Blombäck M - Search Results

1

Effects of the mutant von Willebrand factor gene in von Willebrand disease.

Zhang Z, Lindstedt M, Blombäck M, Anvret M. Zhang Z, et al. Among authors: blomback m. Hum Genet. 1995 Oct;96(4):388-94. doi: 10.1007/BF00191794. Hum Genet. 1995. PMID: 7557958

2

Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish origin.

Zhang ZP, Blombäck M, Egberg N, Falk G, Anvret M. Zhang ZP, et al. Among authors: blomback m. Genomics. 1994 May 1;21(1):188-93. doi: 10.1006/geno.1994.1241. Genomics. 1994. PMID: 8088787

3

Mutations of von Willebrand factor gene in families with von Willebrand disease in the Aland Islands.

Zhang ZP, Blombäck M, Nyman D, Anvret M. Zhang ZP, et al. Among authors: blomback m. Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):7937-40. doi: 10.1073/pnas.90.17.7937. Proc Natl Acad Sci U S A. 1993. PMID: 8367445 Free PMC article.

4

Understanding von Willebrand's disease from gene defects to the patients.

Zhang Z, Blombäck M, Anvret M. Zhang Z, et al. Among authors: blomback m. J Intern Med Suppl. 1997;740:115-9. J Intern Med Suppl. 1997. PMID: 9350192 Review.

5

A new approach to gene therapy.

Zhang Z, Eriksson M, Blombäck M, Anvret M. Zhang Z, et al. Among authors: blomback m. Blood Coagul Fibrinolysis. 1997 Dec;8 Suppl 2:S39-42. Blood Coagul Fibrinolysis. 1997. PMID: 9607112 Review.

6

Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I.

Zhang ZP, Lindstedt M, Falk G, Blombäck M, Egberg N, Anvret M. Zhang ZP, et al. Among authors: blomback m. Am J Hum Genet. 1992 Oct;51(4):850-8. Am J Hum Genet. 1992. PMID: 1415226 Free PMC article.

7

On laboratory problems in diagnosing mild von Willebrand's disease.

Blombäck M, Eneroth P, Andersson O, Anvret M. Blombäck M, et al. Am J Hematol. 1992 Jun;40(2):117-20. doi: 10.1002/ajh.2830400208. Am J Hematol. 1992. PMID: 1585909

8

Identification of a new nonsense mutation in the von Willebrand factor gene in patients with von Willebrand disease type III.

Zhang ZP, Falk G, Blombäck M, Egberg N, Anvret M. Zhang ZP, et al. Among authors: blomback m. Hum Mol Genet. 1992 Apr;1(1):61-2. doi: 10.1093/hmg/1.1.61. Hum Mol Genet. 1992. PMID: 1301136 No abstract available.

9

A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients.

Zhang ZP, Falk G, Blombäck M, Egberg N, Anvret M. Zhang ZP, et al. Among authors: blomback m. Hum Mol Genet. 1992 Dec;1(9):767-8. doi: 10.1093/hmg/1.9.767. Hum Mol Genet. 1992. PMID: 1302613 No abstract available.

10

Dinucleotide repeat polymorphism in the promoter region of the human von Willebrand factor gene (vWF gene).

Zhang ZP, Deng LP, Blombäck M, Anvret M. Zhang ZP, et al. Among authors: blomback m. Hum Mol Genet. 1992 Dec;1(9):780. doi: 10.1093/hmg/1.9.780. Hum Mol Genet. 1992. PMID: 1302623 No abstract available.

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