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5. Mitochondrial myopathy with diffuse activation and focal deficiency of mitochondrial ATPase and carnitine deficiency. Müller-Höcker J; Paetzke I; Pongratz D; Hübner G Virchows Arch B Cell Pathol Incl Mol Pathol; 1985; 48(2):185-96. PubMed ID: 2859691 [TBL] [Abstract][Full Text] [Related]
6. Carnitine deficiency of skeletal muscle: report of a treated case. Angelini C; Lücke S; Cantarutti F Neurology; 1976 Jul; 26(7):633-7. PubMed ID: 945511 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Corticosteroid-responsive skeletal muscle disease associated with partial carnitine deficiency: studies of liver and metabolic alterations. Whitaker JN; Dimauro S; Solomon SS; Sabesin S; Duckworth WC; Mendell JR Am J Med; 1977 Nov; 63(5):805-15. PubMed ID: 201171 [TBL] [Abstract][Full Text] [Related]
9. Systemic carnitine deficiency: clinical, biochemical, and morphological cure with L-carnitine. Di Donato S; Pelucchetti D; Rimoldi M; Mora M; Garavaglia B; Finocchiaro G Neurology; 1984 Feb; 34(2):157-62. PubMed ID: 6538002 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Weakness associated with the pathological presence of lipid in skeletal muscle: a detailed study of a patient with carnitine deficiencey. Isaacs H; Heffron JJ; Badenhorst M; Pickering A J Neurol Neurosurg Psychiatry; 1976 Nov; 39(11):1114-23. PubMed ID: 1011021 [TBL] [Abstract][Full Text] [Related]
12. The syndrome of carnitine deficiency. Di Donato S; Cornelio F Riv Patol Nerv Ment; 1976 Aug; 97(4):181-5. PubMed ID: 1032033 [TBL] [Abstract][Full Text] [Related]
13. The syndrome of carnitine deficiency: morphological and metabolic correlations in two cases. Scarlato G; Pellegrini G; Cerri C; Meola G; Veicsteinas A Can J Neurol Sci; 1978 May; 5(2):205-13. PubMed ID: 667748 [TBL] [Abstract][Full Text] [Related]
14. Familial carnitine deficiency. A fatal case and subclinical state in a sister. Scholte HR; Meijer AE; van Wijngaarden GK; Leenders KL J Neurol Sci; 1979 Jun; 42(1):87-101. PubMed ID: 156248 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Familial oculocranioskeletal neuromuscular disease with abnormal muscle mitochondria. Tamura K; Santa T; Kuroiwa Y Brain; 1974 Dec; 97(4):665-72. PubMed ID: 4154795 [No Abstract] [Full Text] [Related]