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167 related items for PubMed ID: 12656663

  • 1. 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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  • 3. A novel frame shift mutation in the GHRH receptor gene in familial isolated GH deficiency: early occurrence of anterior pituitary hypoplasia.
    Shohreh R, Sherafat-Kazemzadeh R, Jee YH, Blitz A, Salvatori R.
    J Clin Endocrinol Metab; 2011 Oct; 96(10):2982-6. PubMed ID: 21816782
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  • 4. 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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  • 6. Growth hormone releasing hormone receptor (GHRH-r) gene mutation in Indian children with familial isolated growth hormone deficiency: a study from western India.
    Desai MP, Upadhye PS, Kamijo T, Yamamoto M, Ogawa M, Hayashi Y, Seo H, Nair SR.
    J Pediatr Endocrinol Metab; 2005 Oct; 18(10):955-73. PubMed ID: 16355809
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  • 10. Hypothalamic abnormalities: Growth failure due to defects of the GHRH receptor.
    Aguiar-Oliveira MH, Davalos C, Campos VC, Oliveira Neto LA, Marinho CG, Oliveira CRP.
    Growth Horm IGF Res; 2018 Feb; 38():14-18. PubMed ID: 29277338
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  • 11. A new missense mutation in the growth hormone-releasing hormone receptor gene in familial isolated GH deficiency.
    Carakushansky M, Whatmore AJ, Clayton PE, Shalet SM, Gleeson HK, Price DA, Levine MA, Salvatori R.
    Eur J Endocrinol; 2003 Jan; 148(1):25-30. PubMed ID: 12534354
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  • 15. A novel gross indel in the growth hormone releasing hormone receptor gene of Indian IGHD patients.
    Kale S, Budyal S, Kasaliwal R, Shivane V, Raghavan V, Lila A, Bandgar T, Shah N.
    Growth Horm IGF Res; 2014 Dec; 24(6):227-32. PubMed ID: 25153028
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  • 18. 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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