标题
Management of Hereditary Spastic Paraplegia: A Systematic Review of the Literature
作者
关键词
-
出版物
Frontiers in Neurology
Volume 10, Issue -, Pages -
出版商
Frontiers Media SA
发表日期
2019-01-22
DOI
10.3389/fneur.2019.00003
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Hereditary ataxias and paraparesias
- (2018) Livia Parodi et al. CURRENT OPINION IN NEUROLOGY
- Severe 5,10-methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegia
- (2018) A. Perna et al. EUROPEAN JOURNAL OF NEUROLOGY
- Inhibition of Lysosome Membrane Recycling Causes Accumulation of Gangliosides that Contribute to Neurodegeneration
- (2018) Maxime Boutry et al. Cell Reports
- GSK3ß-dependent dysregulation of neurodevelopment in SPG11-patient induced pluripotent stem cell model
- (2016) Himanshu K. Mishra et al. ANNALS OF NEUROLOGY
- Selective dorsal rhizotomy for hereditary spastic paraparesis in children
- (2016) Julia Sharma et al. CHILDS NERVOUS SYSTEM
- Combined Treatment Fkt-Botulinum Toxin Type A (Btx-A) in Patients with Strumpell-Lorrain Disease
- (2016) Marvulli Riccardo et al. CURRENT PHARMACEUTICAL DESIGN
- The Effects of Dalfampridine on Hereditary Spastic Paraparesis
- (2016) Ugur Uygunoglu et al. EUROPEAN NEUROLOGY
- Conserved pharmacological rescue of hereditary spastic paraplegia-related phenotypes across model organisms
- (2016) Carl Julien et al. HUMAN MOLECULAR GENETICS
- Improved Gait Performance in a Patient With Hereditary Spastic Paraplegia After a Continuous Intrathecal Baclofen Test Infusion and Subsequent Pump Implantation: A Case Report
- (2015) Herre W. Heetla et al. ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION
- Treatment of SPG5 with cholesterol-lowering drugs
- (2015) Andrea Mignarri et al. JOURNAL OF NEUROLOGY
- Dalfampridine in hereditary spastic paraplegia: a prospective, open study
- (2015) Matthieu Béreau et al. JOURNAL OF NEUROLOGY
- Functional effects of botulinum toxin type-A treatment and subsequent stretching of spastic calf muscles: A study in patients with hereditary spastic paraplegia
- (2015) M Niet et al. JOURNAL OF REHABILITATION MEDICINE
- Dopa-responsive dystonia—clinical and genetic heterogeneity
- (2015) Subhashie Wijemanne et al. Nature Reviews Neurology
- Robot-Assisted Gait Training in a Patient With Hereditary Spastic Paraplegia
- (2015) Han Gil Seo et al. PM&R
- Intrathecal baclofen therapy for the symptomatic treatment of hereditary spastic paraplegia
- (2014) Konstantinos Margetis et al. CLINICAL NEUROLOGY AND NEUROSURGERY
- Hereditary spastic paraplegia: Clinical-genetic characteristics and evolving molecular mechanisms
- (2014) Temistocle Lo Giudice et al. EXPERIMENTAL NEUROLOGY
- The effect of hydrotherapy treatment on gait characteristics of hereditary spastic paraparesis patients
- (2014) Yanxin Zhang et al. GAIT & POSTURE
- Gene dosage-dependent rescue of HSP neurite defects in SPG4 patients' neurons
- (2014) S. Havlicek et al. HUMAN MOLECULAR GENETICS
- The Global Epidemiology of Hereditary Ataxia and Spastic Paraplegia: A Systematic Review of Prevalence Studies
- (2014) Luis Ruano et al. NEUROEPIDEMIOLOGY
- Severe Methylenetetrahydrofolate Reductase Deficiency
- (2014) Alexander Lossos et al. JAMA Neurology
- Long-term results of selective dorsal rhizotomy for hereditary spastic paraparesis
- (2013) Ma Kai et al. JOURNAL OF CLINICAL NEUROSCIENCE
- Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to l-DOPA treatment
- (2013) Conceição Bettencourt et al. JOURNAL OF NEUROLOGY
- Neurotransmitter abnormalities and response to supplementation in SPG11
- (2012) Adeline Vanderver et al. MOLECULAR GENETICS AND METABOLISM
- Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive Parkinsonism
- (2011) Arianna Guidubaldi et al. MOVEMENT DISORDERS
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now