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Items: 1 to 20 of 142

1.

Contribution of genetical analysis for diagnosis of von Willebrand's disease type 2B.

Victor M, Rugeri L, Nougier C, Meunier S, Fretigny M, Negrier C, Vinciguerra C.

Haemophilia. 2009 Mar;15(2):610-2. doi: 10.1111/j.1365-2516.2008.01966.x. Epub 2009 Feb 1. No abstract available.

PMID:
19187192
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.

PMID:
7833255
4.

Gastrointestinal angiodysplasia in a patient with type 2 von Willebrand's disease and analysis of exon 28 of the von Willebrand factor gene.

Satoh Y, Kita H, Kihira K, Mutoh H, Osawa H, Satoh K, Ido K, Sakata Y, Sugano K.

Am J Gastroenterol. 2004 Dec;99(12):2495-8.

PMID:
15571600
5.

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.

PMID:
11529461
6.

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.

PMID:
9681234
7.

[Digestive hemorrhage disclosing an angiodysplasia and von Willebrand disease type 2].

Lefrançois C, Dubus L, Maurel J, Chiche L, Lavergne JM, Borel-Derlon A.

Ann Fr Anesth Reanim. 1997;16(8):978-81. French.

PMID:
9750649
8.

[Intermittent thrombocytopenia as a manifestation of Von Willebrand's disease].

Gómez García EB, Brouwers GJ, Kappers-Klunne MC, Leebeek FW, van Vliet HH.

Ned Tijdschr Geneeskd. 2002 Jun 22;146(25):1192-5. Dutch.

PMID:
12109311
9.

Molecular misdiagnosis in type 2B von Willebrand disease.

Schmitt S, Trossaert M, Airaud F, Landeau-Trottier G, Talarmain P, Boisseau P, Fressinaud E, Bezieau S.

Am J Hematol. 2006 Oct;81(10):805-6. No abstract available.

10.

[Von Willebrand's disease, with special reference to laboratory diagnosis (the ristomycin test)].

Boda Z, Rák K.

Orv Hetil. 1980 Oct 19;121(42):2563-7. Hungarian. No abstract available.

PMID:
6258126
11.

von Willebrand's disease.

Sarup BM, Walia BN.

J Indian Med Assoc. 1973 Nov 16;61(10):435-8. No abstract available.

PMID:
4545728
12.

Canine von Willebrand's disease type 2 in German wirehair pointers in the Netherlands.

van Dongen AM, van Leeuwen M, Slappendel RJ.

Vet Rec. 2001 Jan 20;148(3):80-2. No abstract available.

PMID:
12503596
13.

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. doi: 10.1111/j.1365-2516.2008.01700.x. Epub 2008 Apr 1. No abstract available.

PMID:
18384353
14.
15.

Homozygous type IIC von Willebrand's disease.

Uno H, Yamazaki T, Suzuki M, Matsuoka H, Yoshioka A, Saito H, Tsubouchi H.

Int J Hematol. 1996 Apr;63(3):243-5. No abstract available.

PMID:
8936339
16.

Type 2B von Willebrand's disease and angiodysplasia.

Hertzberg MS, Facey DA, Favaloro EJ, Koutts J.

Thromb Haemost. 1999 Nov;82(5):1557-8. No abstract available.

PMID:
10595657
17.

Unconventional diagnosis of Normandy-type von Willebrand's disease in a blood donor.

Kashyap S, Nesbitt IM, Makris M.

Transfus Med. 2004 Apr;14(2):181-4.

PMID:
15113383
19.

Von Willebrand's disease in an Icelandic family.

Jensson O, Wallett LH.

Acta Med Scand. 1970 Mar 3;187(3):229-34. No abstract available.

PMID:
5309885
20.

[Case report of a family with von Willebrand's disease and sickle cell anemia].

Rasore-Quartino A, Sciarratta GV, Galletti A, Barone E, Storti G.

Pathologica. 1983;75 Suppl:138-41. Italian. No abstract available.

PMID:
6334834

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