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9. Historical Perspective on Clinical Trials of Carnitine in Children and Adults. Buist NR Ann Nutr Metab; 2016; 68 Suppl 3():1-4. PubMed ID: 27931034 [TBL] [Abstract][Full Text] [Related]
10. L-carnitine: its therapeutic potential. DiPalma JR Am Fam Physician; 1986 Dec; 34(6):127-30. PubMed ID: 3788753 [No Abstract] [Full Text] [Related]
11. L-carnitine Improved the Cardiac Function via the Effect on Myocardial Fatty Acid Metabolism in a Hemodialysis Patient. Kaneko M; Fukasawa H; Ishibuchi K; Niwa H; Yasuda H; Furuya R Intern Med; 2018 Dec; 57(24):3593-3596. PubMed ID: 30146554 [TBL] [Abstract][Full Text] [Related]
12. Dominantly inherited megalencephaly, muscle weakness, and myoliposis: a carnitine-deficient myopathy within the spectrum of the Ruvalcaba-Myhre-Smith syndrome. Powell BR; Budden SS; Buist NR J Pediatr; 1993 Jul; 123(1):70-5. PubMed ID: 8320628 [TBL] [Abstract][Full Text] [Related]
14. Six years' experience with carnitine supplementation in a patient with an inherited defective carnitine transport system. Christensen E; Vikre-Jørgensen J J Inherit Metab Dis; 1995; 18(2):233-6. PubMed ID: 7564256 [No Abstract] [Full Text] [Related]
15. [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]
16. [Pathogenesis and pathophysiology of carnitine deficiency, a predictable risk]. Rodrigues Pereira R; Przyrembel H; Scholte HR Tijdschr Kindergeneeskd; 1990 Oct; 58(5):145-51. PubMed ID: 2247875 [TBL] [Abstract][Full Text] [Related]
17. Urinary propionylcarnitine analysis for monitoring carnitine supplementation in inherited disorders of propionate metabolism. Sugiyama N; Matsuda I; Wada Y; Narisawa K; Kobayashi M; Kidouchi K J Inherit Metab Dis; 1994; 17(5):611-5. PubMed ID: 7837769 [No Abstract] [Full Text] [Related]
18. Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up. Yilmaz BS; Kor D; Mungan NO; Erdem S; Ceylaner S J Pediatr Endocrinol Metab; 2015 Sep; 28(9-10):1179-81. PubMed ID: 26030785 [TBL] [Abstract][Full Text] [Related]
19. [2 causes of muscle ache and reddish-brown urine following exertion]. Jennekens FG; Scholte HR; Koster JF; Bouvy JJ Ned Tijdschr Geneeskd; 1979 Sep; 123(36):1562-8. PubMed ID: 289908 [No Abstract] [Full Text] [Related]