Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Valeria Cerioni"'
Autor:
Norma Tolaba, Yamila Spedalletti, Paola Bazzoni, Macarena Galindez, Valeria Cerioni, Cecilia Santillan, Gilda Richter, Cecilia Herrera, Laura Sanchez, Leopoldo Van Cawulaert, Marta A. Toscano, Marcelo Nallar, Marcelo Monteros Alvi, Christian Martín Moya
Publikováno v:
Endocrinologia, diabetes y nutricion. 69(2)
The study of genetic mutations in thyroid nodules makes it possible to improve the preoperative diagnosis of and reduce unnecessary surgeries on benign nodules. In this study, we analysed the impact of implementing a 7-gene mutation panel that enable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70302eed9a53b4dd21fb65ab5251a1ef
https://pubmed.ncbi.nlm.nih.gov/35256055
https://pubmed.ncbi.nlm.nih.gov/35256055
Autor:
Maddalena Bove, Valeria Cerioni, Luca Albarello, Stefano Mora, Ida Biunno, L. Bosio, Paola Sogno Valin, Claudio Doglioni, Laura Biagiotti, Stefano Grassi, Fabio Gervasi, Maria Carla Proverbio, Ermanna Rovida, Giuseppe Chiumello, I. Zamproni
Publikováno v:
Experimental and molecular pathology
83 (2007): 59–64. doi:10.1016/j.yexmp.2006.11.006
info:cnr-pdr/source/autori:Biagiotti L, Proverbio MC, Bosio L, Gervasi F, Rovida E, Cerioni V, Bove M, Valin PS, Albarello L, Zamproni I, Grassi S, Doglioni C, Mora S, Chiumello G, Biunno I./titolo:Identification of two novel frameshift mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy./doi:10.1016%2Fj.yexmp.2006.11.006/rivista:Experimental and molecular pathology (Print)/anno:2007/pagina_da:59/pagina_a:64/intervallo_pagine:59–64/volume:83
83 (2007): 59–64. doi:10.1016/j.yexmp.2006.11.006
info:cnr-pdr/source/autori:Biagiotti L, Proverbio MC, Bosio L, Gervasi F, Rovida E, Cerioni V, Bove M, Valin PS, Albarello L, Zamproni I, Grassi S, Doglioni C, Mora S, Chiumello G, Biunno I./titolo:Identification of two novel frameshift mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy./doi:10.1016%2Fj.yexmp.2006.11.006/rivista:Experimental and molecular pathology (Print)/anno:2007/pagina_da:59/pagina_a:64/intervallo_pagine:59–64/volume:83
Congenital Hyperinsulinism of Infancy (CHI) is a genetically heterogeneous disorder characterized by profound hypoglycemia related to inappropriate insulin secretion. Two histopathologically and genetically distinct groups are recognized among patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70256aef338d7c559aed222329f40b40
http://www.cnr.it/prodotto/i/55890
http://www.cnr.it/prodotto/i/55890
