Translation and validation into Brazilian Portuguese of the Spastic Paraplegia Rating Scale (SPRS)

Translation and validation into Brazilian Portuguese of the Spastic Paraplegia Rating Scale (SPRS)

Show other versions (1)

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 Paraplegia Rating Scale (SPRS) into Brazilian-Portuguese...

Full description

Saved in:

Bibliographic Details
Main Authors:	Katiane R. Servelhere, Ingrid Faber, Ana Carolina Coan, Marcondes França Junior
Format:	Article
Language:	English
Published:	Thieme Revinter Publicações 2016-06-01
Series:	Arquivos de Neuro-Psiquiatria
Subjects:	spastic paraplegia hereditary scales tranlating
Online Access:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2016000600489&tlng=en
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Translation and validation into Brazilian Portuguese of the Spastic Paraplegia Rating Scale (SPRS)
by: Katiane R. Servelhere, et al.
Published: (2016-06-01)

“Ears of the Lynx” Sign on Brain MRI in Siblings With Spastic Paraplegia: A Case Report
by: Qingqing Wang, et al.
Published: (2025-06-01)

Prevalence of oropharyngeal dysphagia in hereditary spastic paraplegias
by: Laís Alves Jacinto-Scudeiro, et al.
Published: (2020-01-01)

Hereditary spastic paraplegias
by: R. F. Kutlubaeva, et al.
Published: (2024-01-01)

Hereditary spastic paraplegia due to NIPA1 gene mutation: Case report
by: Dary Jizeth Parra-Párraga, et al.
Published: (2022-08-01)

Toxoplasmosis accelerates the progression of hereditary spastic paraplegia
by: James R. Alvin, et al.
Published: (2025-04-01)

Clinical features and management of hereditary spastic paraplegia
by: Ingrid Faber, et al.
Published: (2014-03-01)

Machado-Joseph disease versus hereditary spastic paraplegia: case report
by: Hélio A. Ghizoni Teive, et al.
Published: (2001-09-01)

Editorial: Translational research in hereditary spastic paraplegias: filling the diagnosis gap and therapeutic perspectives
by: Andrea Martinuzzi, et al.
Published: (2025-04-01)

Movement disorders in hereditary spastic paraplegias
by: Jose Luiz Pedroso, et al.
Published: (2023-11-01)

Hereditary spastic paraplegia associated with thin corpus callosum Paraplegia espástica hereditária associada a hipoplasia de corpo caloso
by: Hélio A. Ghizoni Teive, et al.
Published: (2001-09-01)

Spastic Paraplegia Type 78 Associated With ATP13A2 Gene Variants in Compound Heterozygosity
by: R. Bermejo Ramírez, et al.
Published: (2025-02-01)

The epidemiology of hereditary spastic paraplegia and associated common mental health outcomes in England and Northern Ireland
by: Harini Jeyakumar, et al.
Published: (2025-07-01)

A novel SPAST gene splicing variant (c.1617-2A>C) in a heterozygous carrier with hereditary spastic paraplegia
by: Elvira Sbragia, et al.
Published: (2024-06-01)

Intrathecal baclofen therapy in patients with spastic paraplegia: retrospective evaluation of pretreatment drugs, test dosage, dose increments and final therapy
by: Stephan Kurz, et al.
Published: (2025-01-01)

Outcome measures of instrumented gait analysis in hereditary spastic paraplegia: a systematic review
by: Veronika Koch, et al.
Published: (2025-06-01)

Case Report: Hereditary spastic paraplegia associated with monoallelic variant in the motor domain of KIF1A
by: Kathryn Sine, et al.
Published: (2025-05-01)

Entropy, Irreversibility, and Time-Series Deep Learning of Kinematic and Kinetic Data for Gait Classification in Children with Cerebral Palsy, Idiopathic Toe Walking, and Hereditary Spastic Paraplegia
by: Alfonso de Gorostegui, et al.
Published: (2025-07-01)

Genetic Evaluation of Patients with Clinically Suspected Hereditary Spastic Paraplegia with Seven Novel Variants
by: Taha Reşid Özdemir, et al.
Published: (2025-05-01)

Hereditary spastic paraplegia from 1880 to 2017: an historical review
by: Ingrid Faber, et al.

Diagnostic journey and genetic analysis of a novel homozygous CYP2U1 mutation causing autosomal recessive spastic paraplegia type 56 (SPG56) in a consanguineous family
by: Hong-ping Yu, et al.
Published: (2025-05-01)

Motor and functional evaluation of patients with spastic paraplegia, optic atrophy, and neuropathy (SPOAN) Avaliação motora e funcional de pacientes com paraplegia espástica, atrofia óptica e neuropatia (SPOAN)
by: Zodja Graciani, et al.
Published: (2010-02-01)

Hereditary spastic paraplegia: a clinical and epidemiological study of a Brazilian pediatric population
by: Roberta Paiva Magalhães Ortega, et al.

Ataxias in Brazil: 17 years of experience in an ataxia center
by: Breno Kazuo Massuyama, et al.
Published: (2024-08-01)

HPDL Variant Type Correlates With Clinical Disease Onset and Severity
by: Eun Hye Lee, et al.
Published: (2025-07-01)

Comparison Results of Google Translate and Microsoft Translator on the Novel Mughamarah Zahrah Ma'a Ash-Syajarah by Yacoub Al-Sharouni
by: Heniatus Zahroh, et al.
Published: (2023-09-01)

Pathway Analyses of Inherited Neuropathies Identify Putative Common Mechanisms of Axon Degeneration
by: Christopher R. Cashman, et al.
Published: (2025-07-01)

Paraplegia como manifestação inicial de medula presa: relato de caso Paraplegia as initial manifestation of tethered spinal cord: case report
by: ANA GUARDIOLA, et al.
Published: (1999-03-01)

Clinical and socio-demographic characteristics of persons with traumatic paraplegia living in São Paulo, Brazil Características clínicas e sócio demográficas de pessoas com paraplegia traumática na cidade de São Paulo
by: Leila Blanes, et al.
Published: (2009-06-01)

Simultaneous treatment of sacral and ischial pressure ulcers with a single flap: case presentation
by: Antonio Chiquetti Junior, et al.
Published: (2018-12-01)

A complicated intrathecal baclofen pump implantation in a child with spastic Diplegia: Should a genetic mimic of cerebral palsy be Considered?
by: Mohamed Ashraf, et al.
Published: (2025-09-01)

Botulinum toxin for hereditary spastic paraplegia: effects on motor and non-motor manifestations
by: Katiane R. Servelhere, et al.

One gene, many phenotypes: the role of KIF5A in neurodegenerative and neurodevelopmental diseases
by: Marta Cozzi, et al.
Published: (2025-06-01)

Aortic angiosarcoma leading to paraplegia: a case report
by: Jing Li, et al.
Published: (2025-04-01)

Decoding the genetic blueprints of neurological disorders: disease mechanisms and breakthrough gene therapies
by: Umar Saeed, et al.
Published: (2025-04-01)

Selective Dorsal Rhizotomy in Treatment of Spasticity in Patients with Cerebral Palsy
by: Olga A. Klochkova, et al.
Published: (2022-03-01)

Dorsal Spine Extradural Hemangioma with Neurodeficit, Mistaken Pott’s Paraplegia: A Case Report
by: Amit Awachat, et al.
Published: (2025-03-01)

Religion and Spirituality in the Life of Individuals with Paraplegia: Spiritual Journey from Trauma to Spiritual Development
by: Zeynep Şimşir, et al.
Published: (2017-02-01)

Botulinum toxin treatment of lower extremity spasticity
by: S. E. Khat’kova, et al.
Published: (2017-11-01)

Remote Monitoring for the Management of Spasticity: Challenges, Opportunities and Proposed Technological Solution
by: Kavit R. Amin, et al.
Published: (2025-01-01)