Cortical Damage Associated With Cognitive and Motor Impairment in Hereditary Spastic Paraplegia: Evidence of a Novel SPAST Mutation

Neuroimaging in Hereditary Spastic Paraplegias: Current Use and Future Perspectives

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A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegia

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Resting state fMRI studies in SPG4-linked hereditary spastic paraplegia

(2018) Xinxin Liao et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

SPG11 mutations cause widespread white matter and basal ganglia abnormalities, but restricted cortical damage

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Genetic and phenotypic characterization of complex hereditary spastic paraplegia

(2016) Eleanna Kara et al.   BRAIN

Reversible Brain Abnormalities in People Without Signs of Mountain Sickness During High-Altitude Exposure

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Brain magnetic resonance imaging findings and auditory brainstem response in a child with spastic paraplegia 2 due to a PLP1 splice site mutation

(2015) Kazuo Kubota et al.   BRAIN & DEVELOPMENT

Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations

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Multimodal MRI-Based Study in Patients with SPG4 Mutations

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Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms

(2013) John K. Fink   ACTA NEUROPATHOLOGICA

Diffusion tensor imaging inSPG11- andSPG4-linked hereditary spastic paraplegia

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White and grey matter abnormalities in patients withSPG11mutations

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Functional MRI of the cortical sensorimotor system in patients with hereditary spastic paraplegia

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A Bayesian model of shape and appearance for subcortical brain segmentation

(2011) Brian Patenaude et al.   NEUROIMAGE

Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)

(2010) Katherine J. Dick et al.   HUMAN MUTATION

Specific pattern of early white-matter changes in pure hereditary spastic paraplegia

(2010) Thomas Duning et al.   MOVEMENT DISORDERS

SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum

(2009) C. Goizet et al.   NEUROLOGY

Dementia in SPG4 hereditary spastic paraplegia: Clinical, genetic, and neuropathologic evidence

(2009) S. Murphy et al.   NEUROLOGY

Proton magnetic resonance spectroscopy and cognition in patients with spastin mutations

(2008) A.K. Erichsen et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Characterization of seipin/BSCL2, a protein associated with spastic paraplegia 17

(2008) Daisuke Ito et al.   NEUROBIOLOGY OF DISEASE