Divry P - Search Results

1

5-Oxoprolinuria (glutathione synthetase deficiency): a case with neonatal presentation and rapid fatal outcome.

Divry P, Roulaud-Parrot F, Dorche C, Zabot MT, Contraire B, Hagenfeldt L, Larsson A. Divry P, et al. J Inherit Metab Dis. 1991;14(3):341-4. doi: 10.1007/BF01811698. J Inherit Metab Dis. 1991. PMID: 1770788 No abstract available.

2

Isolated 3-methylcrotonyl-CoA carboxylase deficiency in a 16-month-old child.

Rolland MO, Divry P, Zabot MT, Guibaud P, Gomez S, Lachaux A, Loras I. Rolland MO, et al. Among authors: divry p. J Inherit Metab Dis. 1991;14(5):838-9. doi: 10.1007/BF01799962. J Inherit Metab Dis. 1991. PMID: 1779635 No abstract available.

3

A new case of isolated sulphite oxidase deficiency with rapid fatal outcome.

Vianey-Liaud C, Desjacques P, Gaulme J, Dorche C, Vanlieferinghen P, Dechelotte P, Divry P. Vianey-Liaud C, et al. Among authors: divry p. J Inherit Metab Dis. 1988;11(4):425-6. doi: 10.1007/BF01800433. J Inherit Metab Dis. 1988. PMID: 3149702 No abstract available.

4

Infantile form of carnitine palmitoyltransferase II deficiency in a girl with rapid fatal onset.

Vianey-Saban C, Stremler N, Paut O, Buttin T, Divry P, Zabot MT, Camboulives J, Mathieu M, Mousson B. Vianey-Saban C, et al. Among authors: divry p. J Inherit Metab Dis. 1995;18(3):362-3. doi: 10.1007/BF00710434. J Inherit Metab Dis. 1995. PMID: 7474909 No abstract available.

5

Carnitine palmitoyl transferase I deficiency presenting as a Reye-like syndrome without hypoglycaemia.

Vianey-Saban C, Mousson B, Bertrand C, Stamm D, Dumoulin R, Zabot MT, Divry P, Floret D, Mathieu M. Vianey-Saban C, et al. Among authors: divry p. Eur J Pediatr. 1993 Apr;152(4):334-8. doi: 10.1007/BF01956748. Eur J Pediatr. 1993. PMID: 8482285 Review.

6

Combined deficiency of xanthine oxidase and sulphite oxidase: diagnosis of a new case followed by an antenatal diagnosis.

Desjacques P, Mousson B, Vianey-Liaud C, Boulieu R, Bory C, Baltassat P, Divry P, Zabot MT, Cotte J, Lagier P, et al. Desjacques P, et al. Among authors: divry p. J Inherit Metab Dis. 1985;8 Suppl 2:117-8. doi: 10.1007/BF01811486. J Inherit Metab Dis. 1985. PMID: 3930856 No abstract available.

7

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

8

[Beta-ketothiolase deficiency: a case of ketoacidosis with hyperglycinemia].

Elleau C, Parrot-Roulaud F, Perel Y, Divry P, Rolland MO, Zabot MT, Middleton R, Guillard JM. Elleau C, et al. Among authors: divry p. Pediatrie. 1992;47(3):185-9. Pediatrie. 1992. PMID: 1319041 French.

9

L-2-hydroxyglutaric aciduria: two further cases.

Divry P, Jakobs C, Vianey-Saban C, Gibson KM, Michelakakis H, Papadimitriou A, Divari R, Chabrol B, Cournelle MA, Livet MO. Divry P, et al. J Inherit Metab Dis. 1993;16(3):505-7. doi: 10.1007/BF00711666. J Inherit Metab Dis. 1993. PMID: 7609438 No abstract available.

10

Sudden infant death syndrome: organic acid profiles in cerebrospinal fluid from 47 children and the occurrence of N-acetylaspartic acid.

Divry P, Vianey-Liaud C, Jakobs C, ten-Brink HJ, Dutruge J, Gilly R. Divry P, et al. J Inherit Metab Dis. 1990;13(3):330-2. doi: 10.1007/BF01799387. J Inherit Metab Dis. 1990. PMID: 2122095 No abstract available.

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