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Seminars in Reproductive Medicine
|
January 22, 2003
Hypogonadotropic hypogonadism
Leticia F G Silveira, Gavin S MacColl, Pierre M G Bouloux
Frontiers of Hormone Research
|
April 15, 2010
Role of kisspeptin/GPR54 system in human reproductive axis
Leticia F G Silveira, Milena G Teles, Ericka B Trarbach, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 17, 2013
Mutational analysis of KISS1 and KISS1R in idiopathic central precocious puberty
Marina Krstevska-Konstantinova, Jana Jovanovska, Velibor B Tasic, et al.
Annales D'Endocrinologie
|
September 22, 2024
Predictive factors for treatment response in active thyroid eye disease
Nina R Alkmim, Kamilla M A B Rajão, Ana R P Figueiredo, et al.
Fertility and Sterility
|
November 16, 2007
Molecular analysis of the WNT4 gene in 6 patients with Mayer-Rokitansky-Küster-Hauser syndrome
Juliana B Drummond, Fernando M Reis, Wolfanga L M Boson, et al.
Fertility and Sterility
|
June 1, 2013
Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome
Luciana Ribeiro Montenegro, Leticia F G Silveira, Cintia Tusset, et al.
Annales D'Endocrinologie
|
October 16, 2018
Association between KISS1 rs5780218 promoter polymorphism and onset of growth hormone secreting pituitary adenoma
Paulo V G H Amorim, Isabella P P Grande, Rafael L Batista, et al.
The Lancet. Diabetes & Endocrinology
|
March 4, 2024
Classes and predictors of reversal in male patients with congenital hypogonadotropic hypogonadism: a cross-sectional study of six international referral centres
Andrew A Dwyer, Isabella R McDonald, Biagio Cangiano, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 18, 2014
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3
Delanie B Macedo, Ana Paula Abreu, Ana Claudia S Reis, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 25, 2010
TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthood
Elena Gianetti, Cintia Tusset, Sekoni D Noel, et al.
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Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Seminars in Reproductive Medicine
|
January 22, 2003
Hypogonadotropic hypogonadism
Leticia F G Silveira, Gavin S MacColl, Pierre M G Bouloux
Frontiers of Hormone Research
|
April 15, 2010
Role of kisspeptin/GPR54 system in human reproductive axis
Leticia F G Silveira, Milena G Teles, Ericka B Trarbach, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
August 17, 2013
Mutational analysis of KISS1 and KISS1R in idiopathic central precocious puberty
Marina Krstevska-Konstantinova, Jana Jovanovska, Velibor B Tasic, et al.
Annales D'Endocrinologie
|
September 22, 2024
Predictive factors for treatment response in active thyroid eye disease
Nina R Alkmim, Kamilla M A B Rajão, Ana R P Figueiredo, et al.
Fertility and Sterility
|
November 16, 2007
Molecular analysis of the WNT4 gene in 6 patients with Mayer-Rokitansky-Küster-Hauser syndrome
Juliana B Drummond, Fernando M Reis, Wolfanga L M Boson, et al.
Fertility and Sterility
|
June 1, 2013
Combined use of multiplex ligation-dependent probe amplification and automatic sequencing for identification of KAL1 defects in patients with Kallmann syndrome
Luciana Ribeiro Montenegro, Leticia F G Silveira, Cintia Tusset, et al.
Annales D'Endocrinologie
|
October 16, 2018
Association between KISS1 rs5780218 promoter polymorphism and onset of growth hormone secreting pituitary adenoma
Paulo V G H Amorim, Isabella P P Grande, Rafael L Batista, et al.
The Lancet. Diabetes & Endocrinology
|
March 4, 2024
Classes and predictors of reversal in male patients with congenital hypogonadotropic hypogonadism: a cross-sectional study of six international referral centres
Andrew A Dwyer, Isabella R McDonald, Biagio Cangiano, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 18, 2014
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3
Delanie B Macedo, Ana Paula Abreu, Ana Claudia S Reis, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 25, 2010
TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthood
Elena Gianetti, Cintia Tusset, Sekoni D Noel, et al.
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of 1