Heike Hoyer‐Kuhn

Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta

Lutz Garbes, Kyung‐Ho Kim, Angelika Rieß et al. · The American Journal of Human Genetics · 2015 · 174 citations · Full text

Developmental Biology, Cell Division, Bone Morphogenic Protein +12

Vitamin B6 in Primary Hyperoxaluria I

Heike Hoyer‐Kuhn, Sina Kohbrok, Ruth Volland et al. · Clinical Journal of the American Society of Nephrology · 2014 · 134 citations

Two years’ experience with denosumab for children with Osteogenesis imperfecta type VI

Heike Hoyer‐Kuhn, Christian Netzer, Friederike Koerber et al. · Orphanet Journal of Rare Diseases · 2014 · 120 citations · Full text

Safety and efficacy of denosumab in children with osteogenesis imperfect--a first prospective trial.

Heike Hoyer‐Kuhn, Jessica M. Franklin, M. Kron et al. · PubMed · 2016 · 119 citations · Full text

First use of the RANKL antibody denosumab in osteogenesis imperfecta type VI.

Oliver Semler, Christian Netzer, Heike Hoyer‐Kuhn et al. · PubMed · 2012 · 106 citations