Carnitine supplementation for inborn errors of metabolism-Reference-Cited by-同舟云学术

Carnitine supplementation for inborn errors of metabolism

Published:2012-02-15 Issue: Volume: Page:
ISSN:1465-1858
Container-title:Cochrane Database of Systematic Reviews
language:en
Short-container-title:

Author:

Nasser Mona¹,Javaheri Hoda²,Fedorowicz Zbys³,Noorani Zaman⁴

Affiliation:

1. Plymouth University Peninsula Schools of Medicine and Dentistry; Peninsula Dental School; The John Bull Building, Tamar Science Park, Plymouth UK PL6 8BU

2. Animal Science research Institute; Beheshti Street Karaj Iran 31585

3. Cochrane; Bahrain Branch; Box 25438 Awali Bahrain

4. National Iranian Offshore Oil Company (NIOOC); Ciris Clinic; App. 10, No:15, Fifth Alley, Dehghan Villa aval St., Beheshti Ave. Karaj Iran 31398 65161

Publisher

Wiley

Subject

Pharmacology (medical)

Reference55 articles.

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2. Diagnosis and management of glutaric aciduria type I;Baric;Journal of Inherited Metabolic Disease,1998

3. The measurement of carnitine and acyl-carnitines: application to the investigation of patients with suspected inherited disorders of mitochondrial fatty acid oxidation;Bhuiyan;Clinica Chimica Acta,1992

4. Age at symptom onset predicts severity of motor impairment and clinical outcome of glutaric acidemia type 1;Bjugstad;Journal of Pediatrics,2000

5. Inadequate iron availability as a possible cause of low serum carnitine concentrations in patients with phenylketonuria;Bohles;European Journal of Pediatrics,1991

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