Robitaille Y - Search Results

1

Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 gene.

Maquet E, Costagliola S, Parma J, Christophe-Hobertus C, Oligny LL, Fournet JC, Robitaille Y, Vuissoz JM, Payot A, Laberge S, Vassart G, Van Vliet G, Deladoëy J. Maquet E, et al. Among authors: robitaille y. J Clin Endocrinol Metab. 2009 Jan;94(1):197-203. doi: 10.1210/jc.2008-1402. Epub 2008 Oct 28. J Clin Endocrinol Metab. 2009. PMID: 18957494

2

Sudden death in growth hormone-treated children with Prader-Willi syndrome.

Van Vliet G, Deal CL, Crock PA, Robitaille Y, Oligny LL. Van Vliet G, et al. Among authors: robitaille y. J Pediatr. 2004 Jan;144(1):129-31. doi: 10.1016/j.jpeds.2003.09.049. J Pediatr. 2004. PMID: 14722532 Review.

3

Pituitary choriocarcinoma in an adolescent male: tumor-derived CG and GH delay diagnosis.

Wildi-Runge S, Crevier L, Carret AS, Robitaille Y, Deal C. Wildi-Runge S, et al. Among authors: robitaille y. Growth Horm IGF Res. 2011 Jun;21(3):181-4. doi: 10.1016/j.ghir.2011.04.001. Growth Horm IGF Res. 2011. PMID: 21658594

4

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

5

Critical illness polyneuromyopathy in a child with severe demyelinating myelitis.

Adamovic T, Willems A, Vanasse M, D'Anjou G, Robitaille Y, Litalien C, Gauvin F. Adamovic T, et al. Among authors: robitaille y. J Child Neurol. 2009 Jun;24(6):758-62. doi: 10.1177/0883073808330166. Epub 2009 Mar 4. J Child Neurol. 2009. PMID: 19264734

6

Are intratympanic injections of N-acetylcysteine and methylprednisolone protective against Cisplatin-induced ototoxicity?

Saliba I, El Fata F, Ouelette V, Robitaille Y. Saliba I, et al. Among authors: robitaille y. J Otolaryngol Head Neck Surg. 2010 Jun;39(3):236-43. J Otolaryngol Head Neck Surg. 2010. PMID: 20470667

7

The clinical spectrum of nodular heterotopias in children: report of 31 patients.

Srour M, Rioux MF, Varga C, Lortie A, Major P, Robitaille Y, Décarie JC, Michaud J, Carmant L. Srour M, et al. Among authors: robitaille y. Epilepsia. 2011 Apr;52(4):728-37. doi: 10.1111/j.1528-1167.2010.02975.x. Epub 2011 Feb 14. Epilepsia. 2011. PMID: 21320118 Free article.

8

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: robitaille y. 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

9

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: robitaille y. Am J Med Genet. 1999 May 21;84(2):94-101. Am J Med Genet. 1999. PMID: 10323732

10

A liver-specific defect of Acyl-CoA degradation produces hyperammonemia, hypoglycemia and a distinct hepatic Acyl-CoA pattern.

Gauthier N, Wu JW, Wang SP, Allard P, Mamer OA, Sweetman L, Moser AB, Kratz L, Alvarez F, Robitaille Y, Lépine F, Mitchell GA. Gauthier N, et al. Among authors: robitaille y. PLoS One. 2013 Jul 5;8(7):e60581. doi: 10.1371/journal.pone.0060581. Print 2013. PLoS One. 2013. PMID: 23861731 Free PMC article.

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