Acute Ophthalmoplegia with Wernicke-Like MRI Pattern in a Patient with HPDL-Related Disorder.

Sartorelli, Jacopo; Longo, Daniela; Travaglini, Lorena; Orlando, Valeria; D'Amico, Adele; Bertini, Enrico; Nicita, Francesco

Sartorelli, Jacopo; Longo, Daniela; Travaglini, Lorena; Orlando, Valeria; D'Amico, Adele; Bertini, Enrico; Nicita, Francesco.

Afiliação

Sartorelli J; Unit of Neuromuscular and Neurodegenerative Diseases, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Longo D; Neuroradiology Unit, Imaging Department, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Travaglini L; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Orlando V; Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
D'Amico A; Unit of Neuromuscular and Neurodegenerative Diseases, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Bertini E; Unit of Neuromuscular and Neurodegenerative Diseases, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Nicita F; Unit of Neuromuscular and Neurodegenerative Diseases, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Mov Disord Clin Pract ; 2024 Jun 28.

Article em En | MEDLINE | ID: mdl-38940375

Palavras-chave

SPG83; Wernicke encephalopathy; ataxia; hereditary spastic paraplegia; mitochondrial disease; spasticity; thiamine

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Mov Disord Clin Pract Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

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