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Francesca Marta Elli

Showing results (11-20 of 22) with videos related to

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Endocrinology, Diabetes & Metabolism Case Reports|February 1, 2019
Hypercalcitoninaemia in pseudohypo-parathyroidism type 1A and type 1BMaria P Yavropoulou, Efstathios Chronopoulos, George Trovas, et al.
Orphanet Journal of Rare Diseases|February 24, 2022
A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS genePaolo Cavarzere, Andrea Gastaldi, Francesca Marta Elli, et al.
Frontiers in Genetics|October 18, 2019
Improved Molecular Diagnosis of McCune-Albright Syndrome and Bone Fibrous Dysplasia by Digital PCRFrancesca Marta Elli, Luisa de Sanctis, Massimiliano Bergallo, et al.
Orphanet Journal of Rare Diseases|April 20, 2022
Correction to: A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS genePaolo Cavarzere, Andrea Gastaldi, Francesca Marta Elli, et al.
Frontiers in Medicine|December 26, 2022
Fibroblast growth factor 23 level modulates the hepatocyte's alpha-2-HS-glycoprotein transcription through the inflammatory pathway TNFα/NFκBDeborah Mattinzoli, Min Li, Giuseppe Castellano, et al.
Case Reports in Endocrinology|February 8, 2019
Unrecognized Pseudohypoparathyroidism Type 1A as a Cause of Hypocalcemia and Seizures in a 64-Year-Old WomanPatrizia Del Monte, Carla Micaela Cuttica, Alessandro Marugo, et al.
European Journal of Endocrinology|August 25, 2023
Prevalence and clinical features of armadillo repeat-containing 5 mutations carriers in a single center cohort of patients with bilateral adrenal incidentalomasValentina Morelli, Francesca Marta Elli, Sofia Frigerio, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 15, 2016
Screening of PRKAR1A and PDE4D in a Large Italian Series of Patients Clinically Diagnosed With Albright Hereditary Osteodystrophy and/or PseudohypoparathyroidismFrancesca Marta Elli, Paolo Bordogna, Luisa de Sanctis, et al.
Frontiers in Endocrinology|May 16, 2022
Is Encapsulated Medullary Thyroid Carcinoma Associated With a Better Prognosis? A Case Series and a Review of the LiteratureAndrea Contarino, Alessia Dolci, Marco Maggioni, et al.
The Journal of Clinical Endocrinology and Metabolism|July 19, 2016
The Prevalence of GNAS Deficiency-Related Diseases in a Large Cohort of Patients Characterized by the EuroPHP NetworkFrancesca Marta Elli, Agnès Linglart, Intza Garin, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Endocrinology, Diabetes & Metabolism Case Reports|February 1, 2019
Hypercalcitoninaemia in pseudohypo-parathyroidism type 1A and type 1BMaria P Yavropoulou, Efstathios Chronopoulos, George Trovas, et al.
Orphanet Journal of Rare Diseases|February 24, 2022
A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS genePaolo Cavarzere, Andrea Gastaldi, Francesca Marta Elli, et al.
Frontiers in Genetics|October 18, 2019
Improved Molecular Diagnosis of McCune-Albright Syndrome and Bone Fibrous Dysplasia by Digital PCRFrancesca Marta Elli, Luisa de Sanctis, Massimiliano Bergallo, et al.
Orphanet Journal of Rare Diseases|April 20, 2022
Correction to: A complex pheotype in a girl with a novel heterozygous missense variant (p.Ile56Phe) of the GNAS genePaolo Cavarzere, Andrea Gastaldi, Francesca Marta Elli, et al.
Frontiers in Medicine|December 26, 2022
Fibroblast growth factor 23 level modulates the hepatocyte's alpha-2-HS-glycoprotein transcription through the inflammatory pathway TNFα/NFκBDeborah Mattinzoli, Min Li, Giuseppe Castellano, et al.
Case Reports in Endocrinology|February 8, 2019
Unrecognized Pseudohypoparathyroidism Type 1A as a Cause of Hypocalcemia and Seizures in a 64-Year-Old WomanPatrizia Del Monte, Carla Micaela Cuttica, Alessandro Marugo, et al.
European Journal of Endocrinology|August 25, 2023
Prevalence and clinical features of armadillo repeat-containing 5 mutations carriers in a single center cohort of patients with bilateral adrenal incidentalomasValentina Morelli, Francesca Marta Elli, Sofia Frigerio, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 15, 2016
Screening of PRKAR1A and PDE4D in a Large Italian Series of Patients Clinically Diagnosed With Albright Hereditary Osteodystrophy and/or PseudohypoparathyroidismFrancesca Marta Elli, Paolo Bordogna, Luisa de Sanctis, et al.
Frontiers in Endocrinology|May 16, 2022
Is Encapsulated Medullary Thyroid Carcinoma Associated With a Better Prognosis? A Case Series and a Review of the LiteratureAndrea Contarino, Alessia Dolci, Marco Maggioni, et al.
The Journal of Clinical Endocrinology and Metabolism|July 19, 2016
The Prevalence of GNAS Deficiency-Related Diseases in a Large Cohort of Patients Characterized by the EuroPHP NetworkFrancesca Marta Elli, Agnès Linglart, Intza Garin, et al.
Pageof 3