][Full Text] [Related]
6. Re-evaluation of three Israeli families initially diagnosed with type 1 von Willebrand disease in light of the ISTH update on von Willebrand factor pathophysiology and classification.
Hashemi Soteh SM; Anson J; Inbal A; Peake IR; Goodeve AC
Haemophilia; 2008 May; 14(3):621-4. PubMed ID: 18384353
[No Abstract] [Full Text] [Related]
7. Rapid neonatal diagnosis of type IIB von Willebrand disease using the polymerase chain reaction.
Mannhalter C; Kyrle PA; Brenner B; Lechner K
Blood; 1991 Jun; 77(11):2539-40. PubMed ID: 1674891
[No Abstract] [Full Text] [Related]
8. von Willebrand disease phenotype and von Willebrand factor marker genotype in Doberman Pinschers.
Brooks MB; Erb HN; Foureman PA; Ray K
Am J Vet Res; 2001 Mar; 62(3):364-9. PubMed ID: 11277201
[TBL] [Abstract][Full Text] [Related]
9. Effects of the mutant von Willebrand factor gene in von Willebrand disease.
Zhang Z; Lindstedt M; Blombäck M; Anvret M
Hum Genet; 1995 Oct; 96(4):388-94. PubMed ID: 7557958
[TBL] [Abstract][Full Text] [Related]
10. A de novo mutation in exon 28 of the von Willebrand factor gene in a patient with type IIA von Willebrand's disease coincides with an MboI polymorphism in the von Willebrand factor pseudogene.
Pérez-Casal M; Daly M; Peake I
Hum Mol Genet; 1993 Dec; 2(12):2159-61. PubMed ID: 7906590
[No Abstract] [Full Text] [Related]
11. When it comes to von Willebrand disease, does 1 + 1 = 3?
Montgomery RR
J Thromb Haemost; 2006 Oct; 4(10):2162-3. PubMed ID: 16889558
[No Abstract] [Full Text] [Related]
12. Mutations of von Willebrand factor gene in families with von Willebrand disease in the Aland Islands.
Zhang ZP; Blombäck M; Nyman D; Anvret M
Proc Natl Acad Sci U S A; 1993 Sep; 90(17):7937-40. PubMed ID: 8367445
[TBL] [Abstract][Full Text] [Related]
13. Allelic frequencies of three VNTRs in intron 40 of the human von Willebrand factor gene in types 1, 2, and 3 von Willebrand disease patients and controls of a Brazilian population.
Mazzini J; Hackel C; Annichino-Bizzacchi JM
Thromb Res; 2000 Dec; 100(6):489-94. PubMed ID: 11152928
[TBL] [Abstract][Full Text] [Related]
14. Identification of a new nonsense mutation in the von Willebrand factor gene in patients with von Willebrand disease type III.
Zhang ZP; Falk G; Blombäck M; Egberg N; Anvret M
Hum Mol Genet; 1992 Apr; 1(1):61-2. PubMed ID: 1301136
[No Abstract] [Full Text] [Related]
15. Concentration of mRNA for von Willebrand factor in platelets of type I von Willebrand disease.
Takenaka T; Kuribayashi K; Tsukiyama M; Nakamine H; Fukuhara Y; Kuno T
Clin Chim Acta; 1996 Feb; 245(1):125-7. PubMed ID: 8646811
[No Abstract] [Full Text] [Related]
16. Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease.
Miller JL; Cunningham D; Lyle VA; Finch CN
Proc Natl Acad Sci U S A; 1991 Jun; 88(11):4761-5. PubMed ID: 2052556
[TBL] [Abstract][Full Text] [Related]
17. Polymerase chain reaction amplification of two polymorphic simple repeat sequences within the von Willebrand factor gene: application to family studies in von Willebrand disease.
Cumming AM; Armstrong JG; Pendry K; Burn AM; Wensley RT
Hum Genet; 1992 May; 89(2):194-8. PubMed ID: 1587530
[TBL] [Abstract][Full Text] [Related]
18. Von Willebrand gene tracking by single-tube automated fluorescent analysis of four short tandem repeat polymorphisms.
Vidal F; Julià A; Altisent C; Puig L; Gallardo D
Thromb Haemost; 2005 May; 93(5):976-81. PubMed ID: 15886817
[TBL] [Abstract][Full Text] [Related]
19. Characterization of von Willebrand factor gene defects in two unrelated patients with type IIC von Willebrand disease.
Gaucher C; Diéval J; Mazurier C
Blood; 1994 Aug; 84(4):1024-30. PubMed ID: 8049421
[TBL] [Abstract][Full Text] [Related]
20. Family studies in von Willebrand's disease by analysis of restriction fragment length polymorphisms and an intragenic variable number tandem repeat (VNTR) sequence.
Standen GR; Bignell P; Bowen DJ; Peake IR; Bloom AL
Br J Haematol; 1990 Oct; 76(2):242-9. PubMed ID: 1982729
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
