Beauvais P - Search Results

1

Effect of genetically caused excess of brain gamma-hydroxybutyric acid and GABA on sleep.

Arnulf I, Konofal E, Gibson KM, Rabier D, Beauvais P, Derenne JP, Philippe A. Arnulf I, et al. Among authors: beauvais p. Sleep. 2005 Apr;28(4):418-24. doi: 10.1093/sleep/28.4.418. Sleep. 2005. PMID: 16171286

2

The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients.

Gibson KM, Christensen E, Jakobs C, Fowler B, Clarke MA, Hammersen G, Raab K, Kobori J, Moosa A, Vollmer B, Rossier E, Iafolla AK, Matern D, Brouwer OF, Finkelstein J, Aksu F, Weber HP, Bakkeren JA, Gabreels FJ, Bluestone D, Barron TF, Beauvais P, Rabier D, Santos C, Lehnert W, et al. Gibson KM, et al. Among authors: beauvais p. Pediatrics. 1997 Apr;99(4):567-74. doi: 10.1542/peds.99.4.567. Pediatrics. 1997. PMID: 9093300 Free article.

3

First set of gated x-ray imaging diagnostics for the Laser Megajoule facility.

Rosch R, Trosseille C, Caillaud T, Allouche V, Bourgade JL, Briat M, Brunel P, Burillo M, Casner A, Depierreux S, Gontier D, Jadaud JP, Le Breton JP, Llavador P, Loupias B, Miquel JL, Oudot G, Perez S, Raimbourg J, Rousseau A, Rousseaux C, Rubbelynck C, Stemmler P, Troussel P, Ulmer JL, Wrobel R, Beauvais P, Pallet M, Prevot V. Rosch R, et al. Among authors: beauvais p. Rev Sci Instrum. 2016 Mar;87(3):033706. doi: 10.1063/1.4942930. Rev Sci Instrum. 2016. PMID: 27036783

4

A 140 mA cw deuteron electron cyclotron resonance source for the IFMIF-EVEDA project.

Gobin R, Beauvais PY, Delferrière O, De Menezes D, Tuske O, Adroit G, Gauthier Y, Harrault F. Gobin R, et al. Among authors: beauvais py. Rev Sci Instrum. 2008 Feb;79(2 Pt 2):02B303. doi: 10.1063/1.2801976. Rev Sci Instrum. 2008. PMID: 18315169

5

Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum.

Ewenczyk C, Leroux A, Roubergue A, Laugel V, Afenjar A, Saudubray JM, Beauvais P, Billette de Villemeur T, Vidailhet M, Roze E. Ewenczyk C, et al. Among authors: beauvais p. Brain. 2008 Mar;131(Pt 3):760-1. doi: 10.1093/brain/awm337. Epub 2008 Jan 17. Brain. 2008. PMID: 18202104 Review.

6

Phenotypic cellular characterization of an ataxia telangiectasia patient carrying a causal homozygous missense mutation.

Angèle S, Laugé A, Fernet M, Moullan N, Beauvais P, Couturier J, Stoppa-Lyonnet D, Hall J. Angèle S, et al. Among authors: beauvais p. Hum Mutat. 2003 Feb;21(2):169-70. doi: 10.1002/humu.9107. Hum Mutat. 2003. PMID: 12552566

7

[Fragile X syndrome: epidemiology, genetics, diagnosis].

Beauvais P, Houdayer C. Beauvais P, et al. Rev Prat. 2001 Sep 1;51(13):1477-80. Rev Prat. 2001. PMID: 11601079 Review. French. No abstract available.

8

[Duchenne's muscular dystrophy: epidemiology, genetics, diagnosis].

Beauvais P. Beauvais P. Rev Prat. 2001 Sep 1;51(13):1473-6. Rev Prat. 2001. PMID: 11601078 Review. French. No abstract available.

9

Acute clinical events in 299 homozygous sickle cell patients living in France. French Study Group on Sickle Cell Disease.

Neonato MG, Guilloud-Bataille M, Beauvais P, Bégué P, Belloy M, Benkerrou M, Ducrocq R, Maier-Redelsperger M, de Montalembert M, Quinet B, Elion J, Feingold J, Girot R. Neonato MG, et al. Among authors: beauvais p. Eur J Haematol. 2000 Sep;65(3):155-64. doi: 10.1034/j.1600-0609.2000.90210.x. Eur J Haematol. 2000. PMID: 11007050

10

[Hereditary methemoglobinemias].

Beauvais P. Beauvais P. Arch Pediatr. 2000 May;7(5):513-8. doi: 10.1016/S0929-693X(00)89008-9. Arch Pediatr. 2000. PMID: 10855391 French.

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