Christoph J. Mache

Transforming Growth Factor-β Receptor Mutations and Pulmonary Arterial Hypertension in Childhood

Rachel E. Harrison, Rolf M.F. Berger, Sheila G. Haworth et al. · Circulation · 2005 · 230 citations · Full text

Polyhydramnios, Transient Antenatal Bartter’s Syndrome, and<i>MAGED2</i>Mutations

Kamel Laghmani, Bodo B. Beck, Sung-Sen Yang et al. · New England Journal of Medicine · 2016 · 181 citations · Full text

Clinical and genetic predictors of atypical hemolytic uremic syndrome phenotype and outcome

Franz Schaefer, Gianluigi Ardissino, Gema Ariceta et al. · Kidney International · 2018 · 169 citations

Hemodialysis, Genetic Disorder, Medicine +8

Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor

Asif Ali, P. T. Christie, I. V. Grigorieva et al. · Human Molecular Genetics · 2006 · 149 citations

Developmental Biology, Dna Binding, Gata3 Mutations +13

Complement Inhibitor Eculizumab in Atypical Hemolytic Uremic Syndrome

Christoph J. Mache, Birgit Acham‐Roschitz, Véronique Frémeaux‐Bacchi et al. · Clinical Journal of the American Society of Nephrology · 2009 · 149 citations · Full text