Spastic Paraplegia Type 2 Latest Advances

Find the Latest Research About Spastic Paraplegia Type 2

Last Updated: 11/08/2026

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Found 2187 publications

Innovation and practices on case-based genetics teaching focusing on hereditary spastic paraplegia.

Innovation and practices on case-based genetics teaching focusing on hereditary spastic paraplegia.

Journal: Yi chuan = Hereditas
Published: October 18, 2026

Hereditary Spastic Paraplegia Type 11: A Comprehensive Case Report.

Hereditary Spastic Paraplegia Type 11: A Comprehensive Case Report.

Journal: Mymensingh medical journal : MMJ
Published: September 30, 2026

A rare case of hereditary spastic paraplegia with homozygous mutation in the ZFYVE26 gene.

A rare case of hereditary spastic paraplegia with homozygous mutation in the ZFYVE26 gene.

Journal: Ideggyogyaszati szemle
Published: September 28, 2026

Transcutaneous spinal cord stimulation for functional recovery in individuals with hereditary spastic paraplegia: Protocol for a pilot clinical trial.

Transcutaneous spinal cord stimulation for functional recovery in individuals with hereditary spastic paraplegia: Protocol for a pilot clinical trial.

Journal: PloS one
Published: September 07, 2026

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

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

From PLP1 Misfolding to Oligodendrocyte Degeneration: A Proteostasis-Centered Framework for Pelizaeus-Merzbacher Disease.

From PLP1 Misfolding to Oligodendrocyte Degeneration: A Proteostasis-Centered Framework for Pelizaeus-Merzbacher Disease.

Journal: Cells
Published: June 21, 2026

Expanding the adult spectrum of TUBB4A disease: a spasticity-tremor phenotype with network imaging correlates.

Expanding the adult spectrum of TUBB4A disease: a spasticity-tremor phenotype with network imaging correlates.

Journal: Neurogenetics
Published: May 20, 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

Genetic analysis and prenatal diagnosis for a Chinese pedigree affected with Spastic paraplegia type 56 due to variants of CYP2U1 gene

Genetic analysis and prenatal diagnosis for a Chinese pedigree affected with Spastic paraplegia type 56 due to variants of CYP2U1 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 06, 2026
Showing 1-12 of 2,187

Last Updated: 11/08/2026