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972 results

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Page 1
Movement disorders in patients with alternating hemiplegia: "Soft" and "stiff" at the same time.
Panagiotakaki E, Doummar D, Nogue E, Nagot N, Lesca G, Riant F, Nicole S, Delaygue C, Barthez MA, Nassogne MC, Dusser A, Vallée L, Billette T, Bourgeois M, Ioos C, Gitiaux C, Laroche C, Milh M, Portes VD, Arzimanoglou A, Roubertie A; AHC–Movement Disorder Study Group. Panagiotakaki E, et al. Among authors: bourgeois m. Neurology. 2020 Mar 31;94(13):e1378-e1385. doi: 10.1212/WNL.0000000000009175. Epub 2020 Mar 2. Neurology. 2020. PMID: 32123049
Alternating hemiplegia of childhood.
Bourgeois M, Aicardi J, Goutières F. Bourgeois M, et al. J Pediatr. 1993 May;122(5 Pt 1):673-9. doi: 10.1016/s0022-3476(06)80003-x. J Pediatr. 1993. PMID: 8496742 Review.
Topiramate: efficacy and tolerability in children according to epilepsy syndromes.
Mikaeloff Y, de Saint-Martin A, Mancini J, Peudenier S, Pedespan JM, Vallée L, Motte J, Bourgeois M, Arzimanoglou A, Dulac O, Chiron C. Mikaeloff Y, et al. Among authors: bourgeois m. Epilepsy Res. 2003 Mar;53(3):225-32. doi: 10.1016/s0920-1211(03)00028-7. Epilepsy Res. 2003. PMID: 12694931 Clinical Trial.
Heart rate variability during sleep in children with partial epilepsy.
Ferri R, Curzi-Dascalova L, Arzimanoglou A, Bourgeois M, Beaud C, Nunes ML, Elia M, Musumeci SA, Tripodi M. Ferri R, et al. Among authors: bourgeois m. J Sleep Res. 2002 Jun;11(2):153-60. doi: 10.1046/j.1365-2869.2002.00283.x. J Sleep Res. 2002. PMID: 12028480
Electro-clinical features in epileptic children with chromosome 15q duplication syndrome.
Dangles MT, Malan V, Dumas G, Romana S, Raoul O, Coste-Zeitoun D, Soufflet C, Vignolo-Diard P, Bahi-Buisson N, Barnérias C, Chemaly N, Desguerre I, Gitiaux C, Hully M, Bourgeois M, Guimier A, Rio M, Munnich A, Nabbout R, Kaminska A, Eisermann M. Dangles MT, et al. Among authors: bourgeois m. Clin Neurophysiol. 2021 May;132(5):1126-1137. doi: 10.1016/j.clinph.2021.02.010. Epub 2021 Mar 10. Clin Neurophysiol. 2021. PMID: 33773177
Refinement of cortical dysgeneses spectrum associated with TUBA1A mutations.
Bahi-Buisson N, Poirier K, Boddaert N, Saillour Y, Castelnau L, Philip N, Buyse G, Villard L, Joriot S, Marret S, Bourgeois M, Van Esch H, Lagae L, Amiel J, Hertz-Pannier L, Roubertie A, Rivier F, Pinard JM, Beldjord C, Chelly J. Bahi-Buisson N, et al. Among authors: bourgeois m. J Med Genet. 2008 Oct;45(10):647-53. doi: 10.1136/jmg.2008.058073. Epub 2008 Aug 26. J Med Genet. 2008. PMID: 18728072
972 results