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The Journal of Clinical Endocrinology and Metabolism
|
May 2, 2013
Aryl hydrocarbon receptor interacting protein (AIP) mutations occur rarely in sporadic parathyroid adenomas
Elena Pardi, Claudio Marcocci, Simona Borsari, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 28, 2024
Whole-exome Sequencing of Atypical Parathyroid Tumors Detects Novel and Common Genes Linked to Parathyroid Tumorigenesis
Elena Pardi, Anello Marcello Poma, Liborio Torregrossa, et al.
Endocrine
|
May 21, 2017
Clinical profile of juvenile primary hyperparathyroidism: a prospective study
Federica Saponaro, Claudio Marcocci, Federica Cacciatore, et al.
Expert Review of Endocrinology & Metabolism
|
February 14, 2019
HRPT2 gene analysis and the diagnosis of parathyroid carcinoma
Filomena Cetani, Elena Pardi, Chiara Banti, et al.
European Journal of Endocrinology
|
May 14, 2011
A novel mutation in the calcium-sensing receptor in a French family with familial hypocalciuric hypercalcaemia
Abdallah Al-Salameh, Filomena Cetani, Elena Pardi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 29, 2021
Pseudohypoparathyroidism: Focus on Cerebral and Renal Calcifications
Laura Mazoni, Matteo Apicella, Federica Saponaro, et al.
BMC Cancer
|
December 25, 2012
Functioning glucagonoma associated with primary hyperparathyroidism: multiple endocrine neoplasia type 1 or incidental association?
Enrico Erdas, Nicola Aste, Luca Pilloni, 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 literature
Chiara 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 variants
Simone Della Valentina, Laura Pierotti, Chiara Sardella, et al.
Clinical Endocrinology
|
January 25, 2006
Genetic analyses in familial isolated hyperparathyroidism: implication for clinical assessment and surgical management
Filomena Cetani, Elena Pardi, Elena Ambrogini, et al.
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of 5
Search research articles
Search
Showing results (11-20 of 45) with videos related to
Sort By:
Page
of 5
The Journal of Clinical Endocrinology and Metabolism
|
May 2, 2013
Aryl hydrocarbon receptor interacting protein (AIP) mutations occur rarely in sporadic parathyroid adenomas
Elena Pardi, Claudio Marcocci, Simona Borsari, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 28, 2024
Whole-exome Sequencing of Atypical Parathyroid Tumors Detects Novel and Common Genes Linked to Parathyroid Tumorigenesis
Elena Pardi, Anello Marcello Poma, Liborio Torregrossa, et al.
Endocrine
|
May 21, 2017
Clinical profile of juvenile primary hyperparathyroidism: a prospective study
Federica Saponaro, Claudio Marcocci, Federica Cacciatore, et al.
Expert Review of Endocrinology & Metabolism
|
February 14, 2019
HRPT2 gene analysis and the diagnosis of parathyroid carcinoma
Filomena Cetani, Elena Pardi, Chiara Banti, et al.
European Journal of Endocrinology
|
May 14, 2011
A novel mutation in the calcium-sensing receptor in a French family with familial hypocalciuric hypercalcaemia
Abdallah Al-Salameh, Filomena Cetani, Elena Pardi, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 29, 2021
Pseudohypoparathyroidism: Focus on Cerebral and Renal Calcifications
Laura Mazoni, Matteo Apicella, Federica Saponaro, et al.
BMC Cancer
|
December 25, 2012
Functioning glucagonoma associated with primary hyperparathyroidism: multiple endocrine neoplasia type 1 or incidental association?
Enrico Erdas, Nicola Aste, Luca Pilloni, 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 literature
Chiara 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 variants
Simone Della Valentina, Laura Pierotti, Chiara Sardella, et al.
Clinical Endocrinology
|
January 25, 2006
Genetic analyses in familial isolated hyperparathyroidism: implication for clinical assessment and surgical management
Filomena Cetani, Elena Pardi, Elena Ambrogini, et al.
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of 5