Magnetic resonance imaging in lactic acidosis

Journal of Inherited Metabolic Disease

Volumn 19, Issue 4, 1996, Pages 535-547

  Van Der Knaap, M S ^a   Jakobs, C ^a   Valk, J ^a  

^a VU UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN; BRAIN HYPOXIA; BRAIN ISCHEMIA; CONFERENCE PAPER; DIAGNOSTIC VALUE; DISORDERS OF CARBOHYDRATE METABOLISM; GLUCONEOGENESIS; HISTOPATHOLOGY; HUMAN; INBORN ERROR OF METABOLISM; LACTIC ACIDOSIS; NERVE DEGENERATION; NUCLEAR MAGNETIC RESONANCE IMAGING; WHITE MATTER;

EID: 0029785192     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01799114     Document Type: Conference Paper

References (7)

1. Aleck KA, Kaplan AM, Sherwood WG, Robinson BH (1988) In utero central nervous system damage in pyruvate dehydrogenase deficiency. Arch Neurol 45: 987-989.
2. Allard JC, Tilak S, Carter AP (1988) CT and MR of MELAS syndrome. Am J Neuroradiol 9: 1234-1238.
3. Atkin BM, Buist NRM, Utter MF, Leiter AB, Banker BO (1979) Pyruvate carboxylase deficiency and lactic acidosis in a retarded child without Leigh's disease. Pediatr Res 13: 109-116.
4. Bakker HD, Westra M, Overweg-Plandsoen WCG, et al (1994) Normalisation of severe cranial CT scan abnormalities after biotin in a case of biotinidase deficiency. Eur J Pediatr 153: 861.
5. Barkovich AJ, Good WV, Koch TK, Berg BO (1993) Mitochondrial disorders: analysis of their clinical and imaging characteristics. Am J Neuroradiol 14: 1119-1137.
6. Barth PG, Hoffmann GF, Jaeken J, et al (1992) L-2-Hydroxyglutaric acidemia: a novel inherited neurometabolic disease. Ann Neurol 32: 66-71.
7. Baumgartner ER, Suormala M, Wick H, et al (1989) Biotinidase deficiency: a cause of subacute necrotizing encephalomyelopathy (Leigh syndrome). Pediatr Res 26: 260-266.