Striano Pasquale | Epilepsy Center Department Of Neurological Sciences Federico Ii University
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概要
- STRIANO Pasqualeの詳細を見る
- 同名の論文著者
- Epilepsy Center Department Of Neurological Sciences Federico Ii Universityの論文著者
関連著者
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Striano Pasquale
Epilepsy Center Department Of Neurological Sciences Federico Ii University
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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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CASTIGLIA Lucia
Oasi Institute for Research on Mental Retardation and Brain Aging (IRCCS)
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GALESI Ornella
Oasi Institute for Research on Mental Retardation and Brain Aging (IRCCS)
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BEBEK Nerses
Department of Neurology, Istanbul faculty of Medicine
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GURSES Candan
Department of Neurology, Istanbul faculty of Medicine
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BAYKAN Betul
Department of Neurology, Instanbul faculty of Medicine
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GIANOTTI Stefania
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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GENNARO Elena
Laboratory of Human Genetics, E.O. Ospedali Galliera
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Gianotti Stefania
Laboratory Of Human Genetics E. O.
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Guerrini Renzo
Institute Of Child Neurology And Psychiatry University Of Pisa And Irccs Fondazione Stella Maris
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Bebek Nerses
Department Of Neurology Istanbul Faculty Of Medicine
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Bebek Nerses
Department Of Applied Physiology University Of Ulm
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Gennaro Elena
Laboratory Of Human Genetics E.o. Ospedali Galliera
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Zara Federico
Laboratory Of Neurogenetics Department Of Muscular And Neurodegenerative Disease "g. Gaslini&qu
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Gurses Candan
Department Of Neurology Istanbul Faculty Of Medicine
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Guerrini Renzo
Institute Of Child Neurology And Psychiatry University Of Pisa
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Zara Federico
Laboratory Of Neurogenetics Unit Of Neuromuscular Disease Gaslini Institute And University Of Genova
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Baykan Betul
Department Of Neurology Instanbul Faculty Of Medicine
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De Fusco
Stem Cells Research Institute (scri) Dibit- S. Raffaele Hospital
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Michelucci Roberto
Department Of Neurosciences Bellaria Hospital
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Michelucci Roberto
Department Of Neurological Sciences Bellaria Hospital-university Of Bologna
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Striano Pasquale
Epilepsy Center Federico Ii University
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BARTOCCI Arnaldo
Unit of Neurophysiopathology, Hospital of Perugia
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MANCARDI Maria
Muscular and Neurodegenerative Disease Unit, Institute "G. Gaslini", University of Genova
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FICHERA Marco
Oasi Institute for Research on Mental Retardation and Brain Aging (IRCCS)
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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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CASTIGLIA Lucia
Laboratory of Genetic Diagnosis, Oasi Institute for Research on Mental Retardation and Brain Aging (
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GALESI Ornella
Laboratory of Genetic Diagnosis, Oasi Institute for Research on Mental Retardation and Brain Aging (
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PELLIGRA Sabina
Laboratory of Genetic Diagnosis, Oasi Institute for Research on Mental Retardation and Brain Aging (
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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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Mancardi Maria
Muscular And Neurodegenerative Disease Unit Institute "g. Gaslini" University Of Genova
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Bartocci Arnaldo
Unit Of Neurophysiopathology Hospital Of Perugia
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Chifari Rosanna
Epilepsy Center S. Paolo Hospital
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Pelligra Sabina
Laboratory Of Genetic Diagnosis Oasi Institute For Research On Mental Retardation And Brain Aging (i
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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)
著作論文
- Late-onset and Slow-progressing Lafora Disease in Four Siblings with EPM2B Mutation
- Partial monosomy Xq(Xq23→qter) and trisomy 4p(4p15.33→pter) in a woman with intractable focal epilepsy, borderline intellectual functioning, and dysmorphic features
- A New Benign Adult Familial Myoclonic Epilepsy (BAFME) Pedigree Suggesting Linkage to Chromosome 2p11.1-q12.2
- A t(4;9)(q34;p22) Translocation Associated with Partial Epilepsy, Mental Retardation, and Dysmorphism