CHUL
2705, boulevard Laurier
CMES A-1842
Québec, Québec
Canada G1V 4G2

Dernières nouvelles

Information non disponible

19 enregistrements « 2 de 2 »

Preuss C, Capredon M, Wunnemann F, Chetaille P, Prince A, Godard B, Leclerc S, Sobreira N, Ling H, Awadalla P, Thibeault M, Khairy P, Samuels ME, Andelfinger G

Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease.

Article de revue

PLoS Genet, 12 (10), 2016.

Résumé | Liens:

Chetaille P, Preuss C, Burkhard S, Cote JM, Houde C, Castilloux J, Piche J, Gosset N, Leclerc S, Wunnemann F, Thibeault M, Gagnon C, Galli A, Tuck E, Hickson GR, Boufaied I, Lemyre E, de Santa Barbara P, Faure S, Jonzon A, Cameron M, Dietz HC, Gallo-McFarlane E, Benson DW, Moreau C, Labuda D, Zhan SH, Shen Y, Jomphe M, Jones SJ, Bakkers J, Andelfinger G, El Amine N, Boycott K, Friedman J, Michaud J, Bernier F, Brudno M, Fernandez B, Knoppers B, Scherer S

Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm.

Article de revue

Nat Genet, 46 (11), 2014.

Résumé | Liens:

Wessel DL, Berger F, Li JS, Dahnert I, Rakhit A, Fontecave S, Newburger JW, Houde C, Chetaille P, Trentadue J, Gutierrez D, Antoni D, Toledo R, Parodi WC, Guerrero R, Klinger D, Magliola R, Mazzucchelli MT, Moreno M, Bellani P, Couceiro C, Marantz P, Rosselot S, Benmaor L, Elorriaga MS, Peña G, Somoza F, Romero S, Barrea C, Sluysmans T, Nimbona G, Senga J, Moniotte S, Dessy H, Massin M, Milani SM, Mertens L, Gewillig M, Boshoff D, Eyskens B, De Wolf D, De Grote K, Panzer J, Santana MV, Miaiara MA, Santin J, Pontes SC, Guerra AL, Dona TC, Paulista PP, Souza LC, Chaccur P, Pedra CA, Daudt NS, Horowitz E, Kozak MF, Croti UA, Caneo LF, Afiune J, Succi FM, Hincapie MJ, Diniz JD, de Faria GA, Pilla CB, Blacher C, Botta AM, Pereira CA, Luiz RO, Mulinari LA, Navarro F, Pimentel GK, Miyague N, Binotto C, Pelissari EC, Sandrini MK, Lenzi A, Maluf MA, Diógenes S, Carvalho AC, Stocco JC, Silva CM, Piante LS, Trigueiro A, Pasqualucci P, Human D, Potts J, Kakadekar A, Koravangattu S, Cote JM, Delisle G, Jia B, Zhu B, Pan Y, Lv X, Luo Y, Zhang H, Zhuang J, Zeng R, Lei L, Shi C, Xie W, Wang JK, Wu MH, Hsieh KS, Lu WH, Sondergaard L, Reimers J, Helvind M, Shoeb MA, Desoky A, El Sayed MH, Moftah HM, Tynkkynen P, Sairanen H, Rautiainen P, Turanlahti M, Mildh L, Fraisse A, Blanc J, Metras D, Ghez O, Bonello B, Fouilloux V, Paoli F, Chantepie A, Poinsot J, Neuville P, Vaillant MC, Bergoend E, Michel-Behnke I, Billinger K, Hacke P, Ewert P, Abedini M, Kanaan M, Yilmaz S, Paul T, Gravenhorst V, Dann G, Kramer HH, Hoffmann U, Reineker K, Entenmann A, Fischer G, Jung O, Wörner C, Suchowerskyj P, Uhlemann F, Leischner K, Pross L, Kececioglu D, Schaeffler R, Kleideiter U, Kozlik-Feldmann R, Roemer U, Lang N, Nuebel J, Hess J, Balling G, de Winkel N, Cheung YF, Cheng LC, Chau AK, Szatmari A, Ladanyi A, Rao N, Mannam G, Vyas S, Karmalkar M, Manohar K, Dharan BS, Sadiq A, Koneti NR, Swain S, Murthy KS, Koshy S, Anil S, Kurup R, Ranjit M, Kamath S, Gandhi D, Vanaki R, Kural V, Grover V, Gupta V, Agarwal R, Sekar R, Roy C, Vaidyanathan B, Krishna K, Arun N, Supriya S, Xavier J, Bhat S, Joshi S, Sharma M, Suresh PV, Shah S, Mehta A, Manohari M, Rajappa S, Birk E, Berant M, Dagan T, Folgeman R, Bruckheimer E, Razon Y, Amir G, Tirosh N, Beer GB, Zuker N, Vidne BA

Clopidogrel in infants with systemic-to-pulmonary-artery shunts.

Article de revue

N Engl J Med, 368 (25), 2013.

Résumé | Liens:

Côté JM, Chetaille P

Complications rythmiques de la chirurgie des cardiopathies congénitales Arrhythmic complications of surgically corrected congenital cardiac defects

Article de revue

4 (Suppl 1), 2012.

Hitz MP, Lemieux-Perreault LP, Marshall C, Feroz-Zada Y, Davies R, Yang SW, Lionel AC, D'Amours G, Lemyre E, Cullum R, Bigras JL, Thibeault M, Chetaille P, Montpetit A, Khairy P, Overduin B, Klaassen S, Hoodless P, Nemer M, Stewart AF, Boerkoel C, Scherer SW, Richter A, Dube MP, Andelfinger G, Awadalla P, Hussin J, Idaghdour Y

Rare copy number variants contribute to congenital left-sided heart disease.

Article de revue

PLoS Genet, 8 (9), 2012.

Résumé | Liens:

Keshavarz-Motamed Z, Garcia J, Maftoon N, Bedard E, Chetaille P, Kadem L

A new approach for the evaluation of the severity of coarctation of the aorta using Doppler velocity index and effective orifice area: in vitro validation and clinical implications.

Article de revue

J Biomech, 45 (7), 2012.

Résumé | Liens:

Beauchesne LM, Therrien J, Alvarez N, Bergin L, Burggraf G, Chetaille P, Gordon E, Kells CM, Kiess M, Mercier LA, Oechslin EN, Stein J, Tam JW, Taylor D, Williams A, Khairy P, Mackie AS, Silversides CK, Marelli AJ

Structure and process measures of quality of care in adult congenital heart disease patients: a pan-Canadian study.

Article de revue

Int J Cardiol, 157 (1), 2012.

Résumé | Liens:

Rodes-Cabau J, Mineau S, Marrero A, Houde C, Mackey A, Cote JM, Chetaille P, Delisle G, Bertrand OF, Rivest D

Incidence, timing, and predictive factors of new-onset migraine headache attack after transcatheter closure of atrial septal defect or patent foramen ovale.

Article de revue

Am J Cardiol, 101 (5), 2008.

Résumé | Liens:

Bédard E, Rodés-Cabau J, Houde C, Mackey A, Rivest D, Cloutier S, Noël M, Marrero A, Côté JM, Chetaille P, Delisle G, Leblanc MH, Bertrand OF

Enhanced thrombogenesis but not platelet activation is associated with transcatheter closure of patent foramen ovale in patients with cryptogenic stroke.

Article de revue

Stroke, 38 (1), 2007.

Résumé | Liens:

19 enregistrements « 2 de 2 »
Signaler des ajouts ou des modifications

Projets terminés récemment

  • Support au financement du projet de recherche clinique en cardiologie pédiatrique, Subvention, Fondation du CHU de Québec, du 2018-10-17 au 2020-03-31
Information provenant du registre des projets de recherche de l'Université Laval