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Vito Guarnieri

Showing results (21-30 of 79) with videos related to

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Genes|November 29, 2019
Novel <i>TNXB</i> Variants in Two Italian Patients with Classical-Like Ehlers-Danlos SyndromeLucia Micale, Vito Guarnieri, Bartolomeo Augello, 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.
Cells|June 19, 2024
Multiple Endocrine Neoplasia Type 1 Regulates TGFβ-Mediated Suppression of Tumor Formation and Metastasis in MelanomaJulien Boudreault, Lucie Canaff, Mostafa Ghozlan, et al.
Journal of Biomedicine & Biotechnology|August 28, 2010
Small deletion at the 7q21.2 locus in a CCM family detected by real-time quantitative PCRLucia Anna Muscarella, Vito Guarnieri, Michelina Coco, et al.
Bone Reports|January 28, 2021
Imaging technologies in the differential diagnosis and follow-up of brown tumor in primary hyperparathyroidism: Case report and review of the literatureDavide Diacinti, Cristiana Cipriani, Federica Biamonte, et al.
Neurogenetics|October 18, 2006
Identification of two novel mutations and of a novel critical region in the KRIT1 geneVito Guarnieri, Lucia A Muscarella, Rosina Amoroso, et al.
The Journal of Clinical Endocrinology and Metabolism|May 25, 2006
Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: implications for cancer surveillanceVito Guarnieri, Alfredo Scillitani, Lucia Anna Muscarella, et al.
Neurosurgical Focus|July 25, 2006
Supratentorial cerebral cavernous malformations: clinical, surgical, and genetic involvementVincenzo Antonio D'Angelo, Costanzo De Bonis, Rosina Amoroso, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 19, 2017
Expression, function, and regulation of the embryonic transcription factor TBX1 in parathyroid tumorsChiara Verdelli, Laura Avagliano, Vito Guarnieri, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 9, 2014
Calcium-sensing-related gene mutations in hypercalcaemic hypocalciuric patients as differential diagnosis from primary hyperparathyroidism: detection of two novel inactivating mutations in an Italian populationPiero Stratta, Guido Merlotti, Claudio Musetti, et al.
Pageof 8

Showing results (21-30 of 79) with videos related to

Sort By:
Pageof 8
Genes|November 29, 2019
Novel <i>TNXB</i> Variants in Two Italian Patients with Classical-Like Ehlers-Danlos SyndromeLucia Micale, Vito Guarnieri, Bartolomeo Augello, 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.
Cells|June 19, 2024
Multiple Endocrine Neoplasia Type 1 Regulates TGFβ-Mediated Suppression of Tumor Formation and Metastasis in MelanomaJulien Boudreault, Lucie Canaff, Mostafa Ghozlan, et al.
Journal of Biomedicine & Biotechnology|August 28, 2010
Small deletion at the 7q21.2 locus in a CCM family detected by real-time quantitative PCRLucia Anna Muscarella, Vito Guarnieri, Michelina Coco, et al.
Bone Reports|January 28, 2021
Imaging technologies in the differential diagnosis and follow-up of brown tumor in primary hyperparathyroidism: Case report and review of the literatureDavide Diacinti, Cristiana Cipriani, Federica Biamonte, et al.
Neurogenetics|October 18, 2006
Identification of two novel mutations and of a novel critical region in the KRIT1 geneVito Guarnieri, Lucia A Muscarella, Rosina Amoroso, et al.
The Journal of Clinical Endocrinology and Metabolism|May 25, 2006
Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: implications for cancer surveillanceVito Guarnieri, Alfredo Scillitani, Lucia Anna Muscarella, et al.
Neurosurgical Focus|July 25, 2006
Supratentorial cerebral cavernous malformations: clinical, surgical, and genetic involvementVincenzo Antonio D'Angelo, Costanzo De Bonis, Rosina Amoroso, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 19, 2017
Expression, function, and regulation of the embryonic transcription factor TBX1 in parathyroid tumorsChiara Verdelli, Laura Avagliano, Vito Guarnieri, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 9, 2014
Calcium-sensing-related gene mutations in hypercalcaemic hypocalciuric patients as differential diagnosis from primary hyperparathyroidism: detection of two novel inactivating mutations in an Italian populationPiero Stratta, Guido Merlotti, Claudio Musetti, et al.
Pageof 8