Case report: Motor neuron disease phenotype associated with symptomatic copper deficiency: Challenging diagnosis and treatment.

Benkirane, Adam; Warlop, Thibault; Ivanoiu, Adrian; Baret, Pierre; Wiame, Elsa; Haufroid, Vincent; Duprez, Thierry; Hantson, Philippe

Benkirane, Adam; Warlop, Thibault; Ivanoiu, Adrian; Baret, Pierre; Wiame, Elsa; Haufroid, Vincent; Duprez, Thierry; Hantson, Philippe.

Afiliação

Benkirane A; Department of Neurology, Cliniques Universitaires St-Luc, Brussels, Belgium.
Warlop T; Department of Neurology, Cliniques Universitaires St-Luc, Brussels, Belgium.
Ivanoiu A; Institute of Neurosciences, Université Catholique de Louvain, Brussels, Belgium.
Baret P; Department of Neurology, Cliniques Universitaires St-Luc, Brussels, Belgium.
Wiame E; Hospital Pharmacy, Cliniques Universitaires St-Luc, Brussels, Belgium.
Haufroid V; Laboratory of Physiological Chemistry, Université Catholique de Louvain and the Christian de Duve Institute of Cellular Pathology, Brussels, Belgium.
Duprez T; Laboratory of Toxicology, Cliniques Universitaires St-Luc, Brussels, Belgium.
Hantson P; Louvain Centre for Toxicology and Applied Pharmacology, Université Catholique de Louvain, Brussels, Belgium.

Front Neurol ; 13: 1063803, 2022.

Article em En | MEDLINE | ID: mdl-36686537

Palavras-chave

amyotrophic lateral sclerosis (ALS); cerulopasmin; copper deficiency; motoneuron; myelopathy

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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