Search research articles
Contact Us
Filters
Showing results (71-80 of 89) with videos related to
Page
of 9
Sort By:
The Journal of Clinical Endocrinology and Metabolism
|
November 27, 2013
Germline prokineticin receptor 2 (PROKR2) variants associated with central hypogonadism cause differental modulation of distinct intracellular pathways
Domenico Vladimiro Libri, Gunnar Kleinau, Valeria Vezzoli, et al.
JCI Insight
|
February 2, 2023
Defective jagged-1 signaling affects GnRH development and contributes to congenital hypogonadotropic hypogonadism
Ludovica Cotellessa, Federica Marelli, Paolo Duminuco, et al.
Journal of Endocrinological Investigation
|
July 15, 2024
Inositols and female reproduction disorders: a consensus statement from the working group of the Club of the Italian Society of Endocrinology (SIE)-Women's Endocrinology
Costanzo Moretti, Marco Bonomi, Paola Dionese, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 24, 2025
The role of Obstructive Sleep Apnea and CPAP therapy in the functional hypogonadism of male patients with severe obesity
Alessandro Amodeo, Biagio Cangiano, Nicoletta Del Duca, et al.
Clinical Endocrinology
|
August 8, 2018
A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome
Edna F Roche, Anne McGowan, Olympia Koulouri, et al.
European Journal of Endocrinology
|
May 26, 2023
Towards an individualized management of pubertal induction in girls with hypogonadism: insight into the best replacement outcomes from a large multicentre registry
Giulia Rodari, Silvia Federici, Tommaso Todisco, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 31, 2020
Procoagulant Imbalance in Klinefelter Syndrome Assessed by Thrombin Generation Assay and Whole-Blood Thromboelastometry
Rita Indirli, Emanuele Ferrante, Erica Scalambrino, et al.
Human Molecular Genetics
|
April 27, 2017
A frequent oligogenic involvement in congenital hypothyroidism
Tiziana de Filippis, Giulia Gelmini, Elvezia Paraboschi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 4, 2011
Frequent TSH receptor genetic alterations with variable signaling impairment in a large series of children with nonautoimmune isolated hyperthyrotropinemia
Davide Calebiro, Giulia Gelmini, Daniela Cordella, et al.
BMC Infectious Diseases
|
June 15, 2021
Vitamin D and COVID-19 severity and related mortality: a prospective study in Italy
Irene Campi, Luigi Gennari, Daniela Merlotti, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 89) with videos related to
Sort By:
Page
of 9
The Journal of Clinical Endocrinology and Metabolism
|
November 27, 2013
Germline prokineticin receptor 2 (PROKR2) variants associated with central hypogonadism cause differental modulation of distinct intracellular pathways
Domenico Vladimiro Libri, Gunnar Kleinau, Valeria Vezzoli, et al.
JCI Insight
|
February 2, 2023
Defective jagged-1 signaling affects GnRH development and contributes to congenital hypogonadotropic hypogonadism
Ludovica Cotellessa, Federica Marelli, Paolo Duminuco, et al.
Journal of Endocrinological Investigation
|
July 15, 2024
Inositols and female reproduction disorders: a consensus statement from the working group of the Club of the Italian Society of Endocrinology (SIE)-Women's Endocrinology
Costanzo Moretti, Marco Bonomi, Paola Dionese, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 24, 2025
The role of Obstructive Sleep Apnea and CPAP therapy in the functional hypogonadism of male patients with severe obesity
Alessandro Amodeo, Biagio Cangiano, Nicoletta Del Duca, et al.
Clinical Endocrinology
|
August 8, 2018
A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome
Edna F Roche, Anne McGowan, Olympia Koulouri, et al.
European Journal of Endocrinology
|
May 26, 2023
Towards an individualized management of pubertal induction in girls with hypogonadism: insight into the best replacement outcomes from a large multicentre registry
Giulia Rodari, Silvia Federici, Tommaso Todisco, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 31, 2020
Procoagulant Imbalance in Klinefelter Syndrome Assessed by Thrombin Generation Assay and Whole-Blood Thromboelastometry
Rita Indirli, Emanuele Ferrante, Erica Scalambrino, et al.
Human Molecular Genetics
|
April 27, 2017
A frequent oligogenic involvement in congenital hypothyroidism
Tiziana de Filippis, Giulia Gelmini, Elvezia Paraboschi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 4, 2011
Frequent TSH receptor genetic alterations with variable signaling impairment in a large series of children with nonautoimmune isolated hyperthyrotropinemia
Davide Calebiro, Giulia Gelmini, Daniela Cordella, et al.
BMC Infectious Diseases
|
June 15, 2021
Vitamin D and COVID-19 severity and related mortality: a prospective study in Italy
Irene Campi, Luigi Gennari, Daniela Merlotti, et al.
Page
of 9