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Journal Abstract Search

131 related items for PubMed ID: 29571594

  • 21. Effects of depot growth hormone replacement on thyroid function and volume in adults with congenital isolated growth hormone deficiency.
    Leite NT, Salvatori R, Alcântara MR, Alcântara PR, Oliveira CR, Oliveira JL, Anjos-Andrade FD, Farias MI, Britto CT, Nóbrega LM, Nascimento AC, Alves ÉO, Pereira RM, Campos VC, Menezes M, Martinelli CE, Aguiar-Oliveira MH.
    J Endocrinol Invest; 2012 Mar; 35(3):265-8. PubMed ID: 21422802
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  • 22. GH-releasing hormone receptor gene: a novel splice-disrupting mutation and study of founder effects.
    Marui S, Trarbach EB, Boguszewski MC, França MM, Jorge AA, Inoue H, Nishi MY, de Lacerda Filho L, Aguiar-Oliveira MH, Mendonca BB, Arnhold IJ.
    Horm Res Paediatr; 2012 Mar; 78(3):165-72. PubMed ID: 23052699
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  • 23. Vestibular function in severe GH deficiency due to an inactivating mutation in the GH-releasing hormone receptor gene.
    Santos-Carvalho HA, Aguiar-Oliveira MH, Salvatori R, Valença EHO, Andrade-Guimarães AL, Palanch-Repeke CE, Moreira-Cândido LP, Araújo-Daniel CR, de Oliveira-Barreto AC, Andrade BMR, Oliveira AHA, Vieira ER, Gois-Junior MB.
    Endocrine; 2020 Mar; 67(3):659-664. PubMed ID: 31902114
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  • 24. Longevity in untreated congenital growth hormone deficiency due to a homozygous mutation in the GHRH receptor gene.
    Aguiar-Oliveira MH, Oliveira FT, Pereira RM, Oliveira CR, Blackford A, Valenca EH, Santos EG, Gois-Junior MB, Meneguz-Moreno RA, Araujo VP, Oliveira-Neto LA, Almeida RP, Santos MA, Farias NT, Silveira DC, Cabral GW, Calazans FR, Seabra JD, Lopes TF, Rodrigues EO, Porto LA, Oliveira IP, Melo EV, Martari M, Salvatori R.
    J Clin Endocrinol Metab; 2010 Feb; 95(2):714-21. PubMed ID: 19965916
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  • 25. Two siblings with isolated GH deficiency due to loss-of-function mutation in the GHRHR gene: successful treatment with growth hormone despite late admission and severe growth retardation.
    Sıklar Z, Berberoğlu M, Legendre M, Amselem S, Evliyaoğlu O, Hacıhamdioğlu B, Savaş Erdeve S, Oçal G.
    J Clin Res Pediatr Endocrinol; 2010 Feb; 2(4):164-7. PubMed ID: 21274317
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  • 26. Phenotype-genotype correlations in congenital isolated growth hormone deficiency (IGHD).
    Alatzoglou KS, Dattani MT.
    Indian J Pediatr; 2012 Jan; 79(1):99-106. PubMed ID: 22139958
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  • 27. Extensive phenotypic analysis of a family with growth hormone (GH) deficiency caused by a mutation in the GH-releasing hormone receptor gene.
    Netchine I, Talon P, Dastot F, Vitaux F, Goossens M, Amselem S.
    J Clin Endocrinol Metab; 1998 Feb; 83(2):432-6. PubMed ID: 9467553
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  • 28. Growth hormone replacement therapy regulates microRNA-29a and targets involved in insulin resistance.
    Galimov A, Hartung A, Trepp R, Mader A, Flück M, Linke A, Blüher M, Christ E, Krützfeldt J.
    J Mol Med (Berl); 2015 Dec; 93(12):1369-79. PubMed ID: 26199111
    [Abstract] [Full Text] [Related]

  • 29. Molecular and clinical aspects of GHRH receptor mutations.
    Corazzini V, Salvatori R.
    Endocr Dev; 2013 Dec; 24():106-17. PubMed ID: 23392099
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  • 31. Heterozygosity for a mutation in the growth hormone-releasing hormone receptor gene does not influence adult stature, but affects body composition.
    Pereira RM, Aguiar-Oliveira MH, Sagazio A, Oliveira CR, Oliveira FT, Campos VC, Farias CT, Vicente TA, Gois MB, Oliveira JL, Marques-Santos C, Rocha IE, Barreto-Filho JA, Salvatori R.
    J Clin Endocrinol Metab; 2007 Jun; 92(6):2353-7. PubMed ID: 17356054
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  • 36. Familial isolated growth hormone deficiency due to a novel homozygous missense mutation in the growth hormone releasing hormone receptor gene: clinical presentation with hypoglycemia.
    Demirbilek H, Tahir S, Baran RT, Sherif M, Shah P, Ozbek MN, Hatipoglu N, Baran A, Arya VB, Hussain K.
    J Clin Endocrinol Metab; 2014 Dec; 99(12):E2730-4. PubMed ID: 25226297
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  • 37. Expanding the spectrum of mutations in GH1 and GHRHR: genetic screening in a large cohort of patients with congenital isolated growth hormone deficiency.
    Alatzoglou KS, Turton JP, Kelberman D, Clayton PE, Mehta A, Buchanan C, Aylwin S, Crowne EC, Christesen HT, Hertel NT, Trainer PJ, Savage MO, Raza J, Banerjee K, Sinha SK, Ten S, Mushtaq T, Brauner R, Cheetham TD, Hindmarsh PC, Mullis PE, Dattani MT.
    J Clin Endocrinol Metab; 2009 Sep; 94(9):3191-9. PubMed ID: 19567534
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  • 39. Abnormal vascular and neural retinal morphology in congenital lifetime isolated growth hormone deficiency.
    Pereira-Gurgel VM, Faro AC, Salvatori R, Chagas TA, Carvalho-Junior JF, Oliveira CR, Costa UM, Melo GB, Hellström A, Aguiar-Oliveira MH.
    Growth Horm IGF Res; 2016 Sep; 30-31():11-15. PubMed ID: 27552668
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  • 40. Magnetic resonance imaging study of pituitary morphology in subjects homozygous and heterozygous for a null mutation of the GHRH receptor gene.
    Oliveira HA, Salvatori R, Krauss MP, Oliveira CR, Silva PR, Aguiar-Oliveira MH.
    Eur J Endocrinol; 2003 Apr; 148(4):427-32. PubMed ID: 12656663
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