Henry Fehrenbach

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

Karl P. Schlingmann, Martin Kaufmann, Stefanie Weber et al. · New England Journal of Medicine · 2011 · 684 citations · Full text

Medicine, Pediatrics, Pharmacotherapy +17

Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease

Carsten Bergmann, Jennifer von Bothmer, Nadina Ortiz Brüchle et al. · Journal of the American Society of Nephrology · 2011 · 235 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome

Jillian K. Warejko, Weizhen Tan, Ankana Daga et al. · Clinical Journal of the American Society of Nephrology · 2017 · 235 citations · Full text

Life Sciences, Genetics, Nephrology +15

KANK deficiency leads to podocyte dysfunction and nephrotic syndrome

Heon Yung Gee, Fujian Zhang, Shazia Ashraf et al. · Journal of Clinical Investigation · 2015 · 200 citations · Full text

Medicine, Genetics, Pathology +12

A multicenter, randomized, placebo-controlled, double-blind phase 3 trial with open-arm comparison indicates safety and efficacy of nephroprotective therapy with ramipril in children with Alport’s syndrome

Burkhard Tönshoff, Lutz T. Weber, Lars Pape et al. · Kidney International · 2020 · 153 citations · Full text

Pharmacy, Pediatrics, Pharmacotherapy +11