Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review.

Pavone, Piero; Pappalardo, Xena Giada; Ruggieri, Martino; Falsaperla, Raffaele; Parano, Enrico

Pavone, Piero; Pappalardo, Xena Giada; Ruggieri, Martino; Falsaperla, Raffaele; Parano, Enrico.

Afiliação

Pavone P; Pediatric Clinic, Department of Clinical and Experimental Medicine, University Hospital AOU "Policlinico-Vittorio Emanuele", Catania, Italy.
Pappalardo XG; Unit of Catania, National Council of Research, Institute for Research and Biomedical Innovation (IRIB), Catania, Italy.
Ruggieri M; Department of Biomedical and Biotechnological Sciences (BIOMETEC), University of Catania, Catania, Italy.
Falsaperla R; Unit of Rare Diseases of the Nervous System in Childhood, Section of Pediatrics and Child Neuropsychiatry, Department of Catania, Italy, AOU "Policlinico PO San Marco, University of Catania, Catania, Italy.
Parano E; Unit of Pediatrics, Neonatology and Neonatal Intensive Care, and Pediatric Emergency, AOU "Policlinico", PO "San Marco", University of Catania, Catania, Italy.

Medicine (Baltimore) ; 101(31): e29413, 2022 Aug 05.

Article em En | MEDLINE | ID: mdl-35945798

Assuntos

Encefalopatias; Ataxia Cerebelar; Criança; Hemiplegia/terapia; Humanos; Lactente; Mutação; Fenótipo; ATPase Trocadora de Sódio-Potássio/genética; Síndrome

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encefalopatias / Ataxia Cerebelar Tipo de estudo: Prognostic_studies Limite: Child / Humans / Infant Idioma: En Revista: Medicine (Baltimore) Ano de publicação: 2022 Tipo de documento: Article

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