Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Katiane R. Servelhere"'
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 74, Iss 6, Pp 489-494 (2016)
ABSTRACT Hereditary spastic paraplegias (HSP) are characterized by progressive lower limb weakness and spasticity. There are no validated instruments to quantify disease severity in Portuguese. Objective To translate and validate the Spastic Parapleg
Externí odkaz:
https://doaj.org/article/afa4217a249e4776804cac5d099a3839
Autor:
Ingrid Faber, Katiane R. Servelhere, Alberto R. M. Martinez, Anelyssa D?Abreu, Iscia Lopes-Cendes, Marcondes C. França Jr
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 72, Iss 3, Pp 219-226 (2014)
Hereditary spastic paraplegia (HSP) is a group of genetically-determined disorders characterized by progressive spasticity and weakness of lower limbs. An apparently sporadic case of adult-onset spastic paraplegia is a frequent clinical problem and a
Externí odkaz:
https://doaj.org/article/14dcb25bfb1147fb8c90ed19c795ca42
Publikováno v:
Brazilian Neurosurgery, Vol 30, Iss 02, Pp 69-75 (2011)
Introdução: A base do crânio é uma região que pode ser afetada por diferentes tipos de tumores. Os tumores dessa região podem ser benignos ou malignos e se localizarem na cavidade anterior, média ou posterior do crânio. Embora relativamente r
Externí odkaz:
https://doaj.org/article/beaac513b6ee4b23b1b0f98cb3a3cab0
Autor:
Katiane R. Servelhere, Ingrid Faber, Alberto Martinez, Renato Nickel, Adriana Moro, Francisco M. B. Germiniani, Mariana Moscovich, Tatiane R. Blume, Renato P. Munhoz, Hélio A. G. Teive, Marcondes C. França Jr
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 76, Iss 3, Pp 183-188
ABSTRACT Motor and non-motor manifestations are common and disabling features of hereditary spastic paraplegia (HSP). Botulinum toxin type A (Btx-A) is considered effective for spasticity and may improve gait in these patients. Little is known about
Externí odkaz:
https://doaj.org/article/e329a7dbe1444005b8578eef3600a00d
Autor:
Alberto R. M. Martinez, Anamarli Nucci, Katiane R. Servelhere, Ingrid Faber, Fabrício Diniz de Lima, Maria Fernanda Ribeiro Bittar, Luiza Piovesana, Marcondes C. França, Melina Pazian Martins, Benilton S. Carvalho, Tatiana Benaglia, Carlos Roberto Martins
Publikováno v:
Movement Disorders. 36:1654-1663
BACKGROUND Hereditary spastic paraplegia presents spasticity as the main clinical manifestation, reducing gait quality and producing incapacity. Management with botulinum toxin type A (BoNT-A) is not well elucidated. The objective of the current stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f06949ad26286b08195ebbf1957a1fed
https://doi.org/10.1002/mds.28523
https://doi.org/10.1002/mds.28523
Autor:
Thiago Junqueira Ribeiro de Rezende, Raphael F. Casseb, F. D. de Lima, Marcondes C. França, L.P. Ramalho, Katiane R. Servelhere
Publikováno v:
AJNR Am J Neuroradiol
BACKGROUND AND PURPOSE: Spinal cord damage is a hallmark of hereditary spastic paraplegias, but it is still not clear whether specific subtypes of the disease have distinctive patterns of spinal cord gray (GM) and white (WM) matter involvement. We co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b6e0b3dafdeb16e80108edfddf2616b
https://doi.org/10.3174/ajnr.a7017
https://doi.org/10.3174/ajnr.a7017
Autor:
Thiago Junqueira Ribeiro de Rezende, Raphael F. Casseb, Fernando Cendes, Fabrício Diniz de Lima, Renan Flávio de França Nunes, Orlando Graziani Povoas Barsottini, Marcondes C. França, José Luiz Pedroso, Katiane R. Servelhere, Mariana Rabelo de Brito
Publikováno v:
Movement disorders : official journal of the Movement Disorder SocietyReferences. 36(7)
Background Spinal cord has been considered the main target of damage in hereditary spastic paraplegias (HSPs), but mounting evidence indicates that the brain is also affected. Despite this, little is known about the brain signature of HSPs, in partic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d159f1aa20dc6ae0d6137fbd117357b9
https://pubmed.ncbi.nlm.nih.gov/33576112
https://pubmed.ncbi.nlm.nih.gov/33576112
Autor:
Katiane R. Servelhere, Anelyssa D'Abreu, Iscia Lopes-Cendes, Jonas Alex Morales Saute, Ingrid Faber, H.A.G. Teive, Mariana Moscovich, Marcondes C. França, Laura Bannach Jardim
Publikováno v:
European Journal of Neurology. 23:408-411
Background and purpose Non-motor manifestations are frequently overlooked in degenerative disorders and little is known about their frequency and clinical relevance in SPG4 hereditary spastic paraplegia (SPG4-HSP). Methods Thirty patients with SPG4-H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51dce84f325d3302e68fedc365c08a26
https://doi.org/10.1111/ene.12839
https://doi.org/10.1111/ene.12839
Autor:
Renato Nickel, Hélio A.G. Teive, Katiane R. Servelhere, Tatiane R. Blume, Adriana Moro, Marcondes C. França, Francisco M.B. Germiniani, Ingrid Faber, Alberto R. M. Martinez, Renato P. Munhoz, Mariana Moscovich
Publikováno v:
Arquivos de Neuro-Psiquiatria, Volume: 76, Issue: 3, Pages: 183-188, Published: MAR 2018
Arquivos de Neuro-Psiquiatria v.76 n.3 2018
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 76, Iss 3, Pp 183-188
Arquivos de Neuro-Psiquiatria v.76 n.3 2018
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 76, Iss 3, Pp 183-188
Motor and non-motor manifestations are common and disabling features of hereditary spastic paraplegia (HSP). Botulinum toxin type A (Btx-A) is considered effective for spasticity and may improve gait in these patients. Little is known about the effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a83e42ad4a5ef9b97e57b49d108d1a1
https://pubmed.ncbi.nlm.nih.gov/29809239
https://pubmed.ncbi.nlm.nih.gov/29809239
Autor:
Iscia Lopes-Cendes, Marcondes C. França, Anelyssa D’ Abreu, Ingrid Faber, Katiane R. Servelhere, Alberto R. M. Martinez
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 72, Iss 3, Pp 219-226 (2014)
Arquivos de Neuro-Psiquiatria v.72 n.3 2014
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 72, Issue: 3, Pages: 219-226, Published: MAR 2014
Arquivos de Neuro-Psiquiatria v.72 n.3 2014
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 72, Issue: 3, Pages: 219-226, Published: MAR 2014
Hereditary spastic paraplegia (HSP) is a group of genetically-determined disorders characterized by progressive spasticity and weakness of lower limbs. An apparently sporadic case of adult-onset spastic paraplegia is a frequent clinical problem and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df28215d25a044f1d5d8b53b8c8193f2
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2014000300219&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2014000300219&lng=en&tlng=en