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Journal Abstract Search


136 related items for PubMed ID: 33666293

  • 1. 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; 57(4):484-490. PubMed ID: 33666293
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  • 2. 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 Apr; 12():689387. PubMed ID: 34177811
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  • 3. 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
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  • 4. 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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  • 5. 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
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  • 6. 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 01; 88(10):4633-40. PubMed ID: 14557433
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  • 10. 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
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  • 13. Implications of proopiomelanocortin (POMC) mutations in humans: the POMC deficiency syndrome.
    Krude H, Grüters A.
    Trends Endocrinol Metab; 2000 Feb 01; 11(1):15-22. PubMed ID: 10652501
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  • 14. Efficacy and safety of setmelanotide, an MC4R agonist, in individuals with severe obesity due to LEPR or POMC deficiency: single-arm, open-label, multicentre, phase 3 trials.
    Clément K, van den Akker E, Argente J, Bahm A, Chung WK, Connors H, De Waele K, Farooqi IS, Gonneau-Lejeune J, Gordon G, Kohlsdorf K, Poitou C, Puder L, Swain J, Stewart M, Yuan G, Wabitsch M, Kühnen P, Setmelanotide POMC and LEPR Phase 3 Trial Investigators.
    Lancet Diabetes Endocrinol; 2020 Dec 01; 8(12):960-970. PubMed ID: 33137293
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  • 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
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  • 18. Central dysregulation of the hypothalamic-pituitary-adrenal axis in neuron-specific proopiomelanocortin-deficient mice.
    Smart JL, Tolle V, Otero-Corchon V, Low MJ.
    Endocrinology; 2007 Feb 21; 148(2):647-59. PubMed ID: 17095588
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  • 19. Early onset obesity and adrenal insufficiency associated with a homozygous POMC mutation.
    Mendiratta MS, Yang Y, Balazs AE, Willis AS, Eng CM, Karaviti LP, Potocki L.
    Int J Pediatr Endocrinol; 2011 Feb 21; 2011(1):5. PubMed ID: 21860632
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