Zobrazeno 1 - 10
of 105
pro vyhledávání: '"Cacciari, Emanuele"'
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:
SALARDI, SILVANA, ZUCCHINI, STEFANO, BETTOCCHI, ILARIA, ELLERI, DANIELA, SCIPIONE, MIRELLA, CICOGNANI, ALESSANDRO, CACCIARI, EMANUELE, R. Santoni, E. Corbelli
It is far from clear whether hyperhomocysteinemia (HH(e)), when present, is a preexisting marker for diabetic patients predisposed to vascular complications or an acquired condition that may change over time. To try to clarify this question we examin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::e90329a91c127fb6d4c7a43ecbdab535
http://hdl.handle.net/11585/26213
http://hdl.handle.net/11585/26213
Autor:
BALSAMO, ANTONIO, BALDAZZI, LILIA, BARP, LORELLA, BARONIO, FEDERICO, GENNARI, MONIA, CASSIO, ALESSANDRA, CICOGNANI, ALESSANDRO, CACCIARI, EMANUELE, C. Retetangos
BACKGROUND: CYP21 genotyping permits to define better the CAH form of the patients, in particular in males without salt wasting. AIM: Retrospective evaluation of height outcome and pubertal developmental patterns in 22 male patients affected by 21-hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::40404c9c0c4fb63199954fc61d39bc63
http://hdl.handle.net/11585/32072
http://hdl.handle.net/11585/32072
Autor:
ZUCCHINI, STEFANO, BARONIO, FEDERICO, PIRAZZOLI, PIERO, BETTOCCHI, ILARIA, RETETANGOS, CRISTIANA, BAL, MILVA ORQUIDEA, CICOGNANI, ALESSANDRO, CACCIARI, EMANUELE, M. Marsciani
We compared clinical characteristics and final height (FH) data after replacement therapy of 2 groups of pts diagnosed as GHD before puberty and treated either until FH (group 1, persistent deficiency) or until puberty (group 2, transient deficiency)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::c30e64b5cd969a6c439f70529b7214e0
http://hdl.handle.net/11585/26225
http://hdl.handle.net/11585/26225
Autor:
BERGAMASCHI, ROSALBA, MAZZANTI, LAURA, STROCCHI, SIMONA, ROSETTI, VALENTINA, CASTIGLIONI, LAURA, ZAPPULLA, FRANCO, CICOGNANI, ALESSANDRO, CACCIARI, EMANUELE, E. Scarano, I. Neri
There is a wide spectrum of skin anomalies in TS related to fetal lymphoedema, GH therapy or elevated FSH level. AN is characterized by hyperkeratosis, pigmentation and small papillomatous elevation of the skin. Aim of the study: to evaluate the asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::08f68e53cc414a65d4cc6d217855988e
http://hdl.handle.net/11585/26210
http://hdl.handle.net/11585/26210
Autor:
A. Pasini, D. Lazareva, BATTAGLIA, CESARE, BURNELLI, ROBERTA, BARONIO, FEDERICO, RETETANGOS, CRISTIANA, CICOGNANI, ALESSANDRO, CACCIARI, EMANUELE
Aim of the study was to assess the effect of chemo-radiotherapy on gonadal function in males treated for childhood malignancies, adding ultrasonographic and colour Doppler (cD) scanning of the testes to hormonal evaluation. cD allows the measurement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::14dc32e3c81c76fe1c871b3b6973a8f9
http://hdl.handle.net/11585/26198
http://hdl.handle.net/11585/26198
Autor:
MAZZANTI, LAURA, BERGAMASCHI, ROSALBA, MENCARELLI, FRANCESCA, STROCCHI, SIMONA, ROSETTI, VALENTINA, CICOGNANI, ALESSANDRO, CACCIARI, EMANUELE, D. Prandstraller, FATTORI, ROSSELLA, E. Scarano, D. Tassinari
Aortic dilation (AoDil) occurs in Turner syndrome (TS) pts, although in absence of CHD as risk factor. There is limited information on its prevalence and natural history. Aim of our study: to evaluate AoDil prevalence (at echocardiography and MRI) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::17ee66be1ce8fa5932b22e06efd29f58
http://hdl.handle.net/11585/26207
http://hdl.handle.net/11585/26207
Autor:
PIRAZZOLI, PIERO, BARONIO, FEDERICO, ZUCCHINI, STEFANO, GUALANDI, STEFANO, PASINI, ANDREA, CASSIO, ALESSANDRA, SALARDI, SILVANA, CICOGNANI, ALESSANDRO, CACCIARI, EMANUELE
The aim of this study was to evaluate the relationship between final height (FH),relative FH gain (FH-TH) and GH secretion before and after GH therapy in children.We studied 72 short children [chronological age (CA):11.1±2.2 yrs; height (H):-2.0±0.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::d3800007ff0c5921e06553e193d78268
http://hdl.handle.net/11585/26220
http://hdl.handle.net/11585/26220
Autor:
E. Scarano, F. Tamburrino, MAZZANTI, LAURA, MENCARELLI, FRANCESCA, ROSETTI, VALENTINA, CICOGNANI, ALESSANDRO, CACCIARI, EMANUELE
CFC syndrome is characterized by ectodermal abnormalities, coarse face, macrocephaly,postnatal short stature and MR and is in the spectrum of MCA/MR syndromes. Case report: 10 yr old boy with short stature and coarse face. Family history unremarkable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::77b60e8ea67c4b46933fc8a98bb0d1f0
http://hdl.handle.net/11585/26183
http://hdl.handle.net/11585/26183