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22. Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome. Engel AG; Angelini C Science; 1973 Mar; 179(4076):899-902. PubMed ID: 4687787 [TBL] [Abstract][Full Text] [Related]
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27. Metabolic response to exercise and muscle disease. Sahgal V; Solomon R Compr Ther; 1986 Jan; 12(1):31-8. PubMed ID: 2936540 [TBL] [Abstract][Full Text] [Related]
28. Activity of hepatic but not skeletal muscle carnitine palmitoyltransferase enzyme is depressed by intravenous glucose infusions in lactating dairy cows. Al-Trad B; Wittek T; Gäbel G; Fürll M; Reisberg K; Aschenbach JR J Anim Physiol Anim Nutr (Berl); 2010 Dec; 94(6):685-95. PubMed ID: 20546068 [TBL] [Abstract][Full Text] [Related]
29. A patient with lethal cardiomyopathy and a carnitine-acylcarnitine translocase deficiency. Niezen-Koning KE; van Spronsen FJ; Ijlst L; Wanders RJ; Brivet M; Duran M; Reijngoud DJ; Heymans HS; Smit GP J Inherit Metab Dis; 1995; 18(2):230-2. PubMed ID: 7564255 [No Abstract] [Full Text] [Related]
30. Molecular analysis of a presymptomatic case of carnitine palmitoyl transferase I (CPT I) deficiency detected by tandem mass spectrometry newborn screening in Japan. Tsuburaya R; Sakamoto O; Arai N; Kobayashi H; Hasegawa Y; Yamaguchi S; Shigematsu Y; Takayanagi M; Ohura T; Tsuchiya S Brain Dev; 2010 May; 32(5):409-11. PubMed ID: 19345525 [TBL] [Abstract][Full Text] [Related]
31. 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]
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33. 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]