Divry P - Search Results

1

Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene.

Andresen BS, Bross P, Vianey-Saban C, Divry P, Zabot MT, Roe CR, Nada MA, Byskov A, Kruse TA, Neve S, Kristiansen K, Knudsen I, Corydon MJ, Gregersen N. Andresen BS, et al. Among authors: divry p. Hum Mol Genet. 1996 Apr;5(4):461-72. doi: 10.1093/hmg/5.4.461. Hum Mol Genet. 1996. PMID: 8845838

2

The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiency.

Andresen BS, Vianey-Saban C, Bross P, Divry P, Roe CR, Nada MA, Knudsen I, Gregersen N. Andresen BS, et al. Among authors: divry p. J Inherit Metab Dis. 1996;19(2):169-72. doi: 10.1007/BF01799421. J Inherit Metab Dis. 1996. PMID: 8739957 No abstract available.

3

Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients.

Vianey-Saban C, Divry P, Brivet M, Nada M, Zabot MT, Mathieu M, Roe C. Vianey-Saban C, et al. Among authors: divry p. Clin Chim Acta. 1998 Jan 12;269(1):43-62. doi: 10.1016/s0009-8981(97)00185-x. Clin Chim Acta. 1998. PMID: 9498103

4

A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiency.

Touma EH, Rashed MS, Vianey-Saban C, Sakr A, Divry P, Gregersen N, Andresen BS. Touma EH, et al. Among authors: divry p. Arch Dis Child. 2001 Jan;84(1):58-60. doi: 10.1136/adc.84.1.58. Arch Dis Child. 2001. PMID: 11124787 Free PMC article.

5

[Multiple acyl-CoA dehydrogenase deficiency. Report of 2 siblings].

Guffon N, Vianey-Saban C, Berthier JC, Till M, Bertrand C, Divry P, Guibaud P. Guffon N, et al. Among authors: divry p. Pediatrie. 1993;48(5):365-71. Pediatrie. 1993. PMID: 7777389 French.

6

[Generalized epilepsy disclosing medium-chain-acyl-CoA dehydrogenase deficiency].

Chabrol B, Mancini J, Bertrand C, Vianey-Saban C, Divry P, Livet MO, Pinsard N. Chabrol B, et al. Among authors: divry p. Arch Fr Pediatr. 1993 Jun-Jul;50(6):497-500. Arch Fr Pediatr. 1993. PMID: 8135611 French.

7

Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblasts.

Bertrand C, Dumoulin R, Divry P, Mathieu M, Vianey-Saban C. Bertrand C, et al. Among authors: divry p. Clin Chim Acta. 1992 Sep 15;210(1-2):75-91. doi: 10.1016/0009-8981(92)90047-t. Clin Chim Acta. 1992. PMID: 1424161

8

Determination of total fatty acids in plasma: cis-5-tetradecenoic acid (C14:1 omega-9) in the diagnosis of long-chain fatty acid oxidation defects.

Divry P, Vianey-Saban C, Mathieu M. Divry P, et al. J Inherit Metab Dis. 1999 May;22(3):286-8. doi: 10.1023/a:1005567030040. J Inherit Metab Dis. 1999. PMID: 10384388 No abstract available.

9

Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhood.

Divry P, David M, Gregersen N, Kølvraa S, Christensen E, Collet JP, Dellamonica C, Cotte J. Divry P, et al. Acta Paediatr Scand. 1983 Nov;72(6):943-9. doi: 10.1111/j.1651-2227.1983.tb09849.x. Acta Paediatr Scand. 1983. PMID: 6673498

10

Lethal dilated cardiomyopathy due to long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Martins E, Costa A, Silva E, Medina M, Cardoso ML, Vianey-Saban C, Divry P, Vilarinho L. Martins E, et al. Among authors: divry p. J Inherit Metab Dis. 1996;19(3):373-4. doi: 10.1007/BF01799273. J Inherit Metab Dis. 1996. PMID: 8803786 No abstract available.

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