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3. [Studies of the clinicopathological changes of eight patients with lipid storage myopathy]. Wang C; Yin J; Xu X Zhonghua Bing Li Xue Za Zhi; 2001 Feb; 30(1):19-22. PubMed ID: 11866951 [TBL] [Abstract][Full Text] [Related]
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8. 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]
9. 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]
10. Lipid storage myopathies. A review of metabolic defect and of treatment. Angelini C J Neurol; 1976 Nov; 214(1):1-11. PubMed ID: 62824 [TBL] [Abstract][Full Text] [Related]
11. [Lipid storage myopathy--a contribution to the problem of the differential diagnosis of muscle dystrophy (Duchenne)]. Schmidt A; Hässler A Zentralbl Allg Pathol; 1983; 127(3-4):229-36. PubMed ID: 6880434 [TBL] [Abstract][Full Text] [Related]
12. [A case of myopathy with carnitine deficiency]. Martin P; Carrier H; Renaud JF; Kullmann B; Delpont E; Romey G; Cartier B; Bedoucha P Rev Neurol (Paris); 1986; 142(6-7):625-34. PubMed ID: 3797933 [TBL] [Abstract][Full Text] [Related]
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19. Mitochondria-lipid-glycogen myopathy, hyperlactacidemia, and carnitine deficiency. Di Donato S; Cornelio F; Balestrini MR; Bertagnolio B; Peluchetti D Neurology; 1978 Nov; 28(11):1110-6. PubMed ID: 568729 [TBL] [Abstract][Full Text] [Related]
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