Benvenuto sul sito dell’ A.I.N.P. e N.C.

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Combining ischaemic core volume with age and expected imaging-to-reperfusion time will improve assessment of prognosis and might inform endovascular thrombectomy treatment decisions.\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}}s:32:\"http://purl.org/dc/elements/1.1/\";a:5:{s:5:\"title\";a:1:{i:0;a:5:{s:4:\"data\";s:207:\"Penumbral imaging and functional outcome in patients with anterior circulation ischaemic stroke treated with endovascular thrombectomy versus medical therapy: a meta-analysis of individual patient-level data\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:7:\"creator\";a:1:{i:0;a:5:{s:4:\"data\";s:893:\"Bruce C V Campbell, Charles B L M Majoie, Gregory W Albers, Bijoy K Menon, Nawaf Yassi, Gagan Sharma, Wim H van Zwam, Robert J van Oostenbrugge, Andrew M Demchuk, Francis Guillemin, Philip White, Antoni Dávalos, Aad van der Lugt, Kenneth S Butcher, Aboubaker Cherifi, Henk A Marquering, Geoffrey Cloud, Juan M Macho Fernández, Jeremy Madigan, Catherine Oppenheim, Geoffrey A Donnan, Yvo B W E M Roos, Jai Shankar, Hester Lingsma, Alain Bonafé, Hélène Raoult, María Hernández-Pérez, Aditya Bharatha, Reza Jahan, Olav Jansen, Sébastien Richard, Elad I Levy, Olvert A Berkhemer, Marc Soudant, Lucia Aja, Stephen M Davis, Timo Krings, Marie Tisserand, Luis San Román, Alejandro Tomasello, Debbie Beumer, Scott Brown, David S Liebeskind, Serge Bracard, Keith W Muir, Diederik W J Dippel, Mayank Goyal, Jeffrey L Saver, Tudor G Jovin, Michael D Hill, Peter J Mitchell, HERMES collaborators\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:10:\"identifier\";a:1:{i:0;a:5:{s:4:\"data\";s:29:\"10.1016/S1474-4422(18)30314-4\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:6:\"source\";a:1:{i:0;a:5:{s:4:\"data\";s:27:\"The Lancet Neurology (2018)\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:4:\"date\";a:1:{i:0;a:5:{s:4:\"data\";s:20:\"2018-11-06T23:30:02Z\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}}s:46:\"http://prismstandard.org/namespaces/1.2/basic/\";a:3:{s:15:\"publicationName\";a:1:{i:0;a:5:{s:4:\"data\";s:20:\"The Lancet Neurology\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:15:\"publicationDate\";a:1:{i:0;a:5:{s:4:\"data\";s:20:\"2018-11-06T23:30:02Z\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:7:\"section\";a:1:{i:0;a:5:{s:4:\"data\";s:8:\"Articles\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}}}}i:6;a:6:{s:4:\"data\";s:81:\"\n \n \n \n \n \n \n \n \n \n \n \n \";s:7:\"attribs\";a:1:{s:43:\"http://www.w3.org/1999/02/22-rdf-syntax-ns#\";a:1:{s:5:\"about\";s:91:\"https://www.thelancet.com/journals/laneur/article/PIIS1474-4422(18)30404-6/fulltext?rss=yes\";}}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";s:5:\"child\";a:3:{s:24:\"http://purl.org/rss/1.0/\";a:3:{s:5:\"title\";a:1:{i:0;a:5:{s:4:\"data\";s:152:\"[Articles] Global, regional, and national burden of motor neuron diseases 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:4:\"link\";a:1:{i:0;a:5:{s:4:\"data\";s:91:\"https://www.thelancet.com/journals/laneur/article/PIIS1474-4422(18)30404-6/fulltext?rss=yes\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:11:\"description\";a:1:{i:0;a:5:{s:4:\"data\";s:591:\"Motor neuron diseases have low prevalence and incidence, but cause severe disability with a high fatality rate. Incidence of motor neuron diseases has geographical heterogeneity, which is not explained by any risk factors quantified in GBD, suggesting other unmeasured risk factors might have a role. Between 1990 and 2016, the burden of motor neuron diseases has increased substantially. The estimates presented here, as well as future estimates based on data from a greater number of countries, will be important in the planning of services for people with motor neuron diseases worldwide.\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}}s:32:\"http://purl.org/dc/elements/1.1/\";a:5:{s:5:\"title\";a:1:{i:0;a:5:{s:4:\"data\";s:141:\"Global, regional, and national burden of motor neuron diseases 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:7:\"creator\";a:1:{i:0;a:5:{s:4:\"data\";s:43:\"GBD 2016 Motor Neuron Disease Collaborators\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:10:\"identifier\";a:1:{i:0;a:5:{s:4:\"data\";s:29:\"10.1016/S1474-4422(18)30404-6\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:6:\"source\";a:1:{i:0;a:5:{s:4:\"data\";s:27:\"The Lancet Neurology (2018)\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:4:\"date\";a:1:{i:0;a:5:{s:4:\"data\";s:20:\"2018-11-05T23:30:02Z\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}}s:46:\"http://prismstandard.org/namespaces/1.2/basic/\";a:3:{s:15:\"publicationName\";a:1:{i:0;a:5:{s:4:\"data\";s:20:\"The Lancet Neurology\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:15:\"publicationDate\";a:1:{i:0;a:5:{s:4:\"data\";s:20:\"2018-11-05T23:30:02Z\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:7:\"section\";a:1:{i:0;a:5:{s:4:\"data\";s:8:\"Articles\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}}}}i:7;a:6:{s:4:\"data\";s:81:\"\n \n \n \n \n \n \n \n \n \n \n \n \";s:7:\"attribs\";a:1:{s:43:\"http://www.w3.org/1999/02/22-rdf-syntax-ns#\";a:1:{s:5:\"about\";s:91:\"https://www.thelancet.com/journals/laneur/article/PIIS1474-4422(18)30398-3/fulltext?rss=yes\";}}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";s:5:\"child\";a:3:{s:24:\"http://purl.org/rss/1.0/\";a:3:{s:5:\"title\";a:1:{i:0;a:5:{s:4:\"data\";s:63:\"[Comment] Global burden of motor neuron diseases: mind the gaps\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:4:\"link\";a:1:{i:0;a:5:{s:4:\"data\";s:91:\"https://www.thelancet.com/journals/laneur/article/PIIS1474-4422(18)30398-3/fulltext?rss=yes\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:11:\"description\";a:1:{i:0;a:5:{s:4:\"data\";s:595:\"According to the International Classification of Diseases ninth (ICD-9) and tenth (ICD-10) editions, the category of motor neuron diseases comprises amyotrophic lateral sclerosis, progressive muscular atrophy, primary lateral sclerosis, progressive bulbar palsy, spinal muscular atrophy, and hereditary spastic paraparesis. 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Imaging features and safety and efficacy of endovascular stroke treatment: a meta-analysis of individual patient-level data. Lancet Neurol 2018; 17: 895–904—The author listed as Sourour Nader-Antoine should have been Nader-Antoine Sourour. In figure 1, the x axis has been corrected. In figure 2A, the graphical representation of the point estimates for ASPECTS 7 and 8 have been corrected. In figure 3A, the graphical representation of the point estimates for clot burden score 5–7 and hyperdense sign yes have been corrected.\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}}s:32:\"http://purl.org/dc/elements/1.1/\";a:4:{s:5:\"title\";a:1:{i:0;a:5:{s:4:\"data\";s:47:\"Correction to Lancet Neurol 2018; 17: 895–904\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:10:\"identifier\";a:1:{i:0;a:5:{s:4:\"data\";s:29:\"10.1016/S1474-4422(18)30364-8\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:6:\"source\";a:1:{i:0;a:5:{s:4:\"data\";s:27:\"The Lancet Neurology (2018)\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:4:\"date\";a:1:{i:0;a:5:{s:4:\"data\";s:20:\"2018-10-26T22:30:02Z\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}}s:46:\"http://prismstandard.org/namespaces/1.2/basic/\";a:3:{s:15:\"publicationName\";a:1:{i:0;a:5:{s:4:\"data\";s:20:\"The Lancet Neurology\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:15:\"publicationDate\";a:1:{i:0;a:5:{s:4:\"data\";s:20:\"2018-10-26T22:30:02Z\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:7:\"section\";a:1:{i:0;a:5:{s:4:\"data\";s:11:\"Corrections\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}}}}i:9;a:6:{s:4:\"data\";s:81:\"\n \n \n \n \n \n \n \n \n \n \n \n \";s:7:\"attribs\";a:1:{s:43:\"http://www.w3.org/1999/02/22-rdf-syntax-ns#\";a:1:{s:5:\"about\";s:91:\"https://www.thelancet.com/journals/laneur/article/PIIS1474-4422(18)30336-3/fulltext?rss=yes\";}}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";s:5:\"child\";a:3:{s:24:\"http://purl.org/rss/1.0/\";a:3:{s:5:\"title\";a:1:{i:0;a:5:{s:4:\"data\";s:81:\"[Review] Stroke–heart syndrome: clinical presentation and underlying mechanisms\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:4:\"link\";a:1:{i:0;a:5:{s:4:\"data\";s:91:\"https://www.thelancet.com/journals/laneur/article/PIIS1474-4422(18)30336-3/fulltext?rss=yes\";s:7:\"attribs\";a:0:{}s:8:\"xml_base\";s:0:\"\";s:17:\"xml_base_explicit\";b:0;s:8:\"xml_lang\";s:0:\"\";}}s:11:\"description\";a:1:{i:0;a:5:{s:4:\"data\";s:670:\"Cardiac complications are a frequent medical problem during the first few days after an ischaemic stroke, and patients present with a broad range of symptoms including myocardial injury, cardiac dysfunction, and arrhythmia, with varying overlap between these three conditions. 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Risultati immagini per feed  Neuroscience News – Most Recent Links

 

Risultati immagini per feed The Lancet


Cos’è l’AINPeNC

La Neuropatologia cominciò a svilupparsi in Italia all’inizio del secolo XX, coltivata soprattutto negli ospedali psichiatrici dove venivano eseguite autopsie ai pazienti ivi deceduti. Il principale oggetto di studio furono ovviamente le demenze. Più tardi la disciplina allargò i suoi interessi fino a coprire tutto l’ambito della patologia neurologica ed incrementò il suo sviluppo negli Istituti Universitari di Neurologia, includendo nel suo corpo anche interessi di neurobiologia correlati ai funzionamenti nervosi. Oltre al nome del premio Nobel Camillo Golgi, il quale non era soltanto esperto sull’apparato a lui intitolato, ma anche un noto patologo interessato alle correlazioni anatomo-cliniche, altri insigni neurologi e psichiatri acquistarono notorietà.

Dopo l’ultima guerra la Neuropatologia accrebbe la sua importanza e fu introdotta come insegnamento nelle Scuole di Specializzazione di Neurologia e Neurochirurgia e negli ultimi decenni anche nel corso di laurea in Medicina e Chirurgia. Collocata nell’area neurologica, vide incrementare il suo sviluppo parallelamente allo sviluppo dei Dipartimenti di Neurochirurgia. Sia nella pratica che nella ricerca si estese a coprire principalmente, oltre alle demenze, il campo dei tumori cerebrali, della patologia muscolare e nervosa periferica.
Nel 1966 nacque l’Associazione Italiana di Neuropatologia, come Sezione della Società Italiana di Neurologia e poi come Associazione coordinata, con un numero di membri che raggiunse le duecento unità. Nei primi anni del 2000, l’insegnamento della disciplina fu spostato dal Ministero della Pubblica Istruzione dall’area neurologica a quella anatomo-patologica, ma la disciplina continuò ad essere coltivata nei Dipartimenti Neurologici. Negli ultimi anni la Neuropatologia Italiana subì le stesse modificazioni cui andò incontro la Neuropatologia mondiale, legate soprattutto allo sviluppo della genetica e biologia molecolare e più sofisticate disciplini affini. La sua delimitazione dalle Neuroscienze divenne molto meno netta, mentre i suoi legami con la Clinica Neurologica, la Neurochirurgia e la Neuro-immagine divennero più stretti proprio per lo sviluppo di tecniche molecolari raffinate.

283_History of Neuropathology

54° Congresso Associazione Italiana Neuropatologia e Neurobiologia Clinica
44° Congresso Associazione Italiana Ricerca Invecchiamento Cerebrale
17 – 19 Maggio 2018 MILANO
Istituto di Ricerche Farmacologiche Mario Negri – Via La Masa, 19

ISTRUZIONI PER LA CORRETTA STESURA DEL CONTRIBUTO SCIENTIFICO.
Gli abstract dovranno essere sottomessi e presentati esclusivamente in lingua inglese
con un accurato controllo della grammatica e pronti per la pubblicazione. Gli autori
saranno ritenuti responsabili del contenuto dei contributi. Si prega di non sottomettere
più copie dello stesso abstract. Alla fine del file specificare la preferenza tra
comunicazione orale o poster.
Inviare gli abstract come file allegato di WORD entro il 3 aprile 2018 per posta
elettronica al seguente indirizzo:
info@studiocongresslab.it
Al ricevimento dell’abstract verrà inviato un messaggio di ricezione avvenuta.
ORGANIZZAZIONE DEL CONTRIBUTO
• L’abstract dovrà avere una lunghezza massima non superiore a 400 parole non
comprensivo di autori, affiliazioni titolo ecc..
• Strutturare il contributo secondo le seguenti sezioni:
1. Obiettivi
2. Materiali
3. Metodo
4. Risultati
5. Discussione
6. Conclusioni
• Affermazioni come “risultati saranno discussi”, “dati saranno presentati” non
saranno accettati.
• Non si possono inserire illustrazioni o tabelle

Dr. Giorgio Giaccone                             Dr. Gianluigi Forloni

Programma definitivo       Annuncio congresso AINP AIRIC 2018