Friederike Körber

Acetylcholine Receptor Pathway Mutations Explain Various Fetal Akinesia Deformation Sequence Disorders

Anne Michalk, Sigmar Stricker, Jutta Becker et al. · The American Journal of Human Genetics · 2008 · 139 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +8

The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration

Ghada M. H. Abdel‐Salam, Michaela Thoenes, Hanan H. Afifi et al. · Orphanet Journal of Rare Diseases · 2014 · 87 citations · Full text

A homozygous RAB3GAP2 mutation causes Warburg Micro syndrome

Guntram Borck, Heidrun Lioba Wunram, Angela Steiert et al. · Human Genetics · 2010 · 83 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +8

Deep brain stimulation is effective in pediatric patients with GNAO1 associated severe hyperkinesia

Anne Koy, Victoria González, Kerstin Becker et al. · Journal of the Neurological Sciences · 2018 · 74 citations

Deep Brain Stimulation, Neurobiology Of Disease, Neuromodulation (Medicine) +10

Intranasal breast milk for premature infants with severe intraventricular hemorrhage—an observation

Titus Keller, Friederike Körber, André Oberthuer et al. · European Journal of Pediatrics · 2018 · 51 citations · Full text