Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Giancarlo Guazzi"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a7cd97d00cd8e3bb01730475e5951ae
https://doi.org/10.1111/j.1600-0404.1995.tb00152.x
https://doi.org/10.1111/j.1600-0404.1995.tb00152.x
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8856e51acc6f035dcf1fafc768d40de4
https://doi.org/10.1111/j.1600-0404.1994.tb02723.x
https://doi.org/10.1111/j.1600-0404.1994.tb02723.x
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4baea182f8d9ec54d29491ae938d804
https://doi.org/10.1016/0022-510x(95)00321-r
https://doi.org/10.1016/0022-510x(95)00321-r
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da5bb80d41f800ec31fbd3c20303e9e7
https://doi.org/10.1007/bf00867418
https://doi.org/10.1007/bf00867418
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a3996684b43de803e0df5e6b4ab7e00
https://doi.org/10.1016/0022-510x(94)90016-7
https://doi.org/10.1016/0022-510x(94)90016-7
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5db57c1bf73f94dd331ec455d1a2c59b
https://doi.org/10.1007/bf02334901
https://doi.org/10.1007/bf02334901
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35c8fe4feb864ca88e008472b308df79
https://doi.org/10.3109/01658109409024037
https://doi.org/10.3109/01658109409024037
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 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adfcd19544dd1f5f58a664ba192a60e2
https://pubmed.ncbi.nlm.nih.gov/10487912
https://pubmed.ncbi.nlm.nih.gov/10487912
A high frequency of anti-thyroid antibodies has been demonstrated in multiple sclerosis (MS), but there is a lack of data on the possible association of thyroid autoimmunity with disease activity. To assess whether anti-thyroid antibodies are synthes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c376bf7dc24a66f0297e14e1877c670
http://hdl.handle.net/11365/34144
http://hdl.handle.net/11365/34144