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Review 1. Interrelationships of liver and brain with special reference to Reye syndrome.

Authors: J K Brown; H Imam
Journal: J Inherit Metab Dis Date: 1991 Impact factor: 4.982

2. Carnitine deficiency with cardiomyopathy presenting as neonatal hydrops: successful response to carnitine therapy.

Authors: P Steenhout; C Elmer; A Clercx; D Blum; D Gnat; S van Erum; F Vertongen; E Vamos
Journal: J Inherit Metab Dis Date: 1990 Impact factor: 4.982

3. Decreased serum carnitine in valproate induced Reye syndrome.

Authors: H Böhles; K Richter; E Wagner-Thiessen; H Schäfer
Journal: Eur J Pediatr Date: 1982-11 Impact factor: 3.183

Review 4. Defects of fatty acid oxidation in skeletal muscle.

Authors: D M Turnbull; K Bartlett; N J Watmough; I M Shepherd; H S Sherratt
Journal: J Inherit Metab Dis Date: 1987 Impact factor: 4.982

5. Systemic carnitine deficiency: benefit of oral carnitine supplements vs. persisting biochemical abnormalities.

Authors: M Duran; J B de Klerk; S K Wadman; H R Scholte; R P Beekman; F G Jennekens
Journal: Eur J Pediatr Date: 1984-08 Impact factor: 3.183

6. Kinetic compartmental analysis of carnitine metabolism in the human carnitine deficiency syndromes. Evidence for alterations in tissue carnitine transport.

Authors: C J Rebouche; A G Engel
Journal: J Clin Invest Date: 1984-03 Impact factor: 14.808

7. Carnitine metabolism and inborn errors.

Authors: A G Engel; C J Rebouche
Journal: J Inherit Metab Dis Date: 1984 Impact factor: 4.982

Review 8. l-Carnitine. A preliminary review of its pharmacokinetics, and its therapeutic use in ischaemic cardiac disease and primary and secondary carnitine deficiencies in relationship to its role in fatty acid metabolism.

Authors: K L Goa; R N Brogden
Journal: Drugs Date: 1987-07 Impact factor: 9.546

9. Carnitine transport in cultured muscle cells and skin fibroblasts from patients with primary systemic carnitine deficiency.

Authors: C J Rebouche; A G Engel
Journal: In Vitro Date: 1982-05

10. Possible deleterious effect of L-carnitine supplementation in a patient with mild multiple acyl-CoA dehydrogenation deficiency (ethylmalonic-adipic aciduria).

Authors: A Green; M A Preece; C de Sousa; R J Pollitt
Journal: J Inherit Metab Dis Date: 1991 Impact factor: 4.982