Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features-Reference-Cited by-同舟云学术

Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features

Published:2017-10-16 Issue:10 Volume:12 Page:e0186485
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Pardi Elena,Borsari Simona,Saponaro Federica,Bogazzi Fausto,Urbani Claudio,Mariotti Stefano,Pigliaru Francesca,Satta Chiara,Pani Fabiana,Materazzi Gabriele,Miccoli Paolo,Grantaliano Lorena,Marcocci Claudio,Cetani Filomena^ORCID

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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4. No evidence of germline mutation or somatic deletion of the MEN1 gene in a case of familial multiple endocrine neoplasia type 1 (MEN1);H Namihira;Endocr J,1999

5. Analysis of gross deletions in the MEN1 gene in patients with multiple endocrine neoplasia type 1;M Owens;Clin Endocrinol,2008

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1. Case report: Comprehensive follow-up of a Colombian family carrying a novel MEN1 variant linked to a rare ACTH-producing pancreatic neuroendocrine carcinoma;Frontiers in Endocrinology;2024-07-22

2. Familial states of primary hyperparathyroidism: an update;Journal of Endocrinological Investigation;2024-04-18

3. Updates on the genetics of multiple endocrine neoplasia;Annales d'Endocrinologie;2024-04

4. Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort;Frontiers in Endocrinology;2023-09-21

5. Clinical Factors Predicting Multiple Endocrine Neoplasia Type 1 and Type 4 in Patients with Neuroendocrine Tumors;Genes;2023-09-10