Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/29487
Full metadata record
DC FieldValueLanguage
dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorMELO, U. S.-
dc.contributor.authorFREUA, F.-
dc.contributor.authorLYNCH, D. S.-
dc.contributor.authorRIPA, B. D.-
dc.contributor.authorTENORIO, R. B.-
dc.contributor.authorSAUTE, J. A. M.-
dc.contributor.authorLEITE, F. de Souza-
dc.contributor.authorKITAJIMA, J.-
dc.contributor.authorHOULDEN, H.-
dc.contributor.authorZATZ, M.-
dc.contributor.authorKOK, F.-
dc.date.accessioned2018-11-21T17:04:43Z-
dc.date.available2018-11-21T17:04:43Z-
dc.date.issued2018-
dc.identifier.citationCLINICAL GENETICS, v.94, n.5, p.482-483, 2018-
dc.identifier.issn0009-9163-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/29487-
dc.description.sponsorshipFundacao de Amparo a Pesquisa do Estado de Sao Paulo/Centro de Pesquisa, Inovacao e Difusao-
dc.description.sponsorshipNational Council of Technological and Scientific Development-
dc.language.isoeng-
dc.publisherWILEY-
dc.relation.ispartofClinical Genetics-
dc.rightsrestrictedAccess-
dc.subjectggg-
dc.subject.otherataxia-
dc.titleClinical aspects of hereditary spastic paraplegia 76 and novel CAPN1 mutations-
dc.typearticle-
dc.rights.holderCopyright WILEY-
dc.identifier.doi10.1111/cge.13428-
dc.identifier.pmid30198554-
dc.subject.wosGenetics & Heredity-
dc.type.categoryletter-
dc.type.versionpublishedVersion-
hcfmusp.author.externalMELO, U. S.:Univ Sao Paulo, Inst Biociencias, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, BR-05508090 Sao Paulo, SP, Brazil-
hcfmusp.author.externalLYNCH, D. S.:UCL Inst Neurol, Dept Mol Neurosci, London, England-
hcfmusp.author.externalTENORIO, R. B.:Hosp Clin Porto Alegre, Serv Genet Med & Neurol, Porto Alegre, RS, Brazil-
hcfmusp.author.externalSAUTE, J. A. M.:Hosp Clin Porto Alegre, Serv Genet Med & Neurol, Porto Alegre, RS, Brazil-
hcfmusp.author.externalLEITE, F. de Souza:Univ Sao Paulo, Inst Biociencias, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, BR-05508090 Sao Paulo, SP, Brazil-
hcfmusp.author.externalKITAJIMA, J.:Mendelics, Sao Paulo, Brazil-
hcfmusp.author.externalHOULDEN, H.:UCL Inst Neurol, Dept Mol Neurosci, London, England-
hcfmusp.author.externalZATZ, M.:Univ Sao Paulo, Inst Biociencias, Dept Genet & Evolutionary Biol, Human Genome & Stem Cell Res Ctr, BR-05508090 Sao Paulo, SP, Brazil-
hcfmusp.description.beginpage482-
hcfmusp.description.endpage483-
hcfmusp.description.issue5-
hcfmusp.description.volume94-
hcfmusp.origemWOS-
hcfmusp.origem.idWOS:000446554800013-
hcfmusp.origem.id2-s2.0-85053060511-
hcfmusp.publisher.cityHOBOKEN-
hcfmusp.publisher.countryUSA-
hcfmusp.relation.referenceGan-Or Z, 2016, AM J HUM GENET, V98, P1038, DOI 10.1016/j.ajhg.2016.04.002-
hcfmusp.relation.referenceKocoglu C, 2018, NEUROL-GENET, V4, DOI 10.1212/NXG.0000000000000218-
hcfmusp.relation.referenceShetty A, 2018, NEUROLOGY S15, V90-
hcfmusp.relation.referenceTadic V, 2017, J NEUROL, V264, P1008, DOI 10.1007/s00415-017-8464-5-
hcfmusp.relation.referenceTravaglini L, 2017, J NEUROL SCI, V378, P210, DOI 10.1016/j.jns.2017.05.014-
hcfmusp.relation.referenceWang YB, 2016, CELL REP, V16, P79, DOI 10.1016/j.celrep.2016.05.044-
dc.description.indexMEDLINE-
dc.identifier.eissn1399-0004-
hcfmusp.citation.scopus7-
hcfmusp.scopus.lastupdate2022-05-06-
Appears in Collections:

Artigos e Materiais de Revistas Científicas - FM/MNE
Departamento de Neurologia - FM/MNE

Artigos e Materiais de Revistas Científicas - HC/ICHC
Instituto Central - HC/ICHC

Artigos e Materiais de Revistas Científicas - LIM/15
LIM/15 - Laboratório de Investigação em Neurologia


Files in This Item:
File Description SizeFormat 
art_MELO_Clinical_aspects_of_hereditary_spastic_paraplegia_76_and_2018.PDF
  Restricted Access
publishedVersion (English)469.13 kBAdobe PDFView/Open Request a copy

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.