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12. [Carnitine deficiency and carnitine therapy]. Künnert B Z Gesamte Inn Med; 1988 Jan; 43(1):1-5. PubMed ID: 3281380 [TBL] [Abstract][Full Text] [Related]
13. In vitro analysis of hepatic carnitine biosynthesis in human systemic carnitine deficiency. Rebouche CJ; Engel AG Clin Chim Acta; 1980 Oct; 106(3):295-300. PubMed ID: 7418229 [TBL] [Abstract][Full Text] [Related]
14. Autosomal recessive lethal infantile cytochrome C oxidase deficiency. Eshel G; Lahat E; Fried K; Barr J; Barash V; Gutman A; DiMauro S; Aladjem M Am J Dis Child; 1991 Jun; 145(6):661-4. PubMed ID: 1852096 [TBL] [Abstract][Full Text] [Related]
15. Carnitine-deficient myopathy as a presentation of tyrosinemia type I. Nissenkorn A; Korman SH; Vardi O; Levine A; Katzir Z; Ballin A; Lerman-Sagie T J Child Neurol; 2001 Sep; 16(9):642-4. PubMed ID: 11575602 [TBL] [Abstract][Full Text] [Related]
16. Familial congenital fiber type disproportion (CFTD) with an autosomal recessive inheritance. Jaffe M; Shapira J; Borochowitz Z Clin Genet; 1988 Jan; 33(1):33-7. PubMed ID: 3342545 [TBL] [Abstract][Full Text] [Related]
18. Lipid storage myopathy associated with recurrent Reye syndrome-like attacks, but with a normal carnitine level. Matsuishi T; Yuge K; Aramaki S; Yoshino M; Yoshida I; Yamashita F Brain Dev; 1988; 10(2):125-9. PubMed ID: 3389475 [TBL] [Abstract][Full Text] [Related]
19. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome. Bonioli E; Palmieri A; Bertola A; Bellini C Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417 [TBL] [Abstract][Full Text] [Related]