Budde U - Search Results

1

Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD).

Goodeve A, Eikenboom J, Castaman G, Rodeghiero F, Federici AB, Batlle J, Meyer D, Mazurier C, Goudemand J, Schneppenheim R, Budde U, Ingerslev J, Habart D, Vorlova Z, Holmberg L, Lethagen S, Pasi J, Hill F, Hashemi Soteh M, Baronciani L, Hallden C, Guilliatt A, Lester W, Peake I. Goodeve A, et al. Among authors: budde u. Blood. 2007 Jan 1;109(1):112-21. doi: 10.1182/blood-2006-05-020784. Epub 2006 Sep 19. Blood. 2007. PMID: 16985174 Free article.

2

Luminographic detection of von Willebrand factor multimers in agarose gels and on nitrocellulose membranes.

Budde U, Schneppenheim R, Plendl H, Dent J, Ruggeri ZM, Zimmerman TS. Budde U, et al. Thromb Haemost. 1990 Apr 12;63(2):312-5. Thromb Haemost. 1990. PMID: 2363131

3

Luminography--an alternative assay for detection of von Willebrand factor multimers.

Schneppenheim R, Plendl H, Budde U. Schneppenheim R, et al. Among authors: budde u. Thromb Haemost. 1988 Oct 31;60(2):133-6. Thromb Haemost. 1988. PMID: 3064356

4

Subunit composition of plasma von Willebrand factor in patients with the myeloproliferative syndrome.

Budde U, Dent JA, Berkowitz SD, Ruggeri ZM, Zimmerman TS. Budde U, et al. Blood. 1986 Dec;68(6):1213-7. Blood. 1986. PMID: 3535924 Free article.

5

Acquired von Willebrand's disease in the myeloproliferative syndrome.

Budde U, Schaefer G, Mueller N, Egli H, Dent J, Ruggeri Z, Zimmerman T. Budde U, et al. Blood. 1984 Nov;64(5):981-5. Blood. 1984. PMID: 6333259 Free article.

6

Identification of a candidate missense mutation in a family with von Willebrand disease type IIC.

Schneppenheim R, Thomas KB, Krey S, Budde U, Jessat U, Sutor AH, Zieger B. Schneppenheim R, et al. Among authors: budde u. Hum Genet. 1995 Jun;95(6):681-6. doi: 10.1007/BF00209487. Hum Genet. 1995. PMID: 7789955

7

Genetic heterogeneity of severe von Willebrand disease type III in the German population.

Schneppenheim R, Krey S, Bergmann F, Bock D, Budde U, Lange M, Linde R, Mittler U, Meili E, Mertes G, et al. Schneppenheim R, et al. Among authors: budde u. Hum Genet. 1994 Dec;94(6):640-52. doi: 10.1007/BF00206958. Hum Genet. 1994. PMID: 7989040

8

von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure.

Holmberg L, Dent JA, Schneppenheim R, Budde U, Ware J, Ruggeri ZM. Holmberg L, et al. Among authors: budde u. J Clin Invest. 1993 May;91(5):2169-77. doi: 10.1172/JCI116443. J Clin Invest. 1993. PMID: 8486782 Free PMC article.

9

Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease.

Schneppenheim R, Brassard J, Krey S, Budde U, Kunicki TJ, Holmberg L, Ware J, Ruggeri ZM. Schneppenheim R, et al. Among authors: budde u. Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3581-6. doi: 10.1073/pnas.93.8.3581. Proc Natl Acad Sci U S A. 1996. PMID: 8622978 Free PMC article.

10

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. Schneppenheim R, et al. Among authors: budde u. Thromb Haemost. 1996 Oct;76(4):598-602. Thromb Haemost. 1996. PMID: 8903002 Clinical Trial.

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