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。Cerebello-Cortical Alterations Linked to Cognitive and Social Problems in Patients With Spastic Paraplegia Type 7: A Preliminary Study
Michela Lupo et al.
FRONTIERS IN NEUROLOGY (2020)
Multimodal longitudinal study of structural brain involvement in amyotrophic lateral sclerosis
Hannelore K. van der Burgh et al.
NEUROLOGY (2020)
Multimodal MRI Longitudinal Assessment of White and Gray Matter in Different SPG Types of Hereditary Spastic Paraparesis
Domenico Montanaro et al.
FRONTIERS IN NEUROSCIENCE (2020)
Prevalence and phenotype of the c.1529C>T SPG7 variant in adult-onset cerebellar ataxia in Italy
C. Mancini et al.
EUROPEAN JOURNAL OF NEUROLOGY (2019)
Are Cognitive Changes in Hereditary Spastic Paraplegias Restricted to Complicated Forms?
Lais Alves Jacinto-Scudeiro et al.
FRONTIERS IN NEUROLOGY (2019)
Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches
Samuel Shribman et al.
LANCET NEUROLOGY (2019)
Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism
Beatriz De la Casa-Fages et al.
MOVEMENT DISORDERS (2019)
Neuroimaging in Hereditary Spastic Paraplegias: Current Use and Future Perspectives
Felipe Franco da Graca et al.
FRONTIERS IN NEUROLOGY (2019)
Structural signature of SCA3: From presymptomatic to late disease stages
Thiago Junqueira Ribeiro Rezende et al.
ANNALS OF NEUROLOGY (2018)
Converging cellular themes for the hereditary spastic paraplegias
Craig Blackstone
CURRENT OPINION IN NEUROBIOLOGY (2018)
Hereditary ataxias and paraparesias: clinical and genetic update
Livia Parodi et al.
CURRENT OPINION IN NEUROLOGY (2018)
SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage
Ingrid Faber et al.
NEUROIMAGE-CLINICAL (2018)
Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex
Livia Parodi et al.
BRAIN (2018)
SPG11-related parkinsonism: Clinical profile, molecular imaging and l-dopa response
Ingrid Faber et al.
MOVEMENT DISORDERS (2018)
Defects in ER-endosome contacts impact lysosome function in hereditary spastic paraplegia
Rachel Allison et al.
JOURNAL OF CELL BIOLOGY (2017)
Hereditary spastic paraplegia: More than an upper motor neuron disease
L. Parodi et al.
REVUE NEUROLOGIQUE (2017)
Hereditary spastic paraplegia from 1880 to 2017: an historical review
Ingrid Faber et al.
ARQUIVOS DE NEURO-PSIQUIATRIA (2017)
Translation and validation into Brazilian Portuguese of the Spastic Paraplegia Rating Scale (SPRS)
Katiane R. Servelhere et al.
ARQUIVOS DE NEURO-PSIQUIATRIA (2016)
Regional expression of the MAPT gene is associated with loss of hubs in brain networks and cognitive impairment in Parkinson disease and progressive supranuclear palsy
Timothy Rittman et al.
NEUROBIOLOGY OF AGING (2016)
Abnormal Paraplegin Expression in Swollen Neurites, τ- and α-Synuclein Pathology in a Case of Hereditary Spastic Paraplegia SPG7 with an Ala510Val Mutation
Dietmar R. Thal et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2015)
Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations
Tobias Lindig et al.
JOURNAL OF NEUROLOGY (2015)
Canonical genetic signatures of the adult human brain
Michael Hawrylycz et al.
NATURE NEUROSCIENCE (2015)
Hereditary Spastic Paraplegia: Beyond Clinical Phenotypes toward a Unified Pattern of Central Nervous System Damage
Federica Agosta et al.
RADIOLOGY (2015)
Multimodal MRI-Based Study in Patients with SPG4 Mutations
Thiago J. R. Rezende et al.
PLOS ONE (2015)
Brain White Matter Involvement in Hereditary Spastic Paraplegias: Analysis with Multiple Diffusion Tensor Indices
G. Aghakhanyan et al.
AMERICAN JOURNAL OF NEURORADIOLOGY (2014)
Genotype-phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort
Koen L. I. van Gassen et al.
BRAIN (2012)
White and grey matter abnormalities in patients with SPG11 mutations
Marcondes C. Franca et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2012)
An anatomically comprehensive atlas of the adult human brain transcriptome
Michael J. Hawrylycz et al.
NATURE (2012)
Structural and metabolic damage in brains of patients with SPG11-related spastic paraplegia as detected by quantitative MRI
Maria Laura Stromillo et al.
JOURNAL OF NEUROLOGY (2011)
Specific Pattern of Early White-Matter Changes in Pure Hereditary Spastic Paraplegia
Thomas Duning et al.
MOVEMENT DISORDERS (2010)
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia
Paul N. Valdmanis et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Diffusion tensor imaging detects and differentiates axon and myelin degeneration in mouse optic nerve after retinal ischemia
SK Song et al.
NEUROIMAGE (2003)
分享论文
