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Results: 1 to 20 of 38

1.

Autosomal recessive form of isolated growth hormone deficiency is more frequent than the autosomal dominant form in a Brazilian cohort.

Lido AC, França MM, Correa FA, Otto AP, Carvalho LR, Quedas EP, Nishi MY, Mendonca BB, Arnhold IJ, Jorge AA.

Growth Horm IGF Res. 2014 Oct;24(5):180-6. doi: 10.1016/j.ghir.2014.07.001. Epub 2014 Jul 30.

PMID:
25116472
2.

Biphasic response of subscapular skinfold thickness to hGH or IGF-1 administration to patients with congenital IGHD, congenital MPHD and Laron syndrome.

Bisker-Kassif O, Kauli R, Lilos P, Laron Z.

Obes Res Clin Pract. 2014 Jan-Feb;8(1):e55-62. doi: 10.1016/j.orcp.2012.11.001.

PMID:
24548577
3.

Defective minor spliceosome mRNA processing results in isolated familial growth hormone deficiency.

Argente J, Flores R, Gutiérrez-Arumí A, Verma B, Martos-Moreno GÁ, Cuscó I, Oghabian A, Chowen JA, Frilander MJ, Pérez-Jurado LA.

EMBO Mol Med. 2014 Mar;6(3):299-306. doi: 10.1002/emmm.201303573. Epub 2014 Jan 30.

4.

Isolated growth hormone deficiency (GHD) in childhood and adolescence: recent advances.

Alatzoglou KS, Webb EA, Le Tissier P, Dattani MT.

Endocr Rev. 2014 Jun;35(3):376-432. doi: 10.1210/er.2013-1067. Epub 2014 Jan 22. Review.

PMID:
24450934
5.

Hearing status in adult individuals with lifetime, untreated isolated growth hormone deficiency.

Prado-Barreto VM, Salvatori R, Santos Júnior RC, Brandão-Martins MB, Correa EA, Garcez FB, Valença EH, Souza AH, Pereira RM, Nunes MA, D'Avila JS, Aguiar-Oliveira MH.

Otolaryngol Head Neck Surg. 2014 Mar;150(3):464-71. doi: 10.1177/0194599813517987. Epub 2014 Jan 7.

PMID:
24398366
6.

Splice site mutations in GH1 detected in previously (Genetically) undiagnosed families with congenital isolated growth hormone deficiency type II.

Kempers MJ, van der Crabben SN, de Vroede M, Alfen-van der Velden J, Netea-Maier RT, Duim RA, Otten BJ, Losekoot M, Wit JM.

Horm Res Paediatr. 2013;80(6):390-6. doi: 10.1159/000355403. Epub 2013 Nov 23.

PMID:
24280736
7.

The effect of recombinant human growth hormone therapy on left-ventricular chamber size and function in children with growth hormone deficiency.

Esen I, Cetin I, Demirel F, Ekici F.

Pediatr Cardiol. 2013;34(8):1854-9. doi: 10.1007/s00246-013-0727-z. Epub 2013 Jun 13.

PMID:
23760513
8.

Novel compound heterozygous mutations of the growth hormone-releasing hormone receptor gene in a case of isolated growth hormone deficiency.

Soneda A, Adachi M, Muroya K, Asakura Y, Takagi M, Hasegawa T, Inoue H, Itakura M.

Growth Horm IGF Res. 2013 Aug;23(4):89-97. doi: 10.1016/j.ghir.2013.03.003. Epub 2013 Apr 18.

PMID:
23602557
9.

Molecular genetic studies in isolated growth hormone deficiency (IGHD).

Desai MP, Mithbawkar SM, Upadhye PS, Rao SC, Bhatia V, Vijaykumar M.

Indian J Pediatr. 2013 Aug;80(8):623-30. doi: 10.1007/s12098-013-0982-2. Epub 2013 Feb 23.

PMID:
23436191
10.

Type IA isolated growth hormone deficiency (IGHD) consistent with compound heterozygous deletions of 6.7 and 7.6 Kb at the GH1 gene locus.

Keselman A, Scaglia PA, Rodríguez Prieto MS, Ballerini MG, Rodríguez ME, Ropelato MG, Bergadá I, Jasper HG, Domené HM.

Arq Bras Endocrinol Metabol. 2012 Nov;56(8):558-63.

11.

Isolated growth hormone deficiency type 2: from gene to therapy.

Miletta MC, Lochmatter D, Pektovic V, Mullis PE.

Endocr Dev. 2012;23:109-20. doi: 10.1159/000341766. Epub 2012 Nov 23. Review.

PMID:
23182825
13.

Voice quality in short stature with and without GH deficiency.

Valença EH, Souza AH, Oliveira AH, Valença SL, Salvatori R, Gonçalves MI, Oliveira-Neto LA, Barros AD, Nascimento UN, Oliveira CR, Cardoso DF, Melo VA, Aguiar-Oliveira MH.

J Voice. 2012 Sep;26(5):673.e13-9. doi: 10.1016/j.jvoice.2011.12.009. Epub 2012 Jun 13.

PMID:
22698553
14.

Head circumference in untreated and IGF-I treated patients with Laron syndrome: comparison with untreated and hGH-treated children with isolated growth hormone deficiency.

Laron Z, Iluz M, Kauli R.

Growth Horm IGF Res. 2012 Apr;22(2):49-52. doi: 10.1016/j.ghir.2012.02.005. Epub 2012 Mar 11. Review.

PMID:
22414926
15.

Insulin sensitivity and β-cell function in adults with lifetime, untreated isolated growth hormone deficiency.

Oliveira CR, Salvatori R, Barreto-Filho JA, Rocha IE, Mari A, Pereira RM, Campos VC, Menezes M, Gomes E, Meneguz-Moreno RA, Araújo VP, Leite NT, Nascimento-Junior AC, Farias MI, Viscente TA, Araújo RD, Melo EV, Aguiar-Oliveira MH.

J Clin Endocrinol Metab. 2012 Mar;97(3):1013-9. doi: 10.1210/jc.2011-2590. Epub 2011 Dec 14.

PMID:
22170707
16.

Phenotype-genotype correlations in congenital isolated growth hormone deficiency (IGHD).

Alatzoglou KS, Dattani MT.

Indian J Pediatr. 2012 Jan;79(1):99-106. doi: 10.1007/s12098-011-0614-7. Epub 2011 Dec 3. Review.

PMID:
22139958
17.

Effect of growth hormone deficiency on brain structure, motor function and cognition.

Webb EA, O'Reilly MA, Clayden JD, Seunarine KK, Chong WK, Dale N, Salt A, Clark CA, Dattani MT.

Brain. 2012 Jan;135(Pt 1):216-27. doi: 10.1093/brain/awr305. Epub 2011 Nov 26.

18.

Growth hormone (GH-1) gene deletions in children with isolated growth hormone deficiency (IGHD).

Desai MP, Mithbawkar SM, Upadhye PS, Shalia KK.

Indian J Pediatr. 2012 Jul;79(7):875-83. doi: 10.1007/s12098-011-0588-5. Epub 2011 Oct 21.

PMID:
22016154
19.

Cephalometric features in isolated growth hormone deficiency.

Oliveira-Neto LA, Melo Mde F, Franco AA, Oliveira AH, Souza AH, Valença EH, Britto IM, Salvatori R, Aguiar-Oliveira MH.

Angle Orthod. 2011 Jul;81(4):578-83. doi: 10.2319/102210-618.1. Epub 2011 Feb 21.

PMID:
21341997
20.

Genetic causes and treatment of isolated growth hormone deficiency-an update.

Alatzoglou KS, Dattani MT.

Nat Rev Endocrinol. 2010 Oct;6(10):562-76. doi: 10.1038/nrendo.2010.147. Review.

PMID:
20852587
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