Christoph Korenke

Biochemical and molecular characterization of 18 patients with pyridoxine-dependent epilepsy and mutations of the antiquitin (ALDH7A1) gene

Barbara Plecko, Karl Paul, Eduard Paschke et al. · Human Mutation · 2006 · 166 citations

Possible Pde, Molecular Pharmacology, Molecular Characterization +14

Autosomal dominant Glut‐1 deficiency syndrome and familial epilepsy

Knut Brockmann, Dong Wang, Christoph Korenke et al. · Annals of Neurology · 2001 · 161 citations · Full text

Persisting myelin oligodendrocyte glycoprotein antibodies in aquaporin-4 antibody negative pediatric neuromyelitis optica

Kevin Rostásy, Simone Mader, EM Hennes et al. · Multiple Sclerosis Journal · 2012 · 151 citations

Antibodies to MOG and AQP4 in children with neuromyelitis optica and limited forms of the disease

Christian Lechner, Matthias Baumann, Eva-Maria Hennes et al. · Journal of Neurology Neurosurgery & Psychiatry · 2015 · 117 citations · Full text

Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex

Sonja Stahl, Sabine Gaetzner, Bettina Brackertz et al. · Human Mutation · 2008 · 112 citations

Genetics, Splice Variant, Pathology +16