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3. Fatal lipid storage myopathy in an infant: case report and autopsy findings. Esiri MM; Bower BD; Ross BD J Neurol Sci; 1979 Mar; 41(1):93-100. PubMed ID: 438846 [TBL] [Abstract][Full Text] [Related]
4. A hereditary case of lipid storage myopathy with carnitine deficiency. Ultrastructural observation of muscle tissue in parents. Pellegrini G; Scarlato G; Moggio M J Neurol; 1980; 223(2):73-84. PubMed ID: 6157005 [TBL] [Abstract][Full Text] [Related]
5. [Myopathy with carnitine deficiency and lactic acidosis. A contribution to differential diagnosis of carnitine deficiency myopathies and mitochondrial myopathies]. Cammann R; Dunker H; Schumacher H; Ruitenbeek W; Sperner J Z Arztl Fortbild (Jena); 1992 Jul; 86(13):667-71. PubMed ID: 1642019 [No Abstract] [Full Text] [Related]
6. Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult case. Mongini T; Doriguzzi C; Palmucci L; De Francesco A; Bet L; Manfredi L; Ponzetto C; Bresolin N Eur Neurol; 1992; 32(3):170-6. PubMed ID: 1592075 [TBL] [Abstract][Full Text] [Related]
7. Muscle carnitine deficiency in old age. Case report and therapeutic results. Martin JJ; Vercruyssen A; de Barsy T; Ceuterick C Clin Neurol Neurosurg; 1985; 87(4):275-81. PubMed ID: 4092408 [TBL] [Abstract][Full Text] [Related]
8. Cytochrome C oxidase-deficient mitochondria in mitochondrial myopathy. Haginoya K; Miyabayashi S; Iinuma K; Okino E; Maesaka H; Tada K Pediatr Neurol; 1992; 8(1):13-8. PubMed ID: 1313674 [TBL] [Abstract][Full Text] [Related]
9. Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle. Müller-Höcker J; Pongratz D; Deufel T; Trijbels JM; Endres W; Hübner G Virchows Arch A Pathol Anat Histopathol; 1983; 399(1):11-23. PubMed ID: 6298999 [TBL] [Abstract][Full Text] [Related]
10. Fatal systemic carnitine deficiency with lipid storage in skeletal muscle, heart, liver and kidney. Boudin G; Mikol J; Guillard A; Engel AG J Neurol Sci; 1976 Dec; 30(2-3):313-25. PubMed ID: 187738 [TBL] [Abstract][Full Text] [Related]
11. Systemic carnitine deficiency with peripheral nerve involvement morphological and biochemical study. Cornelio F; Peluchetti D; Rimoldi M; Testa D; Mora M; Negri S; DiDonato S Acta Neuropathol Suppl; 1981; 7():226-9. PubMed ID: 6261516 [TBL] [Abstract][Full Text] [Related]
12. Neuromuscular disorders with abnormal muscle mitochondria. Kamieniecka Z; Schmalbruch H Int Rev Cytol; 1980; 65():321-57. PubMed ID: 6993406 [No Abstract] [Full Text] [Related]
14. [A case of mitochondrial encephalomyopathy with a defect in electron transport at complex I and IV in skeletal muscle showing peripheral neuropathy]. Ohnishi A; Nakano S; Hashimoto T; Tsuji S; Murai Y Rinsho Shinkeigaku; 1988 Jan; 28(1):107-11. PubMed ID: 2838209 [No Abstract] [Full Text] [Related]
15. Hypotonia in infancy. Dubowitz V Acta Univ Carol Med Monogr; 1976; (75):13-8. PubMed ID: 1077757 [No Abstract] [Full Text] [Related]
16. Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin. Boustany RN; Aprille JR; Halperin J; Levy H; DeLong GR Ann Neurol; 1983 Oct; 14(4):462-70. PubMed ID: 6314875 [TBL] [Abstract][Full Text] [Related]