Zobrazeno 1 - 10
of 56
pro vyhledávání: '"E. Bacchini"'
Autor:
Angelica Santoro, Carlo Caffarelli, Sergio Bernasconi, Francesca Santamaria, Giovanni Corsello, Virginia Mirra, E. Bacchini
Publikováno v:
Italian Journal of Pediatrics
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-11 (2020)
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-11 (2020)
We highlight the main developments that have been published during the first semester of the last year in the Italian Journal of Pediatrics. We have carefully chosen information from numerous exciting progresses issued in the Journal in the field of
Autor:
Marco Tartaglia, Paola Daniele, Domenico Corradi, Livia Garavelli, Stefania Errico, Sergio Bernasconi, Riccardo Riccardi, Maria E. Street, Giovanni Cazzaniga, Ivan Ivanovski, Eric Legius, Carmine Del Rossi, Alessandro De Luca, Anita Wischmeijer, Simonetta Rosato, Marzia Pollazzon, E. Bacchini, Carlo Dominici, Alfonsa Anna Lombardi, Cesare Rossi, Giancarlo Izzi, Viviana Cordeddu, Giacomo Biasucci, P Bertolini
Publikováno v:
American Journal of Medical Genetics Part A. 167:1902-1907
Noonan-like syndrome with loose anagen hair (NSLH), also known as Mazzanti syndrome, is a RASopathy characterized by craniofacial features resembling Noonan syndrome, cardiac defects, cognitive deficits and behavioral issues, reduced growth generally
Autor:
Giacomo Banchini, Livia Garavelli, Raffaele Virdis, Simonetta Rosato, Chiara Gelmini, Giuseppe Novelli, S. Bernasconi, Andrea Superti-Furga, Enrico Albertini, E. Bacchini, Maria Rosaria D'Apice, Francesca Rivieri, R. Dal Zotto, V. De Nigris, Anita Wischmeijer, Lorenzo Iughetti, M. Bertoli
Publikováno v:
American Journal of Medical Genetics Part A. :2258-2264
Mandibuloacral dysplasia type A (MADA) is characterized by growth retardation, postnatal onset of craniofacial anomalies with mandibular hypoplasia, progressive acral osteolysis, and skin changes including mottled pigmentation, skin atrophy, and lipo
Autor:
Massimo Bellomi, Maria Teresa Tondelli, Francesco Ferrozzi, E. Bacchini, Giancarlo Izzi, Giulio Zuccoli
Publikováno v:
Clinical Imaging. 23:356-360
In 1995, as a result of the observation of Rhabdoid elements among the other components of a Teratoid/Rhabdoid tumor (TRT), a new nomenclature was introduced, Atypical Teratoid/Rhabdoid Tumor (ATRT) of infancy and childhood. We report the clinical hi
Autor:
Davide Bova, G L dè Angelis, M Uccelli, R Grinzcich, F Campodonico, Andrea Battistini, E Bacchini, F De Chiara, Francesco Ferrozzi
Publikováno v:
Radiology. 198:875-879
To evaluate magnetic resonance (MR) imaging for assessment of pancreatic damage in cystic fibrosis.Twenty-seven patients with cystic fibrosis and 12 control subjects underwent T1-weighted imaging for visual assessment for pancreatic hyperintensity an
Autor:
Maria E. Street, Paolo Piazza, Francesco Ferrozzi, E. Bacchini, M. Sigorini, Raffaele Virdis, Giulio Zuccoli, Maurizio Rossi
Publikováno v:
American journal of medical genetics. 93(4)
In subjects with neurofibromatosis type 1 (NF1), we show that a reduction in the visual field is the most sensitive indicator of gliomas along the optic pathway. Therefore, we conclude that a visual field evaluation is the most sensitive clinical tes
Publikováno v:
Clinical imaging. 23(6)
In 1995, as a result of the observation of Rhabdoid elements among the other components of a Teratoid/Rhabdoid tumor (TRT), a new nomenclature was introduced, Atypical Teratoid/Rhabdoid Tumor (ATRT) of infancy and childhood. We report the clinical hi
Publikováno v:
La Radiologia medica. 96(3)
Publikováno v:
European urology. 30(1)
Objectives : To determine : (1) the incidence in newborns of both significant urinary anomalies and mild hydronephrosis ; (2) the degree of inaccuracy of prenatal sonography in our area, and (3) the evolution of neonatal hydronephrosis. Methods : Usi
Autor:
L, Iughetti, E, Bacchini, I, Dodi, A, Bianchi, G, Caselli, A, Cozzini, A, Ottaviani, S, Bernasconi
In adult obese patients both an increase of aminotranspherase values and hepatic steatosis have been frequently showed. Conversely in childhood the existence of a liver's damage is often not investigated. To assess the prevalence of hepatic alteratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::38a76ba97e2707b9dc63da53ddec6929
https://hdl.handle.net/11380/608677
https://hdl.handle.net/11380/608677