Zobrazeno 1 - 10
of 636
pro vyhledávání: '"V. Pietrini"'
Autor:
N. Facciolongo, A. Di Stefano, V. Pietrini, C. Galeone, F. Bellanova, F. Menzella, N. Scichilone, R. Piro, G. L. Bajocchi, B. Balbi, L. Agostini, P. P. Salsi, D. Formisano, M. Lusuardi
Publikováno v:
BMC Pulmonary Medicine, Vol 18, Iss 1, Pp 1-11 (2018)
Abstract Background Bronchial thermoplasty (BT) is a non-pharmacological intervention for severe asthma whose mechanism of action is not completely explained by a reduction of airway smooth muscle (ASM). In this study we analyzed the effect of BT on
Externí odkaz:
https://doaj.org/article/c65a0247861a463fbf4ceba73d39fc41
Publikováno v:
Journal of Movement Disorders, Vol 14, Iss 3, Pp 204-207 (2021)
Journal of Movement Disorders
Journal of Movement Disorders
Autor:
Annarita Capozzi, Stefano Calzetti, V. Pietrini, Elena Saccani, Anna Negrotti, M. F. Bellanova
Publikováno v:
Journal of Clinical Neuroscience. 69:139-142
Background The determinants of restless legs syndrome (RLS) occurring in co-morbid association with Parkinson’s disease (PD) are currently unknown. Methods We performed a skin biopsy in proximal and distal sites of lower limbs in four PD patients,
Autor:
J. Mandrioli, S. Biguzzi, C. Guidi, E. Venturini, E. Sette, E. Terlizzi, A. Ravasio, M. Casmiro, F. Salvi, R. Liguori, R. Rizzi, V. Pietrini, E. Chierici, M. Santangelo, E. Granieri, V. Mussuto, A. Borghi, R. Rinaldi, N. Fini, E. Georgoulopoulou, S. De Pasqua, M. Vinceti, F. Bonvicini, ERRALS Group, S. Ferro, R. D'Alessandro, P. Avoni
Publikováno v:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 15:262-268
Our objective was to describe incidence and clinical features of ALS from a prospective population-based study in Emilia Romagna Region (ERR). From 2009 onwards, a prospective registry recorded all incident cases of ALS among residents in the ERR (po
Autor:
Franco Aversa, Valentina Papa, Benedetta Dalla Palma, Nicola Giuliani, Cristina Mancini, Roberta Costa, Anna Rita Capozzi, Laura Verga, V. Pietrini, Laura Notarfranchi, Fabrizio Accardi, Giovanna Cenacchi, Eugenia Martella, Gian Luca Capello
Publikováno v:
Case Reports in Hematology, Vol 2018 (2018)
Case Reports in Hematology
Case Reports in Hematology
Muscle involvement in AL amyloidosis is a rare condition, and the diagnosis of amyloid myopathy is often delayed and underdiagnosed. Amyloid myopathy may be the initial manifestation and may precede the diagnosis of systemic AL amyloidosis. Here, we
Autor:
Nicola Fini, Anna Odone, Lauren A. Wise, Francesco Patti, Renato Scillieri, Federica Violi, Kenneth J. Rothman, Carlotta Malagoli, Tommaso Filippini, Grazia Ghermandi, Margherita Ferrante, Caterina Ledda, Salvatore Lo Fermo, Sergio Teggi, V. Pietrini, Salvatore Sciacca, Sofia Costanzini, Jessica Mandrioli, Elisa Arcolin, Carlo Signorelli, Maria Fiore, Laura Iacuzio, Cristina Mauceri, Marco Vinceti
Publikováno v:
Environmental Health, Vol 16, Iss 1, Pp 1-14 (2017)
Environmental Health
Environmental Health
Background Epidemiologic studies have raised the possibility that some pesticide compounds induce the neurodegenerative disease amyotrophic lateral sclerosis (ALS), though the available evidence is not entirely consistent. Methods We conducted a popu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::287dddc66ec52e8b7d4900f85562ea5e
https://hdl.handle.net/11380/1144852
https://hdl.handle.net/11380/1144852
Autor:
Adriana V. Pietrini, Pier Luigi Luisi
Publikováno v:
ChemBioChem. 5:1055-1062
This work is aimed at finding conditions under which synthetic compartments used as cell models can fuse with each other and allow reagents contained in the different compartments to react. This goal seems to be best achieved by the use of water in o
Autor:
Barbara Castellotti, Floriano Girotti, Maria Concetta Riggio, Cinzia Gellera, V. Pietrini, Franca Mazzucchelli, Antonella Antonelli, S. Di Donato, Caterina Mariotti, Davide Pareyson
Publikováno v:
Journal of Neurology. 246:389-393
We clinically and genetically evaluated 73 Italian families with autosomal dominant cerebellar ataxia (ADCA) type I. Spinocerebellar ataxia (SCA) type 1 was the most common genotype (SCA1), accounting for 41% of cases (30 families), SCA2 was slightly
Autor:
M. Godani, Barbara Castellotti, Anna Negrotti, Stefano Calzetti, C. Toffoli, V. Pietrini, M. C. Riggio
Publikováno v:
The Italian Journal of Neurological Sciences. 19:345-350
We report a family affected by autosomal dominant ataxia, in which numerous members also showed microcytosis. Genetic analysis demonstrated a CAG expansion in the SCA1 locus in five members, while all subjects with microcytosis revealed a C-T substit
Autor:
V. Pietrini
Publikováno v:
Neurocase. 4:399aj-427