<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(10)</volume><submitter>Pardi E</submitter><pubmed_abstract>The aim of this study was to carry out genetic screening of the MEN1, CDKN1B and AIP genes, both by direct sequencing of the coding region and multiplex ligation-dependent probe amplification (MLPA) assay in the largest monocentric series of Italian patients with Multiple Endocrine Neoplasia type 1 syndrome (MEN1) and Familial Isolated Hyperparathyroidism (FIHP). The study also aimed to describe and compare the clinical features of MEN1 mutation-negative and mutation-positive patients during long-term follow-up and to correlate the specific types and locations of MEN1 gene mutations with onset and aggressiveness of the main MEN1 manifestations. A total of 69 index cases followed at the Endocrinology Unit in Pisa over a period of 19 years, including 54 MEN1 and 15 FIHP kindreds were enrolle</pubmed_abstract><journal>PloS one</journal><pagination>e0186485</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5643132</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features.</pubmed_title><pmcid>PMC5643132</pmcid><pubmed_authors>Mariotti S</pubmed_authors><pubmed_authors>Pardi E</pubmed_authors><pubmed_authors>Pigliaru F</pubmed_authors><pubmed_authors>Borsari S</pubmed_authors><pubmed_authors>Materazzi G</pubmed_authors><pubmed_authors>Cetani F</pubmed_authors><pubmed_authors>Satta C</pubmed_authors><pubmed_authors>Saponaro F</pubmed_authors><pubmed_authors>Urbani C</pubmed_authors><pubmed_authors>Bogazzi F</pubmed_authors><pubmed_authors>Miccoli P</pubmed_authors><pubmed_authors>Grantaliano L</pubmed_authors><pubmed_authors>Pani F</pubmed_authors><pubmed_authors>Marcocci C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features.</name><description>The aim of this study was to carry out genetic screening of the MEN1, CDKN1B and AIP genes, both by direct sequencing of the coding region and multiplex ligation-dependent probe amplification (MLPA) assay in the largest monocentric series of Italian patients with Multiple Endocrine Neoplasia type 1 syndrome (MEN1) and Familial Isolated Hyperparathyroidism (FIHP). The study also aimed to describe and compare the clinical features of MEN1 mutation-negative and mutation-positive patients during long-term follow-up and to correlate the specific types and locations of MEN1 gene mutations with onset and aggressiveness of the main MEN1 manifestations. A total of 69 index cases followed at the Endocrinology Unit in Pisa over a period of 19 years, including 54 MEN1 and 15 FIHP kindreds were enrolle</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017</publication><modification>2026-04-30T18:19:26.323Z</modification><creation>2019-03-27T02:59:04Z</creation></dates><accession>S-EPMC5643132</accession><cross_references><pubmed>29036195</pubmed><doi>10.1371/journal.pone.0186485</doi></cross_references></HashMap>