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23. Carnitine deficiency: clinical, morphological, and biochemical observations in a fatal case. Engel AG; Banker BQ; Eiben RM J Neurol Neurosurg Psychiatry; 1977 Apr; 40(4):313-22. PubMed ID: 874508 [TBL] [Abstract][Full Text] [Related]
24. [Morphological study of muscle fibers stained red by modified Gomori trichrome staining with special reference to smooth red fibers]. Yoshida K Hokkaido Igaku Zasshi; 1997 Mar; 72(2):163-80. PubMed ID: 9145310 [TBL] [Abstract][Full Text] [Related]
25. [Lipid myopathy: a heterogenic familial case]. Kuntzer T; Robert D; Cox J; Meier C; Schwartz A; Guelpa G; Pfister CE Schweiz Med Wochenschr; 1987 Dec; 117(50):2027-9. PubMed ID: 3433086 [TBL] [Abstract][Full Text] [Related]
26. [Lipidic myopathy with severe cardiomyopathy caused by a generalized carnitine deficiency. Favourable course during carnitine hydrochloride treatment]. Morand P; Despert F; Carrier HN; Saudubray BM; Fardeau M; Romieux B; Fauchier C; Combe P Arch Mal Coeur Vaiss; 1979 May; 72(5):536-44. PubMed ID: 115407 [TBL] [Abstract][Full Text] [Related]
27. Plasma and muscle free carnitine deficiency due to renal Fanconi syndrome. Bernardini I; Rizzo WB; Dalakas M; Bernar J; Gahl WA J Clin Invest; 1985 Apr; 75(4):1124-30. PubMed ID: 3988933 [TBL] [Abstract][Full Text] [Related]
28. Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges. Laforêt P; Vianey-Saban C Neuromuscul Disord; 2010 Nov; 20(11):693-700. PubMed ID: 20691590 [TBL] [Abstract][Full Text] [Related]
30. [Primary cardiomyopathy in children with lipid infiltration of the myocardium and skeletal muscles and demonstration of a palmityl-carnitine transferase deficiency. Apropos of 4 cases]. Normand J; Carrier H; Berthillier G; Bozio A; Jocteur-Monrozier D; André M; Joffre B Arch Mal Coeur Vaiss; 1979 May; 72(5):529-35. PubMed ID: 115406 [TBL] [Abstract][Full Text] [Related]
31. Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency. Koga Y; Nonaka I; Kobayashi M; Tojyo M; Nihei K Ann Neurol; 1988 Dec; 24(6):749-56. PubMed ID: 3144939 [TBL] [Abstract][Full Text] [Related]
32. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency. Stanley CA Adv Pediatr; 1987; 34():59-88. PubMed ID: 3318304 [TBL] [Abstract][Full Text] [Related]
33. [A case of progressive myopathy with tubular aggregates]. Kamakura K; Takeshita K; Sunohara N; Arahata K; Nonaka I Rinsho Shinkeigaku; 1989 Jun; 29(6):769-73. PubMed ID: 2684470 [TBL] [Abstract][Full Text] [Related]
34. Intracellular free [Ca2+] in human skeletal muscle with myopathic carnitine deficiency. López JR; Briceño LE; Cordovez G; Sánchez V; Linares N Gen Physiol Biophys; 1989 Apr; 8(2):91-8. PubMed ID: 2777061 [TBL] [Abstract][Full Text] [Related]
35. Muscle carnitine deficiency and lipid storage myopathy in patients with mitochondrial myopathy. Campos Y; Huertas R; Bautista J; Gutiérrez E; Aparicio M; Lorenzo G; Segura D; Villanueva M; Cabello A; Alesso L Muscle Nerve; 1993 Jul; 16(7):778-81. PubMed ID: 8505934 [TBL] [Abstract][Full Text] [Related]