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Usher syndrome type 1: early detection of electroretinographic changes.
Flores-Guevara R, Renault F, Loundon N, Marlin S, Pelosse B, Momtchilova M, Auzoux-Chevé M, Vermersch AI, Richard P. Flores-Guevara R, et al. Among authors: vermersch ai. Eur J Paediatr Neurol. 2009 Nov;13(6):505-7. doi: 10.1016/j.ejpn.2008.10.002. Epub 2008 Nov 9. Eur J Paediatr Neurol. 2009. PMID: 19006676
The epileptology of GNB5 encephalopathy.
Poke G, King C, Muir A, de Valles-Ibáñez G, Germano M, Moura de Souza CF, Fung J, Chung B, Fung CW, Mignot C, Ilea A, Keren B, Vermersch AI, Davis S, Stanley T, Moharir M, Kannu P, Shao Z, Malerba N, Merla G, Mefford HC, Scheffer IE, Sadleir LG. Poke G, et al. Among authors: vermersch ai. Epilepsia. 2019 Nov;60(11):e121-e127. doi: 10.1111/epi.16372. Epub 2019 Oct 20. Epilepsia. 2019. PMID: 31631344
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients.
Le Roux M, Barth M, Gueden S, Desbordes de Cepoy P, Aeby A, Vilain C, Hirsch E, de Saint Martin A, Portes VD, Lesca G, Riquet A, Chaton L, Villeneuve N, Villard L, Cances C, Valton L, Renaldo F, Vermersch AI, Altuzarra C, Nguyen-Morel MA, Van Gils J, Angelini C, Biraben A, Arnaud L, Riant F, Van Bogaert P. Le Roux M, et al. Among authors: vermersch ai. Eur J Paediatr Neurol. 2021 Jul;33:75-85. doi: 10.1016/j.ejpn.2021.05.010. Epub 2021 May 26. Eur J Paediatr Neurol. 2021. PMID: 34102571 Free article.
WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation.
Mignot C, Lambert L, Pasquier L, Bienvenu T, Delahaye-Duriez A, Keren B, Lefranc J, Saunier A, Allou L, Roth V, Valduga M, Moustaïne A, Auvin S, Barrey C, Chantot-Bastaraud S, Lebrun N, Moutard ML, Nougues MC, Vermersch AI, Héron B, Pipiras E, Héron D, Olivier-Faivre L, Guéant JL, Jonveaux P, Philippe C. Mignot C, et al. Among authors: vermersch ai. J Med Genet. 2015 Jan;52(1):61-70. doi: 10.1136/jmedgenet-2014-102748. Epub 2014 Nov 19. J Med Genet. 2015. PMID: 25411445
Early neurological phenotype in 4 children with biallelic PRODH mutations.
Afenjar A, Moutard ML, Doummar D, Guët A, Rabier D, Vermersch AI, Mignot C, Burglen L, Heron D, Thioulouse E, de Villemeur TB, Campion D, Rodriguez D. Afenjar A, et al. Among authors: vermersch ai. Brain Dev. 2007 Oct;29(9):547-52. doi: 10.1016/j.braindev.2007.01.008. Epub 2007 Apr 6. Brain Dev. 2007. PMID: 17412540
Sequences of memory-guided saccades in Parkinson's disease.
Vermersch AI, Rivaud S, Vidailhet M, Bonnet AM, Gaymard B, Agid Y, Pierrot-Deseilligny C. Vermersch AI, et al. Ann Neurol. 1994 Apr;35(4):487-90. doi: 10.1002/ana.410350419. Ann Neurol. 1994. PMID: 8154878
Memory guided saccade deficit after caudate nucleus lesion.
Vermersch AI, Gaymard BM, Rivaud-Pechoux S, Ploner CJ, Agid Y, Pierrot-Deseilligny C. Vermersch AI, et al. J Neurol Neurosurg Psychiatry. 1999 Apr;66(4):524-7. doi: 10.1136/jnnp.66.4.524. J Neurol Neurosurg Psychiatry. 1999. PMID: 10201429 Free PMC article. Clinical Trial.
Cortical control of saccades.
Pierrot-Deseilligny C, Rivaud S, Gaymard B, Müri R, Vermersch AI. Pierrot-Deseilligny C, et al. Among authors: vermersch ai. Ann Neurol. 1995 May;37(5):557-67. doi: 10.1002/ana.410370504. Ann Neurol. 1995. PMID: 7755349 Review.
20 results