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63. [Dietary intake, circulating levels and excretion of carnitine as a function of age in normal children]. Lalau Keraly J; Bougnères PF Arch Fr Pediatr; 1984 Dec; 41(10):715-9. PubMed ID: 6532361 [TBL] [Abstract][Full Text] [Related]
64. 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]
65. Fatty acid beta-oxidation in peroxisomes and mitochondria: the first, unequivocal evidence for the involvement of carnitine in shuttling propionyl-CoA from peroxisomes to mitochondria. Jakobs BS; Wanders RJ Biochem Biophys Res Commun; 1995 Aug; 213(3):1035-41. PubMed ID: 7654220 [TBL] [Abstract][Full Text] [Related]
66. L-carnitine: its therapeutic potential. DiPalma JR Am Fam Physician; 1986 Dec; 34(6):127-30. PubMed ID: 3788753 [No Abstract] [Full Text] [Related]
67. Primary carnitine deficiency in a male adult. Karmaniolas K; Ioannidis P; Liatis S; Dalamanga M; Papalambros T; Migdalis I J Med; 2002; 33(1-4):105-10. PubMed ID: 12939109 [TBL] [Abstract][Full Text] [Related]
68. Different ketogenic response to medium-chain triglycerides and to long-chain triglycerides in a case of muscular carnitine palmitoyltransferase deficiency. Sugiyama N; Wada Y; Morishita H; Nonaka I J Inherit Metab Dis; 1982; 5(4):233-4. PubMed ID: 6820447 [No Abstract] [Full Text] [Related]
69. Effects of dexamethasone on carnitine metabolism in liver and extrahepatic tissues. French TJ; Good AW; Palmer TN; Sugden MC Biosci Rep; 1985 Sep; 5(9):729-34. PubMed ID: 4084672 [TBL] [Abstract][Full Text] [Related]
70. Fuel utilization in subjects with carnitine palmitoyltransferase 2 gene mutations. Ørngreen MC; Dunø M; Ejstrup R; Christensen E; Schwartz M; Sacchetti M; Vissing J Ann Neurol; 2005 Jan; 57(1):60-6. PubMed ID: 15622536 [TBL] [Abstract][Full Text] [Related]
72. [Respiratory and renal dysfunctions due to lipid storage metabolic myopathy: case report]. Campos Filho Wde O; Nicolini E; Auxiliadora Martins M; Zucoloto S; Basile Filho A Arq Neuropsiquiatr; 2002 Sep; 60(3-A):647-50. PubMed ID: 12244409 [TBL] [Abstract][Full Text] [Related]
73. Muscle carnitine palmitoyltransferase II deficiency: clinical and molecular genetic features and diagnostic aspects. Deschauer M; Wieser T; Zierz S Arch Neurol; 2005 Jan; 62(1):37-41. PubMed ID: 15642848 [TBL] [Abstract][Full Text] [Related]
74. Recurrent exertional myalgia and myoglobinuria due to carnitine palmityltransferase deficiency. Argov Z; DiMauro S Isr J Med Sci; 1983 Jun; 19(6):552-4. PubMed ID: 6862863 [No Abstract] [Full Text] [Related]
75. Carnitine-acylcarnitine translocase deficiency with severe hypoglycemia and auriculo ventricular block. Translocase assay in permeabilized fibroblasts. Pande SV; Brivet M; Slama A; Demaugre F; Aufrant C; Saudubray JM J Clin Invest; 1993 Mar; 91(3):1247-52. PubMed ID: 8450053 [TBL] [Abstract][Full Text] [Related]
76. Recurrent metabolic decompensation in profound carnitine palmitoyltransferase II deficiency. Elpeleg ON; Joseph A; Branski D; Christensen E; Holme E; Demaugre F; Saudubray JM; Gutman A J Pediatr; 1993 Jun; 122(6):917-9. PubMed ID: 8501570 [TBL] [Abstract][Full Text] [Related]
77. [Human syndromes of carnitine deficiency (a review)]. Grinio LP Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(8):123-5. PubMed ID: 3057780 [No Abstract] [Full Text] [Related]
78. Carnitine and diseases of skeletal muscle. Nutr Rev; 1979 Jan; 37(1):8-10. PubMed ID: 431900 [No Abstract] [Full Text] [Related]
79. The use of carnitine in pediatric nutrition. Crill CM; Helms RA Nutr Clin Pract; 2007 Apr; 22(2):204-13. PubMed ID: 17374794 [TBL] [Abstract][Full Text] [Related]