Electroclinical and Genetic Findings in a Family with Cortical Tremor, Myoclonus, and Epilepsy
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概要
- 論文の詳細を見る
- 2005-12-01
著者
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MADIA Francesca
Laboratory of Human Genetics, E. O.
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ZARA Federico
Laboratory of Neurogenetics, Unit of Neuromuscular Disease, Gaslini Institute and University of Geno
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Madia Francesca
Laboratory Of Human Genetics E.o. Ospedali Galliera
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Madia Francesca
Laboratory Of Human Genetics Galliera Hospitals
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Zara Federico
Laboratory Of Neurogenetics Department Of Muscular And Neurodegenerative Disease "g. Gaslini&qu
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STRIANO Pasquale
Department of Neurological Sciences, Epilepsy Center, Federico II University
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MINETTI Carlo
Laboratory of Neurogenetics, Department of Muscular and Neurodegenerative disease, "G. Gaslini" Inst
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STRIANO Salvatore
Department of Neurological Sciences, Epilepsy Center, Federico II University
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Striano Salvatore
Department Of Neurological Sciences Epilepsy Center "federico Ii" University
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Striano Salvatore
Department Of Neurological Sciences Epilepsy Center Federico Ii University
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Minetti Carlo
Laboratory Of Neurogenetics Department Of Muscular And Neurodegenerative Disease "g. Gaslini&qu
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STRIANO Pasquale
Muscolar and Neurodegenerative Diseases Unit, G.Gaslini Institute
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Striano Pasquale
Muscolar And Neurodegenerative Diseases Unit G.gaslini Institute
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Striano Pasquale
Department Of Neurological Sciences Epilepsy Center "federico Ii" University
関連論文
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- Electroclinical and Genetic Findings in a Family with Cortical Tremor, Myoclonus, and Epilepsy
- Late-onset and Slow-progressing Lafora Disease in Four Siblings with EPM2B Mutation
- Cutis Verticis Gyrate : Mental Deficincy Syndrome: A Patient with Drug-Resistant Epilepsy and Polymicrogyria
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