Trisomy 12p and epilepsy with myoclonic absences
スポンサーリンク
概要
著者
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Musumeci Sebastiano
Department Of Neurology Oasi Institute For Research On Mental Retardation And Brain Aging (irccs)
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ELIA Maurizio
Department of Neurology, Oasi Institute for Research on Mental Retardation and Brain Aging (IRCCS),
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Ferri Raffaele
Department Of Neurology Oasi Institute For Research On Mental Retardation And Brain Aging (irccs)
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Elia Maurizio
Department Of Neurology Oasi Institute For Research On Mental Retardation And Brain Aging (irccs)
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Elia Maurizio
Department Of Neurology Oasi Institute For Research On Mental Retardation And Brain Aging
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CAMMARATA Marina
Department of Cytogenetics, Oasi Institute for Research on Mental Retardation and Brain Aging (IRCCS
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Musumeci Sebastiano
Department Of Neurology Oasi Institute For Research On Mental Retardation And Brain Aging
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Cammarata Marina
Department Of Cytogenetics Oasi Institute For Research On Mental Retardation And Brain Aging (irccs)
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Ferri Raffaele
Department Of Neurology Oasi Institute For Research On Mental Retardation And Brain Aging
関連論文
- Myoclonic Absence-Like Seizures and Chromosome Abnormality Syndromes
- Chromosome Abnormalities and Epilepsy
- Sleep in subjects with autistic disrder : a neurophysiological and psychological study
- Audiogenic Seizures Susceptibility in Transgenic Mice with Fragile X Syndrome
- Trisomy 12p and epilepsy with myoclonic absences
- A further family with epilepsy, dementia and yellow teeth: the Kohlschutter syndrome
- Leigh syndrome and partial deficit of cytochrome c oxidase associated with epilesia partialis continua
- A New Benign Adult Familial Myoclonic Epilepsy (BAFME) Pedigree Suggesting Linkage to Chromosome 2p11.1-q12.2
- Mild Generalized Epilepsy and Developmental Disorder Associated with Large Inv Dup(15)
- Sleep disturbances in Angelman syndrome : a questionnaire study
- A t(4;9)(q34;p22) Translocation Associated with Partial Epilepsy, Mental Retardation, and Dysmorphism