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Items: 20

1.

Higher cardiovascular fitness level is associated to better cognitive dual-task performance in Master Athletes: Mediation by cardiac autonomic control.

Dupuy O, Bosquet L, Fraser SA, Labelle V, Bherer L.

Brain Cogn. 2018 Aug;125:127-134. doi: 10.1016/j.bandc.2018.06.003. Epub 2018 Jun 30.

PMID:
29990702
2.

Cognitive function in patients with stable coronary heart disease: Related cerebrovascular and cardiovascular responses.

Gayda M, Gremeaux V, Bherer L, Juneau M, Drigny J, Dupuy O, Lapierre G, Labelle V, Fortier A, Nigam A.

PLoS One. 2017 Sep 22;12(9):e0183791. doi: 10.1371/journal.pone.0183791. eCollection 2017.

3.

Cerebral Hemodynamics During Exercise and Recovery in Heart Transplant Recipients.

Gayda M, Desjardins A, Lapierre G, Dupuy O, Fraser S, Bherer L, Juneau M, White M, Gremeaux V, Labelle V, Nigam A.

Can J Cardiol. 2016 Apr;32(4):539-46. doi: 10.1016/j.cjca.2015.07.011. Epub 2015 Jul 22.

PMID:
26577897
4.

Physical activity may improve measures of cognition in children.

Labelle V.

Evid Based Med. 2015 Aug;20(4):143. doi: 10.1136/ebmed-2014-110119. Epub 2015 Jul 3. No abstract available.

PMID:
26141179
5.

The relationship between exercise intensity, cerebral oxygenation and cognitive performance in young adults.

Mekari S, Fraser S, Bosquet L, Bonnéry C, Labelle V, Pouliot P, Lesage F, Bherer L.

Eur J Appl Physiol. 2015 Oct;115(10):2189-97. doi: 10.1007/s00421-015-3199-4. Epub 2015 Jun 11.

PMID:
26063061
6.

Clinical heterogeneity and a high proportion of novel mutations in a Chinese cohort of patients with dysferlinopathy.

Xi J, Blandin G, Lu J, Luo S, Zhu W, Béroud C, Pécheux C, Labelle V, Lévy N, Urtizberea JA, Zhao C, Krahn M.

Neurol India. 2014 Nov-Dec;62(6):635-9. doi: 10.4103/0028-3886.149386.

7.

Fitness level moderates executive control disruption during exercise regardless of age.

Labelle V, Bosquet L, Mekary S, Vu TT, Smilovitch M, Bherer L.

J Sport Exerc Psychol. 2014 Jun;36(3):258-70. doi: 10.1123/jsep.2013-0115.

PMID:
24918309
8.

Decline in executive control during acute bouts of exercise as a function of exercise intensity and fitness level.

Labelle V, Bosquet L, Mekary S, Bherer L.

Brain Cogn. 2013 Feb;81(1):10-7. doi: 10.1016/j.bandc.2012.10.001. Epub 2012 Nov 10.

PMID:
23146780
9.

UMD-DYSF, a novel locus specific database for the compilation and interactive analysis of mutations in the dysferlin gene.

Blandin G, Beroud C, Labelle V, Nguyen K, Wein N, Hamroun D, Williams B, Monnier N, Rufibach LE, Urtizberea JA, Cau P, Bartoli M, Lévy N, Krahn M.

Hum Mutat. 2012 Mar;33(3):E2317-31. doi: 10.1002/humu.22015. Epub 2011 Dec 29.

PMID:
22213072
10.

Single-dose influenza vaccination of patients with egg allergy in a multicenter study.

Webb L, Petersen M, Boden S, LaBelle V, Bird JA, Howell D, Burks AW, Laubach S.

J Allergy Clin Immunol. 2011 Jul;128(1):218-9. doi: 10.1016/j.jaci.2011.02.013. Epub 2011 Apr 2. No abstract available.

11.

Novel ancestral Dysferlin splicing mutation which migrated from the Iberian peninsula to South America.

Vernengo L, Oliveira J, Krahn M, Vieira E, Santos R, Carrasco L, Negrão L, Panuncio A, Leturcq F, Labelle V, Bronze-da-Rocha E, Mesa R, Pizzarossa C, Lévy N, Rodriguez MM.

Neuromuscul Disord. 2011 May;21(5):328-37. doi: 10.1016/j.nmd.2011.02.003. Epub 2011 Mar 9.

PMID:
21392994
12.

A naturally occurring human minidysferlin protein repairs sarcolemmal lesions in a mouse model of dysferlinopathy.

Krahn M, Wein N, Bartoli M, Lostal W, Courrier S, Bourg-Alibert N, Nguyen K, Vial C, Streichenberger N, Labelle V, DePetris D, Pécheux C, Leturcq F, Cau P, Richard I, Lévy N.

Sci Transl Med. 2010 Sep 22;2(50):50ra69. doi: 10.1126/scitranslmed.3000951.

13.

Exclusion of mutations in the dysferlin alternative exons 1 of DYSF-v1, 5a, and 40a in a cohort of 26 patients.

Krahn M, Labelle V, Borges A, Bartoli M, Lévy N.

Genet Test Mol Biomarkers. 2010 Feb;14(1):153-4. doi: 10.1089/gtmb.2009.0131.

PMID:
19929428
14.

Analysis of the DYSF mutational spectrum in a large cohort of patients.

Krahn M, Béroud C, Labelle V, Nguyen K, Bernard R, Bassez G, Figarella-Branger D, Fernandez C, Bouvenot J, Richard I, Ollagnon-Roman E, Bevilacqua JA, Salvo E, Attarian S, Chapon F, Pellissier JF, Pouget J, Hammouda el H, Laforêt P, Urtizberea JA, Eymard B, Leturcq F, Lévy N.

Hum Mutat. 2009 Feb;30(2):E345-75. doi: 10.1002/humu.20910.

PMID:
18853459
15.

Clinical characteristics of peanut-allergic children: recent changes.

Green TD, LaBelle VS, Steele PH, Kim EH, Lee LA, Mankad VS, Williams LW, Anstrom KJ, Burks AW.

Pediatrics. 2007 Dec;120(6):1304-10.

PMID:
18055680
16.

Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes.

Nguyen K, Bassez G, Krahn M, Bernard R, Laforêt P, Labelle V, Urtizberea JA, Figarella-Branger D, Romero N, Attarian S, Leturcq F, Pouget J, Lévy N, Eymard B.

Arch Neurol. 2007 Aug;64(8):1176-82.

PMID:
17698709
17.

Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathies.

Nguyen K, Bassez G, Bernard R, Krahn M, Labelle V, Figarella-Branger D, Pouget J, Hammouda el H, Béroud C, Urtizberea A, Eymard B, Leturcq F, Lévy N.

Hum Mutat. 2005 Aug;26(2):165.

PMID:
16010686
18.

Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease.

Villard L, Lévy N, Xiang F, Kpebe A, Labelle V, Chevillard C, Zhang Z, Schwartz CE, Tardieu M, Chelly J, Anvret M, Fontès M.

J Med Genet. 2001 Jul;38(7):435-42.

19.

Prenatal detection of a 17p11.2 duplication resulting from a rare recombination event and novel PCR-based strategy for molecular identification of Charcot-Marie-Tooth disease type 1A.

Bernard R, Labelle V, Negre P, Tardieu S, Azulay JP, Malzac P, Mattéi JF, Leguern E, Philip N, Lévy N.

Eur J Hum Genet. 2000 Mar;8(3):229-35.

20.

Hair artifacts that may simulate disease.

LaBelle VS, Spock A.

N C Med J. 1992 Apr;53(4):170-1. No abstract available.

PMID:
1594058

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