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Methylmalonic aciduria as a biochemical marker for mitochondrial DNA depletion syndrome in patients with developmental delay and movement disorders: a case series.
Almudhry, Montaha; Saini, Arushi Gahlot; Al-Omari, Mohammed A; Sharma, Yashu; Nouri, Maryam Nabavi; Rupar, C Anthony; Prasad, Chitra; Yu, Andrea C; Attri, Savita Verma; Prasad, Asuri Narayan.
Afiliación
  • Almudhry M; London Health Sciences Centre, London, ON, Canada.
  • Saini AG; Department of Neuroscience, King Fahad Specialist Hospital, Dammam, Saudi Arabia.
  • Al-Omari MA; Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Sharma Y; Department of Pediatrics, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
  • Nouri MN; King Fahad Hospital of the University, Al-Khobar, Saudi Arabia.
  • Rupar CA; Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Prasad C; London Health Sciences Centre, London, ON, Canada.
  • Yu AC; Department of Pediatrics, University of Western Ontario, London, ON, Canada.
  • Attri SV; Department of Clinical Neurological Science, Western University, London, ON, Canada.
  • Prasad AN; London Health Sciences Centre, London, ON, Canada.
Front Neurol ; 14: 1265115, 2023.
Article en En | MEDLINE | ID: mdl-38073635
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Neurol Año: 2023 Tipo del documento: Article País de afiliación: Canadá
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Neurol Año: 2023 Tipo del documento: Article País de afiliación: Canadá