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Luca Persani

Showing results (271-280 of 321) with videos related to

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Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|June 23, 2006
Functional characterization of wild-type and a mutated form of SLC26A4 identified in a patient with Pendred syndromeSilvia Dossena, Valeria Vezzoli, Nadia Cerutti, et al.
The Journal of Clinical Endocrinology and Metabolism|April 6, 2017
Retinal Photoreceptor Functions Are Compromised in Patients With Resistance to Thyroid Hormone Syndrome (RTHβ)Irene Campi, Gabriella Cammarata, Stefania Bianchi Marzoli, et al.
Trends in Endocrinology and Metabolism: TEM|May 1, 2018
Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian InsufficiencyIlpo Huhtaniemi, Outi Hovatta, Antonio La Marca, et al.
Italian Journal of Pediatrics|November 5, 2016
Long-term safety and efficacy of Omnitrope®, a somatropin biosimilar, in children requiring growth hormone treatment: Italian interim analysis of the PATRO Children studyLorenzo Iughetti, Gianluca Tornese, Maria Elisabeth Street, et al.
JCI Insight|February 2, 2023
Defective jagged-1 signaling affects GnRH development and contributes to congenital hypogonadotropic hypogonadismLudovica Cotellessa, Federica Marelli, Paolo Duminuco, 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 obesityAlessandro Amodeo, Biagio Cangiano, Nicoletta Del Duca, et al.
Molecular and Cellular Biology|December 6, 2021
Structure-Guided Approach to Relieving Transcriptional Repression in Resistance to Thyroid Hormone αBeatriz Romartinez-Alonso, Maura Agostini, Heulyn Jones, et al.
The Journal of Clinical Endocrinology and Metabolism|January 14, 2016
JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid DefectsTiziana de Filippis, Federica Marelli, Gabriella Nebbia, et al.
Oncotarget|May 18, 2017
Epigenome-wide association study in hepatocellular carcinoma: Identification of stochastic epigenetic mutations through an innovative statistical approachDavide Gentilini, Stefania Scala, Germano Gaudenzi, 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 syndromeEdna F Roche, Anne McGowan, Olympia Koulouri, et al.
Pageof 33

Showing results (271-280 of 321) with videos related to

Sort By:
Pageof 33
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|June 23, 2006
Functional characterization of wild-type and a mutated form of SLC26A4 identified in a patient with Pendred syndromeSilvia Dossena, Valeria Vezzoli, Nadia Cerutti, et al.
The Journal of Clinical Endocrinology and Metabolism|April 6, 2017
Retinal Photoreceptor Functions Are Compromised in Patients With Resistance to Thyroid Hormone Syndrome (RTHβ)Irene Campi, Gabriella Cammarata, Stefania Bianchi Marzoli, et al.
Trends in Endocrinology and Metabolism: TEM|May 1, 2018
Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian InsufficiencyIlpo Huhtaniemi, Outi Hovatta, Antonio La Marca, et al.
Italian Journal of Pediatrics|November 5, 2016
Long-term safety and efficacy of Omnitrope®, a somatropin biosimilar, in children requiring growth hormone treatment: Italian interim analysis of the PATRO Children studyLorenzo Iughetti, Gianluca Tornese, Maria Elisabeth Street, et al.
JCI Insight|February 2, 2023
Defective jagged-1 signaling affects GnRH development and contributes to congenital hypogonadotropic hypogonadismLudovica Cotellessa, Federica Marelli, Paolo Duminuco, 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 obesityAlessandro Amodeo, Biagio Cangiano, Nicoletta Del Duca, et al.
Molecular and Cellular Biology|December 6, 2021
Structure-Guided Approach to Relieving Transcriptional Repression in Resistance to Thyroid Hormone αBeatriz Romartinez-Alonso, Maura Agostini, Heulyn Jones, et al.
The Journal of Clinical Endocrinology and Metabolism|January 14, 2016
JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid DefectsTiziana de Filippis, Federica Marelli, Gabriella Nebbia, et al.
Oncotarget|May 18, 2017
Epigenome-wide association study in hepatocellular carcinoma: Identification of stochastic epigenetic mutations through an innovative statistical approachDavide Gentilini, Stefania Scala, Germano Gaudenzi, 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 syndromeEdna F Roche, Anne McGowan, Olympia Koulouri, et al.
Pageof 33