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Increased Stroke Risk in Patients with Parkinson's Disease with LRRK2 Mutations
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| Published in: | Movement disorders 2022-01, Vol.37 (1), p.225-227 |
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| Main Authors: | , , , , , , , , , , |
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| cites | cdi_FETCH-LOGICAL-c4283-74f54f6124b4c541c15fb90992399ed205ec7292d5aa76195f86e7c5387a0fdd3 |
| container_end_page | 227 |
| container_issue | 1 |
| container_start_page | 225 |
| container_title | Movement disorders |
| container_volume | 37 |
| creator | Macías‐García, Daniel Periñán, María Teresa Muñoz‐Delgado, Laura Jesús, Silvia Jimenez‐Jaraba, María Valle Buiza‐Rueda, Dolores Bonilla‐Toribio, Marta Adarmes‐Gómez, Astrid Carrillo, Fátima Gómez‐Garre, Pilar Mir, Pablo |
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| doi_str_mv | 10.1002/mds.28863 |
| format | article |
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Periñán, María Teresa ; Muñoz‐Delgado, Laura ; Jesús, Silvia ; Jimenez‐Jaraba, María Valle ; Buiza‐Rueda, Dolores ; Bonilla‐Toribio, Marta ; Adarmes‐Gómez, Astrid ; Carrillo, Fátima ; Gómez‐Garre, Pilar ; Mir, Pablo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4283-74f54f6124b4c541c15fb90992399ed205ec7292d5aa76195f86e7c5387a0fdd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Humans</topic><topic>Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - genetics</topic><topic>LRRK2 protein</topic><topic>Movement disorders</topic><topic>Mutation - genetics</topic><topic>Neurodegenerative diseases</topic><topic>Parkinson Disease - complications</topic><topic>Parkinson Disease - genetics</topic><topic>Parkinson's disease</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Macías‐García, Daniel</creatorcontrib><creatorcontrib>Periñán, María Teresa</creatorcontrib><creatorcontrib>Muñoz‐Delgado, Laura</creatorcontrib><creatorcontrib>Jesús, Silvia</creatorcontrib><creatorcontrib>Jimenez‐Jaraba, María Valle</creatorcontrib><creatorcontrib>Buiza‐Rueda, Dolores</creatorcontrib><creatorcontrib>Bonilla‐Toribio, Marta</creatorcontrib><creatorcontrib>Adarmes‐Gómez, Astrid</creatorcontrib><creatorcontrib>Carrillo, Fátima</creatorcontrib><creatorcontrib>Gómez‐Garre, Pilar</creatorcontrib><creatorcontrib>Mir, Pablo</creatorcontrib><collection>Wiley-Blackwell Open Access Titles</collection><collection>Wiley Online Library Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Movement disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Macías‐García, Daniel</au><au>Periñán, María Teresa</au><au>Muñoz‐Delgado, Laura</au><au>Jesús, Silvia</au><au>Jimenez‐Jaraba, María Valle</au><au>Buiza‐Rueda, Dolores</au><au>Bonilla‐Toribio, Marta</au><au>Adarmes‐Gómez, Astrid</au><au>Carrillo, Fátima</au><au>Gómez‐Garre, Pilar</au><au>Mir, Pablo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased Stroke Risk in Patients with Parkinson's Disease with LRRK2 Mutations</atitle><jtitle>Movement disorders</jtitle><addtitle>Mov Disord</addtitle><date>2022-01</date><risdate>2022</risdate><volume>37</volume><issue>1</issue><spage>225</spage><epage>227</epage><pages>225-227</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><notes>Nothing to report.</notes><notes>Relevant conflicts of interest/financial disclosures</notes><notes>Funding agencies</notes><notes>This work was supported by the Spanish Ministry of Science and Innovation (RTC2019‐007150‐1); the Carlos III Health Institute–The European Regional Development Fund (ISCIII‐FEDER; PI14/01823, PI16/01575, PI18/01898, PI19/01576); the Ministry of Economy, Innovation, Science and Employment of the Government of Andalucía (CVI‐02526, CTS‐7685); the Ministry of Health and Social Welfare of the Government of Andalucía (PI‐0471‐2013, PE‐0210‐2018, PI‐0459‐2018, PE‐0186‐2019); and Fundación Alicia Koplowitz. Pilar Gómez‐Garre was supported by the “Nicolás Monardes” program (C‐0048‐2017; from the Andalusian Regional Ministry of Health). Silvia Jesús was supported by the “Acción B Clínicos Investigadores” program from the Ministry of Health and Families of the Government of Andalucía (B‐0007‐2019). Daniel Macías‐García was supported by the “Río Hortega” program (CM18/00142) from the Carlos III Health Institute (ISCIII‐FEDER). María Teresa Periñán was supported by the Spanish Ministry of Education, Culture and Sports (FPU16/05061).</notes><notes>SourceType-Other Sources-1</notes><notes>ObjectType-Article-2</notes><notes>content type line 63</notes><notes>ObjectType-Correspondence-1</notes><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>34859503</pmid><doi>10.1002/mds.28863</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-8818-1824</orcidid><oa>free_for_read</oa></addata></record> |
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| ispartof | Movement disorders, 2022-01, Vol.37 (1), p.225-227 |
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| language | eng |
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| source | Wiley:Jisc Collections:Wiley Jisc Read and Publish Open Access Agreement 2020-2023 (reading list) |
| subjects | Humans Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - genetics LRRK2 protein Movement disorders Mutation - genetics Neurodegenerative diseases Parkinson Disease - complications Parkinson Disease - genetics Parkinson's disease |
| title | Increased Stroke Risk in Patients with Parkinson's Disease with LRRK2 Mutations |
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