A New Benign Adult Familial Myoclonic Epilepsy (BAFME) Pedigree Suggesting Linkage to Chromosome 2p11.1-q12.2
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概要
- 論文の詳細を見る
- 2004-02-01
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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Striano Pasquale
Epilepsy Center Department Of Neurological Sciences Federico Ii University
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Guerrini Renzo
Institute Of Child Neurology And Psychiatry University Of Pisa
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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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Striano Salvatore
Epilepsy Center Department Of Neurological Sciences University Of Naples Federico Ii
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De Fusco
Stem Cells Research Institute (scri) Dibit- S. Raffaele Hospital
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CHIFARI Rosanna
Epilepsy Center, S. Paolo Hospital
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CASARI Giorgio
Stem Cells Research Institute (SCRI), DIBIT-, S. Raffaele Hospital
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CANEVINI Maria
Epilepsy Center, S. Paolo Hospital
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Canevini Maria
Epilepsy Center S. Paolo Hospital
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Casari Giorgio
Stem Cells Research Institute (scri) Dibit- S. Raffaele Hospital
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Chifari Rosanna
Epilepsy Center S. Paolo Hospital
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Chifari Rosanna
Epilepsy Center Department Of Neurosciences "fatebenefratelli E Oftalmico" Hospital
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ELIA Maurizio
Department of Neurology, Oasi Institute for Research on Mental Retardation and Brain Aging (IRCCS)
関連論文
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- Adolescent Onset of Idiopathic Photosensitive Occipital Epilepsy After Remission of Benign Rolandic Epilepsy
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- A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms
- 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)
- Continuous Spike-and-Wave Activity During Slow-Wave Sleep : Syndrome or EEG Pattern?
- Sleep disturbances in Angelman syndrome : a questionnaire study
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- 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
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