Desbiens R - Search Results

1

Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12.

Berkovic SF, Serratosa JM, Phillips HA, Xiong L, Andermann E, Díaz-Otero F, Gómez-Garre P, Martín M, Fernández-Bullido Y, Andermann F, Lopes-Cendes I, Dubeau F, Desbiens R, Scheffer IE, Wallace RH, Mulley JC, Pandolfo M. Berkovic SF, et al. Among authors: desbiens r. Epilepsia. 2004 Sep;45(9):1054-60. doi: 10.1111/j.0013-9580.2004.30502.x. Epilepsia. 2004. PMID: 15329069 Free article.

2

Genetic linkage studies in familial frontal epilepsy: exclusion of the human chromosome regions homologous to the El-1 mouse locus.

Lopes-Cendes I, Phillips HA, Scheffer IE, Mulley JC, Desbiens R, Andermann E, Cendes F, Verret S, Andermann F, Berkovic SF, et al. Lopes-Cendes I, et al. Among authors: desbiens r. Epilepsy Res. 1995 Nov;22(3):227-33. doi: 10.1016/0920-1211(95)00049-6. Epilepsy Res. 1995. PMID: 8991790

3

Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder.

Scheffer IE, Bhatia KP, Lopes-Cendes I, Fish DR, Marsden CD, Andermann E, Andermann F, Desbiens R, Keene D, Cendes F, et al. Scheffer IE, et al. Among authors: desbiens r. Brain. 1995 Feb;118 ( Pt 1):61-73. doi: 10.1093/brain/118.1.61. Brain. 1995. PMID: 7895015

4

Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder.

Scheffer IE, Bhatia KP, Lopes-Cendes I, Fish DR, Marsden CD, Andermann F, Andermann E, Desbiens R, Cendes F, Manson JI, et al. Scheffer IE, et al. Among authors: desbiens r. Lancet. 1994 Feb 26;343(8896):515-7. doi: 10.1016/s0140-6736(94)91463-x. Lancet. 1994. PMID: 7906762 Review.

5

Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12.

Xiong L, Labuda M, Li DS, Hudson TJ, Desbiens R, Patry G, Verret S, Langevin P, Mercho S, Seni MH, Scheffer I, Dubeau F, Berkovic SF, Andermann F, Andermann E, Pandolfo M. Xiong L, et al. Among authors: desbiens r. Am J Hum Genet. 1999 Dec;65(6):1698-710. doi: 10.1086/302649. Am J Hum Genet. 1999. PMID: 10577924 Free PMC article.

6

Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study.

Koko M, Motelow JE, Stanley KE, Bobbili DR, Dhindsa RS, May P; Canadian Epilepsy Network; Epi4K Consortium; Epilepsy Phenome/Genome Project; EpiPGX Consortium; EuroEPINOMICS-CoGIE Consortium. Koko M, et al. Epilepsia. 2022 Mar;63(3):723-735. doi: 10.1111/epi.17166. Epub 2022 Jan 15. Epilepsia. 2022. PMID: 35032048 Free PMC article.

7

Life-threatening focal status epilepticus due to occult cortical dysplasia.

Desbiens R, Berkovic SF, Dubeau F, Andermann F, Laxer KD, Harvey S, Leproux F, Melanson D, Robitaille Y, Kalnins R, et al. Desbiens R, et al. Arch Neurol. 1993 Jul;50(7):695-700. doi: 10.1001/archneur.1993.00540070015007. Arch Neurol. 1993. PMID: 8323470

8

Orbitofrontal epilepsy: Case series and review of literature.

Chibane IS, Boucher O, Dubeau F, Tran TPY, Mohamed I, McLachlan R, Sadler RM, Desbiens R, Carmant L, Nguyen DK. Chibane IS, et al. Among authors: desbiens r. Epilepsy Behav. 2017 Nov;76:32-38. doi: 10.1016/j.yebeh.2017.08.038. Epub 2017 Sep 18. Epilepsy Behav. 2017. PMID: 28928072

9

A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11.

Kinirons P, Verlaan DJ, Dubé MP, Poirier J, Deacon C, Lortie A, Clément JF, Desbiens R, Carmant L, Cieuta-Walti C, Shevell M, Rouleau GA, Cossette P. Kinirons P, et al. Among authors: desbiens r. Am J Med Genet A. 2008 Mar 1;146A(5):578-84. doi: 10.1002/ajmg.a.32139. Am J Med Genet A. 2008. PMID: 18241056

10

Stages and patterns of centrifugal arrest of diffuse neuronal migration disorders.

Palmini A, Andermann F, de Grissac H, Tampieri D, Robitaille Y, Langevin P, Desbiens R, Andermann E. Palmini A, et al. Among authors: desbiens r. Dev Med Child Neurol. 1993 Apr;35(4):331-9. doi: 10.1111/j.1469-8749.1993.tb11645.x. Dev Med Child Neurol. 1993. PMID: 8335148

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