Spastic Paraplegia Type 7 Latest Advances

Find the Latest Research About Spastic Paraplegia Type 7

Last Updated: 09/26/2026

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Found 2547 publications

Cognitive impairment as a manifestation of SPG7: case report.

Cognitive impairment as a manifestation of SPG7: case report.

Journal: Neurocase
Published: September 06, 2026

Vestibular rehabilitation in hereditary spastic paraplegia: a randomized pilot study.

Vestibular rehabilitation in hereditary spastic paraplegia: a randomized pilot study.

Journal: Arquivos de neuro-psiquiatria
Published: August 31, 2026

Walking aids to improve gait in hereditary spastic paraplegia - effects and predictive parameters in a short-term sensor-based evaluation.

Walking aids to improve gait in hereditary spastic paraplegia - effects and predictive parameters in a short-term sensor-based evaluation.

Journal: Neurodegenerative disease management
Published: August 06, 2026

Hereditary spastic paraplegia in three siblings with distinct genetic mutations.

Hereditary spastic paraplegia in three siblings with distinct genetic mutations.

Journal: The Journal of international medical research
Published: July 14, 2026

Instrumented Three-Dimensional Gait Analysis in an Adult With KIF1A-Associated Neurological Disorder: A Case Report.

Instrumented Three-Dimensional Gait Analysis in an Adult With KIF1A-Associated Neurological Disorder: A Case Report.

Journal: Cureus
Published: July 11, 2026

SPG4-Associated Hereditary Spastic Paraplegia and Dilated Cardiomyopathy: Coincidence or Clue?

SPG4-Associated Hereditary Spastic Paraplegia and Dilated Cardiomyopathy: Coincidence or Clue?

Journal: JACC. Case reports
Published: June 08, 2026

Beyond Binding Affinity: How a Conformation-Specific Salt Bridge Tunes KIF1A Mechanochemistry.

Beyond Binding Affinity: How a Conformation-Specific Salt Bridge Tunes KIF1A Mechanochemistry.

Journal: Cytoskeleton (Hoboken, N.J.)
Published: May 28, 2026

Clinical and genetic characterization of hereditary spastic paraplegia type 4 in a Taiwanese cohort.

Clinical and genetic characterization of hereditary spastic paraplegia type 4 in a Taiwanese cohort.

Journal: Parkinsonism & related disorders
Published: May 25, 2026

CRISPR/Cas9 loss-of-function screen in a neuronal model of AP-4 deficiency identifies ATG9A trafficking modulators.

CRISPR/Cas9 loss-of-function screen in a neuronal model of AP-4 deficiency identifies ATG9A trafficking modulators.

Journal: JCI insight
Published: May 19, 2026

CRISPR/Cas9 loss-of-function screen in a neuronal model of AP-4 deficiency identifies ATG9A trafficking modulators.

CRISPR/Cas9 loss-of-function screen in a neuronal model of AP-4 deficiency identifies ATG9A trafficking modulators.

Journal: JCI insight
Published: May 19, 2026

Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic models.

Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic models.

Journal: Journal of neurogenetics
Published: May 18, 2026

Late-Onset Rapidly Progressive Spastic Paraplegia with Extensive White Matter Abnormalities Associated with an MFN2 Variant.

Late-Onset Rapidly Progressive Spastic Paraplegia with Extensive White Matter Abnormalities Associated with an MFN2 Variant.

Journal: NeuroSci
Published: May 18, 2026
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Last Updated: 09/26/2026