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Person

Sonja Schneppenheim (1968-)

Assistenzärztin

Name	Sonja Schneppenheim
Time	1968- (Date of birth and death)
Place	Itzehoe (Geburtsort) Deutschland
Profession	Assistenzärztin (characteristic profession)
Variant	Sonja Krey (früherer Name)
Further information	Diss. Medizinische Fakultät an der Universität Hamburg
Record type	Person
GND-Identifier	136238041
Record ID	136238041
Involved in show all MAP kinase activating death domain deficiency is a novel cause of impaired lymphocyte cytotoxicity Effect of plasma exchange on COVID-19 associated excess of von Willebrand factor and inflammation in critically ill patients Alteration in GPIIb/IIIa Binding of VWD-Associated von Willebrand Factor Variants with C-Terminal Missense Mutations Advancing multimer analysis of von Willebrand factor by single-molecule AFM imaging Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw–Schulman Syndrome Investigated in Germany Distinct mechanisms account for acquired von Willebrand syndrome in plasma cell dyscrasias von Willebrand disease type 2A phenotypes IIC, IID and IIE: A day in the life of shear-stressed mutant von Willebrand factor Molekulare Grundlage des von Willebrand-Syndroms Subtyp 2A (IID)

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Katalog der Deutschen Nationalbibliothek

Sonja Schneppenheim (1968-)

MAP kinase activating death domain deficiency is a novel cause of impaired lymphocyte cytotoxicity

Effect of plasma exchange on COVID-19 associated excess of von Willebrand factor and inflammation in critically ill patients

Alteration in GPIIb/IIIa Binding of VWD-Associated von Willebrand Factor Variants with C-Terminal Missense Mutations

Advancing multimer analysis of von Willebrand factor by single-molecule AFM imaging

Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw–Schulman Syndrome Investigated in Germany

Distinct mechanisms account for acquired von Willebrand syndrome in plasma cell dyscrasias

von Willebrand disease type 2A phenotypes IIC, IID and IIE: A day in the life of shear-stressed mutant von Willebrand factor

Molekulare Grundlage des von Willebrand-Syndroms Subtyp 2A (IID)