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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 1
2004 1
2009 1
2010 1
2011 1
2012 1
2013 4
2014 2
2015 1
2016 1
2017 1
2022 0
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13 results
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Page 1
[Follow-up networks for preterm neonates: for what purpose?].
Sizun J, Duigou AL, Roué JM; Le Comité Régional de Coordination du réseau « Bien grandir en Bretagne », Bertschy F, Le Gouill I, Bernicot MP, De Baracé C, Busnel A, Bretaudeau G, Le Guillou C, Millet P, Muller JB, Pichon C, Pladys P, Robert H, Tréguier G. Sizun J, et al. Among authors: de barace c. Arch Pediatr. 2013 Sep;20(9):917-20. doi: 10.1016/j.arcped.2013.06.009. Epub 2013 Jul 22. Arch Pediatr. 2013. PMID: 23886869 French. No abstract available.
Prognostic value of EEG in very premature newborns.
Le Bihannic A, Beauvais K, Busnel A, de Barace C, Furby A. Le Bihannic A, et al. Among authors: de barace c. Arch Dis Child Fetal Neonatal Ed. 2012 Mar;97(2):F106-9. doi: 10.1136/adc.2010.204735. Epub 2011 Jun 9. Arch Dis Child Fetal Neonatal Ed. 2012. PMID: 21659622
Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review.
El Khattabi L, Jaillard S, Andrieux J, Pasquier L, Perrin L, Capri Y, Benmansour A, Toutain A, Marcorelles P, Vincent-Delorme C, Journel H, Henry C, De Barace C, Devisme L, Dubourg C, Demurger F, Lucas J, Belaud-Rotureau MA, Amiel J, Malan V, De Blois MC, De Pontual L, Lebbar A, Le Dû N, Germain DP, Pinard JM, Pipiras E, Tabet AC, Aboura A, Verloes A. El Khattabi L, et al. Among authors: de barace c. Am J Med Genet A. 2015 Jun;167(6):1252-61. doi: 10.1002/ajmg.a.36932. Epub 2015 Apr 2. Am J Med Genet A. 2015. PMID: 25847481 Free article. Review.
Clinical, laboratory and molecular findings and long-term follow-up data in 96 French patients with PMM2-CDG (phosphomannomutase 2-congenital disorder of glycosylation) and review of the literature.
Schiff M, Roda C, Monin ML, Arion A, Barth M, Bednarek N, Bidet M, Bloch C, Boddaert N, Borgel D, Brassier A, Brice A, Bruneel A, Buissonnière R, Chabrol B, Chevalier MC, Cormier-Daire V, De Barace C, De Maistre E, De Saint-Martin A, Dorison N, Drouin-Garraud V, Dupré T, Echenne B, Edery P, Feillet F, Fontan I, Francannet C, Labarthe F, Gitiaux C, Héron D, Hully M, Lamoureux S, Martin-Coignard D, Mignot C, Morin G, Pascreau T, Pincemaille O, Polak M, Roubertie A, Thauvin-Robinet C, Toutain A, Viot G, Vuillaumier-Barrot S, Seta N, De Lonlay P. Schiff M, et al. Among authors: de barace c. J Med Genet. 2017 Dec;54(12):843-851. doi: 10.1136/jmedgenet-2017-104903. Epub 2017 Sep 27. J Med Genet. 2017. PMID: 28954837 Review.
Epilepsy diagnostic and treatment needs identified with a collaborative database involving tertiary centers in France.
Chipaux M, Szurhaj W, Vercueil L, Milh M, Villeneuve N, Cances C, Auvin S, Chassagnon S, Napuri S, Allaire C, Derambure P, Marchal C, Caubel I, Ricard-Mousnier B, N'Guyen The Tich S, Pinard JM, Bahi-Buisson N, de Baracé C, Kahane P, Gautier A, Hamelin S, Coste-Zeitoun D, Rosenberg SD, Clerson P, Nabbout R, Kuchenbuch M, Picot MC, Kaminska A; GRENAT Group. Chipaux M, et al. Among authors: de barace c. Epilepsia. 2016 May;57(5):757-69. doi: 10.1111/epi.13368. Epub 2016 Apr 1. Epilepsia. 2016. PMID: 27037674 Free article.
[Understand the neurodevelopment of language: a necessity to prevent learning disabilities in children].
LAMOPRESCO, Charollais A, Marret S, Stumpf MH, Lemarchand M, Delaporte B, Philip E, Monom-Diverre, Guillois B, Datin-Dorriere V, Debillon T, Simon MJ, De Barace C, Pasquet F, Saliba E, Zebhib R. LAMOPRESCO, et al. Among authors: de barace c. Arch Pediatr. 2013 Sep;20(9):994-9. doi: 10.1016/j.arcped.2013.06.004. Epub 2013 Jul 19. Arch Pediatr. 2013. PMID: 23876442 French.
Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age.
Mercier S, Toutain A, Toussaint A, Raynaud M, de Barace C, Marcorelles P, Pasquier L, Blayau M, Espil C, Parent P, Journel H, Lazaro L, Andoni Urtizberea J, Moerman A, Faivre L, Eymard B, Maincent K, Gherardi R, Chaigne D, Ben Yaou R, Leturcq F, Chelly J, Desguerre I. Mercier S, et al. Among authors: de barace c. Eur J Hum Genet. 2013 Aug;21(8):855-63. doi: 10.1038/ejhg.2012.269. Epub 2013 Jan 9. Eur J Hum Genet. 2013. PMID: 23299919 Free PMC article.
Mitochondrial ND5 mutations mimicking brainstem tectal glioma.
Rio M, Lebre AS, de Lonlay P, Valayannopoulos V, Desguerre I, Dufier JL, Grévent D, Zilbovicius M, Tréguier C, Brunelle F, de Baracé C, Kaplan J, Espinase-Berrod MA, Sainte-Rose C, Puget S, Rotig A, Munnich A, Boddaert N. Rio M, et al. Among authors: de barace c. Neurology. 2010 Jul 6;75(1):93. doi: 10.1212/WNL.0b013e3181e6214a. Neurology. 2010. PMID: 20603491 No abstract available.
29 French adult patients with PMM2-congenital disorder of glycosylation: outcome of the classical pediatric phenotype and depiction of a late-onset phenotype.
Monin ML, Mignot C, De Lonlay P, Héron B, Masurel A, Mathieu-Dramard M, Lenaerts C, Thauvin C, Gérard M, Roze E, Jacquette A, Charles P, de Baracé C, Drouin-Garraud V, Khau Van Kien P, Cormier-Daire V, Mayer M, Ogier H, Brice A, Seta N, Héron D. Monin ML, et al. Among authors: de barace c. Orphanet J Rare Dis. 2014 Dec 11;9:207. doi: 10.1186/s13023-014-0207-4. Orphanet J Rare Dis. 2014. PMID: 25497157 Free PMC article.
13 results