These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 9681234)

  • 1. Rapid genotypic diagnosis of type 2A von Willebrand's disease by heteroduplex analysis.
    Culpan D; Goodeve A; Bowen DJ; Standen G; Bidwell J
    Clin Lab Haematol; 1998 Jun; 20(3):177-8. PubMed ID: 9681234
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rapid genotype analysis in type 2B von Willebrand's disease using a universal heteroduplex generator.
    Wood N; Standen GR; Murray EW; Lillicrap D; Holmberg L; Peake IR; Bidwell J
    Br J Haematol; 1995 Jan; 89(1):152-6. PubMed ID: 7833255
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rapid mutation screening in type 2A von Willebrand's disease using universal heteroduplex generators.
    Culpan D; Standen G; Wood N; Mazurier C; Gaucher C; Bidwell J
    Br J Haematol; 1997 Mar; 96(3):464-9. PubMed ID: 9054649
    [TBL] [Abstract][Full Text] [Related]  

  • 4. UHG-based mutation screening in type 2B von Willebrand's disease: detection of a candidate mutation Ser547Phe.
    Wood N; Standen GR; Bowen DJ; Cumming A; Lush C; Lee R; Bidwell J
    Thromb Haemost; 1996 Feb; 75(2):363-7. PubMed ID: 8815591
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ins405AsnPro mutation in the von Willebrand factor propeptide in recessive type 2A (IIC) von Willebrand's disease.
    Holmberg L; Karpman D; Isaksson C; Kristoffersson AC; Lethagen S; Schneppenheim R
    Thromb Haemost; 1998 Apr; 79(4):718-22. PubMed ID: 9569179
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Laboratory diagnosis of von Willebrand's disease.
    Rick ME
    Clin Lab Med; 1994 Dec; 14(4):781-94. PubMed ID: 7874871
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new candidate mutation, G1629R, in a patient with type 2A von Willebrand's disease: basic mechanisms and clinical implications.
    Hilbert L; Federici AB; Baronciani L; Dallagiovanna S; Mazurier C
    Haematologica; 2004 Sep; 89(9):1128-33. PubMed ID: 15377475
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutational analysis of the von Willebrand factor gene in type 1 von Willebrand disease using conformation sensitive gel electrophoresis: a comparison of fluorescent and manual techniques.
    Hashemi Soteh M; Peake IR; Marsden L; Anson J; Batlle J; Meyer D; Fressinaud E; Mazurier C; Goudemand J; Eikenboom J; Goodeve A;
    Haematologica; 2007 Apr; 92(4):550-3. PubMed ID: 17488667
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Laboratory diagnosis of von Willebrand disease type 1/2E (2A subtype IIE), type 1 Vicenza and mild type 1 caused by mutations in the D3, D4, B1-B3 and C1-C2 domains of the von Willebrand factor gene. Role of von Willebrand factor multimers and the von Willebrand factor propeptide/antigen ratio.
    Gadisseur A; Berneman Z; Schroyens W; Michiels JJ
    Acta Haematol; 2009; 121(2-3):128-38. PubMed ID: 19506359
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sulfatide-binding assay for von Willebrand factor. Detection of von Willebrand's disease without discrimination of vWD subtypes.
    Favaloro EJ
    Thromb Res; 2000 Apr; 98(2):213-9. PubMed ID: 10713323
    [TBL] [Abstract][Full Text] [Related]  

  • 12. New mutations in exon 28 of the von Willebrand factor gene detected in patients with different types of von Willebrand's disease.
    Casaña P; Martínez F; Haya S; Tavares A; Aznar JA
    Haematologica; 2001 Apr; 86(4):414-9. PubMed ID: 11325649
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Recessive inheritance of von Willebrand's disease type I.
    Eikenboom JC; Reitsma PH; Peerlinck KM; Briët E
    Lancet; 1993 Apr; 341(8851):982-6. PubMed ID: 8096943
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Type 2B von Willebrand's disease in thirteen individuals from five unrelated Australian families: phenotype and genotype correlations.
    Facey DA; Favaloro EJ; Maxwell E; Baker R; Hertzberg MS
    Am J Hematol; 2000 Apr; 63(4):197-9. PubMed ID: 10706763
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of two point mutations in the von Willebrand factor gene of three families with the 'Normandy' variant of von Willebrand disease.
    Gaucher C; Mercier B; Jorieux S; Oufkir D; Mazurier C
    Br J Haematol; 1991 Aug; 78(4):506-14. PubMed ID: 1832934
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Aberrant multimeric structure of von Willebrand factor in a new variant of von Willebrand's disease (type IIC).
    Ruggeri ZM; Nilsson IM; Lombardi R; Holmberg L; Zimmerman TS
    J Clin Invest; 1982 Nov; 70(5):1124-7. PubMed ID: 6982283
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel candidate mutation (Arg611-->His) in type I 'platelet discordant' von Willebrand's disease with desmopressin-induced thrombocytopenia.
    Castaman G; Eikenboom JC; Rodeghiero F; Briët E; Reitsma PH
    Br J Haematol; 1995 Mar; 89(3):656-8. PubMed ID: 7734373
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Association of the 3467C>T mutation (T1156M) in the von Willebrand's factor gene with dominant type 1 von Willebrand's disease.
    Casaña P; Martínez F; Haya S; Espinós C; Aznar JA
    Ann Hematol; 2001 Jul; 80(7):381-3. PubMed ID: 11529461
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Understanding von Willebrand's disease from gene defects to the patients.
    Zhang Z; Blombäck M; Anvret M
    J Intern Med Suppl; 1997; 740():115-9. PubMed ID: 9350192
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.