R. Kálmánchey

Homozygosity (E140K) in <i>SCO2</i> causes delayed infantile onset of cardiomyopathy and neuropathy

Michaela Jaksch, Rita Horváth, Nina Horn et al. · Neurology · 2001 · 81 citations

Aicardi-Goutières Syndrome Displays Genetic Heterogeneity with One Locus (AGS1) on Chromosome 3p21

Yanick J. Crow, Andrew P. Jackson, Emma Roberts et al. · The American Journal of Human Genetics · 2000 · 78 citations · Full text

Allelic Variant, Genetic Disorder, Genetics +10

Megalencephalic leukoencephalopathy with cysts without <i>MLC1</i> defect

Marjo S. van der Knaap, Vincent Lai, Wolfgang Köhler et al. · Annals of Neurology · 2010 · 61 citations

Neurological Disorder, Corticobasal Degeneration, Pathology +19

Converging evidences on language impairment in Landau–Kleffner Syndrome revealed by behavioral and brain activity measures: A case study

Ferenc Honbolygó, Valéria Csépe, Attila Fekésházy et al. · Clinical Neurophysiology · 2006 · 42 citations

Neuropsychological Functioning, Neurolinguistics, Case Study +9

Evoked potentials in the rett syndrome

R. Kálmánchey · Brain and Development · 1990 · 39 citations

Neurophysiology, Neuroanatomy, Medicine +10