Alpers progressive infantile neuronal poliodystrophy: An acute neonatal form with findings of the fetal akinesia syndrome
- 1 August 1993
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 47 (1) , 31-36
- https://doi.org/10.1002/ajmg.1320470107
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Transmission of Alpers' disease (chronic progressive encephalopathy) produces experimental Creutzfeldt‐Jakob disease in hamstersNeurology, 1989
- Agyria ? pachygyria and Miller-Dieker syndrome: clinical, genetic and chromosome studiesHuman Genetics, 1988
- The Pena-Shokeir syndrome: Report of five cases and further delineation of the syndromeAmerican Journal of Medical Genetics, 1983
- Progressive Infantile PoliodystrophyArchives of Neurology, 1981
- Pyruvate Carboxylase Deficiency and Lactic Acidosis in a Retarded Child without Leigh's DiseasePediatric Research, 1979
- Fatal Lactic Acidosis in a Newborn Attributable to a Congenital Defect of Pyruvate DehydrogenasePediatric Research, 1976
- Familial poliodystrophy, mitochondrial myopathy, and lactate acidemiaNeurology, 1975
- Alpers' disease ? A variant of Creutzfeldt-Jakob disease and subacute spongiform encephalopathy?Acta Neuropathologica, 1968
- The Syndrome of Progressive Cerebral PoliodystrophyArchives of Neurology, 1964
- PROGRESSIVE CEREBRAL DEGENERATION OF INFANCYJournal of Nervous & Mental Disease, 1960