Mitchell GA - Search Results

1

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

2

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.

3

Long-term outcome of Leigh syndrome caused by the NARP-T8993C mtDNA mutation.

Debray FG, Lambert M, Lortie A, Vanasse M, Mitchell GA. Debray FG, et al. Among authors: mitchell ga. Am J Med Genet A. 2007 Sep 1;143A(17):2046-51. doi: 10.1002/ajmg.a.31880. Am J Med Genet A. 2007. PMID: 17663470 Review.

4

Treatment of cobalamin C (cblC) deficiency during pregnancy.

Brunel-Guitton C, Costa T, Mitchell GA, Lambert M. Brunel-Guitton C, et al. Among authors: mitchell ga. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S409-12. doi: 10.1007/s10545-010-9202-7. Epub 2010 Sep 10. J Inherit Metab Dis. 2010. PMID: 20830523

5

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

6

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.

7

Long-term outcome and clinical spectrum of 73 pediatric patients with mitochondrial diseases.

Debray FG, Lambert M, Chevalier I, Robitaille Y, Decarie JC, Shoubridge EA, Robinson BH, Mitchell GA. Debray FG, et al. Among authors: mitchell ga. Pediatrics. 2007 Apr;119(4):722-33. doi: 10.1542/peds.2006-1866. Pediatrics. 2007. PMID: 17403843

8

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.

9

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.

10

LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.

Debray FG, Morin C, Janvier A, Villeneuve J, Maranda B, Laframboise R, Lacroix J, Decarie JC, Robitaille Y, Lambert M, Robinson BH, Mitchell GA. Debray FG, et al. Among authors: mitchell ga. J Med Genet. 2011 Mar;48(3):183-9. doi: 10.1136/jmg.2010.081976. Epub 2011 Jan 25. J Med Genet. 2011. PMID: 21266382

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