Výsledky vyhledávání - "sclerosi laterale amiotrofica"

Akademický článek

Clinical features and lifestyle of patients with amyotrophic lateral sclerosis in Campania: brief overview of an Italian database

Autor: Francesca Trojsi, Anna Sagnelli, Nicola Vanacore, Giovanni Piccirillo, Luca Daniele, Francesco Izzo, Anna Laiola, Alfonso Di Costanzo, Giovanni Savettieri, Maria Rosaria Monsurrò, Gioacchino Tedeschi

Publikováno v: Annali dell'Istituto Superiore di Sanità, Vol 48, Iss 3, Pp 287-291 (2012)

BACKGROUND: Physical activity and occupational exposures appeared to play a relevant role in pathogenesis of amyotrophic lateral sclerosis (ALS), a neurodegenerative disease of unknown origin. MATERIALS AND METHODS: We aimed to make an overview of th

Externí odkaz: https://doaj.org/article/00a82054b55f495b81a84363eac4b0d2

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Akademický článek

Possible involvement of overexposure to environmental selenium in the etiology of amyotrophic lateral sclerosis: a short review

Autor: Marco Vinceti, Francesca Bonvicini, Margherita Bergomi, Carlotta Malagoli

Publikováno v: Annali dell'Istituto Superiore di Sanità, Vol 46, Iss 3, Pp 279-283 (2010)

Excess exposure to the metalloid selenium (Se), a trace element with both toxicological and nutritional properties, has been implicated in the etiology of a human motor neuron disease of unknown origin and extremely severe prognosis, sporadic amyotro

Externí odkaz: https://doaj.org/article/bd2fd395451f4bc5b73d40246713a978

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Akademický článek

Exposure to pesticides and risk of amyotrophic lateral sclerosis: a population-based case-control study

Autor: Francesca Bonvicini, Norina Marcello, Jessica Mandrioli, Vladimiro Pietrini, Marco Vinceti

Publikováno v: Annali dell'Istituto Superiore di Sanità, Vol 46, Iss 3, Pp 284-287 (2010)

A few epidemiologic studies have suggested an association of agricultural work and pesticides exposure with a severe degenerative disease of the motor neurons, amyotrophic lateral sclerosis (ALS), though conflicting results have also been provided. W

Externí odkaz: https://doaj.org/article/35c41fd953ef4ad0bf7e45f3ca55fe93

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Integrative multi-omic analysis identifies new drivers and pathways in molecularly distinct subtypes of ALS

Autor: Sebastiano Cavallaro, Maria Guarnaccia, Francesca Luisa Conforti, Antonio Gianmaria Spampinato, Velia D'Agata, Giovanna Morello, Eleonora Aronica, Salvatore Salomone

Publikováno v: Scientific Reports, Vol 9, Iss 1, Pp 1-18 (2019)
Scientific reports, 9(1):9968. Nature Publishing Group
Scientific reports (Nature Publishing Group) 9 (2019). doi:10.1038/s41598-019-46355-w
info:cnr-pdr/source/autori:Giovanna Morello; Maria Guarnaccia; Antonio Gianmaria Spampinato; Salvatore Salomone; Velia D'Agata; Francesca Luisa Conforti; Eleonora Aronica; Sebastiano Cavallaro/titolo:Integrative multi-omic analysis identifies new drivers and pathways in molecularly distinct subtypes of ALS/doi:10.1038%2Fs41598-019-46355-w/rivista:Scientific reports (Nature Publishing Group)/anno:2019/pagina_da:/pagina_a:/intervallo_pagine:/volume:9
Scientific Reports

Amyotrophic lateral sclerosis (ALS) is an incurable and fatal neurodegenerative disease. Increasing the chances of success for future clinical strategies requires more in-depth knowledge of the molecular basis underlying disease heterogeneity. We rec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e4028ec4c5db6ea1caaf8ad6e072365
https://doaj.org/article/2c47732928ac47b9af5ea01a9f35d762

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Abstractive skills of mnd patients neuropsychological assessment by means of an eye tracking system approach

Autor: Susanna, Nanni, Enrica, Armienti, Azzollini, Valentina, Paolo, Bongioanni, Carboncini, MARIA CHIARA

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3728::1d66c7ac49a91a0cd877c0d8d1ecb527
http://hdl.handle.net/11568/940158

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Studio della localizzazione nucleo-citosol degli RNA messaggeri in modelli cellulari di Sclerosi Laterale Amiotrofica associata a mutazione nel gene C9ORF72

Autor: Francesca Di Vozzo

Amyotrophic lateral sclerosis (ALS) is the most common adult-onset motor neuron disease. It is characterized by the neurodegeneration of motor neurons in the brain and spinal cord. The result for patients is the inability to coordinate the voluntary

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::e3ef2c604fffa532710764b5979d18f0
https://publications.cnr.it/doc/405924

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Psychological and neuropsychological advances in Motor neuron diseases: Amyotrophic lateral sclerosis and X-linked spinal-bulbar muscular atrophy

Autor: Grasso, Irene

Motor neuron disease (MND) is a heterogeneous family of neurodegenerative diseases, rare, characterized by an early involvement of motor neurons and can be hereditary or sporadic, including Amyotrophic lateral sclerosis (ALS) and X-linked spinal-bulb

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::680f26dcd037efb73e5dff5c566f8b4e
http://hdl.handle.net/11577/3424187

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Endotelina-1: un nuovo target farmacologico per la Sclerosi Laterale Amiotrofica?

Autor: D'Antoni S.1, Ranno E.1, M. Spatuzza M.1, Catania M.V.1, 2

Publikováno v: 56° Congresso Nazionale SNO, Acicastello, Catania, 18-21/05/2016
info:cnr-pdr/source/autori:D'Antoni S.1, Ranno E.1, M. Spatuzza M.1, Catania M.V.1,2/congresso_nome:56° Congresso Nazionale SNO/congresso_luogo:Acicastello, Catania/congresso_data:18-21%2F05%2F2016/anno:2016/pagina_da:/pagina_a:/intervallo_pagine

La Sclerosi Laterale Amiotrofica (SLA) è una malattia neurodegenerativa che colpisce i motoneuroni (MN). Evidenze sperimentali indicano che fattori rilasciati dalla glia reattiva possono contribuire alla morte dei MN. Il nostro gruppo ha recentement

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::b7a7f4dc4464b7b0268e6b477c97a5d8
http://www.cnr.it/prodotto/i/356157

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Alterazioni nel meccanismo di esporto nucleare degli mRNA nella patogenesi della Sclerosi Laterale Amiotrofica associata a mutazioni nel gene C9orf72

Autor: Gioa Cappelletti

Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disease that affects both lower motor neurons i n the brainstem and spinal cord, and the upper motor neurons i n the motor cortex. Loss of these neurons leads to muscle atrophy a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::d955f1bbca0e21ed133867fbbc08c936
https://publications.cnr.it/doc/405623

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Classificazione molecolare di pazienti affetti da sclerosi laterale amiotrofica attraverso l'analisi ed integrazione di dati multi-omici

Autor: Antonio Gianmaria Spampinato, Giovanna Morello, Sebastiano Cavallaro

Publikováno v: 56° Congresso Nazionale SNO, Catania, 18-21/05/2016
info:cnr-pdr/source/autori:Antonio Gianmaria Spampinato, Giovanna Morello, Sebastiano Cavallaro/congresso_nome:56° Congresso Nazionale SNO/congresso_luogo:Catania/congresso_data:18-21%2F05%2F2016/anno:2016/pagina_da:/pagina_a:/intervallo_pagine

Il recente perfezionamento delle tecnologie di caratterizzazione molecolare ha permesso di monitorare i diversi livelli del flusso di informazione biologica. Tali tecnologie, dette -omiche, hanno consentito lo sviluppo di una tassonomia molecolare de

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::165109e7a4fbebb94552456303363a81
http://www.cnr.it/prodotto/i/356225

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