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Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy.
Amadori, Elisabetta; Pellino, Giuditta; Bansal, Lalit; Mazzone, Serena; Møller, Rikke S; Rubboli, Guido; Striano, Pasquale; Russo, Angelo.
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  • Amadori E; Pediatric Neurology and Muscular Disease Unit, IRCCS G. Gaslini Institute, 16147, Genoa, Italy; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Italy.
  • Pellino G; Pediatric Unit, Azienda USL Ferrara - Sant'Anna University Hospital of Ferrara, Ferrara, Italy; Department of Neuroscience and Rehabilitation, University of Ferrara, Ferrara, Italy.
  • Bansal L; Division of Neurology, Children's Mercy Hospital, University of Missouri Kansas City, Missouri, United States.
  • Mazzone S; IRCCS, Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
  • Møller RS; Department for genetics and Personalized Medicine, Danish Epilepsy Centre, Dianalund, Denmark; Institute for Regional Health Services Research, University of Southern Denmark, Odense, Denmark.
  • Rubboli G; Department of Neurology, Danish Epilepsy Center (Member of the European Reference Network EpiCARE), Dianalund, Denmark; University of Copenhagen, Copenhagen, Denmark.
  • Striano P; Pediatric Neurology and Muscular Disease Unit, IRCCS G. Gaslini Institute, 16147, Genoa, Italy; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Italy.
  • Russo A; IRCCS, Istituto delle Scienze Neurologiche di Bologna, UOC Neuropsichiatria dell'età pediatrica, Bologna, Italy. Electronic address: russo.neuroped@gmail.com.
Eur J Med Genet ; 65(4): 104450, 2022 Apr.
Article en En | MEDLINE | ID: mdl-35219921
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Ataxia / Epilepsia Límite: Humans Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Italia
Texto completo
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XML
PubMed Links
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Ataxia / Epilepsia Límite: Humans Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Italia