Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Scognamiglio, D."'
Autor:
Olivieri, A, Fazzini, C, Medda, E, Altamura, R, Angeloni, A, Bernasconi, S, Bona, G, Bucci, I, Calaciura, F, Camilot, M, Cappa, M, Carducci, C, Caruso, U, Cavallo, L, Cesaretti, G, Chiarelli, F, Ciannamea, B, Ciatti, R, Cicciò, Mp, Corbetta, C, Costa, P, De Luca, F, Gallicchio, G, Gastaldi, R, Grasso, G, Gurrado, R, Lelli, A, Leonardi, D, Loche, S, Lorini, R, Minelli, G, Napolitano, G, Narducci, P, Oggiano, N, Pafundi, V, Pagliardini, S, Parlato, G, Pasquini, E, Pilia, S, Pizzolante, M, Radetti, G, Righetti, F, Rizzo, A, Salerno, Mc, Scognamiglio, D, Stoppioni, V, Tonacchera, M, Vignola, G, Vigone, Mc, Weber, G., CASSIO, ALESSANDRA
Publikováno v:
Hormone Research in Paediatrics. 83:86-93
Background/Aims: Over the years a rise in the incidence of congenital hypothyroidism (CH) has been described worldwide. The aim of our study was to investigate trends in the incidence of CH in Italy over the period 1987-2008, and to investigate which
Autor:
Olivieri, A, Radetti, G, Medda, E, Altamura, R, Angeloni, A, Bernasconi, S, Bona, G, Bucci, I, Calaciura, F, Camilot, M, Cappa, M, Carducci, C, Caruso, U, Cassio, A, Cavallo, L, Cesaretti, G, Chiarelli, F, Ciannamea, B, Ciatti, R, Cicciò, Mp, Corbetta, C, Costa, P, De Luca, F, Gallicchio, G, Gastaldi, R, Grasso, G, Gurrado, R, Lelli, A, Leonardi, D, Loche, S, Lorini, R, Minelli, G, Napolitano, G, Narducci, P, Oggiano, N, Pafundi, V, Pagliardini, S, Parlato, G, Pasquini, E, Pilia, S, Pizzolante, M, Righetti, F, Rizzo, A, Salerno, Mc, Scognamiglio, D, Stoppioni, V, Tonacchera, Massimo, Vignola, G, Vigone, Mc, Weber, G.
Publikováno v:
Journal of Endocrinological Investigation. 38:185-187
PURPOSE: Although a nation-wide salt iodization program on voluntary basis was implemented in 2005, many areas in our country are still characterized by mild iodine deficiency. Differently from the rest of Italy, an efficient program of iodine prophy
Autor:
Olivieri A, Corbetta C, Weber G, Vigone MC, Fazzini C, Medda E, Angeloni U, Antonozzi I, Baserga M, Bernasconi S, Bona G, Bucci I, Calaciura F, Caldarera R, Camilot M, Cappa M, Caruso U, Casini M, Cavallo L, Cesaretti G, Chiarelli F, Ciannamea B, Ciatti R, Cicciò M, Cordova R, Correra A, Costa P, De Santis C, Di Maio S, Gallicchio G, Gastaldi R, Grasso G, Gurrado R, Lelli A, Leonardi D, Loche S, Lorini R, Manente G, Monaco F, Minelli G, Narducci P, Oggiano N, Pagliardini S, Parlato G, Pasquini E, Pinchera A, Pizzolante M, Radetti G, Righetti F, Rizzo A, Saggese G, Sala D, Salerno C, Sava L, Scognamiglio D, Stoppioni V, Tonacchera M, Vigneri R, Vignola G, De Luca F., CASSIO, ALESSANDRA
Context: Over the years lower TSH cutoffs have been adopted in some screening programs for congenital hypothyroidism (CH) worldwide. This has resulted in a progressive increase in detecting additional mild forms of the disease, essentially with norma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8812a4891679fc36154ab785cb8358b
Autor:
Olivieri A, Altamura R, Angeloni U, Antonozzi I, Baserga M, Bernasconi S, Bona G, Bucci I, Calaciura F, Caldarera R, Camilot M, Cappa M, Caruso U, Casini MR, Cassio A, Cavallo L, Cesaretti G, Chiarelli F, Ciannamea B, Ciatti R, Cicciò M, Civolani P, Corbetta C, Cordova R, Correra A, Costa P, De Luca F, De Santis C, Fazzini C, Gallicchio G, Gastaldi R, Grasso G, Gurrado R, Lelli A, Leonardi D, Loche S, Lorini R, Medda E, Monaco F, Minelli G, Narducci P, Oggiano N, Pagliardini S, Parlato G, Pasquini E, Pinchera A, Pizzolante M, Radetti G, Righetti F, Rizzo A, Saggese G, Salerno C, Sava L, Scognamiglio D, Stoppioni V, Tonacchera M, Vigneri R, Vignola G, Vigone MC, WEBER , GIOVANNA
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 25:7-9
"In Italy, the nationwide newborn screening programme for congenital hypothyroidism (CH) represents an integrated approach to the disease including screening tests, diagnosis, treatment, follow up and nation-wide surveillance of the disease. The latt
Autor:
Olivieri A., Medda E, De Angelis S, Valensise H, De Felice M, Fazzini C, Cascino I, Cordeddu V, Sorcini M, Stazi M, Altamura R, Angeloni U, Antonozzi I, Baserga M, Berardi R, Bernasconi S, Bona G, Burroni M, Calaciura F, Caldarera R, Cappa M, Casini M, Cavallo L, Cherubini V, Chiumello G, Chiovato L, Cicchetti M, Cicciò M, Coppa G, Coppola A, Corbetta C, Cordova R, Correra A, Costa P, Dammacco F, De Luca F, De Santis C, Di Maio S, Gallicchio G, Gastaldi R, Giovannelli G, Grasso G, Gurrado R, Lasciarrea L, Lelli A, Leonardi D, Liotta A, Loche S, Lorini R, Manente G, Minelli G, Monaco F, Moschini L, Musarò M, Mussa G, Narducci T, Pagliardini S, Palillo L, Parlato G, Pasquini E, Peruzzi L, Piazzi S, Pinchera A, Pizzolante M, Puggioni R, Rizzo A, Saggese G, Sala D, Salerno C, Salti R, Sava L, Scognamiglio D, Stoppioni V, Tatò L, Tonacchera M, Vigneri R, Vignola G, Vigone M, Volta C, Weber G., CACCIARI, EMANUELE, CASSIO, ALESSANDRA, CICOGNANI, ALESSANDRO
Publikováno v:
92(8) (2007): 3141–3147.
info:cnr-pdr/source/autori:Olivieri A., Medda E., De Angelis S., Valensise H., De Felice M., Fazzini C., Cascino I., Cordeddu V., Sorcini M., Stazi M.A. and the Study Group for Congenital Hypothyroidism./titolo:High risk of congenital hypothyroidism in multiple pregnancies./doi:/rivista:/anno:2007/pagina_da:3141/pagina_a:3147/intervallo_pagine:3141–3147/volume:92(8)
info:cnr-pdr/source/autori:Olivieri A., Medda E., De Angelis S., Valensise H., De Felice M., Fazzini C., Cascino I., Cordeddu V., Sorcini M., Stazi M.A. and the Study Group for Congenital Hypothyroidism./titolo:High risk of congenital hypothyroidism in multiple pregnancies./doi:/rivista:/anno:2007/pagina_da:3141/pagina_a:3147/intervallo_pagine:3141–3147/volume:92(8)
CONTEXT: In Italy, the surveillance of congenital hypothyroidism (CH) is performed by the Italian National Registry of Infants with CH (INRICH). Up to now, about 3600 infants with CH are recorded in the INRICH, and a high number of twins are included
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76e9f87856dce704bd328a55155c3d2d
http://hdl.handle.net/11588/138480
http://hdl.handle.net/11588/138480
Autor:
A. Correra, Giuseppe Castaldo, Francesco Salvatore, Aurora Daniele, A. Pignero, Giuseppe Cardillo, C. Pennino, M. T. Carbone, D. Scognamiglio
Hyperphenylalaninemia (HPA) comprises a group of autosomal recessive disorders mainly caused by phenylalanine hydroxylase (PAH) gene mutations. We investigated PAH mutations in 126 HPA patients from Southern Italy who were identified in a neonatal sc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::731ab1475653aa66f727ea6847974679
http://hdl.handle.net/11588/102258
http://hdl.handle.net/11588/102258