Zobrazeno 1 - 6
of 6
pro vyhledávání: '"N. A. Curtò"'
Autor:
Franco Carrara, Jacopo C. DiFrancesco, L Brighina, Massimo Zeviani, L. Marzorati, Carlo Ferrarese, N. A. Curtò, Enrico Saracchi, Costanza Lamperti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f2e4ab653d1e1cb5ca72620c2ab09f4
http://hdl.handle.net/10281/32836
http://hdl.handle.net/10281/32836
Autor:
Jacopo C. DiFrancesco, M. Brioschi, Mario Savoiardo, C. Ruffmann, E. Saracchi, N. A. Curtò, Gloria Galimberti, G. Costantino, L Brighina, Paolo Remida, Elisa Conti, Fabrizio Tagliavini, Carlo Ferrarese, L. Marzorati
Publikováno v:
Neurology. 76(9)
A 68-year-old man presented with a 4-month history of progressive memory loss and mood disorders. Neurologic examination revealed severe impairment of attention and verbal skills, without motor and sensory deficits. His medical history included mild
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d60d65f2c01f3f5ce4508bfa43be2a2d
https://pubmed.ncbi.nlm.nih.gov/21357829
https://pubmed.ncbi.nlm.nih.gov/21357829
Autor:
Barbara Frigeni, M. Brioschi, L. Marzorati, Enrico Saracchi, Carlo Ferrarese, Lorenzo Fumagalli, L Brighina, Lucio Tremolizzo, Jacopo C. DiFrancesco, N. A. Curtò, Maria Luisa Piatti, G Costantino
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is often related to the A3243G mutation of the mitochondrial DNA, accounting for about 80% of typical cases, with a relevant phenotypic variability. Hemorrhagic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::202217555c6b46922f1ea0f20f0a997f
http://hdl.handle.net/10281/33170
http://hdl.handle.net/10281/33170
Autor:
Grazia Annesi, L. Marzorati, Patrizia Tarantino, Lucio Tremolizzo, N. A. Curtò, F. Lanzani, Carlo Ferrarese
Publikováno v:
Neurological sciences (Testo stamp.) (2011).
info:cnr-pdr/source/autori:Tremolizzo L, Curtò NA, Marzorati L, Lanzani F, Tarantino P, Annesi G, Ferrarese C./titolo:Early-onset SCA17 with 43 TBP repeats: expanding the phenotype?/doi:/rivista:Neurological sciences (Testo stamp.)/anno:2011/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Tremolizzo L, Curtò NA, Marzorati L, Lanzani F, Tarantino P, Annesi G, Ferrarese C./titolo:Early-onset SCA17 with 43 TBP repeats: expanding the phenotype?/doi:/rivista:Neurological sciences (Testo stamp.)/anno:2011/pagina_da:/pagina_a:/intervallo_pagine:/volume
The SCA17 clinical phenotype includes characteristics associated with cerebellar and cortical atrophy such as ataxia, dementia, epilepsy, chorea and parkinsonian features. Here we describe the case of a 38-year-old male presenting with ataxia, cognit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb34488a171403d0aaf67bae27e2e4ef
https://pubmed.ncbi.nlm.nih.gov/21710129
https://pubmed.ncbi.nlm.nih.gov/21710129
Autor:
Carlo Ferrarese, E. Tagliabue, S. Fermi, Costanza Lamperti, M. Moggio, Lucio Tremolizzo, N. A. Curtò, Ildebrando Appollonio, A. Galbussera, M. Bruttini
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 28(6)
Here we report the case of a 73-year-old Italian woman affected by genetically confirmed oculopharyngeal muscular dystrophy (OPMD) with a negative family history. As OPMD is usually transmitted as an autosomal-dominant meiotically stable trait, this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a118741ea0ff3dd5986b74e807f928e
https://pubmed.ncbi.nlm.nih.gov/18175083
https://pubmed.ncbi.nlm.nih.gov/18175083
Autor:
S Rota, M Colombo, D Massimini, F Lanzani, N. A. Curtò, Lucio Tremolizzo, L. Marzorati, Patrizia Perego, Giorgio Gelosa, Jacopo C. DiFrancesco, Carlo Ferrarese
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 80:698-699
Here we report a case of steroid responsive encephalopathy associated with autoimmune thyroiditis (SREAT), a rare neurological condition characterised by acute or subacute onset of cognitive impairment, psychiatric disorders, seizures, myoclonus and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82e3bb85c10e21ac76ef3b6d5d625ff9
https://doi.org/10.1136/jnnp.2008.152413
https://doi.org/10.1136/jnnp.2008.152413