A.-E. Lehesjoki

<i>SCN2A</i> mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain

Yunxiang Liao, Anna-Kaisa Anttonen, Esa Liukkonen et al. · Neurology · 2010 · 161 citations

Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.

A.-E. Lehesjoki, Marjaleena Koskiniemi, P. Sistonen et al. · Proceedings of the National Academy of Sciences · 1991 · 153 citations · Full text

Close Linkage, Systems Biology, Mendelian Disorder +13

Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia

Niklas Schwarz, Andreas Hahn, Thomas Bast et al. · Journal of Neurology · 2015 · 91 citations · Full text

Channelopathies, Neurophysiology, Genetic Disorder +7

The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8.

Esa Tahvanainen, Susanna Ranta, Aune Hirvasniemi et al. · Proceedings of the National Academy of Sciences · 1994 · 82 citations · Full text

Gene Locus, Cytogenetics, Childhood Epilepsy +15

Motor cortex and thalamic atrophy in Unverricht–Lundborg disease

Päivi Koskenkorva, Jelena Khyuppenen, Eini Niskanen et al. · Neurology · 2009 · 54 citations