Increased brain lactate during stroke-like episode in a patient with congenital disorder of glycosylation type Ia
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health
Reference5 articles.
1. Neurological presentation in pediatric patients with congenital disorders of glycosylation type Ia;Miossec-Chauvet;Neuropediatrics,2003
2. Ishikawa N, Tajima G, Ono H, Kobayashi M. Different neuroradiological findings during two stroke-like episodes in a patient with a congenital disorder of glycosylation type Ia. Brain Dev (2008), doi:10.1016/j.braindev.2008.03.012.
3. Congenital disorders of glycosylation: a review;Grünewald;Pediatr Res,2002
4. Congenital disorders of glycosylation (CDG) may be underdiagnosed when mimicking mitochondrial disease;Briones;Eur J Paediatr Neurol,2001
5. Regulation of mitochondrial oxidative phosphorylation through cell signaling;Hüttemann;Biochim Biophys Acta,2007
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5. International clinical guidelines for the management of phosphomannomutase 2‐congenital disorders of glycosylation: Diagnosis, treatment and follow up;Journal of Inherited Metabolic Disease;2019-01
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