Budde U - Search Results

1

Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD.

Eikenboom J, Van Marion V, Putter H, Goodeve A, Rodeghiero F, Castaman G, Federici AB, Batlle J, Meyer D, Mazurier C, Goudemand J, Schneppenheim R, Budde U, Ingerslev J, Vorlova Z, Habart D, Holmberg L, Lethagen S, Pasi J, Hill F, Peake I. Eikenboom J, et al. Among authors: budde u. J Thromb Haemost. 2006 Apr;4(4):774-82. doi: 10.1111/j.1538-7836.2006.01823.x. J Thromb Haemost. 2006. PMID: 16634746 Free article.

2

Luminography--a new, highly sensitive visualization method for electrophoresis.

Schneppenheim R, Budde U, Dahlmann N, Rautenberg P. Schneppenheim R, et al. Among authors: budde u. Electrophoresis. 1991 May;12(5):367-72. doi: 10.1002/elps.1150120508. Electrophoresis. 1991. PMID: 1682145

3

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

4

Type IIB von Willebrand factor with normal sialic acid content induces platelet aggregation in the absence of ristocetin. Role of platelet activation, fibrinogen, and two distinct membrane receptors.

De Marco L, Mazzuccato M, Grazia Del Ben M, Budde U, Federici AB, Girolami A, Ruggeri ZM. De Marco L, et al. Among authors: budde u. J Clin Invest. 1987 Aug;80(2):475-82. doi: 10.1172/JCI113095. J Clin Invest. 1987. PMID: 3038958 Free PMC article.

5

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

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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