Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Virginia Vicenzi"'
Autor:
Eva Trevisson, Giacomo Miglionico, Raffaele Parrozzani, Rodica Mardari, Virginia Vicenzi, Maurizio Clementi, Marta Lucchetta, Elisabetta Viscardi, Edoardo Midena, Matteo Cassina, Enrico Opocher
Publikováno v:
Journal of Neuro-Oncology. 134:279-287
Optic pathway glioma (OPG) represents the most common central nervous system tumor in children with Neurofibromatosis type-1 (NF1). Although overall survival is usually good, no clear prognostic factors have been identified so far. We assessed the na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::053061ce102847cf2c90298d74d82015
https://doi.org/10.1007/s11060-017-2517-6
https://doi.org/10.1007/s11060-017-2517-6
Autor:
Virginia Vicenzi, Maria Donata Benedetti, Antonio Marangi, Marika Vianello, Gianola Stenta, Gabriele Farina, Antonio Forgione, Francesca Calabria, Stefano Forlivesi, Fabio Marchioretto, Alberto Gajofatto, Francesca Rossi
Publikováno v:
Multiple sclerosis and related disorders. 41
Background The availability of new disease-modifying treatments (DMTs) in the last years has changed the therapeutic strategies used in Multiple Sclerosis (MS). We aimed to describe trend in DMTs utilization and persistence to treatment in a large sa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6b6e9707e64828dfb14f18f44579c19
https://pubmed.ncbi.nlm.nih.gov/32078935
https://pubmed.ncbi.nlm.nih.gov/32078935
Autor:
Maurizio Clementi, Paola Midrio, Virginia Vicenzi, Piergiorgio Gamba, Matteo Cassina, Mario Saugo, Michele Ruol, Carmen Fiorella Stocco, Silvano Piffer, Riccardo Pertile
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 106:542-548
Background Esophageal atresia (EA) is a congenital malformation of the upper gastrointestinal tract with an estimated prevalence varying from 1 in 2500 to 1 in 4500 births. The aim of this study was to describe the epidemiology of EA between 1981 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fce5601bbb66de12df6334082efb5bc3
https://doi.org/10.1002/bdra.23493
https://doi.org/10.1002/bdra.23493
Autor:
Antonio Marangi, Matteo Tagliapietra, Alessandro Salviati, Isabella Pasquin, Virginia Vicenzi
A 58-year-old woman with genetically confirmed adult GM1 gangliosidosis (aGM1-g) presented with generalized dystonia that was later followed by akinetic-rigid parkinsonism. Brain MRI revealed hyperintensities in the bilateral putamen typically observ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::306a1a83ac71ac022f9f422ff80184e2
http://hdl.handle.net/11562/983688
http://hdl.handle.net/11562/983688
Autor:
Virginia Vicenzi, Matteo Cassina, Chiara Rigon, Alberto Casarin, Leonardo Salviati, Maurizio Clementi
Publikováno v:
American journal of medical genetics. Part A. 167(6)
Au et al. [2014] reported on a girl with a 590 Kb deletion within chromosome 1q41q42 and suggested that FBXO28 is a major gene contributing to the neurodevelopmental, epileptic, and dysmorphologic phenotype of patients with 1q41q42 microdeletion synd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f856a520af852d9a0b633f9166a21198
https://pubmed.ncbi.nlm.nih.gov/25900767
https://pubmed.ncbi.nlm.nih.gov/25900767