Dubern B - Search Results

1

Implication of Heterozygous Variants in Genes of the Leptin-Melanocortin Pathway in Severe Obesity.

Courbage S, Poitou C, Le Beyec-Le Bihan J, Karsenty A, Lemale J, Pelloux V, Lacorte JM, Carel JC, Lecomte N, Storey C, De Filippo G, Coupaye M, Oppert JM, Tounian P, Clément K, Dubern B. Courbage S, et al. Among authors: dubern b. J Clin Endocrinol Metab. 2021 Sep 27;106(10):2991-3006. doi: 10.1210/clinem/dgab404. J Clin Endocrinol Metab. 2021. PMID: 34097736 Free article.

2

Mutational analysis of melanocortin-4 receptor, agouti-related protein, and alpha-melanocyte-stimulating hormone genes in severely obese children.

Dubern B, Clément K, Pelloux V, Froguel P, Girardet JP, Guy-Grand B, Tounian P. Dubern B, et al. J Pediatr. 2001 Aug;139(2):204-9. doi: 10.1067/mpd.2001.116284. J Pediatr. 2001. PMID: 11487744

3

Presence of increased stiffness of the common carotid artery and endothelial dysfunction in severely obese children: a prospective study.

Tounian P, Aggoun Y, Dubern B, Varille V, Guy-Grand B, Sidi D, Girardet JP, Bonnet D. Tounian P, et al. Among authors: dubern b. Lancet. 2001 Oct 27;358(9291):1400-4. doi: 10.1016/S0140-6736(01)06525-4. Lancet. 2001. PMID: 11705484

4

Melanocortin 4 receptor mutations in a large cohort of severely obese adults: prevalence, functional classification, genotype-phenotype relationship, and lack of association with binge eating.

Lubrano-Berthelier C, Dubern B, Lacorte JM, Picard F, Shapiro A, Zhang S, Bertrais S, Hercberg S, Basdevant A, Clement K, Vaisse C. Lubrano-Berthelier C, et al. Among authors: dubern b. J Clin Endocrinol Metab. 2006 May;91(5):1811-8. doi: 10.1210/jc.2005-1411. Epub 2006 Feb 28. J Clin Endocrinol Metab. 2006. PMID: 16507637

5

Cart overexpression is the only identifiable cause of high bone mass in melanocortin 4 receptor deficiency.

Ahn JD, Dubern B, Lubrano-Berthelier C, Clement K, Karsenty G. Ahn JD, et al. Among authors: dubern b. Endocrinology. 2006 Jul;147(7):3196-202. doi: 10.1210/en.2006-0281. Epub 2006 Apr 13. Endocrinology. 2006. PMID: 16614075

6

Pulmonary function and sleep-related breathing disorders in severely obese children.

Dubern B, Tounian P, Medjadhi N, Maingot L, Girardet JP, Boulé M. Dubern B, et al. Clin Nutr. 2006 Oct;25(5):803-9. doi: 10.1016/j.clnu.2005.12.001. Epub 2006 May 15. Clin Nutr. 2006. PMID: 16698133

7

[Genetic aspects of obesity].

Dubern B, Clément K. Dubern B, et al. Presse Med. 2007 Nov;36(11 Pt 2):1598-605. doi: 10.1016/j.lpm.2007.04.013. Epub 2007 May 21. Presse Med. 2007. PMID: 17513079 Review. French.

8

Homozygous null mutation of the melanocortin-4 receptor and severe early-onset obesity.

Dubern B, Bisbis S, Talbaoui H, Le Beyec J, Tounian P, Lacorte JM, Clément K. Dubern B, et al. J Pediatr. 2007 Jun;150(6):613-7, 617.e1. doi: 10.1016/j.jpeds.2007.01.041. J Pediatr. 2007. PMID: 17517245

9

Insulin resistance and ferritin as major determinants of abnormal serum aminotransferase in severely obese children.

Dubern B, Girardet JP, Tounian P. Dubern B, et al. Int J Pediatr Obes. 2006;1(2):77-82. doi: 10.1080/17477160600569594. Int J Pediatr Obes. 2006. PMID: 17907318

10

Mutational analysis of the pro-opiomelanocortin gene in French obese children led to the identification of a novel deleterious heterozygous mutation located in the alpha-melanocyte stimulating hormone domain.

Dubern B, Lubrano-Berthelier C, Mencarelli M, Ersoy B, Frelut ML, Bouglé D, Costes B, Simon C, Tounian P, Vaisse C, Clement K. Dubern B, et al. Pediatr Res. 2008 Feb;63(2):211-6. doi: 10.1203/PDR.0b013e31815ed62b. Pediatr Res. 2008. PMID: 18091355

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