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High risk of congenital hypothyroidism in multiple pregnancies

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)

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

Characterization of Phenylketonuria Alleles in the Italian Population

Autor: Alliaudi C, Alberto Burlina, Paolo Lattanzio, Dionisi Vici C, Gianfranco Sebastio, de Sanctis L, Irma Dianzani, Sergio Giannattasio, Carnevale F, Burroni M

Publikováno v: European Journal of Human Genetics. 3:294-302

In order to identify the molecular basis of phenylketonuria (PKU) in Italy, we screened the entire coding sequence of the phenylalanine hydroxylase gene in 20 Italian PKU patients, whose origins are scattered throughout Italy. The frequency of each i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab6668e68ba59aa81e6c56efa65a46df
https://doi.org/10.1159/000472313

Objective melanoma progression

Autor: Rubegni, Pietro, Burroni, M, Nami, N, Cevenini, Gabriele, Bono, R, Sbano, P, Fimiani, Michele

Publikováno v: Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI). 17(1)

Many aspects of the natural history of malignant melanoma (MM) are still unclear, specifically its appearance at onset and particularly how it changes in time. The purpose of our study was to retrospectively determine objective changes in melanoma ov

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3052ce2a1f5422676f75866ab2a2eca6
https://pubmed.ncbi.nlm.nih.gov/20923468

The Italian National Register of infants with congenital hypothyroidism: twenty years of surveillance and study of congenital hypothyroidism

Autor: Olivieri, A., Altamura, R., Angeloni, U., Antonozzi, I., Baserga, M., Berardi, R., Bernasconi, S., Bona, G., Bucci, I., Burroni, M., Calaciura, F., Caldarera, R., Cappa, M., Caruso, U., Casini, M. R., Cassio, A., Cavallo, L., Cerone, R., Cesaretti, G., Cherubini, V., Chiarelli, F., Chiumello, G., Cicchetti, M., Ciccio', M. P., Cicognani, A., Coppola, A., Corbetta, C., Cordova, R., Correra, A., Costa, P., Dammacco, F., Sala, D., De Luca, F., De Santis, C., Di Maio, S., Gallicchio, G., Gastaldi, R., Grasso, G., Gurrado, R., Lasciarrea, L., Lelli, A., Leonardi, D., Liotta, A., Loche, S., Monaco, F., Lorini, R., Manente, G., Minelli, G., Moschini, L., Musaro', M. A., Narducci, T., Pagliardini, S., Palillo, L., Parlato, G., Pasquini, E., Peruzzi, L., Pinchera, Aldo, Pizzolante, M., Radetti, G., Righetti, F., Rizzo, A., Saggese, Giuseppe, Salerno, M. C., Salti, R., Sava, L., Scognamiglio, D., Stoppioni, V., Tato', L., Tonacchera, Massimo, Vigneri, R., Vignola, G., Vigone, M. C., Volta, C., Weber, G., Medda, E., Fazzini, C., De Angelis, S., Stazi, M. A., Sorcini, M.

Publikováno v: Italian Journal of Pediatrics, Vol 35, Iss 1, p 2 (2009)
Italian Journal of Pediatrics

All the Italian Centres in charge of screening, diagnosis, and follow-up of infants with congenital hypothyroidism participate in the Italian National Registry of affected infants, which performs the nationwide surveillance of the disease. It was est

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bddf4f1c8449fdc0bb086c8aaf874ed
http://www.ijponline.net/content/35/1/2