193 related articles for article (PubMed ID: 3152100)
1. [Hemophilia A and von Willebrand disease].
Tanimoto M; Saito H
Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):964-9. PubMed ID: 3152100
[No Abstract] [Full Text] [Related]
2. [Physiopathology and therapy of hemophilia and von Willebrand's disease].
Fukui H
Nihon Naika Gakkai Zasshi; 1991 Jun; 80(6):866-74. PubMed ID: 1919201
[No Abstract] [Full Text] [Related]
3. Factor VIII-von Willebrand factor binding defects in autosomal recessive von Willebrand disease type Normandy and in mild hemophilia A. New insights into factor VIII-von Willebrand factor interactions.
Jacquemin M
Acta Haematol; 2009; 121(2-3):102-5. PubMed ID: 19506355
[TBL] [Abstract][Full Text] [Related]
4. von Willebrand disease masquerading as haemophilia A.
Mazurier C
Thromb Haemost; 1992 Apr; 67(4):391-6. PubMed ID: 1631785
[No Abstract] [Full Text] [Related]
5. [Importance of the study of the binding of factor VIII to von Willebrand factor in hemophilia A].
Batlle J; Blanco-López MJ; Castiñeira MP; López-Fernández MF
Sangre (Barc); 1992 Jun; 37(3):211-24. PubMed ID: 1359656
[No Abstract] [Full Text] [Related]
6. Using genetic diagnostics in hemophilia and von Willebrand disease.
Swystun LL; James P
Hematology Am Soc Hematol Educ Program; 2015; 2015():152-9. PubMed ID: 26637715
[TBL] [Abstract][Full Text] [Related]
7. [Molecular biology of blood coagulation disorders].
Saito H
Nihon Naika Gakkai Zasshi; 1991 Oct; 80(10):1682-6. PubMed ID: 1685509
[No Abstract] [Full Text] [Related]
8. Characterisation of type 2N von Willebrand disease using phenotypic and molecular techniques.
Nesbitt IM; Goodeve AC; Guilliatt AM; Makris M; Preston FE; Peake IR
Thromb Haemost; 1996 Jun; 75(6):959-64. PubMed ID: 8822593
[TBL] [Abstract][Full Text] [Related]
9. Von Willebrand factor, factor VIII and the factor VIII/von Willebrand factor complex.
Ingerslev J
Dan Med Bull; 1990 Oct; 37(5):385-406. PubMed ID: 2125548
[No Abstract] [Full Text] [Related]
10. Factor viii and hemorrhagic disease.
Kahn A
J Ark Med Soc; 1979 Apr; 75(11):439-40. PubMed ID: 155683
[No Abstract] [Full Text] [Related]
11. Something new about type Normandy von Willebrand disease (type 2N VWD)?
Mazurier C
Thromb Haemost; 2004 Jul; 92(1):1-2. PubMed ID: 15213838
[No Abstract] [Full Text] [Related]
12. Recessive von Willebrand disease type 2 Normandy: variable expression of mild hemophilia and VWD type 1.
Michiels JJ; Gadisseur A; Vangenegten I; Schroyens W; Berneman Z
Acta Haematol; 2009; 121(2-3):119-27. PubMed ID: 19506358
[TBL] [Abstract][Full Text] [Related]
13. Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type 1 von Willebrand disease.
Gallinaro L; Sartorello F; Pontara E; Cattini MG; Bertomoro A; Bartoloni L; Pagnan A; Casonato A
Thromb Haemost; 2006 Dec; 96(6):711-6. PubMed ID: 17139363
[TBL] [Abstract][Full Text] [Related]
14. Combined hemophilia A and type 2 von Willebrand's disease: defect of both factor VIII level and factor VIII binding capacity of von Willebrand factor.
Casonato A; Pontara E; Sartorello F; Gemmati D; Cattini MG; Girolami A
Haematologica; 2001 Oct; 86(10):1110-1. PubMed ID: 11602423
[No Abstract] [Full Text] [Related]
15. The role of molecular genetics in diagnosing von Willebrand disease.
James P; Lillicrap D
Semin Thromb Hemost; 2008 Sep; 34(6):502-8. PubMed ID: 19085649
[TBL] [Abstract][Full Text] [Related]
16. Molecular basis of von Willebrand disease and its clinical implications.
Haematologica; 2004 Sep; 89(9):1036. PubMed ID: 15377463
[No Abstract] [Full Text] [Related]
17. Genetic diagnosis in hemophilia and von Willebrand disease.
Swystun LL; James PD
Blood Rev; 2017 Jan; 31(1):47-56. PubMed ID: 27596108
[TBL] [Abstract][Full Text] [Related]
18. Identification of a His54Gln substitution in von Willebrand factor from a patient with defective binding of factor VIII.
Rick ME; Krizek DM
Am J Hematol; 1996 Apr; 51(4):302-6. PubMed ID: 8602631
[TBL] [Abstract][Full Text] [Related]
19. [DNA analysis in the diagnosis of hemorrhagic diathesis].
Tanimoto M; Saito H
Rinsho Byori; 1987 Apr; Spec No 70():64-9. PubMed ID: 2886678
[No Abstract] [Full Text] [Related]
20. Variations in the hereditary patterns of factor VIII complex in a large kindred: coexistence of hemophilia A with Von Willebrand.
Tavori S; Tatarsky I
Am J Hematol; 1984 Jul; 17(1):1-9. PubMed ID: 6430067
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
