Expanding MAPT p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy

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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorPARMERA, Jacy Bezerra
dc.contributor.authorCOUTINHO, Artur Martins
dc.contributor.authorGUIMARAES, Thiago Goncalves
dc.contributor.authorYAMAMOTO, Joyce Yuri Silvestre
dc.contributor.authorTAKADA, Leonel Tadao
dc.contributor.authorNITRINI, Ricardo
dc.contributor.authorBARBOSA, Egberto Reis
dc.contributor.authorBRUCKI, Sonia Maria Dozzi
dc.date.accessioned2023-06-21T14:11:34Z
dc.date.available2023-06-21T14:11:34Z
dc.date.issued2023
dc.description.indexPubMed
dc.description.indexWoS
dc.description.indexScopus
dc.description.sponsorshipSao Paulo Research Foundation (FAPESP) in Brazil [2017/10033-4]
dc.identifier.citationMOVEMENT DISORDERS CLINICAL PRACTICE, v.10, n.4, p.716-718, 2023
dc.identifier.doi10.1002/mdc3.13671
dc.identifier.issn2330-1619
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/53947
dc.language.isoeng
dc.publisherWILEYeng
dc.relation.ispartofMovement Disorders Clinical Practice
dc.rightsrestrictedAccesseng
dc.rights.holderCopyright WILEYeng
dc.subjectMAPT geneeng
dc.subjectcorticobasal degenerationeng
dc.subjectprogressive supranuclear palsyeng
dc.subjectcorticobasal syndromeeng
dc.subjectfrontotemporal lobar degenerationeng
dc.subject.otherdiagnosiseng
dc.subject.wosClinical Neurologyeng
dc.titleExpanding MAPT p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophyeng
dc.typearticleeng
dc.type.categorylettereng
dc.type.versionpublishedVersioneng
dspace.entity.typePublication
hcfmusp.citation.scopus1
hcfmusp.contributor.author-fmusphcJACY BEZERRA PARMERA
hcfmusp.contributor.author-fmusphcARTUR MARTINS NOVAES COUTINHO
hcfmusp.contributor.author-fmusphcTHIAGO GONCALVES GUIMARAES
hcfmusp.contributor.author-fmusphcJOYCE YURI SILVESTRE YAMAMOTO
hcfmusp.contributor.author-fmusphcLEONEL TADAO TAKADA
hcfmusp.contributor.author-fmusphcRICARDO NITRINI
hcfmusp.contributor.author-fmusphcEGBERTO REIS BARBOSA
hcfmusp.contributor.author-fmusphcSONIA MARIA DOZZI BRUCKI
hcfmusp.description.beginpage716
hcfmusp.description.endpage718
hcfmusp.description.issue4
hcfmusp.description.volume10
hcfmusp.origemWOS
hcfmusp.origem.pubmed37070053
hcfmusp.origem.scopus2-s2.0-85148341703
hcfmusp.origem.wosWOS:000936629400001
hcfmusp.publisher.cityHOBOKENeng
hcfmusp.publisher.countryUSAeng
hcfmusp.relation.referenceAhmed S, 2019, NEUROL-GENET, V5, DOI 10.1212/NXG.0000000000000347eng
hcfmusp.relation.referenceAnfossi M, 2011, ALZ DIS ASSOC DIS, V25, P96, DOI 10.1097/WAD.0b013e3181eff860eng
hcfmusp.relation.referenceArmstrong MJ, 2013, NEUROLOGY, V80, P496, DOI 10.1212/WNL.0b013e31827f0fd1eng
hcfmusp.relation.referenceBessi V, 2010, J NEUROL SCI, V296, P112, DOI 10.1016/j.jns.2010.06.007eng
hcfmusp.relation.referenceCrutch SJ, 2017, ALZHEIMERS DEMENT, V13, P870, DOI 10.1016/j.jalz.2017.01.014eng
hcfmusp.relation.referenceHoglinger GU, 2017, MOVEMENT DISORD, V32, P853, DOI 10.1002/mds.26987eng
hcfmusp.relation.referenceRossi G, 2014, NEUROBIOL AGING, V35, P408, DOI 10.1016/j.neurobiolaging.2013.08.004eng
hcfmusp.scopus.lastupdate2024-05-17
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Artigos e Materiais de Revistas Científicas - FM/MNE
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