Huot C - Search Results

1

A novel mechanism for isolated central hypothyroidism: inactivating mutations in the thyrotropin-releasing hormone receptor gene.

Collu R, Tang J, Castagné J, Lagacé G, Masson N, Huot C, Deal C, Delvin E, Faccenda E, Eidne KA, Van Vliet G. Collu R, et al. Among authors: huot c. J Clin Endocrinol Metab. 1997 May;82(5):1561-5. doi: 10.1210/jcem.82.5.3918. J Clin Endocrinol Metab. 1997. PMID: 9141550

2

Severe autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy in an adolescent girl with a novel AIRE mutation: response to immunosuppressive therapy.

Ward L, Paquette J, Seidman E, Huot C, Alvarez F, Crock P, Delvin E, Kämpe O, Deal C. Ward L, et al. Among authors: huot c. J Clin Endocrinol Metab. 1999 Mar;84(3):844-52. doi: 10.1210/jcem.84.3.5580. J Clin Endocrinol Metab. 1999. PMID: 10084559

3

Primary adrenal insufficiency in children: twenty years experience at the Sainte-Justine Hospital, Montreal.

Perry R, Kecha O, Paquette J, Huot C, Van Vliet G, Deal C. Perry R, et al. Among authors: huot c. J Clin Endocrinol Metab. 2005 Jun;90(6):3243-50. doi: 10.1210/jc.2004-0016. Epub 2005 Apr 5. J Clin Endocrinol Metab. 2005. PMID: 15811934

4

Severe cortisol deficiency associated with reversible growth hormone deficiency in two infants: what is the link?

McEachern R, Drouin J, Metherell L, Huot C, Van Vliet G, Deal C. McEachern R, et al. Among authors: huot c. J Clin Endocrinol Metab. 2011 Sep;96(9):2670-4. doi: 10.1210/jc.2011-0129. Epub 2011 Jul 13. J Clin Endocrinol Metab. 2011. PMID: 21752888

5

Bioinactive ACTH causing glucocorticoid deficiency.

Samuels ME, Gallo-Payet N, Pinard S, Hasselmann C, Magne F, Patry L, Chouinard L, Schwartzentruber J, René P, Sawyer N, Bouvier M, Djemli A, Delvin E, Huot C, Eugene D, Deal CL, Van Vliet G, Majewski J, Deladoëy J; FORGE Canada Consortium. Samuels ME, et al. Among authors: huot c. J Clin Endocrinol Metab. 2013 Feb;98(2):736-42. doi: 10.1210/jc.2012-3199. Epub 2013 Jan 4. J Clin Endocrinol Metab. 2013. PMID: 23293326

6

Severe congenital hypopituitarism with low prolactin levels and age-dependent anterior pituitary hypoplasia: a clue to a PIT-1 mutation.

Ward L, Chavez M, Huot C, Lecocq P, Collu R, Décarie JC, Martial JA, Van Vliet G. Ward L, et al. Among authors: huot c. J Pediatr. 1998 Jun;132(6):1036-8. doi: 10.1016/s0022-3476(98)70405-6. J Pediatr. 1998. PMID: 9627600 Review.

7

Outcome of pediatric Graves' disease after treatment with antithyroid medication and radioiodine.

Ward L, Huot C, Lambert R, Deal C, Collu R, Van Vliet G. Ward L, et al. Among authors: huot c. Clin Invest Med. 1999 Aug;22(4):132-9. Clin Invest Med. 1999. PMID: 10497711

8

Cognition and behavior at school entry in children with congenital hypothyroidism treated early with high-dose levothyroxine.

Simoneau-Roy J, Marti S, Deal C, Huot C, Robaey P, Van Vliet G. Simoneau-Roy J, et al. Among authors: huot c. J Pediatr. 2004 Jun;144(6):747-52. doi: 10.1016/j.jpeds.2004.02.021. J Pediatr. 2004. PMID: 15192621 Clinical Trial.

9

Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum.

Cole LW, Sidis Y, Zhang C, Quinton R, Plummer L, Pignatelli D, Hughes VA, Dwyer AA, Raivio T, Hayes FJ, Seminara SB, Huot C, Alos N, Speiser P, Takeshita A, Van Vliet G, Pearce S, Crowley WF Jr, Zhou QY, Pitteloud N. Cole LW, et al. Among authors: huot c. J Clin Endocrinol Metab. 2008 Sep;93(9):3551-9. doi: 10.1210/jc.2007-2654. Epub 2008 Jun 17. J Clin Endocrinol Metab. 2008. PMID: 18559922 Free PMC article.

10

Hyperfunctioning malignant thyroid nodule in an 11-year-old girl: pathologic and molecular studies.

Mircescu H, Parma J, Huot C, Deal C, Oligny LL, Vassart G, Van Vliet G. Mircescu H, et al. Among authors: huot c. J Pediatr. 2000 Oct;137(4):585-7. doi: 10.1067/mpd.2000.108437. J Pediatr. 2000. PMID: 11035845 Review.

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