Search Results - "Lommi, Markus"

Dravet syndrome: New potential genetic modifiers, imaging abnormalities, and ictal findings by Gaily, Eija, Anttonen, Anna‐Kaisa, Valanne, Leena, Liukkonen, Elina, Träskelin, Ann‐Liz, Polvi, Anne, Lommi, Markus, Muona, Mikko, Eriksson, Kai, Lehesjoki, Anna‐Elina

“…Summary Purpose Dravet syndrome is an autosomal dominant epileptic encephalopathy of childhood, which is caused mainly by SCN1A and PCHD19 mutations. Although…”
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Incidence and outcome of epilepsy syndromes with onset in the first year of life: A retrospective population‐based study by Gaily, Eija, Lommi, Markus, Lapatto, Risto, Lehesjoki, Anna‐Elina

“…Summary Objective Population‐based studies on infantile epilepsy syndromes are scarce. Our aim was to provide syndrome‐specific data on the incidence and…”
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