Mathieu J - Search Results

1

Epidemiological surveillance of myotonic dystrophy type 1: a 25-year population-based study.

Mathieu J, Prévost C. Mathieu J, et al. Neuromuscul Disord. 2012 Nov;22(11):974-9. doi: 10.1016/j.nmd.2012.05.017. Epub 2012 Aug 1. Neuromuscul Disord. 2012. PMID: 22858159

2

Psychosocial impact of predictive testing for myotonic dystrophy type 1.

Prévost C, Veillette S, Perron M, Laberge C, Tremblay C, Auclair J, Villeneuve J, Tremblay M, Mathieu J. Prévost C, et al. Among authors: mathieu j. Am J Med Genet A. 2004 Apr 1;126A(1):68-77. doi: 10.1002/ajmg.a.20560. Am J Med Genet A. 2004. PMID: 15039975

3

Anticipation in myotonic dystrophy type 1 parents with small CTG expansions.

Pratte A, Prévost C, Puymirat J, Mathieu J. Pratte A, et al. Among authors: mathieu j. Am J Med Genet A. 2015 Apr;167A(4):708-14. doi: 10.1002/ajmg.a.36950. Epub 2015 Feb 25. Am J Med Genet A. 2015. PMID: 25712547

4

Myotonic dystrophy: clinical assessment of muscular disability in an isolated population with presumed homogeneous mutation.

Mathieu J, De Braekeleer M, Prévost C, Boily C. Mathieu J, et al. Neurology. 1992 Jan;42(1):203-8. doi: 10.1212/wnl.42.1.203. Neurology. 1992. PMID: 1734305

5

A 10-year study of mortality in a cohort of patients with myotonic dystrophy.

Mathieu J, Allard P, Potvin L, Prévost C, Bégin P. Mathieu J, et al. Neurology. 1999 May 12;52(8):1658-62. doi: 10.1212/wnl.52.8.1658. Neurology. 1999. PMID: 10331695 Clinical Trial.

6

Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions.

Arsenault ME, Prévost C, Lescault A, Laberge C, Puymirat J, Mathieu J. Arsenault ME, et al. Among authors: mathieu j. Neurology. 2006 Apr 25;66(8):1248-50. doi: 10.1212/01.wnl.0000208513.48550.08. Neurology. 2006. PMID: 16636244

7

A 9-year follow-up study of the natural progression of upper limb performance in myotonic dystrophy type 1: A similar decline for phenotypes but not for gender.

Raymond K, Levasseur M, Mathieu J, Desrosiers J, Gagnon C. Raymond K, et al. Among authors: mathieu j. Neuromuscul Disord. 2017 Jul;27(7):673-682. doi: 10.1016/j.nmd.2017.04.007. Epub 2017 May 2. Neuromuscul Disord. 2017. PMID: 28527585

8

Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada).

Mathieu J, De Braekeleer M, Prévost C. Mathieu J, et al. Neurology. 1990 May;40(5):839-42. doi: 10.1212/wnl.40.5.839. Neurology. 1990. PMID: 2330114

9

Myotonic dystrophy: linkage with apolipoprotein E and estimation of the gene carrier status with genetic markers.

Thibault MC, Mathieu J, Moorjani S, Lescault A, Prévost C, Gaudet D, Morissette J, Laberge C. Thibault MC, et al. Among authors: mathieu j. Can J Neurol Sci. 1989 Feb;16(1):134-40. doi: 10.1017/s0317167100028687. Can J Neurol Sci. 1989. PMID: 2924208

10

Sibship stability of genotype and phenotype in myotonic dystrophy.

Brisson D, Tremblay M, Prévost C, Laberge C, Puymirat J, Mathieu J. Brisson D, et al. Among authors: mathieu j. Clin Genet. 2002 Sep;62(3):220-5. doi: 10.1034/j.1399-0004.2002.620306.x. Clin Genet. 2002. PMID: 12220437

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