Secondary inhibition of multiple NAD-requiring dehydrogenases in respiratory chain complex I deficiency: Possible metabolic markers for the primary defect-Reference-Cited by-同舟云学术

Secondary inhibition of multiple NAD-requiring dehydrogenases in respiratory chain complex I deficiency: Possible metabolic markers for the primary defect

Published:1993 Issue:3 Volume:16 Page:560-562
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Bennett M. J.,Sherwood W. G.,Gibson K. M.,Burlina A. B.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://www.springerlink.com/index/pdf/10.1007/BF00711681

Reference7 articles.

1. Bakkeren JAJM, Sengers RCA, Ruitenbeek W, Trijbels JMF (1992) 3-Methylglutaconic aciduria in a patient with disturbed mitochondrial energy metabolism.Eur J Pediatr 152: 313.

2. Chalmers RA (1984) Organic acids in urine of patient with congenital lactic acidosis: An aid to differential diagnosis.J Inher Metab Dis 7(Suppl 1): 179?189.

3. Christodoulou J, Petrova-Benedict R, Robinson B, Clarke J (1991) A unique patient with the neonatal Marfan syndrome and Complex I deficiency.Abstracts 29th Symposium SSIEM, P- 92.

4. Ribes A, Ridor E, Sancho S et al (1990) Tiglylglycine in two patients with C6?C14 3-hydroxydicarboxylic aciduria.Abstracts 28th Symposium SSIEM, P- 104.

5. Robinson BH (1989) Lactic acidemia. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic Basis of Inherited Disease, 6th edn. New York: McGraw-Hill, 869?888.

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