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Journal Abstract Search

105 related items for PubMed ID: 23431750

  • 1. Early-onset severe obesity with ACTH deficiency and red hair in a boy: the POMC deficiency.
    Ozen S, Aldemir O.
    Genet Couns; 2012; 23(4):493-5. PubMed ID: 23431750
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  • 2. A novel mutation in the proopiomelanocortin (POMC) gene of a Hispanic child: metformin treatment shows a beneficial impact on the body mass index.
    Hilado MA, Randhawa RS.
    J Pediatr Endocrinol Metab; 2018 Jul 26; 31(7):815-819. PubMed ID: 29858905
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  • 3. Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans.
    Krude H, Biebermann H, Luck W, Horn R, Brabant G, Grüters A.
    Nat Genet; 1998 Jun 26; 19(2):155-7. PubMed ID: 9620771
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  • 4. Transient salt wasting in POMC-deficiency due to infection induced stress.
    Darcan S, Can S, Goksen D, Asar G.
    Exp Clin Endocrinol Diabetes; 2010 Apr 26; 118(4):281-3. PubMed ID: 19998238
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  • 12. Obesity in the mouse model of pro-opiomelanocortin deficiency responds to peripheral melanocortin.
    Yaswen L, Diehl N, Brennan MB, Hochgeschwender U.
    Nat Med; 1999 Sep 26; 5(9):1066-70. PubMed ID: 10470087
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  • 17. Unexpected endocrine features and normal pigmentation in a young adult patient carrying a novel homozygous mutation in the POMC gene.
    Clément K, Dubern B, Mencarelli M, Czernichow P, Ito S, Wakamatsu K, Barsh GS, Vaisse C, Leger J.
    J Clin Endocrinol Metab; 2008 Dec 26; 93(12):4955-62. PubMed ID: 18765507
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