Ludwig Stapenhorst

Successful plasma therapy for atypical hemolytic uremic syndrome caused by factor H deficiency owing to a novel mutation in the complement cofactor protein domain 15

Christoph Licht, Annic Weyersberg, Stefan Heinen et al. · American Journal of Kidney Diseases · 2005 · 113 citations

Medicine, Hematology, Nephrology +17

Hypocitraturia as a risk factor for nephrocalcinosis after kidney transplantation

Ludwig Stapenhorst, Robert Sassen, Bodo B. Beck et al. · Pediatric Nephrology · 2005 · 63 citations

Medicine, Nephrology, Pathology +7

Two novel ADAMTS13 gene mutations in thrombotic thrombocytopenic purpura/hemolytic-uremic syndrome (TTP/HUS)

Christoph Licht, Ludwig Stapenhorst, Thorsten Simon et al. · Kidney International · 2004 · 52 citations · Full text

Medicine, Genetics, Hematology +10

A Novel Point Mutation in the 3’ Region of the Prothrombin Gene at Position 20221 in a Lebanese/Syrian Family

Ludwig Stapenhorst, Klaus Wielckens, Mark Wylenzek et al. · Thrombosis and Haemostasis · 2001 · 39 citations

Life Sciences, Genetics, Molecular Genetics +9

Type I IgE receptor, interleukin 4 receptor and interleukin 13 polymorphisms in children with nephrotic syndrome

Klaus Tenbrock, Angela R. Schubert, Ludwig Stapenhorst et al. · Clinical Science · 2002 · 33 citations

Medicine, Immunology, Nephrology +15