512 related articles for article (PubMed ID: 19085650)
21. The clinical manifestations of bleeding.
Schwartz SO
Med Clin North Am; 1972 Jan; 56(1):17-24. PubMed ID: 4536634
[No Abstract] [Full Text] [Related]
22. Common bleeding problems.
Moake JL; Funicella T
Clin Symp; 1983; 35(3):1-32. PubMed ID: 6336273
[No Abstract] [Full Text] [Related]
23. [Thrombasthenia, thrombopathy, von Willebrand's disease (hemorrhagic diathesis caused by the congenital disorder of primary hemostasis)].
Rák K
Orv Hetil; 1969 Mar; 110(12):637-45. PubMed ID: 4889625
[No Abstract] [Full Text] [Related]
24. Rare bleeding disorders: genetic, laboratory, clinical, and molecular aspects. Preface.
Othman M
Semin Thromb Hemost; 2013 Sep; 39(6):575-8. PubMed ID: 23982907
[No Abstract] [Full Text] [Related]
25. Screening women with menorrhagia for underlying bleeding disorders: the utility of the platelet function analyser and bleeding time.
Philipp CS; Miller CH; Faiz A; Dilley A; Michaels LA; Ayers C; Bachmann G; Dowling N; Saidi P
Haemophilia; 2005 Sep; 11(5):497-503. PubMed ID: 16128894
[TBL] [Abstract][Full Text] [Related]
26. Phenotypic implications of a co-existent haemorrhagic and thrombotic genotype.
Thachil J; Martlew V
Blood Coagul Fibrinolysis; 2012 Apr; 23(3):232-4. PubMed ID: 22343681
[TBL] [Abstract][Full Text] [Related]
27. [Problems of haemostasis and coagulation. Diagnostic orientation].
Bezeaud A; Guillin MC; Fischer AM
Rev Prat; 2007 Feb; 57(3):327-35. PubMed ID: 17578036
[No Abstract] [Full Text] [Related]
28. Bleeding diatheses in the orthopedic patient.
Cederbaum AI; Zimbler S
Orthop Clin North Am; 1978 Jul; 9(3):781-90. PubMed ID: 308626
[No Abstract] [Full Text] [Related]
29. Genetic diagnosis of haemophilia and other inherited bleeding disorders.
Peyvandi F; Jayandharan G; Chandy M; Srivastava A; Nakaya SM; Johnson MJ; Thompson AR; Goodeve A; Garagiola I; Lavoretano S; Menegatti M; Palla R; Spreafico M; Tagliabue L; Asselta R; Duga S; Mannucci PM
Haemophilia; 2006 Jul; 12 Suppl 3():82-9. PubMed ID: 16684001
[TBL] [Abstract][Full Text] [Related]
30. Congenital disorders of platelet function.
Weiss HJ
Semin Hematol; 1980 Oct; 17(4):228-41. PubMed ID: 7003719
[No Abstract] [Full Text] [Related]
31. Clinical hemostasis practice: the major impact of laboratory automation.
Bick RL
Semin Thromb Hemost; 1983 Jul; 9(3):139-71. PubMed ID: 6412362
[TBL] [Abstract][Full Text] [Related]
32. Inherited platelet disorders: a clinical approach to diagnosis and management.
Cox K; Price V; Kahr WH
Expert Rev Hematol; 2011 Aug; 4(4):455-72. PubMed ID: 21801136
[TBL] [Abstract][Full Text] [Related]
33. Laboratory diagnosis and molecular classification of von Willebrand disease.
Gadisseur A; Hermans C; Berneman Z; Schroyens W; Deckmyn H; Michiels JJ
Acta Haematol; 2009; 121(2-3):71-84. PubMed ID: 19506352
[TBL] [Abstract][Full Text] [Related]
34. Lung-angiodysplasia and von Willebrand's disease in a family with Rendu-Osler disease. A case report.
Girola SS; Cusa C; Di Giulio G; Marti A; Mazzone A
Recenti Prog Med; 1996 Dec; 87(12):589-91. PubMed ID: 9066252
[TBL] [Abstract][Full Text] [Related]
35. Hereditary disorders of platelet function.
Hardisty RM
Clin Haematol; 1983 Feb; 12(1):153-73. PubMed ID: 6340879
[No Abstract] [Full Text] [Related]
36. Von Willebrand's disease.
Quast GL; Schoettger JD
J Oral Surg; 1974 Nov; 32(11):840-6. PubMed ID: 4547793
[No Abstract] [Full Text] [Related]
37. Genetics of haemostasis.
Goodeve AC; Perry DJ; Cumming T; Hill M; Jennings I; Kitchen S; Walker I; Gray E; Jayandharan GR; Tuddenham E
Haemophilia; 2012 Jul; 18 Suppl 4():73-80. PubMed ID: 22726087
[TBL] [Abstract][Full Text] [Related]
38. [Biological diagnosis of Von Willebrand disease and its difficulties].
Znazen R; Guermazi S; Karoui M
Tunis Med; 2007 Jun; 85(6):445-9. PubMed ID: 17644894
[TBL] [Abstract][Full Text] [Related]
39. [Principal symptoms in hemostasis disorders].
Coninx S; Beck EA
Schweiz Med Wochenschr; 1979 Feb; 109(5):137-41. PubMed ID: 312528
[TBL] [Abstract][Full Text] [Related]
40. How to evaluate phenotype-genotype relationship in rare coagulation haemorrhagic disorders: examples from FVII deficiency.
Bernardi F; Marchetti G; Dolce A; Mariani G
Haemophilia; 2004 Oct; 10 Suppl 4():177-9. PubMed ID: 15479394
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]