Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/29696
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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.authorGUSMAO, Claudio M. de-
dc.contributor.authorKOK, Fernando-
dc.contributor.authorCASELLA, Erasmo Barbante-
dc.contributor.authorWAUGH, Jeff L.-
dc.date.accessioned2018-11-21T17:09:39Z-
dc.date.available2018-11-21T17:09:39Z-
dc.date.issued2016-
dc.identifier.citationNEUROLOGY-GENETICS, v.2, n.1, article ID UNSP e40, 2p, 2016-
dc.identifier.issn2376-7839-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/29696-
dc.description.sponsorshipMarshall Wolff Neurology Fellowship-
dc.description.sponsorshipSilverman Family Bachman-Strauss Fellowship for Movement-
dc.language.isoeng-
dc.publisherLIPPINCOTT WILLIAMS & WILKINS-
dc.relation.ispartofNeurology-Genetics-
dc.rightsopenAccess-
dc.titleBENIGN HEREDITARY CHOREA RELATED TO NKX2-1 WITH ATAXIA AND DYSTONIA-
dc.typearticle-
dc.rights.holderCopyright LIPPINCOTT WILLIAMS & WILKINS-
dc.identifier.doi10.1212/NXG.0000000000000040-
dc.identifier.pmid27066577
dc.subject.wosClinical Neurology-
dc.type.categoryeditorial material-
dc.type.versionpublishedVersion-
hcfmusp.author.externalGUSMAO, Claudio M. de:Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA-
hcfmusp.author.externalKOK, Fernando:Mendel Genom Anal, Sao Paulo, Brazil-
hcfmusp.author.externalWAUGH, Jeff L.:Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA; Boston Childrens Hosp, Dept Neurol, Boston, MA USA-
hcfmusp.description.articlenumberUNSP e40-
hcfmusp.description.issue1-
hcfmusp.description.volume2-
hcfmusp.origemWOS-
hcfmusp.origem.idWOS:000445307200002-
hcfmusp.origem.id2-s2.0-85046599399-
hcfmusp.publisher.cityPHILADELPHIA-
hcfmusp.publisher.countryUSA-
hcfmusp.relation.referenceArmstrong MJ, 2011, MOVEMENT DISORD, V26, P2296, DOI 10.1002/mds.23822-
hcfmusp.relation.referenceAsmus F, 2007, MOVEMENT DISORD, V22, P2104, DOI 10.1002/mds.21692-
hcfmusp.relation.referenceBreedveld GJ, 2002, HUM MOL GENET, V11, P971, DOI 10.1093/hmg/11.8.971-
hcfmusp.relation.referenceChen YZ, 2014, ANN NEUROL, V75, P542, DOI 10.1002/ana.24119-
hcfmusp.relation.referenceDoyle DA, 2004, J PEDIATR-US, V145, P190, DOI 10.1016/j.jpeds.2004.04.011-
hcfmusp.relation.referenceFerrara AM, 2008, THYROID, V18, P1005, DOI 10.1089/thy.2008.0085-
hcfmusp.relation.referenceGras D, 2012, J NEUROL NEUROSUR PS, V83, P956, DOI 10.1136/jnnp-2012-302505-
hcfmusp.relation.referencePeall KJ, 2014, DEV MED CHILD NEUROL, V56, P642, DOI 10.1111/dmcn.12323-
hcfmusp.relation.referenceVeneziano L, 2014, CEREBELLUM, V13, P588, DOI 10.1007/s12311-014-0570-7-
dc.description.indexPubMed-
hcfmusp.citation.scopus8-
hcfmusp.scopus.lastupdate2024-03-29-
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