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Rodolfo A Rey

Showing results (101-110 of 109) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|February 11, 2025
FSH and Sertoli cell biomarkers accurately distinguish hypogonadotropic hypogonadism from self-limited delayed pubertySebastián Castro, Lourdes Correa Brito, Patricia Bedecarrás, et al.
The Journal of Clinical Endocrinology and Metabolism|November 19, 2025
A novel POR G88S mutation causes severe PORD and establishes a critical pharmacogenomic risk profileMaria Natalia Rojas Velazquez, Jimena Lopez Dacal, Flemming S Jørgensen, et al.
Hormone Research in Paediatrics|December 17, 2013
Heterozygous IGFALS gene variants in idiopathic short stature and normal children: impact on height and the IGF systemHoracio M Domené, Paula A Scaglia, Alicia S Martínez, et al.
Frontiers in Endocrinology|November 20, 2025
Variation spectra in mild isolated hyperthyrotropinemia: pilot cohort and systematic reviewValentina Ricci, María E Masnata, María D Villanueva Gonzalez, et al.
Clinical Endocrinology|April 27, 2017
Characterization of four Latin American families confirms previous findings and reveals novel features of acid-labile subunit deficiencyPaula A Scaglia, Ana C Keselman, Débora Braslavsky, et al.
European Journal of Endocrinology|September 21, 2019
A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiencyAna Claudia Keselman, Ayelen Martin, Paula Alejandra Scaglia, et al.
Hormone Research in Paediatrics|July 10, 2017
Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org PortalLaura J C Kranenburg, Sam T H Reerds, Martine Cools, et al.
European Journal of Endocrinology|April 7, 2025
Deleterious variants in intolerant genes reveal new candidates for self-limited delayed pubertyRaíssa C Rezende, Wen He, Lena R Kaisinger, et al.
The Journal of Clinical Endocrinology and Metabolism|June 20, 2023
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and PubertyKatie Duckett, Alice Williamson, John W R Kincaid, et al.
Pageof 11

Showing results (101-110 of 109) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 109 results.
The Journal of Clinical Endocrinology and Metabolism|February 11, 2025
FSH and Sertoli cell biomarkers accurately distinguish hypogonadotropic hypogonadism from self-limited delayed pubertySebastián Castro, Lourdes Correa Brito, Patricia Bedecarrás, et al.
The Journal of Clinical Endocrinology and Metabolism|November 19, 2025
A novel POR G88S mutation causes severe PORD and establishes a critical pharmacogenomic risk profileMaria Natalia Rojas Velazquez, Jimena Lopez Dacal, Flemming S Jørgensen, et al.
Hormone Research in Paediatrics|December 17, 2013
Heterozygous IGFALS gene variants in idiopathic short stature and normal children: impact on height and the IGF systemHoracio M Domené, Paula A Scaglia, Alicia S Martínez, et al.
Frontiers in Endocrinology|November 20, 2025
Variation spectra in mild isolated hyperthyrotropinemia: pilot cohort and systematic reviewValentina Ricci, María E Masnata, María D Villanueva Gonzalez, et al.
Clinical Endocrinology|April 27, 2017
Characterization of four Latin American families confirms previous findings and reveals novel features of acid-labile subunit deficiencyPaula A Scaglia, Ana C Keselman, Débora Braslavsky, et al.
European Journal of Endocrinology|September 21, 2019
A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiencyAna Claudia Keselman, Ayelen Martin, Paula Alejandra Scaglia, et al.
Hormone Research in Paediatrics|July 10, 2017
Global Application of the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org PortalLaura J C Kranenburg, Sam T H Reerds, Martine Cools, et al.
European Journal of Endocrinology|April 7, 2025
Deleterious variants in intolerant genes reveal new candidates for self-limited delayed pubertyRaíssa C Rezende, Wen He, Lena R Kaisinger, et al.
The Journal of Clinical Endocrinology and Metabolism|June 20, 2023
Prevalence of Deleterious Variants in MC3R in Patients With Constitutional Delay of Growth and PubertyKatie Duckett, Alice Williamson, John W R Kincaid, et al.
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