M Tetreault
Overview
Explore the profile of M Tetreault including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
268
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Recent Articles
1.
Kerwin A, Burhans W, Mann S, Tetreault M, Nydam D, Overton T
J Dairy Sci
. 2022 Apr;
105(6):5327-5348.
PMID: 35469639
Our objective was to describe management and herd characteristics of the transition period on freestall dairy herds in the northeastern United States using an on-farm survey and prospective cohort design....
2.
Perrier S, Gauquelin L, Tetreault M, Tran L, Webb N, Srour M, et al.
Clin Genet
. 2017 Sep;
93(2):396-400.
PMID: 28857146
Deficiencies of mitochondrial respiratory chain complex I frequently result in leukoencephalopathy in young patients, and different mutations in the genes encoding its subunits are still being uncovered. We report 2...
3.
Hartley T, Wagner J, Warman-Chardon J, Tetreault M, Brady L, Baker S, et al.
Clin Genet
. 2017 Jul;
93(2):301-309.
PMID: 28708278
The inherited peripheral neuropathies (IPNs) are characterized by marked clinical and genetic heterogeneity and include relatively frequent presentations such as Charcot-Marie-Tooth disease and hereditary motor neuropathy, as well as more...
4.
Balci T, Hartley T, Xi Y, Dyment D, Beaulieu C, Bernier F, et al.
Clin Genet
. 2017 Feb;
92(3):281-289.
PMID: 28170084
Background: Recent clinical whole exome sequencing (WES) cohorts have identified unanticipated multiple genetic diagnoses in single patients. However, the frequency of multiple genetic diagnoses in families is largely unknown. Aims:...
5.
Dyment D, Tetreault M, Beaulieu C, Hartley T, Ferreira P, Chardon J, et al.
Clin Genet
. 2014 Jul;
88(1):34-40.
PMID: 25046240
Whole-exome sequencing (WES) has transformed our ability to detect mutations causing rare diseases. FORGE (Finding Of Rare disease GEnes) and Care4Rare Canada are nation-wide projects focused on identifying disease genes...
6.
Thiffault I, Dicaire M, Tetreault M, Huang K, Demers-Lamarche J, Bernard G, et al.
Can J Neurol Sci
. 2012 Dec;
40(1):61-6.
PMID: 23250129
Background: The growing number of spastic ataxia of Charlevoix-Saguenay (SACS) gene mutations reported worldwide has broadened the clinical phenotype of autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS). The identification of...
7.
Tetreault M, Srour M, Allyson J, Thiffault I, Loisel L, Robitaille Y, et al.
Can J Neurol Sci
. 2011 Aug;
38(5):747-52.
PMID: 21856579
Background: We have recruited a group of four living and reviewed the records of six deceased distantly related French-Canadians of Acadian descent affected by a childhood-onset form of recessive limb-girdle...
8.
Rossignol E, Mathieu J, Thiffault I, Tetreault M, Dicaire M, Chrestian N, et al.
Neurology
. 2007 Nov;
69(20):1937-41.
PMID: 17998485
Background: Myotonia is observed in classic congenital myotonia caused by CLCN1 mutations and in sodium-channel myotonia (SCM) due to SCN4A mutations. Methods: We assessed 66 electrically proven cases of myotonia...
9.
A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12
Jarry J, Rioux M, Bolduc V, Robitaille Y, Khoury V, Thiffault I, et al.
Brain
. 2006 Sep;
130(Pt 2):368-80.
PMID: 17008331
Limb-girdle muscular dystrophies (LGMD) are a heterogeneous group of pathologies. We have identified a cohort of 14 French-Canadian patients from eight different families displaying a novel form of LGMD with...
10.
Tetreault M, Duquette A, Thiffault I, Bherer C, Jarry J, Loisel L, et al.
Brain
. 2006 Jun;
129(Pt 8):2077-84.
PMID: 16760198
Congenital muscular dystrophies (CMDS) are a heterogeneous group of disorders. A growing number of CMDS have been found to be associated with joint hyperlaxity. We recruited 14 French-Canadian cases belonging...