Briët E - Search Results

1

Recessive inheritance of von Willebrand's disease type I.

Eikenboom JC, Reitsma PH, Peerlinck KM, Briët E. Eikenboom JC, et al. Among authors: briet e. Lancet. 1993 Apr 17;341(8851):982-6. doi: 10.1016/0140-6736(93)91070-3. Lancet. 1993. PMID: 8096943

2

Seeming homozygosity in type-IIB von Willebrand's disease due to a polymorphism within the sequence of a commonly used primer.

Eikenboom JC, Reitsma PH, Briët E. Eikenboom JC, et al. Among authors: briet e. Ann Hematol. 1994 Mar;68(3):139-41. doi: 10.1007/BF01727418. Ann Hematol. 1994. PMID: 7909449

3

Increased risk of venous thrombosis in oral-contraceptive users who are carriers of factor V Leiden mutation.

Vandenbroucke JP, Koster T, Briët E, Reitsma PH, Bertina RM, Rosendaal FR. Vandenbroucke JP, et al. Among authors: briet e. Lancet. 1994 Nov 26;344(8935):1453-7. doi: 10.1016/s0140-6736(94)90286-0. Lancet. 1994. PMID: 7968118 Free article.

4

Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect.

Allaart CF, Poort SR, Rosendaal FR, Reitsma PH, Bertina RM, Briët E. Allaart CF, et al. Among authors: briet e. Lancet. 1993 Jan 16;341(8838):134-8. doi: 10.1016/0140-6736(93)90003-y. Lancet. 1993. PMID: 8093743

5

Instability of repeats of the von Willebrand factor gene variable number tandem repeat sequence in intron 40.

Eikenboom JC, Reitsma PH, van der Velden PA, Briët E. Eikenboom JC, et al. Among authors: briet e. Br J Haematol. 1993 Jul;84(3):533-5. doi: 10.1111/j.1365-2141.1993.tb03114.x. Br J Haematol. 1993. PMID: 8105872

6

Multiple substitutions in the von Willebrand factor gene that mimic the pseudogene sequence.

Eikenboom JC, Vink T, Briët E, Sixma JJ, Reitsma PH. Eikenboom JC, et al. Among authors: briet e. Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2221-4. doi: 10.1073/pnas.91.6.2221. Proc Natl Acad Sci U S A. 1994. PMID: 8134377 Free PMC article.

7

Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor.

Eikenboom JC, Matsushita T, Reitsma PH, Tuley EA, Castaman G, Briët E, Sadler JE. Eikenboom JC, et al. Among authors: briet e. Blood. 1996 Oct 1;88(7):2433-41. Blood. 1996. PMID: 8839833 Free article.

8

The inheritance and molecular genetics of von Willebrand's disease.

Eikenboom JC, Reitsma PH, Briët E. Eikenboom JC, et al. Among authors: briet e. Haemophilia. 1995 Apr;1(2):77-90. doi: 10.1111/j.1365-2516.1995.tb00045.x. Haemophilia. 1995. PMID: 27214314 No abstract available.

9

A novel candidate mutation (Arg611-->His) in type I 'platelet discordant' von Willebrand's disease with desmopressin-induced thrombocytopenia.

Castaman G, Eikenboom JC, Rodeghiero F, Briët E, Reitsma PH. Castaman G, et al. Among authors: briet e. Br J Haematol. 1995 Mar;89(3):656-8. doi: 10.1111/j.1365-2141.1995.tb08383.x. Br J Haematol. 1995. PMID: 7734373

10

Acquired von Willebrand's disease due to excessive fibrinolysis.

Eikenboom JC, van der Meer FJ, Briët E. Eikenboom JC, et al. Among authors: briet e. Br J Haematol. 1992 Aug;81(4):618-20. doi: 10.1111/j.1365-2141.1992.tb03005.x. Br J Haematol. 1992. PMID: 1390254 No abstract available.

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