Houang M - Search Results

1

Perrault syndrome: report of four new cases, review and exclusion of candidate genes.

Marlin S, Lacombe D, Jonard L, Leboulanger N, Bonneau D, Goizet C, de Villemeur TB, Cabrol S, Houang M, Moatti L, Feldmann D, Denoyelle F. Marlin S, et al. Among authors: houang m. Am J Med Genet A. 2008 Mar 1;146A(5):661-4. doi: 10.1002/ajmg.a.32180. Am J Med Genet A. 2008. PMID: 18241061

2

[Physiopathology of the somatotropin axis in chronic renal insufficiency].

Cabrol S, Houang M, Le Bouc Y. Cabrol S, et al. Among authors: houang m. Arch Pediatr. 1998;5 Suppl 4:348S-353S. doi: 10.1016/s0929-693x(99)80189-4. Arch Pediatr. 1998. PMID: 9853082 Review. French.

3

Insulin-like growth factor-I (IGF-I), insulin-like growth factor binding proteins (IGFBP) and insulin-like growth factor type I receptor in children with various status of chronic renal failure.

Houang M, Cabrol S, Perin L, Ducos B, Bensman A, Le Bouc Y. Houang M, et al. Growth Horm IGF Res. 2000 Dec;10(6):332-41. doi: 10.1054/ghir.2000.0178. Growth Horm IGF Res. 2000. PMID: 11161964

4

IGF type 1 receptor ligand binding characteristics are altered in a subgroup of children with intrauterine growth retardation.

Ducos B, Cabrol S, Houang M, Perin L, Holzenberger M, Le Bouc Y. Ducos B, et al. Among authors: houang m. J Clin Endocrinol Metab. 2001 Nov;86(11):5516-24. doi: 10.1210/jcem.86.11.7985. J Clin Endocrinol Metab. 2001. PMID: 11701730 Clinical Trial.

5

Hypogonadotrophic hypogonadism associated with prelingual deafness due to a connexin 26 gene mutation.

Houang M, Gourmelen M, Moatti L, Le BY, Garabédian EN, Denoyelle F. Houang M, et al. J Pediatr Endocrinol Metab. 2002 Feb;15(2):219-23. doi: 10.1515/jpem.2002.15.2.219. J Pediatr Endocrinol Metab. 2002. PMID: 11874189

6

Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.

Blons H, Feldmann D, Duval V, Messaz O, Denoyelle F, Loundon N, Sergout-Allaoui A, Houang M, Duriez F, Lacombe D, Delobel B, Leman J, Catros H, Journel H, Drouin-Garraud V, Obstoy MF, Toutain A, Oden S, Toublanc JE, Couderc R, Petit C, Garabédian EN, Marlin S. Blons H, et al. Among authors: houang m. Clin Genet. 2004 Oct;66(4):333-40. doi: 10.1111/j.1399-0004.2004.00296.x. Clin Genet. 2004. PMID: 15355436

7

Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.

Gicquel C, Rossignol S, Cabrol S, Houang M, Steunou V, Barbu V, Danton F, Thibaud N, Le Merrer M, Burglen L, Bertrand AM, Netchine I, Le Bouc Y. Gicquel C, et al. Among authors: houang m. Nat Genet. 2005 Sep;37(9):1003-7. doi: 10.1038/ng1629. Epub 2005 Aug 7. Nat Genet. 2005. PMID: 16086014

8

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome with renal failure: impact of posttransplant immunosuppression on disease activity.

Ulinski T, Perrin L, Morris M, Houang M, Cabrol S, Grapin C, Chabbert-Buffet N, Bensman A, Deschênes G, Giurgea I. Ulinski T, et al. Among authors: houang m. J Clin Endocrinol Metab. 2006 Jan;91(1):192-5. doi: 10.1210/jc.2005-1538. Epub 2005 Nov 1. J Clin Endocrinol Metab. 2006. PMID: 16263818

9

SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.

Albert S, Blons H, Jonard L, Feldmann D, Chauvin P, Loundon N, Sergent-Allaoui A, Houang M, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Dollfus H, Eliot MM, David A, Calais C, Drouin-Garraud V, Obstoy MF, Tran Ba Huy P, Lacombe D, Duriez F, Francannet C, Bitoun P, Petit C, Garabédian EN, Couderc R, Marlin S, Denoyelle F. Albert S, et al. Among authors: houang m. Eur J Hum Genet. 2006 Jun;14(6):773-9. doi: 10.1038/sj.ejhg.5201611. Eur J Hum Genet. 2006. PMID: 16570074

10

11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations.

Netchine I, Rossignol S, Dufourg MN, Azzi S, Rousseau A, Perin L, Houang M, Steunou V, Esteva B, Thibaud N, Demay MC, Danton F, Petriczko E, Bertrand AM, Heinrichs C, Carel JC, Loeuille GA, Pinto G, Jacquemont ML, Gicquel C, Cabrol S, Le Bouc Y. Netchine I, et al. Among authors: houang m. J Clin Endocrinol Metab. 2007 Aug;92(8):3148-54. doi: 10.1210/jc.2007-0354. Epub 2007 May 15. J Clin Endocrinol Metab. 2007. PMID: 17504900

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