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Items: 1 to 50 of 120

1.

Clinical and translational advances in esophageal squamous cell carcinoma.

Reichenbach ZW, Murray MG, Saxena R, Farkas D, Karassik EG, Klochkova A, Patel K, Tice C, Hall TM, Gang J, Parkman HP, Ward SJ, Tétreault MP, Whelan KA.

Adv Cancer Res. 2019;144:95-135. doi: 10.1016/bs.acr.2019.05.004. Epub 2019 Jun 10.

PMID:
31349905
2.

GI Manifestations With a Focus on the Esophagus: Recent Progress in Understanding Pathogenesis.

Tétreault MP, Kahrilas P.

Curr Rheumatol Rep. 2019 Jul 3;21(8):42. doi: 10.1007/s11926-019-0841-x. Review.

PMID:
31270707
3.

Inpatient Versus Outpatient Arthroplasty: A Single-Surgeon, Matched Cohort Analysis of 90-Day Complications.

Darrith B, Frisch NB, Tetreault MW, Fice MP, Culvern CN, Della Valle CJ.

J Arthroplasty. 2019 Feb;34(2):221-227. doi: 10.1016/j.arth.2018.10.015. Epub 2018 Oct 17.

PMID:
30415832
4.

Reply: TDP-43 mutations increase HNRNP A1-7B through gain of splicing function.

Tétreault M, Deshaies JE, Semmler S, Sidibé H, Shkreta L, Volkening K, Soreq H, Strong MJ, Chabot B, Vande Velde C.

Brain. 2018 Dec 1;141(12):e84. doi: 10.1093/brain/awy261. No abstract available.

PMID:
30364932
5.

Analysis of Player Statistics in Major League Baseball Players Before and After Achilles Tendon Repair.

Saltzman BM, Tetreault MW, Bohl DD, Tetreault D, Lee S, Bach BR Jr.

HSS J. 2018 Jul;14(2):223-224. doi: 10.1007/s11420-017-9603-3. Epub 2018 Feb 27. No abstract available.

6.

Are patients being evaluated for periprosthetic joint infection prior to referral to a tertiary care center?

Tetreault MW, Estrera KA, Kayupov E, Brander C, Della Valle CJ.

Arthroplast Today. 2017 Nov 10;4(2):216-220. doi: 10.1016/j.artd.2017.10.001. eCollection 2018 Jun.

7.

Short-term Complications After Revision Hip Arthroplasty for Prosthetic Joint Infection Are Increased Relative to Noninfectious Revisions.

Boddapati V, Fu MC, Tetreault MW, Blevins JL, Richardson SS, Su EP.

J Arthroplasty. 2018 Sep;33(9):2997-3002. doi: 10.1016/j.arth.2018.05.001. Epub 2018 May 9.

PMID:
29853307
8.

Indoleamine 2,3-dioxygenase 1 and overall survival of patients diagnosed with esophageal cancer.

Rosenberg AJ, Wainwright DA, Rademaker A, Galvez C, Genet M, Zhai L, Lauing KL, Mulcahy MF, Hayes JP, Odell DD, Horbinski C, Komanduri S, Tetreault MP, Kim KA, Villaflor VM.

Oncotarget. 2018 May 4;9(34):23482-23493. doi: 10.18632/oncotarget.25235. eCollection 2018 May 4.

9.

Autophagy as a cytoprotective mechanism in esophageal squamous cell carcinoma.

Hall TM, Tétreault MP, Hamilton KE, Whelan KA.

Curr Opin Pharmacol. 2018 Aug;41:12-19. doi: 10.1016/j.coph.2018.04.003. Epub 2018 Apr 17. Review.

10.

A three-way inter-molecular network accounts for the CaVα2δ1-induced functional modulation of the pore-forming CaV1.2 subunit.

Briot J, Mailhot O, Bourdin B, Tétreault MP, Najmanovich R, Parent L.

J Biol Chem. 2018 May 11;293(19):7176-7188. doi: 10.1074/jbc.RA118.001902. Epub 2018 Mar 27.

11.

Clinical, biochemical, and genetic features of four patients with short-chain enoyl-CoA hydratase (ECHS1) deficiency.

Fitzsimons PE, Alston CL, Bonnen PE, Hughes J, Crushell E, Geraghty MT, Tetreault M, O'Reilly P, Twomey E, Sheikh Y, Walsh R, Waterham HR, Ferdinandusse S, Wanders RJA, Taylor RW, Pitt JJ, Mayne PD.

Am J Med Genet A. 2018 May;176(5):1115-1127. doi: 10.1002/ajmg.a.38658. Epub 2018 Mar 25.

12.

Adverse Local Tissue Reaction After a Metal-on-Metal Total Hip Prosthesis Without Elevated Serum Metal Ion Levels.

Tetreault MW, Jacobs JJ, Mahmud W, Nam D.

Orthopedics. 2018 May 1;41(3):e438-e441. doi: 10.3928/01477447-20171213-05. Epub 2017 Dec 19.

PMID:
29257191
13.

POLR3A variants in hereditary spastic paraplegia and ataxia.

Gauquelin L, Tétreault M, Thiffault I, Farrow E, Miller N, Yoo B, Bareke E, Yoon G, Suchowersky O, Dupré N, Tarnopolsky M, Brais B, Wolf NI, Majewski J, Rouleau GA, Gan-Or Z, Bernard G.

Brain. 2018 Jan 1;141(1):e1. doi: 10.1093/brain/awx290. No abstract available.

14.

Same-Day Discharge Compared with Inpatient Hospitalization Following Hip and Knee Arthroplasty.

Basques BA, Tetreault MW, Della Valle CJ.

J Bone Joint Surg Am. 2017 Dec 6;99(23):1969-1977. doi: 10.2106/JBJS.16.00739.

PMID:
29206786
15.

A classification-based approach to the patella in revision total knee arthroplasty.

Tetreault MW, Gross CE, Yi PH, Bohl DD, Sporer SM, Della Valle CJ.

Arthroplast Today. 2017 Aug 7;3(4):264-268. doi: 10.1016/j.artd.2017.05.002. eCollection 2017 Dec.

16.

Orthostatic hypotension associated with executive dysfunction in mild cognitive impairment.

Bocti C, Pépin F, Tétreault M, Cossette P, Langlois F, Imbeault H, Duval N, Lacombe G, Fulop T.

J Neurol Sci. 2017 Nov 15;382:79-83. doi: 10.1016/j.jns.2017.09.028. Epub 2017 Sep 27.

PMID:
29111025
17.

A de novo mutation in RPL10 causes a rare X-linked ribosomopathy characterized by syndromic intellectual disability and epilepsy: A new case and review of the literature.

Bourque DK, Hartley T, Nikkel SM, Pohl D, Tétreault M, Kernohan KD; Care4Rare Canada Consortium, Dyment DA.

Eur J Med Genet. 2018 Feb;61(2):89-93. doi: 10.1016/j.ejmg.2017.10.011. Epub 2017 Oct 21. Review.

PMID:
29066376
18.

TRMT5 mutations are associated with features of complex hereditary spastic paraparesis.

Tarnopolsky MA, Brady L, Tetreault M; Care4Rare Canada Consortium.

Neurology. 2017 Nov 21;89(21):2210-2211. doi: 10.1212/WNL.0000000000004657. Epub 2017 Oct 11. No abstract available.

19.

SHORT syndrome due to a novel de novo mutation in PRKCE (Protein Kinase Cɛ) impairing TORC2-dependent AKT activation.

Alcantara D, Elmslie F, Tetreault M, Bareke E, Hartley T; Care4Rare Consortium, Majewski J, Boycott K, Innes AM, Dyment DA, O'Driscoll M.

Hum Mol Genet. 2017 Oct 1;26(19):3713-3721. doi: 10.1093/hmg/ddx256.

PMID:
28934384
20.

Negatively charged residues in the first extracellular loop of the L-type CaV1.2 channel anchor the interaction with the CaVα2δ1 auxiliary subunit.

Bourdin B, Briot J, Tétreault MP, Sauvé R, Parent L.

J Biol Chem. 2017 Oct 20;292(42):17236-17249. doi: 10.1074/jbc.M117.806893. Epub 2017 Sep 1.

21.

Recessive mutations in NDUFA2 cause mitochondrial leukoencephalopathy.

Perrier S, Gauquelin L, Tétreault M, Tran LT, Webb N, Srour M, Mitchell JJ, Brunel-Guitton C, Majewski J, Long V, Keller S, Gambello MJ, Simons C; Care4Rare Canada Consortium, Vanderver A, Bernard G.

Clin Genet. 2018 Feb;93(2):396-400. doi: 10.1111/cge.13126. Epub 2017 Dec 21.

PMID:
28857146
22.

Whole-exome sequencing is a valuable diagnostic tool for inherited peripheral neuropathies: Outcomes from a cohort of 50 families.

Hartley T, Wagner JD, Warman-Chardon J, Tétreault M, Brady L, Baker S, Tarnopolsky M, Bourque PR, Parboosingh JS, Smith C, McInnes B, Innes AM, Bernier F, Curry CJ, Yoon G, Horvath GA, Bareke E, Gillespie M; FORGE Canada Consortium; Care4Rare Canada Consortium, Majewski J, Bulman DE, Dyment DA, Boycott KM.

Clin Genet. 2018 Feb;93(2):301-309. doi: 10.1111/cge.13101. Epub 2017 Dec 12.

PMID:
28708278
23.

Analysis of Player Statistics in Major League Baseball Players Before and After Achilles Tendon Repair.

Saltzman BM, Tetreault MW, Bohl DD, Tetreault D, Lee S, Bach BR Jr.

HSS J. 2017 Jul;13(2):108-118. doi: 10.1007/s11420-016-9540-6. Epub 2017 Feb 1.

24.

Sepsis Within 30 Days of Geriatric Hip Fracture Surgery.

Bohl DD, Iantorno SE, Saltzman BM, Tetreault MW, Darrith B, Della Valle CJ.

J Arthroplasty. 2017 Oct;32(10):3114-3119. doi: 10.1016/j.arth.2017.05.024. Epub 2017 May 19.

PMID:
28634098
25.

MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability.

Ylikallio E, Woldegebriel R, Tumiati M, Isohanni P, Ryan MM, Stark Z, Walsh M, Sawyer SL, Bell KM, Oshlack A, Lockhart PJ, Shcherbii M, Estrada-Cuzcano A, Atkinson D, Hartley T, Tetreault M, Cuppen I, van der Pol WL, Candayan A, Battaloglu E, Parman Y, van Gassen KLI, van den Boogaard MH, Boycott KM, Kauppi L, Jordanova A, Lönnqvist T, Tyynismaa H.

Brain. 2017 Aug 1;140(8):2093-2103. doi: 10.1093/brain/awx138.

PMID:
28633435
26.

Proteolytic cleavage of the hydrophobic domain in the CaVα2δ1 subunit improves assembly and activity of cardiac CaV1.2 channels.

Segura E, Bourdin B, Tétreault MP, Briot J, Allen BG, Mayer G, Parent L.

J Biol Chem. 2017 Jun 30;292(26):11109-11124. doi: 10.1074/jbc.M117.784355. Epub 2017 May 11.

27.

Medial Gastrocnemius Flap in the Course of Treatment for an Infection at the Site of a Total Knee Arthroplasty.

Tetreault MW, Della Valle CJ, Hellman MD, Wysocki RW.

JBJS Essent Surg Tech. 2017 May 10;7(2):e14. doi: 10.2106/JBJS.ST.17.00005. eCollection 2017 Jun 28.

28.

A Prospective Randomized Trial of Mini-Incision Posterior and 2-Incision Total Hip Arthroplasty: Minimum 5-Year Follow-Up.

Sershon RA, Tetreault MW, Della Valle CJ.

J Arthroplasty. 2017 Aug;32(8):2462-2465. doi: 10.1016/j.arth.2017.03.038. Epub 2017 Mar 23.

PMID:
28434694
29.

Compound heterozygous mutations in the gene PIGP are associated with early infantile epileptic encephalopathy.

Johnstone DL, Nguyen TT, Murakami Y, Kernohan KD, Tétreault M, Goldsmith C, Doja A, Wagner JD, Huang L, Hartley T, St-Denis A, le Deist F, Majewski J, Bulman DE; Care4Rare Canada Consortium, Kinoshita T, Dyment DA, Boycott KM, Campeau PM.

Hum Mol Genet. 2017 May 1;26(9):1706-1715. doi: 10.1093/hmg/ddx077.

PMID:
28334793
30.

Inherited Ventricular Arrhythmias: The Role of the Multi-Subunit Structure of the L-Type Calcium Channel Complex.

Briot J, Tétreault MP, Bourdin B, Parent L.

Adv Exp Med Biol. 2017;966:55-64. doi: 10.1007/5584_2016_186. Review.

PMID:
28315127
31.

Matchmaking facilitates the diagnosis of an autosomal-recessive mitochondrial disease caused by biallelic mutation of the tRNA isopentenyltransferase (TRIT1) gene.

Kernohan KD, Dyment DA, Pupavac M, Cramer Z, McBride A, Bernard G, Straub I, Tetreault M, Hartley T, Huang L, Sell E, Majewski J, Rosenblatt DS, Shoubridge E, Mhanni A, Myers T, Proud V, Vergano S, Spangler B, Farrow E, Kussman J, Safina N; Care4Rare Consortium, Saunders C, Boycott KM, Thiffault I.

Hum Mutat. 2017 May;38(5):511-516. doi: 10.1002/humu.23196. Epub 2017 Mar 6.

PMID:
28185376
32.

Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole-exome sequencing.

Balci TB, Hartley T, Xi Y, Dyment DA, Beaulieu CL, Bernier FP, Dupuis L, Horvath GA, Mendoza-Londono R, Prasad C, Richer J, Yang XR, Armour CM, Bareke E, Fernandez BA, McMillan HJ, Lamont RE, Majewski J, Parboosingh JS, Prasad AN, Rupar CA, Schwartzentruber J, Smith AC, Tétreault M; FORGE Canada Consortium; Care4Rare Canada Consortium, Innes AM, Boycott KM.

Clin Genet. 2017 Sep;92(3):281-289. doi: 10.1111/cge.12987. Epub 2017 Mar 13.

PMID:
28170084
33.

Identification and functional characterization of a novel MTFMT mutation associated with selective vulnerability of the visual pathway and a mild neurological phenotype.

La Piana R, Weraarpachai W, Ospina LH, Tetreault M, Majewski J; Care4Rare Canada Consortium, Bruce Pike G, Decarie JC, Tampieri D, Brais B, Shoubridge EA.

Neurogenetics. 2017 Apr;18(2):97-103. doi: 10.1007/s10048-016-0506-0. Epub 2017 Jan 5.

PMID:
28058511
34.

Perceived Leg-Length Discrepancy After Primary Total Knee Arthroplasty: Does Knee Alignment Play a Role?

Goldstein ZH, Yi PH, Batko B, Kearns S, Tetreault MW, Levine BR, Della Valle CJ, Sporer SM.

Am J Orthop (Belle Mead NJ). 2016 Nov/Dec;45(7):E429-E433.

PMID:
28005109
35.

XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia.

Hoch NC, Hanzlikova H, Rulten SL, Tétreault M, Komulainen E, Ju L, Hornyak P, Zeng Z, Gittens W, Rey SA, Staras K, Mancini GM, McKinnon PJ, Wang ZQ, Wagner JD; Care4Rare Canada Consortium, Yoon G, Caldecott KW.

Nature. 2017 Jan 5;541(7635):87-91. doi: 10.1038/nature20790. Epub 2016 Dec 21.

36.

RMND1-Related Leukoencephalopathy With Temporal Lobe Cysts and Hearing Loss-Another Mendelian Mimicker of Congenital Cytomegalovirus Infection.

Ulrick N, Goldstein A, Simons C, Taft RJ, Helman G, Pizzino A, Bloom M, Vogt J, Pysden K, Diodato D, Martinelli D, Monavari A, Buhas D, van Karnebeek CD, Dorboz I, Boespflug-Tanguy O, Rodriguez D, Tétreault M, Majewski J, Bernard G, Ng YS; Care4Rare Canada Consortium, McFarland R, Vanderver A.

Pediatr Neurol. 2017 Jan;66:59-62. doi: 10.1016/j.pediatrneurol.2016.09.003. Epub 2016 Sep 13.

PMID:
27843092
37.

Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion.

Vasli N, Harris E, Karamchandani J, Bareke E, Majewski J, Romero NB, Stojkovic T, Barresi R, Tasfaout H, Charlton R, Malfatti E, Bohm J, Marini-Bettolo C, Choquet K, Dicaire MJ, Shao YH, Topf A, O'Ferrall E, Eymard B, Straub V, Blanco G, Lochmüller H, Brais B, Laporte J, Tétreault M.

Brain. 2017 Jan;140(1):37-48. doi: 10.1093/brain/aww257. Epub 2016 Nov 5.

38.

A cost comparison of unicompartmental and total knee arthroplasty.

Shankar S, Tetreault MW, Jegier BJ, Andersson GB, Della Valle CJ.

Knee. 2016 Dec;23(6):1016-1019. doi: 10.1016/j.knee.2015.11.012. Epub 2016 Oct 31.

PMID:
27810433
39.

Determination of the Relative Cell Surface and Total Expression of Recombinant Ion Channels Using Flow Cytometry.

Bourdin B, Segura E, Tétreault MP, Lesage S, Parent L.

J Vis Exp. 2016 Sep 28;(115). doi: 10.3791/54732.

40.

Concordance between whole-exome sequencing and clinical Sanger sequencing: implications for patient care.

Hamilton A, Tétreault M, Dyment DA, Zou R, Kernohan K, Geraghty MT; FORGE Canada Consortium; Care4Rare Canada Consortium, Hartley T, Boycott KM.

Mol Genet Genomic Med. 2016 May 10;4(5):504-12. doi: 10.1002/mgg3.223. eCollection 2016 Sep.

41.

KLF4 transcriptionally activates non-canonical WNT5A to control epithelial stratification.

Tetreault MP, Weinblatt D, Shaverdashvili K, Yang Y, Katz JP.

Sci Rep. 2016 May 17;6:26130. doi: 10.1038/srep26130.

42.

Mutations in GALC cause late-onset Krabbe disease with predominant cerebellar ataxia.

Shao YH, Choquet K, La Piana R, Tétreault M, Dicaire MJ; Care4Rare Canada Consortium, Boycott KM, Majewski J, Brais B.

Neurogenetics. 2016 Apr;17(2):137-41. doi: 10.1007/s10048-016-0476-2. Epub 2016 Feb 26.

PMID:
26915362
43.

Esophageal Expression of Active IκB Kinase-β in Mice Up-Regulates Tumor Necrosis Factor and Granulocyte-Macrophage Colony-Stimulating Factor, Promoting Inflammation and Angiogenesis.

Tétreault MP, Weinblatt D, Ciolino JD, Klein-Szanto AJ, Sackey BK, Twyman-Saint Victor C, Karakasheva T, Teal V, Katz JP.

Gastroenterology. 2016 Jun;150(7):1609-1619.e11. doi: 10.1053/j.gastro.2016.02.025. Epub 2016 Feb 17.

44.

Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation.

Ejaz R, Qin W, Huang L, Blaser S, Tetreault M, Hartley T, Boycott KM, Carter MT; Care4Rare Canada Consortium.

Am J Med Genet A. 2016 Apr;170A(4):1070-5. doi: 10.1002/ajmg.a.37541. Epub 2016 Jan 11.

PMID:
26754023
45.

Identification of Glycosylation Sites Essential for Surface Expression of the CaVα2δ1 Subunit and Modulation of the Cardiac CaV1.2 Channel Activity.

Tétreault MP, Bourdin B, Briot J, Segura E, Lesage S, Fiset C, Parent L.

J Biol Chem. 2016 Feb 26;291(9):4826-43. doi: 10.1074/jbc.M115.692178. Epub 2016 Jan 7.

46.

Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability.

Stray-Pedersen A, Cobben JM, Prescott TE, Lee S, Cang C, Aranda K, Ahmed S, Alders M, Gerstner T, Aslaksen K, Tétreault M, Qin W, Hartley T, Jhangiani SN, Muzny DM, Tarailo-Graovac M, van Karnebeek CD; Care4Rare Canada Consortium; Baylor-Hopkins Center for Mendelian Genomics, Lupski JR, Ren D, Yoon G.

Am J Hum Genet. 2016 Jan 7;98(1):202-9. doi: 10.1016/j.ajhg.2015.11.004. Epub 2015 Dec 17.

47.

Autosomal recessive cerebellar ataxia caused by a homozygous mutation in PMPCA.

Choquet K, Zurita-Rendón O, La Piana R, Yang S, Dicaire MJ; Care4Rare Consortium, Boycott KM, Majewski J, Shoubridge EA, Brais B, Tétreault M.

Brain. 2016 Mar;139(Pt 3):e19. doi: 10.1093/brain/awv362. Epub 2015 Dec 10. No abstract available.

PMID:
26657514
48.

Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8.

Boycott KM, Beaulieu CL, Kernohan KD, Gebril OH, Mhanni A, Chudley AE, Redl D, Qin W, Hampson S, Küry S, Tetreault M, Puffenberger EG, Scott JN, Bezieau S, Reis A, Uebe S, Schumacher J, Hegele RA, McLeod DR, Gálvez-Peralta M, Majewski J, Ramaekers VT; Care4Rare Canada Consortium, Nebert DW, Innes AM, Parboosingh JS, Abou Jamra R.

Am J Hum Genet. 2015 Dec 3;97(6):886-93. doi: 10.1016/j.ajhg.2015.11.002.

49.

SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases.

Choquet K, Tétreault M, Yang S, La Piana R, Dicaire MJ, Vanstone MR, Mathieu J, Bouchard JP, Rioux MF, Rouleau GA; Care4Rare Canada Consortium, Boycott KM, Majewski J, Brais B.

Eur J Hum Genet. 2016 Jul;24(7):1016-21. doi: 10.1038/ejhg.2015.240. Epub 2015 Dec 2.

50.

DNM1L-related mitochondrial fission defect presenting as refractory epilepsy.

Vanstone JR, Smith AM, McBride S, Naas T, Holcik M, Antoun G, Harper ME, Michaud J, Sell E, Chakraborty P, Tetreault M; Care4Rare Consortium, Majewski J, Baird S, Boycott KM, Dyment DA, MacKenzie A, Lines MA.

Eur J Hum Genet. 2016 Jul;24(7):1084-8. doi: 10.1038/ejhg.2015.243. Epub 2015 Nov 25.

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