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9. [Alpers' infantile cerebral poliodystrophy. A case with abnormal hepatic pyruvate carboxylase]. Tommasi M; Jouvet-Telinge A; Kopp N; Pialat J; Gilly J Ann Anat Pathol (Paris); 1977; 22(4):337-42. PubMed ID: 615502 [TBL] [Abstract][Full Text] [Related]
10. A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q. Fischer JC; Ruitenbeek W; Gabreëls FJ; Janssen AJ; Renier WO; Sengers RC; Stadhouders AM; ter Laak HJ; Trijbels JM; Veerkamp JH Eur J Pediatr; 1986 Feb; 144(5):441-4. PubMed ID: 3956532 [TBL] [Abstract][Full Text] [Related]
11. Childhood mitochondrial myopathy with ophthalmoplegia. Land JM; Hockaday JM; Hughes JT; Ross BD J Neurol Sci; 1981 Sep; 51(3):371-82. PubMed ID: 7276984 [TBL] [Abstract][Full Text] [Related]
12. Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions. Kuriyama M; Umezaki H; Fukuda Y; Osame M; Koike K; Tateishi J; Igata A Neurology; 1984 Jan; 34(1):72-7. PubMed ID: 6537855 [TBL] [Abstract][Full Text] [Related]
13. [Cerebral poliodystrophy in childhood. Anatomo-clinical study of a case]. Guidugli Neto J; Mattosinho França LC; Scarante O; Melaragno R Arq Neuropsiquiatr; 1973 Dec; 31(4):313-8. PubMed ID: 4785065 [No Abstract] [Full Text] [Related]
14. [Mitochondrial myopathy with increased blood lactate and pyruvate levels among siblings in familial thiamine deficiency]. Sato Y; Kaji M; Osame M; Matsuishi T; Itokawa Y Rinsho Shinkeigaku; 1983 Aug; 23(8):668-77. PubMed ID: 6661867 [No Abstract] [Full Text] [Related]
16. A large head in a 2-year-old boy. Becker LE; Armstrong JB; Meloff KL J Pediatr; 1977 Sep; 91(3):499-502. PubMed ID: 894429 [No Abstract] [Full Text] [Related]
17. Familial chronic acidosis due to an error in lactate and pyruvate metabolism. Haworth JC; Ford JD; Younoszai MK Can Med Assoc J; 1967 Sep; 97(13):773-9. PubMed ID: 6050895 [No Abstract] [Full Text] [Related]
18. [Tapetoretinal degeneration, deafness, myoclonus, dementia, epilepsy with the presence of excess alpha-amino-n-butyric acid. Contribution to the study of leptomeningeal angiomatosis with leukodystrophy sudanophil and abiotrophic complexes]. Martin L; Martin JJ; Guazzi GC; Lowenthal A; Maniewski J J Neurol Sci; 1968; 6(2):217-36. PubMed ID: 4180009 [No Abstract] [Full Text] [Related]
19. Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature. Fukuhara N; Tokiguchi S; Shirakawa K; Tsubaki T J Neurol Sci; 1980 Jul; 47(1):117-33. PubMed ID: 6774061 [TBL] [Abstract][Full Text] [Related]
20. Familial progressive poliodystrophy with cirrhosis of the liver. Wefring KW; Lamvik JO Acta Paediatr Scand; 1967 May; 56(3):295-300. PubMed ID: 6033104 [No Abstract] [Full Text] [Related] [Next] [New Search]