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1.
Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.
Clin Endocrinol (Oxf)
; 87(6): 725-732, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-28734020
2.
Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single center.
Pituitary
; 18(4): 561-7, 2015 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-25315032
3.
Relatively high frequency of non-synonymous GLI2 variants in patients with congenital hypopituitarism without holoprosencephaly.
Clin Endocrinol (Oxf)
; 78(4): 551-7, 2013 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-22967285
4.
Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency.
PLoS One
; 15(10): e0240795, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33095795
5.
A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD).
Eur J Endocrinol
; 175(2): K7-K15, 2016 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-27252485
6.
FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies.
Endocr Connect
; 4(2): 100-7, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-25759380
7.
Study of the association between 3111T/C polymorphism of the CLOCK gene and the presence of overweight in schoolchildren.
J Pediatr (Rio J)
; 90(5): 500-5, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24818524
8.
Uremic leontiasis ossea.
Endocrine
; 65(3): 707-709, 2019 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-31175578
9.
Genetic predictors of long-term response to growth hormone (GH) therapy in children with GH deficiency and Turner syndrome: the influence of a SOCS2 polymorphism.
J Clin Endocrinol Metab
; 99(9): E1808-13, 2014 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-24905066
10.
The sitting height/height ratio for age in healthy and short individuals and its potential role in selecting short children for SHOX analysis.
Horm Res Paediatr
; 80(6): 449-56, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-24296787
11.
The interactive effect of GHR-exon 3 and -202 A/C IGFBP3 polymorphisms on rhGH responsiveness and treatment outcomes in patients with Turner syndrome.
J Clin Endocrinol Metab
; 97(4): E671-7, 2012 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-22278433
12.
Novel heterozygous nonsense GLI2 mutations in patients with hypopituitarism and ectopic posterior pituitary lobe without holoprosencephaly.
J Clin Endocrinol Metab
; 95(11): E384-91, 2010 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-20685856
13.
Study of the association between 3111T/C polymorphism of the CLOCK gene and the presence of overweight in schoolchildren, / Estudo da associação entre o polimorfismo 3111T/C do gene CLOCK e a presença de excesso de peso em escolares,
J. pediatr. (Rio J.)
; 90(5): 500-505, Sep-Oct/2014. tab, graf
Artículo
en Inglés
| LILACS | ID: lil-723174
14.
[Mathematical models for predicting growth responses to growth hormone replacement therapy]. / Modelos matemáticos para previsão de resposta ao tratamento com hormônio de crescimento.
Arq Bras Endocrinol Metabol
; 52(5): 839-49, 2008 Jul.
Artículo
en Portugués
| MEDLINE | ID: mdl-18797591
15.
Exon 3-deleted genotype of growth hormone receptor (GHRd3) positively influences IGF-1 increase at generation test in children with idiopathic short stature.
Clin Endocrinol (Oxf)
; 67(4): 500-4, 2007 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-17555512
16.
Modelos matemáticos para previsão de resposta ao tratamento com hormônio de crescimento: [revisão] / Mathematical models for predicting growth responses to growth hormone replacement therapy: [review]
Arq. bras. endocrinol. metab
; 52(5): 839-849, jul. 2008. tab
Artículo
en Portugués
| LILACS | ID: lil-491851
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