Detalhe da pesquisa
1.
SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.
Hum Reprod
; 27(5): 1460-5, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22416012
2.
Reproductive Phenotypes in Men With Acquired or Congenital Hypogonadotropic Hypogonadism: A Comparative Study.
J Clin Endocrinol Metab
; 107(7): e2812-e2824, 2022 06 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35358314
3.
Efficacy and safety of dopamine agonists in patients treated with antipsychotics and presenting a macroprolactinoma.
Eur J Endocrinol
; 183(2): 221-231, 2020 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32583656
4.
Severe Congenital Adrenal Hyperplasia Presenting as Bilateral Testicular Tumors and Azoospermia in the Third Decade of Life.
J Endocr Soc
; 2(9): 997-1000, 2018 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30140784
5.
Pituitary Adenoma Recurrence Suspected on Central Hyperthyroidism Despite Empty Sella and Confirmed by 68Ga-DOTA-TOC PET/CT.
Clin Nucl Med
; 42(6): 454-455, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28263215
6.
Heterogeneous Prognoses for pT3 Papillary Thyroid Carcinomas and Impact of Delayed Risk Stratification.
Thyroid
; 27(6): 778-786, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28351220
7.
Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life.
Orphanet J Rare Dis
; 10: 71, 2015 Jun 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26051373
8.
Sex steroids, precursors, and metabolite deficiencies in men with isolated hypogonadotropic hypogonadism and panhypopituitarism: a GCMS-based comparative study.
J Clin Endocrinol Metab
; 100(2): E292-6, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25393641
9.
Hypertrophic Osteoarthropathy and Follicular Thyroid Cancer: A Rare Paraneoplastic Syndrome.
Eur Thyroid J
; 4(4): 266-70, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26835431
10.
Congenital hypogonadotropic hypogonadism and Kallmann syndrome as models for studying hormonal regulation of human testicular endocrine functions.
Ann Endocrinol (Paris)
; 75(2): 79-87, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24815726
11.
Insulin-like peptide 3 (INSL3) in men with congenital hypogonadotropic hypogonadism/Kallmann syndrome and effects of different modalities of hormonal treatment: a single-center study of 281 patients.
J Clin Endocrinol Metab
; 99(2): E268-75, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24243640
12.
The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.
J Clin Endocrinol Metab
; 99(10): E2138-43, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25077900
13.
Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients.
Eur J Endocrinol
; 169(6): 805-9, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24031091
14.
Impact of clinical, hormonal, radiological, and immunohistochemical studies on the diagnosis of postmenopausal hyperandrogenism.
Eur J Endocrinol
; 165(5): 779-88, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21896622
15.
Pituitary stalk interruption and olfactory bulbs aplasia/hypoplasia in a man with Kallmann syndrome and reversible gonadotrope and somatotrope deficiencies.
Endocrine
; 49(3): 865-6, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25381604
16.
Kallmann syndrome caused by mutations in the PROK2 and PROKR2 genes: pathophysiology and genotype-phenotype correlations.
Front Horm Res
; 39: 121-132, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20389090
17.
A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genes.
J Clin Endocrinol Metab
; 95(2): 659-69, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20022991
18.
Impact of combined and progestogen-only contraceptives on bone mineral density.
Joint Bone Spine
; 76(2): 134-8, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19181558