Klaus Mohnike

A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets

Fiona Francis, Steffen Hennig, Bernd Korn et al. · Nature Genetics · 1995 · 1.1K citations

Genetic Disorder, Genetics, X–linked Hypophosphatemic Rickets +3

Once-daily, subcutaneous vosoritide therapy in children with achondroplasia: a randomised, double-blind, phase 3, placebo-controlled, multicentre trial

Ravi Savarirayan, Louise Tofts, Melita Irving et al. · The Lancet · 2020 · 184 citations

Subcutaneous Vosoritide Therapy, Pediatrics, Multicentre Trial +2

Genomic Organization of the Human <i>PEX</i> Gene Mutated in X-Linked Dominant Hypophosphatemic Rickets

Fiona Francis, Tim M. Strom, Steffen Hennig et al. · Genome Research · 1997 · 162 citations · Full text

Genetics, Genomic Mechanism, Molecular Biology +19

Clinical studies of IGFBP-2 by radioimmunoassay.

W. F. Blum, Nanette Horn, Jüergen Kratzsch et al. · PubMed · 1993 · 140 citations

Human Growth, Immunology, Pathology +17

Serum MEPE-ASARM-peptides are elevated in X-linked rickets (HYP): implications for phosphaturia and rickets

Doron Bresler, Jan Bruder, Klaus Mohnike et al. · Journal of Endocrinology · 2004 · 113 citations · Full text

Sclerostin, Immunology, Osteoporosis +23