Marina Schlicke

Heterozygous Mutation within a Kinase-Conserved Motif of the Insulin-Like Growth Factor I Receptor Causes Intrauterine and Postnatal Growth Retardation

Tassilo Kruis, Jürgen Klammt, Assimina Galli‐Τsinopoulou et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 79 citations · Full text

Medicine, Genetics, Molecular Genetics +17

A Heterozygous Mutation of the Insulin-Like Growth Factor-I Receptor Causes Retention of the Nascent Protein in the Endoplasmic Reticulum and Results in Intrauterine and Postnatal Growth Retardation

Tillmann Wallborn, Stefan Wüller, Jürgen Klammt et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 76 citations

Life Sciences, Genetics, Molecular Genetics +17

Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes

Eleonore Bertko, Jürgen Klammt, Petra Dušátková et al. · Journal of Human Genetics · 2017 · 29 citations · Full text

Medicine, Endocrinology, Genetics +16

A Comprehensive Cohort Analysis Comparing Growth and GH Therapy Response in IGF1R Mutation Carriers and SGA Children

Eric Göpel, Denise Rockstroh, Heike Pfäffle et al. · The Journal of Clinical Endocrinology & Metabolism · 2019 · 22 citations

Medicine, Endocrinology, Pediatrics +17

Novel heterozygous IGF1R mutation in two brothers with developing impaired glucose tolerance

Sebastian Burkhardt, Julia Gesing, Thomas Kapellen et al. · Journal of Pediatric Endocrinology and Metabolism · 2014 · 16 citations

Medicine, Endocrinology, Genetics +17