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3. [Myopathies related to lipid metabolism disorders (review of the literature)]. Aingorn ED; Zhurba LT; Koroleva IA; Timonina OV; Sitnikov VF Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(10):1441-4. PubMed ID: 494923 [No Abstract] [Full Text] [Related]
4. Effect of carnitine deprivation on carnitine homeostasis and energy metabolism in mice with systemic carnitine deficiency. Knapp AC; Todesco L; Torok M; Beier K; Krähenbühl S Ann Nutr Metab; 2008; 52(2):136-44. PubMed ID: 18417958 [TBL] [Abstract][Full Text] [Related]
5. Primary and secondary carnitine deficiency in man. Di Donato S Ital J Biochem; 1984; 33(4):285A-291A. PubMed ID: 6511302 [No Abstract] [Full Text] [Related]
8. Postpartum manifestation of a necrotising lipid storage myopathy associated with muscle carnitine deficiency. Köller H; Stoll G; Neuen-Jacob E J Neurol Neurosurg Psychiatry; 1998 Mar; 64(3):407-8. PubMed ID: 9527165 [No Abstract] [Full Text] [Related]
9. Carnitine and the twins. Bressler R N Engl J Med; 1970 Mar; 282(13):745-6. PubMed ID: 5416207 [No Abstract] [Full Text] [Related]
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]
11. [Exercise-induced malignant hyperthermia in a patient with familial ichthyosis vulgaris. Muscular carnitine deficiency as contributing factor (author's transl)]. Haegy JM; Laplatte G; Gollner JL; Eulry F; Clement R; Schneider F Nouv Presse Med; 1982 Jan; 11(2):115-7. PubMed ID: 7058128 [TBL] [Abstract][Full Text] [Related]
16. In vivo stable isotope studies in three patients affected with mitochondrial fatty acid oxidation disorders: limited diagnostic use of 1-13C fatty acid breath test using bolus technique. Jakobs C; Kneer J; Martin D; Boulloche J; Brivet M; Poll-The BT; Saudubray JM Eur J Pediatr; 1997 Aug; 156 Suppl 1():S78-82. PubMed ID: 9266222 [TBL] [Abstract][Full Text] [Related]
17. Carnitine-acylcarnitine carrier deficiency: identification of the molecular defect in a patient. Huizing M; Wendel U; Ruitenbeek W; Iacobazzi V; IJlst L; Veenhuizen P; Savelkoul P; van den Heuvel LP; Smeitink JA; Wanders RJ; Trijbels JM; Palmieri F J Inherit Metab Dis; 1998 Jun; 21(3):262-7. PubMed ID: 9686371 [No Abstract] [Full Text] [Related]
18. A biochemical approach to lipid storage myopathies. Di Donato S; Rimoldi M; Bertagnolio B; Uziel G; Wiesmann UN Biochem Exp Biol; 1977; 13(1):85-91. PubMed ID: 614047 [No Abstract] [Full Text] [Related]
19. [Carnitine deficiency in inborn errors of metabolism]. Sela BA; Lerman-Sagie T; Berkovitz M Harefuah; 1997 Nov; 133(10):419-23, 504. PubMed ID: 9418309 [TBL] [Abstract][Full Text] [Related]