Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Giancarlo Guazzi"'
Autor:
Martin, Liliane, Martin, Jean-Jacques
Publikováno v:
Libro giubilare dedicato a G.C. Guazzi / Rossi, A. [edit.]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2097::836c9e215ee38f5a5092db5032aba0c5
https://hdl.handle.net/10067/205840151162165141
https://hdl.handle.net/10067/205840151162165141
Publikováno v:
Acta Neurologica Scandinavica. 92:387-393
Introduction The significance of the association of motor neuron syndromes with anti-GM1 antibodies remains unclear. We report the immunological study of a juvenile case of amyotrophic lateral sclerosis (ALS). Materials and methods Serum anti-Gm1 and
Publikováno v:
Acta Neurologica Scandinavica. 90:285-292
Human immunodeficiency virus type 1 (HIV-1)-infected individuals frequently develop a broad spectrum of neurological syndromes, classified as HIV-1-associated cognitive/motor complex. Diffuse demyelination of hemispheric white matter is a commonly ob
Autor:
Gian Maria Fabrizi, Bruno Barbiroli, Alessandro Malandrini, Michele D'Ettorre, Raffaele Lodi, Marco Rimoldi, P. Zaniol, Giancarlo Guazzi, Tiziana Cavallaro
Publikováno v:
Journal of the Neurological Sciences. 137:20-27
We describe a late-onset autosomal dominant limb girdle myopathy, associated with dilated cardiomyopathy and mental deterioration. In two affected members of the pedigree with histochemical (ragged-red and cytocrome c oxidase — negative fibers) and
Autor:
Alessandro Malandrini, Stefano DiDonato, Massimo Zeviani, Caterina Mariotti, Giancarlo Guazzi, Valeria Tiranti, G. M. Fabrizi
Publikováno v:
Journal of Neurology. 242:490-496
A heteroplasmic insertion of a 9-bp tandem repeat element was detected in the mitochondrial DNA of the maternal members of a large family. The mutation was contained within the non-coding region between the genes specifying subunit II of cytochrome c
Autor:
Alessandro Bucalossi, Claudio Salvadori, Francesco Moschini, Giuseppe Di Pietro, Gian Maria Fabrizi, Paola Bartalucci, Giancarlo Guazzi, Alessandro Malandrini, Fabio Truschi, Gianna Berti
Publikováno v:
Journal of the Neurological Sciences. 124:89-94
We report a family with three members affected by a typically X-linked McLeod syndrome. In the proband a very weak positivity for antigens of the Kell group was detected. His sister showed a normal antigenic pattern. We emphasize the prominent neurol
Publikováno v:
The Italian Journal of Neurological Sciences. 11:21-29
Serum and cerebrospinal fluid (CSF) from patients with multiple sclerosis (MS), patients with other (non-inflammatory) neurological diseases (OND), patients with non-inflammatory non-neurological diseases, and normal controls were assayed for lymphoc
Autor:
Nevia Caputo, A. M. Bardelli, Giancarlo Guazzi, Maria Teresa Dotti, Antonio Federico, Enrico Signorini, G Ciacci
Publikováno v:
Neuro-Ophthalmology. 14:131-133
Marinesco-Sjogren syndrome is an inherited neuro-ocular disease with spinocerebellar symptoms and cataracts. The authors report three cases, two of them belonging to the same family, with unusual magnetic resonance imaging findings, consisting of atr
Autor:
Alessandro Malandrini, Danilo DeFalco, Jean G.M. Huijmans, Silvia Palmeri, Giancarlo Guazzi, Chantal Ceuterick, Jean Jacques Martin, Alessandra Rufa, Otto P. van Diggelen, G Ciacci, Marcello Villanova
Publikováno v:
European Neurology, 43, 88-94. Karger
European neurology
European neurology
We report biochemical, morphological and neuroradiological findings in a 40-year-old woman affected with type I sialidosis. The clinical symptoms, consisting of a cerebellar syndrome, were first noted at the age of 17 years. The macular cherry-red sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43277aed60dafa4b38e6ba6bd880798d
http://hdl.handle.net/11365/38022
http://hdl.handle.net/11365/38022
Autor:
Mirella Bruttini, Alessandro Malandrini, Francesca Vitelli, Giancarlo Guazzi, Alessandra Renieri, Monica Piccini, Luciano Merlini, Marcello Villanova
Publikováno v:
Musclenerve. 22(10)
Facioscapulohumeral dystrophy (FSHD) is an autosomal-dominant muscular disorder associated with a short (