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Results: 1 to 20 of 56

1.

Enhanced EEG connectivity in children with febrile seizures.

Birca A, Lassonde M, Lippé S, Lortie A, Vannasing P, Carmant L.

Epilepsy Res. 2015 Feb;110:32-8. doi: 10.1016/j.eplepsyres.2014.11.008. Epub 2014 Nov 22.

PMID:
25616453
[PubMed - in process]
2.

Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness.

Perrault I, Hamdan FF, Rio M, Capo-Chichi JM, Boddaert N, Décarie JC, Maranda B, Nabbout R, Sylvain M, Lortie A, Roux PP, Rossignol E, Gérard X, Barcia G, Berquin P, Munnich A, Rouleau GA, Kaplan J, Rozet JM, Michaud JL.

Am J Hum Genet. 2014 Jun 5;94(6):891-7. doi: 10.1016/j.ajhg.2014.04.012. Epub 2014 May 8.

PMID:
24814191
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

The genetic landscape of infantile spasms.

Michaud JL, Lachance M, Hamdan FF, Carmant L, Lortie A, Diadori P, Major P, Meijer IA, Lemyre E, Cossette P, Mefford HC, Rouleau GA, Rossignol E.

Hum Mol Genet. 2014 Sep 15;23(18):4846-58. doi: 10.1093/hmg/ddu199. Epub 2014 Apr 29.

PMID:
24781210
[PubMed - in process]
4.

Clinical and magnetic resonance imaging (MRI) distinctions between tumefactive demyelination and brain tumors in children.

Yiu EM, Laughlin S, Verhey LH, Banwell BL; Canadian Pediatric Demyelinating Disease Network.

J Child Neurol. 2014 May;29(5):654-65. doi: 10.1177/0883073813500713. Epub 2013 Oct 3.

PMID:
24092896
[PubMed - indexed for MEDLINE]
5.

Diagnosis of migraine in the pediatric emergency department.

Trottier ED, Bailey B, Lucas N, Lortie A.

Pediatr Neurol. 2013 Jul;49(1):40-5. doi: 10.1016/j.pediatrneurol.2013.03.003.

PMID:
23827425
[PubMed - indexed for MEDLINE]
6.

Psychogenic nonepileptic seizures.

Lortie A.

Handb Clin Neurol. 2013;112:875-9. doi: 10.1016/B978-0-444-52910-7.00009-X. Review.

PMID:
23622297
[PubMed - indexed for MEDLINE]
7.

[Surgical treatment of paediatric epileptic patients].

Lortie A.

Rev Prat. 2012 Dec;62(10):1401-5. Review. French.

PMID:
23424921
[PubMed - indexed for MEDLINE]
8.

Children with a history of atypical febrile seizures show abnormal steady state visual evoked potential brain responses.

Sheppard E, Birca A, Carmant L, Lortie A, Vannassing P, Lassonde M, Lippé S.

Epilepsy Behav. 2013 Apr;27(1):90-4. doi: 10.1016/j.yebeh.2012.12.023. Epub 2013 Feb 5.

PMID:
23391502
[PubMed - indexed for MEDLINE]
9.

2010 McDonald criteria for diagnosing pediatric multiple sclerosis.

Sadaka Y, Verhey LH, Shroff MM, Branson HM, Arnold DL, Narayanan S, Sled JG, Bar-Or A, Sadovnick AD, McGowan M, Marrie RA, Banwell B; Canadian Pediatric Demyelinating Disease Network.

Ann Neurol. 2012 Aug;72(2):211-23. doi: 10.1002/ana.23575.

PMID:
22926854
[PubMed - indexed for MEDLINE]
10.

A condensed performance-validation strategy for multiplex detection kits used in studies of human clinical samples.

Belabani C, Rajasekharan S, Poupon V, Johnson T, Bar-Or A; CIHR/MSSC NET in Clinical Autoimmunity; Canadian Pediatric Demyelinating Disease Network.

J Immunol Methods. 2013 Jan 31;387(1-2):1-10. doi: 10.1016/j.jim.2012.08.002. Epub 2012 Aug 11.

PMID:
22917931
[PubMed - indexed for MEDLINE]
11.

Discontinuation of antiepileptic drugs after successful epilepsy surgery. a Canadian survey.

Téllez-Zenteno JF, Ronquillo LH, Jette N, Burneo JG, Nguyen DK, Donner EJ, Sadler M, Javidan M M, Gross DW, Wiebe S; Canadian Epilepsy Surgery Study Group.

Epilepsy Res. 2012 Nov;102(1-2):23-33. doi: 10.1016/j.eplepsyres.2012.04.018. Epub 2012 May 15.

PMID:
22595484
[PubMed - indexed for MEDLINE]
12.

Masquerades of acquired demyelination in children: experiences of a national demyelinating disease program.

O'Mahony J, Bar-Or A, Arnold DL, Sadovnick AD, Marrie RA, Banwell B; Canadian Pediatric Demyelinating Disease Network.

J Child Neurol. 2013 Feb;28(2):184-97. doi: 10.1177/0883073812443006. Epub 2012 May 9.

PMID:
22573735
[PubMed - indexed for MEDLINE]
13.

Ataxia-telangiectasia presenting with a novel immunodeficiency.

Perreault S, Bernard G, Lortie A, Le Deist F, Decaluwe H.

Pediatr Neurol. 2012 May;46(5):322-4. doi: 10.1016/j.pediatrneurol.2012.02.027.

PMID:
22520355
[PubMed - indexed for MEDLINE]
14.

Implication of perturbed axoglial apparatus in early pediatric multiple sclerosis.

Dhaunchak AS, Becker C, Schulman H, De Faria O Jr, Rajasekharan S, Banwell B, Colman DR, Bar-Or A; Canadian Pediatric Demyelinating Disease Group.

Ann Neurol. 2012 May;71(5):601-13. doi: 10.1002/ana.22693. Epub 2012 Apr 4.

PMID:
22473675
[PubMed - indexed for MEDLINE]
15.

Hemimegalencephaly in an adult with normal intellectual function and mild epilepsy.

Beaulieu-Boire I, Lortie A, Bissonnette J, Prevost S, Bergeron D, Bocti C.

Dev Med Child Neurol. 2012 Mar;54(3):284-6. doi: 10.1111/j.1469-8749.2011.04136.x. Epub 2011 Dec 21.

PMID:
22188130
[PubMed - indexed for MEDLINE]
16.

Novel α1 and γ2 GABAA receptor subunit mutations in families with idiopathic generalized epilepsy.

Lachance-Touchette P, Brown P, Meloche C, Kinirons P, Lapointe L, Lacasse H, Lortie A, Carmant L, Bedford F, Bowie D, Cossette P.

Eur J Neurosci. 2011 Jul;34(2):237-49. doi: 10.1111/j.1460-9568.2011.07767.x. Epub 2011 Jun 30.

PMID:
21714819
[PubMed - indexed for MEDLINE]
17.

Developmental outcome after a single episode of status epilepticus.

Roy H, Lippé S, Lussier F, Sauerwein HC, Lortie A, Lacroix J, Lassonde M.

Epilepsy Behav. 2011 Aug;21(4):430-6. doi: 10.1016/j.yebeh.2011.05.009. Epub 2011 Jun 25.

PMID:
21705280
[PubMed - indexed for MEDLINE]
18.

Clinical, environmental, and genetic determinants of multiple sclerosis in children with acute demyelination: a prospective national cohort study.

Banwell B, Bar-Or A, Arnold DL, Sadovnick D, Narayanan S, McGowan M, O'Mahony J, Magalhaes S, Hanwell H, Vieth R, Tellier R, Vincent T, Disanto G, Ebers G, Wambera K, Connolly MB, Yager J, Mah JK, Booth F, Sebire G, Callen D, Meaney B, Dilenge ME, Lortie A, Pohl D, Doja A, Venketaswaran S, Levin S, Macdonald EA, Meek D, Wood E, Lowry N, Buckley D, Yim C, Awuku M, Cooper P, Grand'maison F, Baird JB, Bhan V, Marrie RA.

Lancet Neurol. 2011 May;10(5):436-45. doi: 10.1016/S1474-4422(11)70045-X. Epub 2011 Mar 31.

PMID:
21459044
[PubMed - indexed for MEDLINE]
19.

Intellectual disability without epilepsy associated with STXBP1 disruption.

Hamdan FF, Gauthier J, Dobrzeniecka S, Lortie A, Mottron L, Vanasse M, D'Anjou G, Lacaille JC, Rouleau GA, Michaud JL.

Eur J Hum Genet. 2011 May;19(5):607-9. doi: 10.1038/ejhg.2010.183. Epub 2011 Mar 2.

PMID:
21364700
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

The clinical spectrum of nodular heterotopias in children: report of 31 patients.

Srour M, Rioux MF, Varga C, Lortie A, Major P, Robitaille Y, Décarie JC, Michaud J, Carmant L.

Epilepsia. 2011 Apr;52(4):728-37. doi: 10.1111/j.1528-1167.2010.02975.x. Epub 2011 Feb 14.

PMID:
21320118
[PubMed - indexed for MEDLINE]
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