Mild Generalized Epilepsy and Developmental Disorder Associated with Large Inv Dup(15)
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概要
- 論文の詳細を見る
- 2002-09-01
著者
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Guerrini Renzo
Institute Of Child Neurology And Psychiatry University Of Pisa And Irccs Fondazione Stella Maris
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Elia Maurizio
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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Sgro Vincenzo
Regional Centre Of Epilepsy San Paolo Hospital Milano
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CHIFARI Rosanna
Epilepsy Center, S. Paolo Hospital
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CHIFARI Rosanna
Regional Centre of Epilepsy, San Paolo Hospital Milano
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GUERRINI Renzo
Nuroscieces Unit, Institute of Child Health and Great Ormond Street Hospital for Children, Universit
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CAVANI Simona
Laboratory of Human Genetics, Hospital Galliera
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CANGER Raffaele
Regional Centre of Epilepsy, San Paolo Hospital Milano
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CANEVINI Maria
Regional Centre of Epilepsy, San Paolo Hospital Milano
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Canger Raffaele
Regional Centre Of Epilepsy San Paolo Hospital Milano
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Canevini Maria
Epilepsy Center S. Paolo Hospital
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Cavani Simona
Laboratory Of Human Genetics Hospital Galliera
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Chifari Rosanna
Epilepsy Center S. Paolo Hospital
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Canevini Maria
Regional Centre Of Epilepsy San Paolo Hospital Milano
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ELIA Maurizio
Department of Neurology, Oasi Institute for Research on Mental Retardation and Brain Aging (IRCCS)
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
- Partial monosomy Xq(Xq23→qter) and trisomy 4p(4p15.33→pter) in a woman with intractable focal epilepsy, borderline intellectual functioning, and dysmorphic features
- 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
- Chromosome 20 Ring : A Chromosomal Disorder Associated with a Particular Electroclinical Pattern
- 4p^- Syndrome: A Chromosomal Disorder Associated with a Particular EEG Pattern
- Ictal EEG patterns in epilepsy with centro-temporal spikes