Lambert M - Search Results

1

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: lambert m. 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.

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

4

Disorders of mitochondrial function.

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

5

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: lambert m. J Child Neurol. 2010 Aug;25(8):1000-2. doi: 10.1177/0883073809351983. Epub 2010 May 14. J Child Neurol. 2010. PMID: 20472868

6

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: lambert m. 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

7

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. Among authors: lambert m. Clin Chem. 2007 May;53(5):916-21. doi: 10.1373/clinchem.2006.081166. Epub 2007 Mar 23. Clin Chem. 2007. PMID: 17384007

8

Acute tubular dysfunction with Fanconi syndrome: a new manifestation of mitochondrial cytopathies.

Debray FG, Merouani A, Lambert M, Brochu P, Bernard C, Robinson BH, Mitchell GA. Debray FG, et al. Among authors: lambert m. Am J Kidney Dis. 2008 Apr;51(4):691-6. doi: 10.1053/j.ajkd.2007.11.024. Am J Kidney Dis. 2008. PMID: 18371545 Free article. No abstract available.

9

Treatment of cobalamin C (cblC) deficiency during pregnancy.

Brunel-Guitton C, Costa T, Mitchell GA, Lambert M. Brunel-Guitton C, et al. Among authors: lambert m. 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

10

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: lambert m. 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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

2,758 results

Search Page

Filters