Please use this identifier to cite or link to this item:
https://observatorio.fm.usp.br/handle/OPI/29696
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | - |
dc.contributor.author | GUSMAO, Claudio M. de | - |
dc.contributor.author | KOK, Fernando | - |
dc.contributor.author | CASELLA, Erasmo Barbante | - |
dc.contributor.author | WAUGH, Jeff L. | - |
dc.date.accessioned | 2018-11-21T17:09:39Z | - |
dc.date.available | 2018-11-21T17:09:39Z | - |
dc.date.issued | 2016 | - |
dc.identifier.citation | NEUROLOGY-GENETICS, v.2, n.1, article ID UNSP e40, 2p, 2016 | - |
dc.identifier.issn | 2376-7839 | - |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/29696 | - |
dc.description.sponsorship | Marshall Wolff Neurology Fellowship | - |
dc.description.sponsorship | Silverman Family Bachman-Strauss Fellowship for Movement | - |
dc.language.iso | eng | - |
dc.publisher | LIPPINCOTT WILLIAMS & WILKINS | - |
dc.relation.ispartof | Neurology-Genetics | - |
dc.rights | openAccess | - |
dc.title | BENIGN HEREDITARY CHOREA RELATED TO NKX2-1 WITH ATAXIA AND DYSTONIA | - |
dc.type | article | - |
dc.rights.holder | Copyright LIPPINCOTT WILLIAMS & WILKINS | - |
dc.identifier.doi | 10.1212/NXG.0000000000000040 | - |
dc.identifier.pmid | 27066577 | |
dc.subject.wos | Clinical Neurology | - |
dc.type.category | editorial material | - |
dc.type.version | publishedVersion | - |
hcfmusp.author.external | GUSMAO, Claudio M. de:Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA | - |
hcfmusp.author.external | KOK, Fernando:Mendel Genom Anal, Sao Paulo, Brazil | - |
hcfmusp.author.external | WAUGH, Jeff L.:Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA; Boston Childrens Hosp, Dept Neurol, Boston, MA USA | - |
hcfmusp.description.articlenumber | UNSP e40 | - |
hcfmusp.description.issue | 1 | - |
hcfmusp.description.volume | 2 | - |
hcfmusp.origem | WOS | - |
hcfmusp.origem.id | WOS:000445307200002 | - |
hcfmusp.origem.id | 2-s2.0-85046599399 | - |
hcfmusp.publisher.city | PHILADELPHIA | - |
hcfmusp.publisher.country | USA | - |
hcfmusp.relation.reference | Armstrong MJ, 2011, MOVEMENT DISORD, V26, P2296, DOI 10.1002/mds.23822 | - |
hcfmusp.relation.reference | Asmus F, 2007, MOVEMENT DISORD, V22, P2104, DOI 10.1002/mds.21692 | - |
hcfmusp.relation.reference | Breedveld GJ, 2002, HUM MOL GENET, V11, P971, DOI 10.1093/hmg/11.8.971 | - |
hcfmusp.relation.reference | Chen YZ, 2014, ANN NEUROL, V75, P542, DOI 10.1002/ana.24119 | - |
hcfmusp.relation.reference | Doyle DA, 2004, J PEDIATR-US, V145, P190, DOI 10.1016/j.jpeds.2004.04.011 | - |
hcfmusp.relation.reference | Ferrara AM, 2008, THYROID, V18, P1005, DOI 10.1089/thy.2008.0085 | - |
hcfmusp.relation.reference | Gras D, 2012, J NEUROL NEUROSUR PS, V83, P956, DOI 10.1136/jnnp-2012-302505 | - |
hcfmusp.relation.reference | Peall KJ, 2014, DEV MED CHILD NEUROL, V56, P642, DOI 10.1111/dmcn.12323 | - |
hcfmusp.relation.reference | Veneziano L, 2014, CEREBELLUM, V13, P588, DOI 10.1007/s12311-014-0570-7 | - |
dc.description.index | PubMed | - |
hcfmusp.citation.scopus | 8 | - |
hcfmusp.scopus.lastupdate | 2024-03-29 | - |
Appears in Collections: | Artigos e Materiais de Revistas Científicas - HC/ICr |
Files in This Item:
File | Description | Size | Format | |
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art_GUSMAO_BENIGN_HEREDITARY_CHOREA_RELATED_TO_NKX21_WITH_ATAXIA_2016.PDF | publishedVersion (English) | 191.33 kB | Adobe PDF | View/Open |
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