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Items: 1 to 20 of 89

1.

[Mild haemophilia A in Iceland.].

Jensson O, Jonsdottir S.

Laeknabladid. 1995 Jun;81(6):477-83. Icelandic.

PMID:
20065483
2.

Mild haemophilia A in Iceland: clinical genetic studies of three families with the same mutation.

Jensson O, Stenbjerg Bernvil S, Jónsdóttir S, Ingerslev J.

J Intern Med. 1994 May;235(5):443-50.

PMID:
8182400
3.

Detection of carriers of haemophilia A: use of bioassays and restriction fragment length polymorphisms (RFLP).

Rudzki Z, Rodgers SE, Sheffield LJ, Lloyd JV.

Aust N Z J Med. 1996 Apr;26(2):195-205.

PMID:
8744618
4.

Current strategy for genetic analysis of haemophilia A families.

Dardik R, Peretz H, Usher S, Seligsohn U, Martinowitz U.

Haemophilia. 1996 Jan;2(1):11-7. doi: 10.1111/j.1365-2516.1996.tb00003.x.

PMID:
27213899
5.
6.

Haemophilia A in a female: study of a family using intragenic and extragenic restriction site polymorphisms.

Piétu G, Thomas-Maison N, Sié P, Larrieu MJ, Meyer D.

Thromb Haemost. 1988 Aug 30;60(1):102-6.

PMID:
2903574
7.

Characterization, classification, and treatment of von Willebrand diseases: a critical appraisal of the literature and personal experiences.

Michiels JJ, Gadisseur A, Budde U, Berneman Z, van der Planken M, Schroyens W, van de Velde A, van Vliet H.

Semin Thromb Hemost. 2005 Nov;31(5):577-601. Review.

PMID:
16276467
8.

Results of a screening for von Willebrand disease type 2N in patients with suspected haemophilia A or von Willebrand disease type 1.

Schneppenheim R, Budde U, Krey S, Drewke E, Bergmann F, Lechler E, Oldenburg J, Schwaab R.

Thromb Haemost. 1996 Oct;76(4):598-602.

PMID:
8903002
9.

Carrier detection and prenatal diagnosis in families with haemophilia.

Shetty S, Ghosh K, Bhide A, Mohanty D.

Natl Med J India. 2001 Mar-Apr;14(2):81-3.

PMID:
11396323
10.

DDAVP infusion in haemophilia A carriers: different behaviour of plasma factor VIII and von Willebrand factor.

Casonato A, Dannhauser D, Pontara E, Bertomoro A, Orazi B, Santarossa L, Zerbinati P, Girolami A.

Blood Coagul Fibrinolysis. 1996 Jul;7(5):549-53.

PMID:
8874865
11.

Factor VIII inhibitors in mild and moderate-severity haemophilia A. UK Haemophilia Centre Directors Organisation.

Hay CR, Ludlam CA, Colvin BT, Hill FG, Preston FE, Wasseem N, Bagnall R, Peake IR, Berntorp E, Mauser Bunschoten EP, Fijnvandraat K, Kasper CK, White G, Santagostino E.

Thromb Haemost. 1998 Apr;79(4):762-6.

PMID:
9569189
13.
14.

Prevalence and spectrum of von Willebrand disease from western India.

Trasi S, Shetty S, Ghosh K, Mohanty D.

Indian J Med Res. 2005 May;121(5):653-8.

PMID:
15937368
15.

Carrier and prenatal diagnostic strategy and newly identified mutations in Hungarian haemophilia A and B families.

Bors A, Andrikovics H, Illés Z, Jáger R, Kardos M, Marosi A, Nemes L, Tordai A.

Blood Coagul Fibrinolysis. 2015 Mar;26(2):161-6. doi: 10.1097/MBC.0000000000000212.

PMID:
25255241
17.

Diagnosis of inherited von Willebrand disease: a clinical perspective.

Federici AB.

Semin Thromb Hemost. 2006 Sep;32(6):555-65. Review.

19.

Carrier detection and prenatal diagnosis in haemophilia A and B.

Chistolini A, Papacchini M, Mazzucconi MG, La Verde G, Arcieri R, Ferrari A, Paesano R, Pachi A, Mariani G.

Haematologica. 1990 Sep-Oct;75(5):424-8.

PMID:
1982946
20.

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