Leigh's encephalomyelopathy: an inborn error of gluconeogenesis.
about
Alaninuria, associated with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus in two sistersA guide to diagnosis and treatment of Leigh syndrome.Familial dystonia and visual failure with striatal CT lucenciesThiamine metabolism in disease.An inherited defect affecting the tricarboxylic acid cycle in a patient with congenital lactic acidosis.Inborn errors of metabolism. Vitamin-responsive genetic disease.Mitochondrial defects in neurodegenerative disease.Erythrocyte transketolase activity in suspected cases of Leigh's disease, or subacute necrotising encephalomyelopathyThe biotin-dependent carboxylase deficienciesA defect in pyruvate decarboxylase in a child with an intermittent movement disorder.Biotinidase deficiency: a survey of 10 casesNecrotizing encephalomyelopathy of Leigh. Neuropathological findings in 8 cases.Leigh's disease: significance of the biochemical changes in brain.A randomized double-blind placebo-controlled trial of thioctic acid in migraine prophylaxis.Acute respiratory failure precipitated by general anesthesia in Leigh's syndrome.Comparative appraisal of CT scan and MRI in the diagnosis of Leigh encephalomyelopathy in two siblings.Molecular characterization of pyruvate carboxylase deficiency in two consanguineous families.Neurologic presentations of mitochondrial disorders.
P2860
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P2860
Leigh's encephalomyelopathy: an inborn error of gluconeogenesis.
description
1968 nî lūn-bûn
@nan
1968年の論文
@ja
1968年論文
@yue
1968年論文
@zh-hant
1968年論文
@zh-hk
1968年論文
@zh-mo
1968年論文
@zh-tw
1968年论文
@wuu
1968年论文
@zh
1968年论文
@zh-cn
name
Leigh's encephalomyelopathy: an inborn error of gluconeogenesis.
@en
type
label
Leigh's encephalomyelopathy: an inborn error of gluconeogenesis.
@en
prefLabel
Leigh's encephalomyelopathy: an inborn error of gluconeogenesis.
@en
P2093
P2860
P356
P1476
Leigh's encephalomyelopathy: an inborn error of gluconeogenesis.
@en
P2093
P2860
P304
P356
10.1136/ADC.43.230.423
P407
P577
1968-08-01T00:00:00Z