Ethylmalonic encephalopathy: phenotype-genotype description and review of its management.

Cardelo Autero, N; Cordón Martínez, A M; Ramos-Fernández, J M

Cardelo Autero, N; Cordón Martínez, A M; Ramos-Fernández, J M.

Affiliation

Cardelo Autero N; Servicio de Pediatría, Hospital Regional Universitario Materno-Infantil de Málaga, Málaga, Spain.
Cordón Martínez AM; Servicio de Pediatría (lactantes), Hospital Regional Universitario Materno-Infantil de Málaga, Málaga, Spain.
Ramos-Fernández JM; Sección de Neurología Pediátrica, Grupo IBIMA, Servicio de Pediatría, Hospital Regional Universitario Materno-Infantil de Málaga, Málaga, Spain. Electronic address: dr.jmramos@gmail.com.

Neurologia (Engl Ed) ; 36(9): 729-731, 2021.

Article in En | MEDLINE | ID: mdl-34274260

Subject(s)

Brain Diseases, Metabolic, Inborn; Purpura; Genotype; Humans; Phenotype

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Purpura / Brain Diseases, Metabolic, Inborn Limits: Humans Language: En Journal: Neurologia (Engl Ed) Year: 2021 Document type: Article Affiliation country: Spain

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