Herbert Schreiber

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott et al. · The American Journal of Human Genetics · 2019 · 298 citations · Full text

Allelic Variant, Ultra-rare Genetic Variation, Whole-exome Sequencing Study +10

Timing function of the frontal cortex in sequential motor and learning tasks.

L. Deecke, H. H. Kornhuber, Wilfried Lang et al. · PubMed · 1985 · 181 citations

Motor Learning, Neuropsychology, Motor Skill +24

Cognitive function in bulbar– and spinal–onset amyotrophic lateral sclerosis

Herbert Schreiber, Tanja Gaigalat, Ursula Wiedemuth-Catrinescu et al. · Journal of Neurology · 2005 · 169 citations

Neurodegenerative Diseases, Neuropsychology, Neurological Functioning +10

X-linked bulbospinal neuronopathy: Kennedy disease.

Anne D. Sperfeld, J Karitzky, Dagmar Brummer et al. · PubMed · 2002 · 154 citations

Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial

Maggie C. Walter, Peter Reilich, Simone Thiele et al. · Orphanet Journal of Rare Diseases · 2013 · 102 citations · Full text