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Phenotype-genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature.
Am J Med Genet A. 2015 Jan;167A(1):111-22. doi: 10.1002/ajmg.a.36807. Epub 2014 Nov 25.
Am J Med Genet A. 2015.
PMID: 25425167
Review.
Type I hyperprolinemia: genotype/phenotype correlations.
Guilmatre A, Legallic S, Steel G, Willis A, Di Rosa G, Goldenberg A, Drouin-Garraud V, Guet A, Mignot C, Des Portes V, Valayannopoulos V, Van Maldergem L, Hoffman JD, Izzi C, Espil-Taris C, Orcesi S, Bonafé L, Le Galloudec E, Maurey H, Ioos C, Afenjar A, Blanchet P, Echenne B, Roubertie A, Frebourg T, Valle D, Campion D.
Guilmatre A, et al. Among authors: le galloudec e.
Hum Mutat. 2010 Aug;31(8):961-5. doi: 10.1002/humu.21296.
Hum Mutat. 2010.
PMID: 20524212
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Thyroid hormone and folinic acid in young children with Down syndrome: the phase 3 ACTHYF trial.
Mircher C, Sacco S, Bouis C, Gallard J, Pichot A, Le Galloudec E, Cieuta C, Marey I, Greiner-Mahler O, Dorison N, Gambarini A, Stora S, Durand S, Polak M, Baruchel A, Schlumberger E, Dewailly J, Azar-Kolakez A, Guéant-Rodriguez RM, Guéant JL, Borderie D, Bonnefont-Rousselot D, Blondiaux E, Ravel A, Sturtz FG.
Mircher C, et al. Among authors: le galloudec e.
Genet Med. 2020 Jan;22(1):44-52. doi: 10.1038/s41436-019-0597-8. Epub 2019 Jul 8.
Genet Med. 2020.
PMID: 31281181
Free article.
Clinical Trial.
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A disorder of axonal development, necrotizing myopathy, cardiomyopathy, and cataracts: a new familial disease.
Lyon G, Arita F, Le Galloudec E, Vallée L, Misson JP, Ferrière G.
Lyon G, et al. Among authors: le galloudec e.
Ann Neurol. 1990 Feb;27(2):193-9. doi: 10.1002/ana.410270216.
Ann Neurol. 1990.
PMID: 2317015
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Cardiovascular changes induced by the local application of glutamate-related drugs in the rat nucleus tractus solitarii.
Le Galloudec E, Merahi N, Laguzzi R.
Le Galloudec E, et al.
Brain Res. 1989 Dec 4;503(2):322-5. doi: 10.1016/0006-8993(89)91683-1.
Brain Res. 1989.
PMID: 2575008
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