Idiopathic lactic acidemia with developmental delay and type 1 muscle fiber atrophy: report of two patients
- 30 September 1993
- journal article
- case report
- Published by Elsevier in Brain & Development
- Vol. 15 (5) , 384-386
- https://doi.org/10.1016/0387-7604(93)90127-t
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Leigh encephalopathy: Histologic and biochemical analyses of muscle biopsiesPediatric Neurology, 1992
- Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigationsThe Journal of Pediatrics, 1991
- Strongly succinate dehydrogenase–reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodesAnnals of Neurology, 1991
- Benign reversible muscle cytochrome c oxidase deficiencyNeurology, 1986
- The Genetic Heterogeneity of Lactic Acidosis: Occurrence of Recognizable Inborn Errors of Metabolism in a Pediatric Population with Lactic AcidosisPediatric Research, 1980