Bery A - Search Results

1

Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic encephalopathy.

Vegas N, Cavallin M, Maillard C, Boddaert N, Toulouse J, Schaefer E, Lerman-Sagie T, Lev D, Magalie B, Moutton S, Haan E, Isidor B, Heron D, Milh M, Rondeau S, Michot C, Valence S, Wagner S, Hully M, Mignot C, Masurel A, Datta A, Odent S, Nizon M, Lazaro L, Vincent M, Cogné B, Guerrot AM, Arpin S, Pedespan JM, Caubel I, Pontier B, Troude B, Rivier F, Philippe C, Bienvenu T, Spitz MA, Bery A, Bahi-Buisson N. Vegas N, et al. Among authors: bery a. Neurol Genet. 2018 Nov 7;4(6):e281. doi: 10.1212/NXG.0000000000000281. eCollection 2018 Dec. Neurol Genet. 2018. PMID: 30533527 Free PMC article.

2

TLE1, a key player in neurogenesis, a new candidate gene for autosomal recessive postnatal microcephaly.

Cavallin M, Maillard C, Hully M, Philbert M, Boddaert N, Reilly ML, Nitschké P, Bery A, Bahi-Buisson N. Cavallin M, et al. Among authors: bery a. Eur J Med Genet. 2018 Dec;61(12):729-732. doi: 10.1016/j.ejmg.2018.05.002. Epub 2018 May 25. Eur J Med Genet. 2018. PMID: 29758293

3

Recurrent RTTN mutation leading to severe microcephaly, polymicrogyria and growth restriction.

Cavallin M, Bery A, Maillard C, Salomon LJ, Bole C, Reilly ML, Nitschké P, Boddaert N, Bahi-Buisson N. Cavallin M, et al. Among authors: bery a. Eur J Med Genet. 2018 Dec;61(12):755-758. doi: 10.1016/j.ejmg.2018.08.001. Epub 2018 Aug 16. Eur J Med Genet. 2018. PMID: 30121372

4

Mutations in TBR1 gene leads to cortical malformations and intellectual disability.

Vegas N, Cavallin M, Kleefstra T, de Boer L, Philbert M, Maillard C, Boddaert N, Munnich A, Hubert L, Bery A, Besmond C, Bahi-Buisson N. Vegas N, et al. Among authors: bery a. Eur J Med Genet. 2018 Dec;61(12):759-764. doi: 10.1016/j.ejmg.2018.09.012. Epub 2018 Sep 27. Eur J Med Genet. 2018. PMID: 30268909

5

Genes expressed in mouse cortical progenitors are enriched in Pax, Lhx, and Sox transcription factor putative binding sites.

Bery A, Mérot Y, Rétaux S. Bery A, et al. Brain Res. 2016 Feb 15;1633:37-51. doi: 10.1016/j.brainres.2015.12.022. Epub 2015 Dec 23. Brain Res. 2016. PMID: 26721689

6

Characterization of enhancers active in the mouse embryonic cerebral cortex suggests Sox/Pou cis-regulatory logics and heterogeneity of cortical progenitors.

Bery A, Martynoga B, Guillemot F, Joly JS, Rétaux S. Bery A, et al. Cereb Cortex. 2014 Nov;24(11):2822-34. doi: 10.1093/cercor/bht126. Epub 2013 May 29. Cereb Cortex. 2014. PMID: 23720416

7

Assessing cell cycle progression of neural stem and progenitor cells in the mouse developing brain after genotoxic stress.

Etienne O, Bery A, Roque T, Desmaze C, Boussin FD. Etienne O, et al. Among authors: bery a. J Vis Exp. 2014 May 7;(87):51209. doi: 10.3791/51209. J Vis Exp. 2014. PMID: 24837791 Free PMC article.

8

Structure of the central nervous system of a juvenile acoel, Symsagittifera roscoffensis.

Bery A, Cardona A, Martinez P, Hartenstein V. Bery A, et al. Dev Genes Evol. 2010 Sep;220(3-4):61-76. doi: 10.1007/s00427-010-0328-2. Epub 2010 Jun 15. Dev Genes Evol. 2010. PMID: 20549514 Free PMC article.

9

Development of novel resistivity-chargeability statistical relationships for subsurface characterization at Langkawi, Kedah.

Bala GA, Bery AA, Gnapragasan J, Akingboye AS. Bala GA, et al. Among authors: bery aa. Environ Sci Pollut Res Int. 2024 Mar 27. doi: 10.1007/s11356-024-32867-0. Online ahead of print. Environ Sci Pollut Res Int. 2024. PMID: 38532213

10

Acute rehabilitation following traumatic anterior shoulder dislocation (ARTISAN): pragmatic, multicentre, randomised controlled trial.

Kearney RS, Ellard DR, Parsons H, Haque A, Mason J, Nwankwo H, Bradley H, Drew S, Modi C, Bush H, Torgerson D, Underwood M; The ARTISAN collaborators; ARTISAN collaborators. Kearney RS, et al. BMJ. 2024 Jan 17;384:e076925. doi: 10.1136/bmj-2023-076925. BMJ. 2024. PMID: 38233068 Free PMC article. Clinical Trial.

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