Lambert MA - Search Results

1

Stroke-like episodes in autosomal recessive cytochrome oxidase deficiency.

Morin C, Dubé J, Robinson BH, Lacroix J, Michaud J, De Braekeleer M, Geoffroy G, Lortie A, Blanchette C, Lambert MA, Mitchell GA. Morin C, et al. Among authors: lambert ma. Ann Neurol. 1999 Mar;45(3):389-92. Ann Neurol. 1999. PMID: 10072055

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. 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

Diagnostic accuracy of blood lactate-to-pyruvate molar ratio in the differential diagnosis of congenital lactic acidosis.

Debray FG, Mitchell GA, Allard P, Robinson BH, Hanley JA, Lambert M. Debray FG, et al. Clin Chem. 2007 May;53(5):916-21. doi: 10.1373/clinchem.2006.081166. Epub 2007 Mar 23. Clin Chem. 2007. PMID: 17384007

4

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. 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

5

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. 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.

6

Disorders of mitochondrial function.

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

7

Treatment of cobalamin C (cblC) deficiency during pregnancy.

Brunel-Guitton C, Costa T, Mitchell GA, Lambert M. Brunel-Guitton C, et al. 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

8

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. 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

9

Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patients.

Lemay JF, Lambert MA, Mitchell GA, Vanasse M, Valle D, Arbour JF, Dubé J, Flessas J, Laberge M, Lafleur L, et al. Lemay JF, et al. Among authors: lambert ma. J Pediatr. 1992 Nov;121(5 Pt 1):725-30. doi: 10.1016/s0022-3476(05)81900-6. J Pediatr. 1992. PMID: 1432421 Free article.

10

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. Pediatrics. 2007 Apr;119(4):722-33. doi: 10.1542/peds.2006-1866. Pediatrics. 2007. PMID: 17403843

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