Bougnères P - Search Results

1

Retroviral transfer and long-term expression of the adrenoleukodystrophy gene in human CD34+ cells.

Doerflinger N, Miclea JM, Lopez J, Chomienne C, Bougnères P, Aubourg P, Cartier N. Doerflinger N, et al. Among authors: bougneres p. Hum Gene Ther. 1998 May 1;9(7):1025-36. doi: 10.1089/hum.1998.9.7-1025. Hum Gene Ther. 1998. PMID: 9607414

2

Retroviral-mediated gene transfer corrects very-long-chain fatty acid metabolism in adrenoleukodystrophy fibroblasts.

Cartier N, Lopez J, Moullier P, Rocchiccioli F, Rolland MO, Jorge P, Mosser J, Mandel JL, Bougnères PF, Danos O, et al. Cartier N, et al. Among authors: bougneres pf. Proc Natl Acad Sci U S A. 1995 Feb 28;92(5):1674-8. doi: 10.1073/pnas.92.5.1674. Proc Natl Acad Sci U S A. 1995. PMID: 7878038 Free PMC article.

3

[Gene therapy of adrenoleukodystrophy].

Cartier N, Micléa JM, Chomienne C, Bougnères PF, Aubourg P. Cartier N, et al. Among authors: bougneres pf. Arch Pediatr. 1996;3 Suppl 1:77s-81s. doi: 10.1016/0929-693x(96)85998-7. Arch Pediatr. 1996. PMID: 8795973 Review. French. No abstract available.

4

Deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase: a cause of lethal myopathy and cardiomyopathy in early childhood.

Rocchiccioli F, Wanders RJ, Aubourg P, Vianey-Liaud C, Ijlst L, Fabre M, Cartier N, Bougneres PF. Rocchiccioli F, et al. Among authors: bougneres pf. Pediatr Res. 1990 Dec;28(6):657-62. doi: 10.1203/00006450-199012000-00023. Pediatr Res. 1990. PMID: 2284166

5

[Medium-chain acyl-CoA dehydrogenase deficiency: contribution of molecular biology].

Cartier N, Lepetit N, Rocchiccioli F, Bougnères PF. Cartier N, et al. Among authors: bougneres pf. Arch Pediatr. 1994 Mar;1(3):243-8. Arch Pediatr. 1994. PMID: 7994331 French.

6

Capillary gas-liquid chromatographic-mass spectrometric measurement of very long chain (C22 to C26) fatty acids in microliter samples of plasma.

Aubourg P, Bougnères PF, Rocchiccioli F. Aubourg P, et al. Among authors: bougneres pf. J Lipid Res. 1985 Feb;26(2):263-7. J Lipid Res. 1985. PMID: 3989386 Free article.

7

Medium- and long-chain dicarboxylic aciduria in patients with Zellweger syndrome and neonatal adrenoleukodystrophy.

Rocchiccioli F, Aubourg P, Bougnères PF. Rocchiccioli F, et al. Among authors: bougneres pf. Pediatr Res. 1986 Jan;20(1):62-6. doi: 10.1203/00006450-198601000-00018. Pediatr Res. 1986. PMID: 3945517

8

Mass spectrometric identification of 2-hydroxy-sebacic acid in the urines of patients with neonatal adrenoleukodystrophy and Zellweger syndrome.

Rocchiccioli F, Cartier PH, Aubourg P, Bougnères PF. Rocchiccioli F, et al. Among authors: bougneres pf. Biomed Environ Mass Spectrom. 1986 Jun;13(6):315-8. doi: 10.1002/bms.1200130609. Biomed Environ Mass Spectrom. 1986. PMID: 2943344

9

An AAVrh10-CAG-CYP21-HA vector allows persistent correction of 21-hydroxylase deficiency in a Cyp21^-/- mouse model.

Perdomini M, Dos Santos C, Goumeaux C, Blouin V, Bougnères P. Perdomini M, et al. Among authors: bougneres p. Gene Ther. 2017 May;24(5):275-281. doi: 10.1038/gt.2017.10. Epub 2017 Feb 6. Gene Ther. 2017. PMID: 28165447

10

Long-term results of early cyclosporin therapy in juvenile IDDM.

De Filippo G, Carel JC, Boitard C, Bougnères PF. De Filippo G, et al. Among authors: bougneres pf. Diabetes. 1996 Jan;45(1):101-4. doi: 10.2337/diab.45.1.101. Diabetes. 1996. PMID: 8522052 Clinical Trial.

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