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Filomena Cetani

Showing results (51-60 of 120) with videos related to

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Acta Haematologica|September 9, 2020
Concomitant Primary Hyperparathyroidism in Patients with Multiple Myeloma: A Possible Link?Laura Notarfranchi, Valentina Marchica, Benedetta Dalla Palma, et al.
European Journal of Endocrinology|March 12, 2004
TSH receptor antibodies do not alter the function of gonadotropin receptors stably expressed in eukaryotic cellsMassimo Tonacchera, Eleonora Ferrarini, Antonio Dimida, et al.
Surgery|December 17, 2008
Re: Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutationsVito Guarnieri, Michele Bisceglia, Nazzario Bonfitto, et al.
Clinical Endocrinology|November 18, 2003
Impaired GH secretion to provocative stimuli in two families with hypocalciuric hypercalcaemiaElisabetta Cecconi, Fausto Bogazzi, Filomena Cetani, et al.
The Journal of Clinical Endocrinology and Metabolism|May 15, 2022
Long-term Efficacy and Safety of Rifampin in the Treatment of a Patient Carrying a CYP24A1 Loss-of-Function VariantAlessandro Brancatella, Daniele Cappellani, Martin Kaufmann, et al.
Frontiers in Oncology|September 3, 2024
Persistent primary hyperparathyroidism caused by an ectopic adenoma in the piriform sinus: case report and review of the literatureChiara Sardella, Veronica Seccia, Massimo Giambalvo, et al.
Journal of Endocrinological Investigation|June 1, 2026
Clinical and genetic insights into Autosomal Dominant Hypocalcemia type 1: a single-center case series including genotype-phenotype correlations, pregnancy outcomes, and novel CASR variantsSimone Della Valentina, Laura Pierotti, Chiara Sardella, et al.
Case Reports in Endocrinology|May 16, 2019
Hereditary Hypercalcemia Caused by a Homozygous Pathogenic Variant in the <i>CYP24A1</i> Gene: A Case Report and Review of the LiteratureDaniele Cappellani, Alessandro Brancatella, Martin Kaufmann, et al.
The Journal of Clinical Endocrinology and Metabolism|April 30, 2009
Morphometric vertebral fractures in postmenopausal women with primary hyperparathyroidismEdda Vignali, Giuseppe Viccica, Daniele Diacinti, et al.
Clinical Endocrinology|January 25, 2006
Genetic analyses in familial isolated hyperparathyroidism: implication for clinical assessment and surgical managementFilomena Cetani, Elena Pardi, Elena Ambrogini, et al.
Pageof 12

Showing results (51-60 of 120) with videos related to

Sort By:
Pageof 12
Acta Haematologica|September 9, 2020
Concomitant Primary Hyperparathyroidism in Patients with Multiple Myeloma: A Possible Link?Laura Notarfranchi, Valentina Marchica, Benedetta Dalla Palma, et al.
European Journal of Endocrinology|March 12, 2004
TSH receptor antibodies do not alter the function of gonadotropin receptors stably expressed in eukaryotic cellsMassimo Tonacchera, Eleonora Ferrarini, Antonio Dimida, et al.
Surgery|December 17, 2008
Re: Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutationsVito Guarnieri, Michele Bisceglia, Nazzario Bonfitto, et al.
Clinical Endocrinology|November 18, 2003
Impaired GH secretion to provocative stimuli in two families with hypocalciuric hypercalcaemiaElisabetta Cecconi, Fausto Bogazzi, Filomena Cetani, et al.
The Journal of Clinical Endocrinology and Metabolism|May 15, 2022
Long-term Efficacy and Safety of Rifampin in the Treatment of a Patient Carrying a CYP24A1 Loss-of-Function VariantAlessandro Brancatella, Daniele Cappellani, Martin Kaufmann, et al.
Frontiers in Oncology|September 3, 2024
Persistent primary hyperparathyroidism caused by an ectopic adenoma in the piriform sinus: case report and review of the literatureChiara Sardella, Veronica Seccia, Massimo Giambalvo, et al.
Journal of Endocrinological Investigation|June 1, 2026
Clinical and genetic insights into Autosomal Dominant Hypocalcemia type 1: a single-center case series including genotype-phenotype correlations, pregnancy outcomes, and novel CASR variantsSimone Della Valentina, Laura Pierotti, Chiara Sardella, et al.
Case Reports in Endocrinology|May 16, 2019
Hereditary Hypercalcemia Caused by a Homozygous Pathogenic Variant in the <i>CYP24A1</i> Gene: A Case Report and Review of the LiteratureDaniele Cappellani, Alessandro Brancatella, Martin Kaufmann, et al.
The Journal of Clinical Endocrinology and Metabolism|April 30, 2009
Morphometric vertebral fractures in postmenopausal women with primary hyperparathyroidismEdda Vignali, Giuseppe Viccica, Daniele Diacinti, et al.
Clinical Endocrinology|January 25, 2006
Genetic analyses in familial isolated hyperparathyroidism: implication for clinical assessment and surgical managementFilomena Cetani, Elena Pardi, Elena Ambrogini, et al.
Pageof 12