Transcranial sonography findings in spinocerebellar ataxia type 3 (Machado-Joseph disease): A cross-sectional study
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | PEDROSO, Jose Luiz | |
dc.contributor.author | BOR-SENG-SHU, Edson | |
dc.contributor.author | FELICIO, Andre Carvalho | |
dc.contributor.author | BRAGA-NETO, Pedro | |
dc.contributor.author | TEIXEIRA, Manoel Jacobsen | |
dc.contributor.author | BARSOTTINI, Orlando Graziani | |
dc.date.accessioned | 2017-11-27T16:29:02Z | |
dc.date.available | 2017-11-27T16:29:02Z | |
dc.date.issued | 2011 | |
dc.description.abstract | Few studies on transcranial brain sonography have been performed in hereditary and non-hereditary ataxias. The objective of the present study was to report transcranial brain sonography findings in a sample of clinically and molecularly proven Machado-Joseph disease patients and to compare these data against those of an age- and gender-matched control group. A cross-sectional study on transcranial brain sonography was conducted in 30 Machado-Joseph disease patients. Transcranial brain sonography was performed by an experienced sonographer blinded to the clinical, genetic, and neuroimaging data. The results were compared with those of a control group of 44 healthy subjects matched for age and gender. The sonographic findings were also correlated with clinical features and genetic data in Machado-Joseph disease group. A significantly higher frequency of substantia nigra and lenticular nucleus hyperechogenicity was found in the Machado-Joseph disease group compared to an age- and gender-matched healthy control group (p < 0.001). The substantia nigra echogenic area proved to be the best predictor for differentiating cases from controls. Third and lateral ventricles were significantly larger in the Machado-Joseph disease patients than in the control subjects. No significant correlations were found between transcranial brain sonography findings and Machado-Joseph disease demographic/clinical data. Transcranial brain sonography findings in Machado-Joseph disease patients differed significantly to those in age- and gender-matched controls. Substantia nigra hyperechogenicity occurred frequently in Machado-Joseph disease patients and was found to be the best predictor for differentiating cases from controls. Additionally, this data describes the occurrence of brain atrophy in Machado-Joseph disease group. | |
dc.description.index | MEDLINE | |
dc.identifier.citation | NEUROSCIENCE LETTERS, v.504, n.2, p.98-101, 2011 | |
dc.identifier.doi | 10.1016/j.neulet.2011.09.006 | |
dc.identifier.issn | 0304-3940 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/23152 | |
dc.language.iso | eng | |
dc.publisher | ELSEVIER IRELAND LTD | |
dc.relation.ispartof | Neuroscience Letters | |
dc.rights | restrictedAccess | |
dc.rights.holder | Copyright ELSEVIER IRELAND LTD | |
dc.subject | Spinocerebellar ataxia type 3 | |
dc.subject | Machado-Joseph disease | |
dc.subject | Transcranial sonography | |
dc.subject | Substantia nigra hyperechogenicity | |
dc.subject | Brain ultrasound | |
dc.subject.other | brain parenchyma sonography | |
dc.subject.other | real-time sonography | |
dc.subject.other | parkinsons-disease | |
dc.subject.other | movement-disorders | |
dc.subject.other | substantia-nigra | |
dc.subject.other | huntingtons-disease | |
dc.subject.other | ultrasound | |
dc.subject.other | echogenicity | |
dc.subject.other | pathogenesis | |
dc.subject.other | translation | |
dc.subject.wos | Neurosciences | |
dc.title | Transcranial sonography findings in spinocerebellar ataxia type 3 (Machado-Joseph disease): A cross-sectional study | |
dc.type | article | |
dc.type.category | original article | |
dc.type.version | publishedVersion | |
dspace.entity.type | Publication | |
hcfmusp.author.external | PEDROSO, Jose Luiz:Univ Fed Sao Paulo, Dept Neurol & Neurosurg, Sao Paulo, Brazil | |
hcfmusp.author.external | FELICIO, Andre Carvalho:Univ Fed Sao Paulo, Dept Neurol & Neurosurg, Sao Paulo, Brazil | |
hcfmusp.author.external | BRAGA-NETO, Pedro:Univ Fed Sao Paulo, Dept Neurol & Neurosurg, Sao Paulo, Brazil | |
hcfmusp.author.external | BARSOTTINI, Orlando Graziani:Univ Fed Sao Paulo, Dept Neurol & Neurosurg, Sao Paulo, Brazil | |
hcfmusp.citation.scopus | 19 | |
hcfmusp.contributor.author-fmusphc | EDSON BOR-SENG SHU | |
hcfmusp.contributor.author-fmusphc | MANOEL JACOBSEN TEIXEIRA | |
hcfmusp.description.beginpage | 98 | |
hcfmusp.description.endpage | 101 | |
hcfmusp.description.issue | 2 | |
hcfmusp.description.volume | 504 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 21939734 | |
hcfmusp.origem.scopus | 2-s2.0-80054005992 | |
hcfmusp.origem.wos | WOS:000297535000005 | |
hcfmusp.publisher.city | CLARE | |
hcfmusp.publisher.country | IRELAND | |
hcfmusp.relation.reference | Schols L, 2004, LANCET NEUROL, V3, P291, DOI 10.1016/S1474-4422(04)00737-9 | |
hcfmusp.relation.reference | Riess O, 2008, CEREBELLUM, V7, P125, DOI 10.1007/s12311-008-0013-4 | |
hcfmusp.relation.reference | Stiasny-Kolster K, 2007, MOVEMENT DISORD, V22, P2386, DOI 10.1002/mds.21740 | |
hcfmusp.relation.reference | Berg D, 2005, MOVEMENT DISORD, V20, P383, DOI 10.1002/mds.20311 | |
hcfmusp.relation.reference | Braga-Neto P, 2010, ARQ NEURO-PSIQUIAT, V68, P228, DOI 10.1590/S0004-282X2010000200014 | |
hcfmusp.relation.reference | Yen TC, 2000, J NUCL MED, V41, P994 | |
hcfmusp.relation.reference | Walter U, 2007, ARCH NEUROL-CHICAGO, V64, P1635, DOI 10.1001/archneur.64.11.1635 | |
hcfmusp.relation.reference | Gaenslen A, 2008, LANCET NEUROL, V7, P417, DOI 10.1016/S1474-4422(08)70067-X | |
hcfmusp.relation.reference | Berg D, 2008, LANCET NEUROL, V7, P1044, DOI 10.1016/S1474-4422(08)70239-4 | |
hcfmusp.relation.reference | BECKER G, 1995, NEUROLOGY, V45, P182 | |
hcfmusp.relation.reference | Kagi G, 2010, J NEUROL NEUROSUR PS, V81, P5, DOI 10.1136/jnnp.2008.157370 | |
hcfmusp.relation.reference | D'Abreu A, 2010, PARKINSONISM RELAT D, V16, P2, DOI 10.1016/j.parkreldis.2009.08.012 | |
hcfmusp.relation.reference | van Gaalen J, 2011, MOVEMENT DISORD, V26, P792, DOI 10.1002/mds.23584 | |
hcfmusp.relation.reference | Berg D, 2002, ARCH NEUROL-CHICAGO, V59, P999, DOI 10.1001/archneur.59.6.999 | |
hcfmusp.relation.reference | Walter U, 2007, ULTRASOUND MED BIOL, V33, P15, DOI 10.1016/j.ultrasmedbio.2006.07.021 | |
hcfmusp.relation.reference | Godau J, 2010, NEUROIMAG CLIN N AM, V20, P87, DOI 10.1016/j.nic.2009.08.003 | |
hcfmusp.relation.reference | Rub U, 2008, CURR OPIN NEUROL, V21, P111, DOI 10.1097/WCO.0b013e3282f7673d | |
hcfmusp.relation.reference | Masuko AH, 2008, ARQ NEURO-PSIQUIAT, V66, P832, DOI 10.1590/S0004-282X2008000600011 | |
hcfmusp.relation.reference | Barsottini OGP, 2011, CLIN NEUROL NEUROSUR, V113, P404, DOI 10.1016/j.clineuro.2010.11.015 | |
hcfmusp.relation.reference | Berg D, 2001, BIOL PSYCHIAT, V50, P463, DOI 10.1016/S0006-3223(01)01190-8 | |
hcfmusp.relation.reference | Bor-Seng-Shu E, 2010, ACTA NEUROCHIR, V152, P2085, DOI 10.1007/s00701-010-0736-0 | |
hcfmusp.relation.reference | Carbon M, 2006, J NEUROL SCI, V248, P72, DOI 10.1016/j.jns.2006.05.005 | |
hcfmusp.relation.reference | Felicio AC, 2010, J NEUROL SCI, V291, P64, DOI 10.1016/j.jns.2009.12.024 | |
hcfmusp.relation.reference | Gaenslen A, 2010, INT REV NEUROBIOL, V90, P179, DOI 10.1016/S0074-7742(10)90013-5 | |
hcfmusp.relation.reference | Jardim LB, 2001, ACTA NEUROL SCAND, V104, P224, DOI 10.1034/j.1600-0404.2001.00020.x | |
hcfmusp.relation.reference | Krogias C, 2010, INT REV NEUROBIOL, V90, P217, DOI 10.1016/S0074-7742(10)90016-0 | |
hcfmusp.relation.reference | Lu CS, 2004, PARKINSONISM RELAT D, V10, P369, DOI 10.1016/j.parkreldis.2004.03.009 | |
hcfmusp.relation.reference | Mijajlovic M, 2008, J NEUROL, V255, P1164, DOI [10.1007/s00415-008-0862-2, 10.1007/500415-008-0862-2] | |
hcfmusp.relation.reference | Postert T, 1999, J NEUROL NEUROSUR PS, V67, P457, DOI 10.1136/jnnp.67.4.457 | |
hcfmusp.relation.reference | Postert T., 2004, J NEURO ONCOL S, V68, P123 | |
hcfmusp.relation.reference | Ricciardi MC, 2010, J ULTRAS MED, V29, P1143 | |
hcfmusp.relation.reference | Roos RAC, 2010, ORPHANET J RARE DIS, V5, DOI 10.1186/1750-1172-5-40 | |
hcfmusp.relation.reference | Walter U, 2007, MOVEMENT DISORD, V22, P48, DOI 10.1002/mds.21197 | |
hcfmusp.relation.reference | Wolters A, 2005, KLIN NEUROPHYSIOL, V36, P9, DOI 10.1055/s-2004-834704 | |
hcfmusp.scopus.lastupdate | 2024-05-17 | |
relation.isAuthorOfPublication | d4fbc9d0-c5c7-45b8-a47a-2c2db2b7bc16 | |
relation.isAuthorOfPublication | b665cf91-624e-4b90-92bc-9df755eeeaaf | |
relation.isAuthorOfPublication.latestForDiscovery | d4fbc9d0-c5c7-45b8-a47a-2c2db2b7bc16 |
Arquivos
Pacote Original
1 - 1 de 1
Nenhuma Miniatura disponível
- Nome:
- art_PEDROSO_Transcranial_sonography_findings_in_spinocerebellar_ataxia_type_3_2011.PDF
- Tamanho:
- 335.26 KB
- Formato:
- Adobe Portable Document Format
- Descrição:
- publishedVersion (English)