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Leticia F G Silveira

Showing results (1-10 of 10) with videos related to

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Seminars in Reproductive Medicine|January 22, 2003
Hypogonadotropic hypogonadismLeticia 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 axisLeticia 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 pubertyMarina Krstevska-Konstantinova, Jana Jovanovska, Velibor B Tasic, et al.
Annales D'Endocrinologie|September 22, 2024
Predictive factors for treatment response in active thyroid eye diseaseNina 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 syndromeJuliana 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 syndromeLuciana 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 adenomaPaulo 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 centresAndrew 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 3Delanie 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 adulthoodElena Gianetti, Cintia Tusset, Sekoni D Noel, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Seminars in Reproductive Medicine|January 22, 2003
Hypogonadotropic hypogonadismLeticia 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 axisLeticia 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 pubertyMarina Krstevska-Konstantinova, Jana Jovanovska, Velibor B Tasic, et al.
Annales D'Endocrinologie|September 22, 2024
Predictive factors for treatment response in active thyroid eye diseaseNina 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 syndromeJuliana 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 syndromeLuciana 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 adenomaPaulo 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 centresAndrew 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 3Delanie 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 adulthoodElena Gianetti, Cintia Tusset, Sekoni D Noel, et al.
Pageof 1