Richard DesbiensM.D., FRCP(C)

May P, Girard S, Harrer M, Bobbili DR, Schubert J, Wolking S, Becker F, Lachance-Touchette P, Meloche C, Gravel M, Niturad CE, Knaus J, De Kovel C, Toliat M, Polvi A, Iacomino M, Guerrero-Lopez R, Baulac S, Marini C, Thiele H, Altmuller J, Jabbari K, Ruppert AK, Jurkowski W, Lal D, Rusconi R, Cestele S, Terragni B, Coombs ID, Reid CA, Striano P, Caglayan H, Siren A, Everett K, Hjalgrim H, Muhle H, Helbig I, Kunz WS, Weber YG, Weckhuysen S, Jonghe P, Sisodiya SM, Nabbout R, Franceschetti S, Coppola A, Vari MS, Kasteleijn-Nolst Trenite D, Baykan B, Ozbek U, Bebek N, Klein KM, Rosenow F, Nguyen DK, Dubeau F, Carmant L, Lortie A, Desbiens R, Clement JF, Cieuta-Walti C, Sills GJ, Auce P, Francis B, Johnson MR, Marson AG, Berghuis B, Sander JW, Avbersek A, McCormack M, Cavalleri GL, Delanty N, Depondt C, Krenn M, Zimprich F, Peter S, Nikanorova M, Kraaij R, van Rooij J, Balling R, Ikram MA, Uitterlinden AG, Avanzini G, Schorge S, Petrou S, Mantegazza M, Sander T, LeGuern E, Serratosa JM, Koeleman BPC, Palotie A, Lehesjoki AE, Nothnagel M, Nurnberg P, Maljevic S, Zara F, Cossette P, Krause R, Lerche H, Møller RS, De Jonghe P, Arfan Ikram M, Ferlazzo E, di Bonaventura C, La Neve A, Tinuper P, Bisulli F, Vignoli A, Capovilla G, Crichiutti G, Gambardella A, Belcastro V, Bianchi A, Yalçın D, Dizdarer G, Arslan K, Yapıcı Z, Kuşcu D, Leu C, Heggeli K, Willis J, Langley SR, Jorgensen A, Srivastava P, Rau S, Hengsbach C, Sonsma ACM

Rare coding variants in genes encoding GABA receptors in genetic generalised epilepsies: an exome-based case-control study.

Lancet Neurol, 17 (8), 2018.

Résumé | Liens:

Chibane IS, Boucher O, Dubeau F, Tran TPY, Mohamed I, McLachlan R, Sadler RM, Desbiens R, Carmant L, Nguyen DK

Orbitofrontal epilepsy: Case series and review of literature.

Epilepsy Behav, 76 , 2017.

Résumé | Liens:

Savard M, Desbiens R

Status epilepticus - où que tu sois, je te traiterai.

Le Médecin du Québec, 48 (7), 2013.

Desbiens R, Savard M

Le traitement pharmacologique de l'épilepsie comme s'y retrouver

Le Médecin du Québec, 48 (7), 2013.

Savard M, Dupre N, Turgeon AF, Desbiens R, Langevin S, Brunet D

Propofol-related infusion syndrome heralding a mitochondrial disease: case report.

Neurology, 81 (8), 2013.

| Liens:

Tayah T, Savard M, Desbiens R, Nguyen DK

Ictal bradycardia and asystole in an adult with a focal left insular lesion.

Clin Neurol Neurosurg, 115 (9), 2013.

| Liens:

Nadeau Y, Desbiens R

The EEG correlates of cerebellar fits.

Can J Neurol Sci, 36 (4), 2009.

| Liens:

Kinirons P, Verlaan DJ, Dube MP, Poirier J, Deacon C, Lortie A, Clement JF, Desbiens R, Carmant L, Cieuta-Walti C, Shevell M, Rouleau GA, Cossette P

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

Am J Med Genet A, 146A (5), 2008.

Résumé | Liens:

Daleau P, Morgado DC, Iriarte CA, Desbiens R

New epilepsy seizure at high altitude without signs of acute mountain sickness or high altitude cerebral edema.

High Alt Med Biol, 7 (1), 2006.

Résumé | Liens:

Berkovic SF, Serratosa JM, Phillips HA, Xiong L, Andermann E, Diaz-Otero F, Gomez-Garre P, Martin M, Fernandez-Bullido Y, Andermann F, Lopes-Cendes I, Dubeau F, Desbiens R, Scheffer IE, Wallace RH, Mulley JC, Pandolfo M

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

Epilepsia, 45 (9), 2004.

Résumé | Liens: