Allard P - Search Results

1

Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation.

Tétreault M, Gonzalez M, Dicaire MJ, Allard P, Gehring K, Leblanc D, Leclerc N, Schondorf R, Mathieu J, Zuchner S, Brais B. Tétreault M, et al. Among authors: allard p. Brain. 2015 Jun;138(Pt 6):1477-83. doi: 10.1093/brain/awv074. Epub 2015 Mar 28. Brain. 2015. PMID: 25818867 Free PMC article.

2

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. Among authors: allard p. Neurology. 1999 May 12;52(8):1658-62. doi: 10.1212/wnl.52.8.1658. Neurology. 1999. PMID: 10331695 Clinical Trial.

3

Anesthetic and surgical complications in 219 cases of myotonic dystrophy.

Mathieu J, Allard P, Gobeil G, Girard M, De Braekeleer M, Bégin P. Mathieu J, et al. Among authors: allard p. Neurology. 1997 Dec;49(6):1646-50. doi: 10.1212/wnl.49.6.1646. Neurology. 1997. PMID: 9409361

4

The incidence and carrier frequency of Tay-Sachs disease in the French-Canadian population of Quebec based on retrospective data from 24 years, 1992-2015.

Sillon G, Allard P, Drury S, Rivière JB, De Bie I. Sillon G, et al. Among authors: allard p. J Genet Couns. 2020 Dec;29(6):1173-1185. doi: 10.1002/jgc4.1284. Epub 2020 Apr 17. J Genet Couns. 2020. PMID: 32302469

5

Epidemiological study of reptured intracranial aneurysms in the Saguenay-Lac-Saint-Jean region (Quebec, Canada).

Mathieu J, Pérusse L, Allard P, Prévost C, Cantin L, Bouchard JM, DeBraekeleer M. Mathieu J, et al. Among authors: allard p. Can J Neurol Sci. 1996 Aug;23(3):184-8. doi: 10.1017/s0317167100038488. Can J Neurol Sci. 1996. PMID: 8862839

6

Biosynthesis of glycosaminoglycans: associated disorders and biochemical tests.

Sasarman F, Maftei C, Campeau PM, Brunel-Guitton C, Mitchell GA, Allard P. Sasarman F, et al. Among authors: allard p. J Inherit Metab Dis. 2016 Mar;39(2):173-88. doi: 10.1007/s10545-015-9903-z. Epub 2015 Dec 21. J Inherit Metab Dis. 2016. PMID: 26689402 Review.

7

Low citrulline in Leigh disease: still a biomarker of maternally inherited Leigh syndrome.

Debray FG, Lambert M, Allard P, Mitchell GA. Debray FG, et al. Among authors: allard p. J Child Neurol. 2010 Aug;25(8):1000-2. doi: 10.1177/0883073809351983. Epub 2010 May 14. J Child Neurol. 2010. PMID: 20472868

8

Risk factors for peak dose dyskinesia in 100 levodopa-treated parkinsonian patients.

Blanchet PJ, Allard P, Grégoire L, Tardif F, Bédard PJ. Blanchet PJ, et al. Among authors: allard p. Can J Neurol Sci. 1996 Aug;23(3):189-93. doi: 10.1017/s031716710003849x. Can J Neurol Sci. 1996. PMID: 8862840

9

Distribution of fasting plasma insulin, free fatty acids, and glucose concentrations and of homeostasis model assessment of insulin resistance in a representative sample of Quebec children and adolescents.

Allard P, Delvin EE, Paradis G, Hanley JA, O'Loughlin J, Lavallée C, Levy E, Lambert M. Allard P, et al. Clin Chem. 2003 Apr;49(4):644-9. doi: 10.1373/49.4.644. Clin Chem. 2003. PMID: 12651818

10

Normal Cerebrospinal Fluid Pyridoxal 5'-Phosphate Level in a PNPO-Deficient Patient with Neonatal-Onset Epileptic Encephalopathy.

Levtova A, Camuzeaux S, Laberge AM, Allard P, Brunel-Guitton C, Diadori P, Rossignol E, Hyland K, Clayton PT, Mills PB, Mitchell GA. Levtova A, et al. Among authors: allard p. JIMD Rep. 2015;22:67-75. doi: 10.1007/8904_2015_413. Epub 2015 Mar 12. JIMD Rep. 2015. PMID: 25762494 Free PMC article.

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