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2006 | 1 |
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Page 1
Early and long-term electroclinical features of patients with epilepsy and PCDH19 mutation.
Epileptic Disord. 2018 Dec 1;20(6):457-467. doi: 10.1684/epd.2018.1009.
Epileptic Disord. 2018.
PMID: 30530412
Familial rectal pain: a familial autonomic disorder as a cause of paroxysmal attacks in the newborn baby.
Bednarek N, Arbuès AS, Motte J, Sabouraud P, Plouin P, Morville P.
Bednarek N, et al. Among authors: arbues as.
Epileptic Disord. 2005 Dec;7(4):360-2.
Epileptic Disord. 2005.
PMID: 16338680
Free article.
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Cognitive functions in children with benign childhood epilepsy with centrotemporal spikes (BECTS).
Pinton F, Ducot B, Motte J, Arbuès AS, Barondiot C, Barthez MA, Chaix Y, Cheminal R, Livet MO, Penniello MJ, Peudenier S, de Saint-Martin A, Billard C.
Pinton F, et al. Among authors: arbues as.
Epileptic Disord. 2006 Mar;8(1):11-23.
Epileptic Disord. 2006.
PMID: 16567321
Free article.
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Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients.
Panagiotakaki E, De Grandis E, Stagnaro M, Heinzen EL, Fons C, Sisodiya S, de Vries B, Goubau C, Weckhuysen S, Kemlink D, Scheffer I, Lesca G, Rabilloud M, Klich A, Ramirez-Camacho A, Ulate-Campos A, Campistol J, Giannotta M, Moutard ML, Doummar D, Hubsch-Bonneaud C, Jaffer F, Cross H, Gurrieri F, Tiziano D, Nevsimalova S, Nicole S, Neville B, van den Maagdenberg AM, Mikati M, Goldstein DB, Vavassori R, Arzimanoglou A; Italian IBAHC Consortium; French AHC Consortium; International AHC Consortium.
Panagiotakaki E, et al.
Orphanet J Rare Dis. 2015 Sep 26;10:123. doi: 10.1186/s13023-015-0335-5.
Orphanet J Rare Dis. 2015.
PMID: 26410222
Free PMC article.
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Progressive megalencephaly due to specific EIF2Bepsilon mutations in two unrelated families.
Passemard S, Gelot A, Fogli A, N'Guyen S, Barnerias C, Niel F, Doummar D, Arbues AS, Mignot C, de Villemeur TB, Ponsot G, Boespflug-Tanguy O, Rodriguez D.
Passemard S, et al. Among authors: arbues as.
Neurology. 2007 Jul 24;69(4):400-2. doi: 10.1212/01.wnl.0000266388.02772.f8.
Neurology. 2007.
PMID: 17646634
No abstract available.
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Chiari type I malformation causing central apnoeas in a 4-month-old boy.
Van den Broek MJ, Arbues AS, Chalard F, Pinto Da Costa NM, Trang H, Dorfmuller G, Evrard PP, Husson I, Servais LJ.
Van den Broek MJ, et al. Among authors: arbues as.
Eur J Paediatr Neurol. 2009 Sep;13(5):463-5. doi: 10.1016/j.ejpn.2008.07.012. Epub 2008 Sep 10.
Eur J Paediatr Neurol. 2009.
PMID: 18783970
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