Kottler ML - Search Results

1

Progressive osseous heteroplasia: a model for the imprinting effects of GNAS inactivating mutations in humans.

Lebrun M, Richard N, Abeguilé G, David A, Coëslier Dieux A, Journel H, Lacombe D, Pinto G, Odent S, Salles JP, Taieb A, Gandon-Laloum S, Kottler ML. Lebrun M, et al. Among authors: kottler ml. J Clin Endocrinol Metab. 2010 Jun;95(6):3028-38. doi: 10.1210/jc.2009-1451. Epub 2010 Apr 28. J Clin Endocrinol Metab. 2010. PMID: 20427508

2

[Epigenetics and pseudohypoparathyroidism].

Richard N, Abéguilé G, Coudray N, Kottler ML. Richard N, et al. Among authors: kottler ml. Pathol Biol (Paris). 2010 Oct;58(5):367-71. doi: 10.1016/j.patbio.2009.09.007. Epub 2009 Nov 25. Pathol Biol (Paris). 2010. PMID: 19942373 Review. French.

3

CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait.

Molin A, Baudoin R, Kaufmann M, Souberbielle JC, Ryckewaert A, Vantyghem MC, Eckart P, Bacchetta J, Deschenes G, Kesler-Roussey G, Coudray N, Richard N, Wraich M, Bonafiglia Q, Tiulpakov A, Jones G, Kottler ML. Molin A, et al. Among authors: kottler ml. J Clin Endocrinol Metab. 2015 Oct;100(10):E1343-52. doi: 10.1210/jc.2014-4387. Epub 2015 Jul 27. J Clin Endocrinol Metab. 2015. PMID: 26214117

4

Albright hereditary osteodystrophy: report of a particular clinical phenotype caused by a novel GNAS mutation.

Alvarez F, Kottler ML, Paul C, Gennero I, Salles JP, Mazereeuw-Hautier J. Alvarez F, et al. Among authors: kottler ml. J Eur Acad Dermatol Venereol. 2010 Aug;24(8):974-5. doi: 10.1111/j.1468-3083.2009.03539.x. Epub 2009 Dec 15. J Eur Acad Dermatol Venereol. 2010. PMID: 20015054 No abstract available.

5

FSHbeta gene mutation in a female with delayed puberty and hypogonadism: response to recombinant human FSH.

Kottler ML, Richard N, Chabre O, Alain S, Young J. Kottler ML, et al. Folia Histochem Cytobiol. 2009;47(5):S55-8. doi: 10.2478/v10042-009-0054-7. Folia Histochem Cytobiol. 2009. PMID: 20067895

6

KiSS-1 and GPR54 genes are co-expressed in rat gonadotrophs and differentially regulated in vivo by oestradiol and gonadotrophin-releasing hormone.

Richard N, Galmiche G, Corvaisier S, Caraty A, Kottler ML. Richard N, et al. Among authors: kottler ml. J Neuroendocrinol. 2008 Mar;20(3):381-93. doi: 10.1111/j.1365-2826.2008.01653.x. Epub 2008 Jan 17. J Neuroendocrinol. 2008. PMID: 18208554

7

Seasonal expression of KiSS-1 and the pituitary gonadotropins LHβ and FSHβ in adult male Libyan jird (Meriones libycus).

Boufermes R, Richard N, Le Moguen K, Amirat Z, Khammar F, Kottler ML. Boufermes R, et al. Among authors: kottler ml. Anim Reprod Sci. 2014 Jun 10;147(1-2):56-63. doi: 10.1016/j.anireprosci.2014.04.001. Epub 2014 Apr 13. Anim Reprod Sci. 2014. PMID: 24786546

8

Human gene mutations. Gene symbol: CYP19. Disease: Aromatase deficiency.

Mittre Hervé MH, Kottler ML, Pura M. Mittre Hervé MH, et al. Among authors: kottler ml. Hum Genet. 2004 Jan;114(2):224. Hum Genet. 2004. PMID: 15046111 No abstract available.

9

[Epigenetic mechanisms in metabolic disorders].

Kottler ML. Kottler ML. Ann Biol Clin (Paris). 2006 Nov-Dec;64(6):588-90. Ann Biol Clin (Paris). 2006. PMID: 17256238 Free article. French. No abstract available.

10

[Overdose or hypersensitivity to vitamin D?].

Hmami F, Oulmaati A, Amarti A, Kottler ML, Bouharrou A. Hmami F, et al. Among authors: kottler ml. Arch Pediatr. 2014 Oct;21(10):1115-9. doi: 10.1016/j.arcped.2014.06.025. Epub 2014 Aug 13. Arch Pediatr. 2014. PMID: 25129320 French.

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