Klaus Marquard

Prognostic relevance of MOG antibodies in children with an acquired demyelinating syndrome

Eva-Maria Hennes, Matthias Baumann, Kathrin Schanda et al. · Neurology · 2017 · 336 citations · Full text

Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy

Robert Kopajtich, Thomas J. Nicholls, Joanna Rorbach et al. · The American Journal of Human Genetics · 2014 · 152 citations · Full text

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

Homozygous dystroglycan mutation associated with a novel muscle–eye–brain disease-like phenotype with multicystic leucodystrophy

Tobias Geis, Klaus Marquard, Tanja Rödl et al. · Neurogenetics · 2013 · 79 citations

Homozygous Dystroglycan Mutation, Neurodegenerative Diseases, Mendelian Disorder +12

PROTON SPECTROSCOPY IN FIVE PATIENTS WITH LEIGH'S DISEASE AND MITOCHONDRIAL ENZYME DEFICIENCY

Ingeborg Krägeloh‐Mann, Wolfgang Grodd, M. Schöning et al. · Developmental Medicine & Child Neurology · 1993 · 52 citations

Neurological Disorder, Corticobasal Degeneration, Pathology +19