Ingeborg Krägeloh‐Mann

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Markus Wolff, Katrine M. Johannesen, Ulrike B. S. Hedrich et al. · Brain · 2017 · 558 citations · Full text

Decreasing prevalence in cerebral palsy: a multi‐site European population‐based study, 1980 to 2003

Élodie Sellier, Mary Jane Platt, Guro L. Andersen et al. · Developmental Medicine & Child Neurology · 2015 · 466 citations · Full text

Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation

Gert C. Scheper, Thom van der Klok, Rob J. van Andel et al. · Nature Genetics · 2007 · 450 citations

Amyotrophic Lateral Sclerosis, Mitochondrial Function, Neurological Disorder +13

Reorganization in congenital hemiparesis acquired at different gestational ages

Martin Staudt, Christian Gerloff, Wolfgang Grodd et al. · Annals of Neurology · 2004 · 266 citations · Full text

tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia

Birgit Budde, Yasmin Namavar, P. G. Barth et al. · Nature Genetics · 2008 · 251 citations

Genetic Disorder, Natural Sciences, Genetics +5