Mitchell GA - Search Results

1

Population history and its impact on medical genetics in Quebec.

Laberge AM, Michaud J, Richter A, Lemyre E, Lambert M, Brais B, Mitchell GA. Laberge AM, et al. Among authors: mitchell ga. Clin Genet. 2005 Oct;68(4):287-301. doi: 10.1111/j.1399-0004.2005.00497.x. Clin Genet. 2005. PMID: 16143014 Review.

2

The Delta>15 Kb deletion French Canadian founder mutation in familial hypercholesterolemia: rapid polymerase chain reaction-based diagnostic assay and prevalence in Quebec.

Simard LR, Viel J, Lambert M, Paradis G, Levy E, Delvin EE, Mitchell GA. Simard LR, et al. Among authors: mitchell ga. Clin Genet. 2004 Mar;65(3):202-8. doi: 10.1111/j.0009-9163.2004.00223.x. Clin Genet. 2004. PMID: 14756670

3

Long-term follow-up of a new case of liver glycogen synthase deficiency.

Laberge AM, Mitchell GA, van de Werve G, Lambert M. Laberge AM, et al. Among authors: mitchell ga. Am J Med Genet A. 2003 Jul 1;120A(1):19-22. doi: 10.1002/ajmg.a.20110. Am J Med Genet A. 2003. PMID: 12794686

4

Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15.

Debray FG, Lambert M, Lemieux B, Soucy JF, Drouin R, Fenyves D, Dubé J, Maranda B, Laframboise R, Mitchell GA. Debray FG, et al. Among authors: mitchell ga. J Med Genet. 2008 Nov;45(11):759-64. doi: 10.1136/jmg.2008.059097. J Med Genet. 2008. PMID: 18978333 Free article.

5

Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.

Bétard C, Rasquin-Weber A, Brewer C, Drouin E, Clark S, Verner A, Darmond-Zwaig C, Fortin J, Mercier J, Chagnon P, Fujiwara TM, Morgan K, Richter A, Hudson TJ, Mitchell GA. Bétard C, et al. Among authors: mitchell ga. Am J Hum Genet. 2000 Jul;67(1):222-8. doi: 10.1086/302993. Epub 2000 May 11. Am J Hum Genet. 2000. PMID: 10820129 Free PMC article.

6

Recurrent pancreatitis in mitochondrial cytopathy.

Debray FG, Drouin E, Herzog D, Lortie A, Lambert M, Garel L, Mitchell GA, Michaud JL. Debray FG, et al. Among authors: mitchell ga. Am J Med Genet A. 2006 Nov 1;140(21):2330-5. doi: 10.1002/ajmg.a.31457. Am J Med Genet A. 2006. PMID: 17022070 Review.

7

Disorders of mitochondrial function.

Debray FG, Lambert M, Mitchell GA. Debray FG, et al. Among authors: mitchell ga. Curr Opin Pediatr. 2008 Aug;20(4):471-82. doi: 10.1097/MOP.0b013e328306ebb6. Curr Opin Pediatr. 2008. PMID: 18622207 Free article. Review.

8

Pyruvate carboxylase deficiency: prenatal onset of ischemia-like brain lesions in two sibs with the acute neonatal form.

Brun N, Robitaille Y, Grignon A, Robinson BH, Mitchell GA, Lambert M. Brun N, et al. Among authors: mitchell ga. Am J Med Genet. 1999 May 21;84(2):94-101. Am J Med Genet. 1999. PMID: 10323732

9

Diversity of ARSACS mutations in French-Canadians.

Thiffault I, Dicaire MJ, Tetreault M, Huang KN, Demers-Lamarche J, Bernard G, Duquette A, Larivière R, Gehring K, Montpetit A, McPherson PS, Richter A, Montermini L, Mercier J, Mitchell GA, Dupré N, Prévost C, Bouchard JP, Mathieu J, Brais B. Thiffault I, et al. Among authors: mitchell ga. Can J Neurol Sci. 2013 Jan;40(1):61-6. doi: 10.1017/s0317167100012968. Can J Neurol Sci. 2013. PMID: 23250129

10

Clinical, metabolic, and genetic aspects of cytochrome C oxidase deficiency in Saguenay-Lac-Saint-Jean.

Morin C, Mitchell G, Larochelle J, Lambert M, Ogier H, Robinson BH, De Braekeleer M. Morin C, et al. Am J Hum Genet. 1993 Aug;53(2):488-96. Am J Hum Genet. 1993. PMID: 8392291 Free PMC article.

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