Aguiar-Oliveira MH - Search Results

1

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. Aguiar-Oliveira MH, et al. J Clin Endocrinol Metab. 2010 Feb;95(2):714-21. doi: 10.1210/jc.2009-1879. Epub 2009 Dec 4. J Clin Endocrinol Metab. 2010. PMID: 19965916 Free PMC article.

2

Cardiovascular Prognosis of Subclinical Chronic Obstructive Pulmonary Disease in Patients with Suspected or Confirmed Coronary Artery Disease.

Ferreira EJP, Cardoso LVSC, de Matos CJO, Mota IL, Lira JMC, Lopes MEG, Santos GV, Dória Almeida ML, Aguiar-Oliveira MH, Sousa ACS, de Melo EV, Oliveira JLM. Ferreira EJP, et al. Among authors: aguiar oliveira mh. Int J Chron Obstruct Pulmon Dis. 2023 Aug 29;18:1899-1908. doi: 10.2147/COPD.S410416. eCollection 2023. Int J Chron Obstruct Pulmon Dis. 2023. PMID: 37662489 Free PMC article.

3

Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene.

Salvatori R, Hayashida CY, Aguiar-Oliveira MH, Phillips JA 3rd, Souza AH, Gondo RG, Toledo SP, Conceicão MM, Prince M, Maheshwari HG, Baumann G, Levine MA. Salvatori R, et al. J Clin Endocrinol Metab. 1999 Mar;84(3):917-23. doi: 10.1210/jcem.84.3.5599. J Clin Endocrinol Metab. 1999. PMID: 10084571

4

Effect of severe growth hormone (GH) deficiency due to a mutation in the GH-releasing hormone receptor on insulin-like growth factors (IGFs), IGF-binding proteins, and ternary complex formation throughout life.

Aguiar-Oliveira MH, Gill MS, de A Barretto ES, Alcântara MR, Miraki-Moud F, Menezes CA, Souza AH, Martinelli CE, Pereira FA, Salvatori R, Levine MA, Shalet SM, Camacho-Hubner C, Clayton PE. Aguiar-Oliveira MH, et al. J Clin Endocrinol Metab. 1999 Nov;84(11):4118-26. doi: 10.1210/jcem.84.11.6133. J Clin Endocrinol Metab. 1999. PMID: 10566659

5

Serum leptin and body composition in children with familial GH deficiency (GHD) due to a mutation in the growth hormone-releasing hormone (GHRH) receptor.

de A Barretto ES, Gill MS, De Freitas ME, Magalhães MM, Souza AH, Aguiar-Oliveira MH, Clayton PE. de A Barretto ES, et al. Clin Endocrinol (Oxf). 1999 Nov;51(5):559-64. doi: 10.1046/j.1365-2265.1999.00837.x. Clin Endocrinol (Oxf). 1999. PMID: 10594516

6

Growth hormone-releasing peptide-2 stimulates GH secretion in GH-deficient patients with mutated GH-releasing hormone receptor.

Gondo RG, Aguiar-Oliveira MH, Hayashida CY, Toledo SP, Abelin N, Levine MA, Bowers CY, Souza AH, Pereira RM, Santos NL, Salvatori R. Gondo RG, et al. J Clin Endocrinol Metab. 2001 Jul;86(7):3279-83. doi: 10.1210/jcem.86.7.7694. J Clin Endocrinol Metab. 2001. PMID: 11443201

7

Familial isolated growth hormone deficiency is associated with increased systolic blood pressure, central obesity, and dyslipidemia.

Barreto-Filho JA, Alcântara MR, Salvatori R, Barreto MA, Sousa AC, Bastos V, Souza AH, Pereira RM, Clayton PE, Gill MS, Aguiar-Oliveira MH. Barreto-Filho JA, et al. J Clin Endocrinol Metab. 2002 May;87(5):2018-23. doi: 10.1210/jcem.87.5.8474. J Clin Endocrinol Metab. 2002. PMID: 11994335

8

Detection of a recurring mutation in the human growth hormone-releasing hormone receptor gene.

Salvatori R, Aguiar-Oliveira MH, Monte LV, Hedges L, Santos NL, Pereira RM, Phillips JA. Salvatori R, et al. Clin Endocrinol (Oxf). 2002 Jul;57(1):77-80. doi: 10.1046/j.1365-2265.2002.01565.x. Clin Endocrinol (Oxf). 2002. PMID: 12100073

9

Lipid profiles in untreated severe congenital isolated growth hormone deficiency through the lifespan.

Gleeson HK, Souza AH, Gill MS, Wieringa GE, Barretto ES, Barretto-Filho JA, Shalet SM, Aguiar-Oliveira MH, Clayton PE. Gleeson HK, et al. Clin Endocrinol (Oxf). 2002 Jul;57(1):89-95. doi: 10.1046/j.1365-2265.2002.01568.x. Clin Endocrinol (Oxf). 2002. PMID: 12100075

10

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. Oliveira HA, et al. Eur J Endocrinol. 2003 Apr;148(4):427-32. doi: 10.1530/eje.0.1480427. Eur J Endocrinol. 2003. PMID: 12656663

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