Eberhard Kuwertz-Bröking

Mutations in<i>CYP24A1</i>and Idiopathic Infantile Hypercalcemia

Karl P. Schlingmann, Martin Kaufmann, Stefanie Weber et al. · New England Journal of Medicine · 2011 · 663 citations · Full text

Novel Paracellin-1 Mutations in 25 Families with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

Stefanie Weber, Linda Schneider, Melanie Peters et al. · Journal of the American Society of Nephrology · 2001 · 269 citations

Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders

K Hasselbacher, Roger C. Wiggins, Verena Matejas et al. · Kidney International · 2006 · 210 citations · Full text

Mendelian Disorder, Genetic Disorder, Animal Science +12

Immunosuppression and Renal Outcome in Congenital and Pediatric Steroid-Resistant Nephrotic Syndrome

Anja Büscher, Birgitta Kranz, Rainer Büscher et al. · Clinical Journal of the American Society of Nephrology · 2010 · 180 citations · Full text

Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations

Valerié Schumacher, K Schärer, Elke Wühl et al. · Kidney International · 1998 · 160 citations

Glomerulonephritis, Mendelian Disorder, Genetic Disorder +9