Bonnefont JP - Search Results

1

Improvement of cystic fibrosis using antitumoral drugs: a hypothesis.

Faivre L, Bonnefont JP, Lyonnet S, Munnich A, Vekemans M. Faivre L, et al. Among authors: bonnefont jp. Med Hypotheses. 2000 Apr;54(4):580-1. doi: 10.1054/mehy.1999.0899. Med Hypotheses. 2000. PMID: 10859642

2

Approach to the patient with a fatty acid oxidation disorder.

Saudubray JM, Mitchell G, Bonnefont JP, Schwartz G, Nuttin C, Munnich A, Brivet M, Vassault A, Demaugre F, Rabier D, et al. Saudubray JM, et al. Among authors: bonnefont jp. Prog Clin Biol Res. 1992;375:271-88. Prog Clin Biol Res. 1992. PMID: 1438373 Review. No abstract available.

3

Clinical aspects of mitochondrial disorders.

Munnich A, Rustin P, Rötig A, Chretien D, Bonnefont JP, Nuttin C, Cormier V, Vassault A, Parvy P, Bardet J, et al. Munnich A, et al. Among authors: bonnefont jp. J Inherit Metab Dis. 1992;15(4):448-55. doi: 10.1007/BF01799603. J Inherit Metab Dis. 1992. PMID: 1528005

4

Alpha-ketoglutarate dehydrogenase deficiency presenting as congenital lactic acidosis.

Bonnefont JP, Chretien D, Rustin P, Robinson B, Vassault A, Aupetit J, Charpentier C, Rabier D, Saudubray JM, Munnich A. Bonnefont JP, et al. J Pediatr. 1992 Aug;121(2):255-8. doi: 10.1016/s0022-3476(05)81199-0. J Pediatr. 1992. PMID: 1640293

5

Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation.

Mitchell GA, Labuda D, Fontaine G, Saudubray JM, Bonnefont JP, Lyonnet S, Brody LC, Steel G, Obie C, Valle D. Mitchell GA, et al. Among authors: bonnefont jp. Proc Natl Acad Sci U S A. 1991 Feb 1;88(3):815-9. doi: 10.1073/pnas.88.3.815. Proc Natl Acad Sci U S A. 1991. PMID: 1992472 Free PMC article.

6

Clinical approach to inherited metabolic disorders in neonates.

Saudubray JM, Narcy C, Lyonnet L, Bonnefont JP, Poll The BT, Munnich A. Saudubray JM, et al. Among authors: bonnefont jp. Biol Neonate. 1990;58 Suppl 1:44-53. doi: 10.1159/000243299. Biol Neonate. 1990. PMID: 2265219 Review.

7

The fasting test in paediatrics: application to the diagnosis of pathological hypo- and hyperketotic states.

Bonnefont JP, Specola NB, Vassault A, Lombes A, Ogier H, de Klerk JB, Munnich A, Coude M, Paturneau-Jouas M, Saudubray JM. Bonnefont JP, et al. Eur J Pediatr. 1990 Dec;150(2):80-5. doi: 10.1007/BF02072043. Eur J Pediatr. 1990. PMID: 2279514

8

Clinical approach to inherited metabolic diseases in the neonatal period: a 20-year survey.

Saudubray JM, Ogier H, Bonnefont JP, Munnich A, Lombes A, Hervé F, Mitchel G, Thé BP, Specola N, Parvy P, et al. Saudubray JM, et al. Among authors: bonnefont jp. J Inherit Metab Dis. 1989;12 Suppl 1:25-41. doi: 10.1007/BF01799284. J Inherit Metab Dis. 1989. PMID: 2509810

9

[Respiratory chain diseases in infancy. Clinical presentation and diagnosis].

García Silva MT, Bonnefont JP, Rotig A, Romero N, Vassault A, Colonna M, Coude M, Rabier D, Munnich A, Fardeau M, et al. García Silva MT, et al. Among authors: bonnefont jp. An Esp Pediatr. 1989 Nov;31(5):421-30. An Esp Pediatr. 1989. PMID: 2559637 Review. Spanish.

10

[Urgent needs in genetics: clinical diagnosis of acute amino acid disorders of delayed onset].

Saudubray JM, Lyonnet S, Lombes A, Hervé F, Bonnefont JP, Munnich A, Ogier H. Saudubray JM, et al. Among authors: bonnefont jp. J Genet Hum. 1989 Dec;37(4-5):299-310. J Genet Hum. 1989. PMID: 2635710 French. No abstract available.

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