Detalhe da pesquisa
1.
Vasculometabolic effects in patients with congenital growth hormone deficiency with and without GH replacement therapy during adulthood.
Pituitary
; 24(2): 216-228, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33098037
2.
Genetic Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing.
J Pediatr
; 215: 192-198, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31630891
3.
Cushing disease due to a somatic USP8 mutation in a patient with evolving pituitary hormone deficiencies due to a germline GH1 splicing variant.
Arch Endocrinol Metab
; 66(1): 104-111, 2022 Mar 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35029852
4.
Allelic Variants in Established Hypopituitarism Genes Expand Our Knowledge of the Phenotypic Spectrum.
Genes (Basel)
; 12(8)2021 07 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-34440302
5.
Genetic investigation of patients with tall stature.
Eur J Endocrinol
; 182(2): 139-147, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31751304
6.
Analysis of craniofacial and extremity growth in patients with growth hormone deficiency during growth hormone therapy.
Horm Res
; 71(3): 173-7, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19188743
7.
Factors determining normal adult height in girls with gonadotropin-dependent precocious puberty treated with depot gonadotropin-releasing hormone analogs.
J Clin Endocrinol Metab
; 93(7): 2662-9, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18460564
8.
Long-term treatment of familial male-limited precocious puberty (testotoxicosis) with cyproterone acetate or ketoconazole.
Clin Endocrinol (Oxf)
; 69(1): 93-8, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18088394
9.
High prevalence of pituitary magnetic resonance abnormalities and gene mutations in a cohort of Brazilian children with growth hormone deficiency and response to treatment.
J Pediatr Endocrinol Metab
; 21(7): 673-80, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18780602
10.
Androgen insensitivity syndrome: a review.
Arch Endocrinol Metab
; 62(2): 227-235, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29768628
11.
Cushing disease due to a somatic USP8 mutation in a patient with evolving pituitary hormone deficiencies due to a germline GH1 splicing variant
Arch. endocrinol. metab. (Online)
; 66(1): 104-111, Jan.-Feb. 2022. tab, graf
Artigo
em Inglês
| LILACS | ID: biblio-1364312
12.
Triple A Syndrome: Preliminary Response to the Antioxidant N-Acetylcysteine Treatment in a Child.
Horm Res Paediatr
; 88(2): 167-171, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28395280
13.
Preclinical diagnosis of testotoxicosis in a boy with an activating mutation of the luteinizing hormone receptor.
J Pediatr Endocrinol Metab
; 19(4): 541-4, 2006 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-16759041
14.
Inactivating mutations of LH and FSH receptors--from genotype to phenotype.
Pediatr Endocrinol Rev
; 4(1): 28-31, 2006 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17021580
15.
Frequency of the allelic variant (Trp8Arg/Ile15Thr) of the luteinizing hormone gene in a Brazilian cohort of healthy subjects and in patients with hypogonadotropic hypogonadism.
Clinics (Sao Paulo)
; 60(6): 461-4, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16358135
16.
[Leydig cell hypoplasia]. / Hipoplasia das células de Leydig.
Arq Bras Endocrinol Metabol
; 49(1): 83-6, 2005 Feb.
Artigo
em Português
| MEDLINE | ID: mdl-16544038
17.
Gonadotropin resistance.
Endocr Dev
; 24: 25-32, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23392092
18.
Androgen insensitivity syndrome: a review
Arch. endocrinol. metab. (Online)
; 62(2): 227-235, Mar.-Apr. 2018. tab, graf
Artigo
em Inglês
| LILACS | ID: biblio-887640
19.
[Mutations in insulin-like growth factor receptor 1 gene (IGF1R) resulting in intrauterine and postnatal growth retardation]. / Mutações no gene do receptor do fator de crescimento insulina-símile 1 (IGF1R) como causa de retardo do crescimento pré- e pós-natal.
Arq Bras Endocrinol Metabol
; 55(8): 541-9, 2011 Nov.
Artigo
em Português
| MEDLINE | ID: mdl-22218435
20.
Comparison between weight-based and IGF-I-based growth hormone (GH) dosing in the treatment of children with GH deficiency and influence of exon 3 deleted GH receptor variant.
Growth Horm IGF Res
; 19(2): 179-86, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19036620