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4. Fatal cases of lipid storage myopathy with carnitine deficiency. Cornelio F; Di Donato S; Peluchetti D; Bizze A; Bertagnolio B; D'Angelo A; Wiesmann U J Neurol Neurosurg Psychiatry; 1977 Feb; 40(2):170-8. PubMed ID: 194020 [TBL] [Abstract][Full Text] [Related]
5. Successful treatment of familial idiopathic lipid storage myopathy with L-carnitine and modified lipid diet. Snyder TM; Little BW; Roman-Campos G; McQuillen JB Neurology; 1982 Oct; 32(10):1106-15. PubMed ID: 6889698 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Lipid storage myopathy: successful treatment with propranolol. Martyn C; Jellinek EH; Webb JN Br Med J (Clin Res Ed); 1981 Jun; 282(6281):1997-9. PubMed ID: 6788163 [TBL] [Abstract][Full Text] [Related]
8. Short-chain acyl-CoA dehydrogenase deficiency associated with a lipid-storage myopathy and secondary carnitine deficiency. Turnbull DM; Bartlett K; Stevens DL; Alberti KG; Gibson GJ; Johnson MA; McCulloch AJ; Sherratt HS N Engl J Med; 1984 Nov; 311(19):1232-6. PubMed ID: 6493275 [No Abstract] [Full Text] [Related]
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10. [Carnitine deficiency myopathy: a case of late diagnosis]. Rico Corral MA; de la Vega Vázquez JM; Holgado Silva C; Aznar Martín A; Zamora Madaría E An Med Interna; 2002 Aug; 19(8):415-8. PubMed ID: 12244790 [TBL] [Abstract][Full Text] [Related]