These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

281 related items for PubMed ID: 14557433

  • 1. Obesity due to proopiomelanocortin deficiency: three new cases and treatment trials with thyroid hormone and ACTH4-10.
    Krude H, Biebermann H, Schnabel D, Tansek MZ, Theunissen P, Mullis PE, Grüters A.
    J Clin Endocrinol Metab; 2003 Oct; 88(10):4633-40. PubMed ID: 14557433
    [Abstract] [Full Text] [Related]

  • 2. 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; 19(2):155-7. PubMed ID: 9620771
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. A case of early-onset obesity, hypocortisolism, and skin pigmentation problem due to a novel homozygous mutation in the proopiomelanocortin (POMC) gene in an Indian boy.
    Hung CN, Poon WT, Lee CY, Law CY, Chan AY.
    J Pediatr Endocrinol Metab; 2012 Jul 26; 25(1-2):175-9. PubMed ID: 22570972
    [Abstract] [Full Text] [Related]

  • 5. Mutations in the human proopiomelanocortin gene.
    Krude H, Biebermann H, Gruters A.
    Ann N Y Acad Sci; 2003 Jun 26; 994():233-9. PubMed ID: 12851321
    [Abstract] [Full Text] [Related]

  • 6. Two Cases With an Early Presented Proopiomelanocortin Deficiency-A Long-Term Follow-Up and Systematic Literature Review.
    Gregoric N, Groselj U, Bratina N, Debeljak M, Zerjav Tansek M, Suput Omladic J, Kovac J, Battelino T, Kotnik P, Avbelj Stefanija M.
    Front Endocrinol (Lausanne); 2021 Jun 26; 12():689387. PubMed ID: 34177811
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. [Monogenic forms of obesity: from mice to human].
    Clément K.
    Ann Endocrinol (Paris); 2000 Dec 26; 61 Suppl 6():39-49. PubMed ID: 11148335
    [Abstract] [Full Text] [Related]

  • 9. Late Diagnosis of POMC Deficiency and In Vitro Evidence of Residual Translation From Allele With c.-11C>A Mutation.
    Anisimova AS, Rubtsov PM, Akulich KA, Dmitriev SE, Frolova E, Tiulpakov A.
    J Clin Endocrinol Metab; 2017 Feb 01; 102(2):359-362. PubMed ID: 27906547
    [Abstract] [Full Text] [Related]

  • 10. 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 01; 93(12):4955-62. PubMed ID: 18765507
    [Abstract] [Full Text] [Related]

  • 11. Preservation of eumelanin hair pigmentation in proopiomelanocortin-deficient mice on a nonagouti (a/a) genetic background.
    Slominski A, Plonka PM, Pisarchik A, Smart JL, Tolle V, Wortsman J, Low MJ.
    Endocrinology; 2005 Mar 01; 146(3):1245-53. PubMed ID: 15564334
    [Abstract] [Full Text] [Related]

  • 12. Delayed diagnosis of proopiomelanocortin (POMC) deficiency with type 1 diabetes in a 9-year-old girl and her infant sibling.
    Ozsu E, Bahm A.
    J Pediatr Endocrinol Metab; 2017 Oct 26; 30(10):1137-1140. PubMed ID: 28915118
    [Abstract] [Full Text] [Related]

  • 13. A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make.
    Çetinkaya S, Güran T, Kurnaz E, Keskin M, Sağsak E, Savaş Erdeve S, Suntharalingham JP, Buonocore F, Achermann JC, Aycan Z.
    J Clin Res Pediatr Endocrinol; 2018 Mar 01; 10(1):68-73. PubMed ID: 28739551
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Proopiomelanocortin Deficiency Treated with a Melanocortin-4 Receptor Agonist.
    Kühnen P, Clément K, Wiegand S, Blankenstein O, Gottesdiener K, Martini LL, Mai K, Blume-Peytavi U, Grüters A, Krude H.
    N Engl J Med; 2016 Jul 21; 375(3):240-6. PubMed ID: 27468060
    [Abstract] [Full Text] [Related]

  • 16. Implications of proopiomelanocortin (POMC) mutations in humans: the POMC deficiency syndrome.
    Krude H, Grüters A.
    Trends Endocrinol Metab; 2000 Jul 21; 11(1):15-22. PubMed ID: 10652501
    [Abstract] [Full Text] [Related]

  • 17. Pro-opiomelanocortin (POMC) deficiency and peripheral melanocortins in obesity.
    Zemel MB, Shi H.
    Nutr Rev; 2000 Jun 21; 58(6):177-80. PubMed ID: 10885325
    [Abstract] [Full Text] [Related]

  • 18. Melanocortin activation of nucleus of the solitary tract avoids anorectic tachyphylaxis and induces prolonged weight loss.
    Li G, Zhang Y, Rodrigues E, Zheng D, Matheny M, Cheng KY, Scarpace PJ.
    Am J Physiol Endocrinol Metab; 2007 Jul 21; 293(1):E252-8. PubMed ID: 17389713
    [Abstract] [Full Text] [Related]

  • 19. Mice lacking pro-opiomelanocortin are sensitive to high-fat feeding but respond normally to the acute anorectic effects of peptide-YY(3-36).
    Challis BG, Coll AP, Yeo GS, Pinnock SB, Dickson SL, Thresher RR, Dixon J, Zahn D, Rochford JJ, White A, Oliver RL, Millington G, Aparicio SA, Colledge WH, Russ AP, Carlton MB, O'Rahilly S.
    Proc Natl Acad Sci U S A; 2004 Mar 30; 101(13):4695-700. PubMed ID: 15070780
    [Abstract] [Full Text] [Related]

  • 20. Proopiomelanocortin deficiency diagnosed in infancy in two boys and a review of the known cases.
    Graves LE, Khouri JM, Kristidis P, Verge CF.
    J Paediatr Child Health; 2021 Apr 30; 57(4):484-490. PubMed ID: 33666293
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.