Hereditary Spastic Paraparesis Latest Advances

Cognitive impairment as a manifestation of SPG7: case report.

Journal: Neurocase

Published: September 06, 2026

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

Journal: Cureus

Published: July 11, 2026

Expanding the ABCD1 mutation spectrum: a novel variant in X-linked adrenomyeloneuropathy.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: May 27, 2026

Macular Dystrophy Associated With Hereditary Spastic Paraplegia Type 11 (Kjellin Syndrome): A Multidisciplinary Case Report.

Journal: Cureus

Published: March 31, 2026

X-linked adrenoleukodystrophy as an etiological cause of progressive spastic paraplegia: A case report.

Journal: The Journal of international medical research

Published: March 23, 2026

Reorganization of functional brain network architecture in SPG4: Evidence from resting-state fMRI.

Journal: Parkinsonism & related disorders

Published: March 09, 2026

The m.14484T>C MT-ND6 Mutation Presenting with a Hereditary Spastic-Paraparesis Phenotype.

Journal: Movement disorders clinical practice

Published: February 19, 2026

Late-Onset X-linked Adrenoleukodystrophy: A Rare Cause of Progressive Spastic Paraparesis.

Journal: Cureus

Published: December 16, 2025

Essential genetic testing in movement disorders - results from a Delphi study.

Journal: Parkinsonism & related disorders

Published: November 24, 2025

MT-ATP6 variant as a cause of adult-onset hereditary spastic paraparesis: A case report and literature review.

Journal: Journal of neuromuscular diseases

Published: November 12, 2025

Clinical and Electrodiagnostic Characterization of Pediatric Triple A Syndrome: A Cohort of 17 Patients.

Journal: Muscle & nerve

Published: October 31, 2025

Finite Element-Based Biomechanical Evaluation of Patient-Specific Insoles for a Pediatric Patient with Hereditary Spastic Paraplegia Using the Taguchi Method.

Journal: Bioengineering (Basel, Switzerland)

Published: October 07, 2025

Hereditary Spastic Paraparesis Latest Advances

Find the Latest Research About Hereditary Spastic Paraparesis

Cognitive impairment as a manifestation of SPG7: case report.

Cognitive impairment as a manifestation of SPG7: case report.

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.

Expanding the ABCD1 mutation spectrum: a novel variant in X-linked adrenomyeloneuropathy.

Expanding the ABCD1 mutation spectrum: a novel variant in X-linked adrenomyeloneuropathy.

Macular Dystrophy Associated With Hereditary Spastic Paraplegia Type 11 (Kjellin Syndrome): A Multidisciplinary Case Report.

Macular Dystrophy Associated With Hereditary Spastic Paraplegia Type 11 (Kjellin Syndrome): A Multidisciplinary Case Report.

X-linked adrenoleukodystrophy as an etiological cause of progressive spastic paraplegia: A case report.

X-linked adrenoleukodystrophy as an etiological cause of progressive spastic paraplegia: A case report.

Reorganization of functional brain network architecture in SPG4: Evidence from resting-state fMRI.

Reorganization of functional brain network architecture in SPG4: Evidence from resting-state fMRI.

The m.14484T>C MT-ND6 Mutation Presenting with a Hereditary Spastic-Paraparesis Phenotype.

The m.14484T>C MT-ND6 Mutation Presenting with a Hereditary Spastic-Paraparesis Phenotype.

Late-Onset X-linked Adrenoleukodystrophy: A Rare Cause of Progressive Spastic Paraparesis.

Late-Onset X-linked Adrenoleukodystrophy: A Rare Cause of Progressive Spastic Paraparesis.

Essential genetic testing in movement disorders - results from a Delphi study.

Essential genetic testing in movement disorders - results from a Delphi study.

MT-ATP6 variant as a cause of adult-onset hereditary spastic paraparesis: A case report and literature review.

MT-ATP6 variant as a cause of adult-onset hereditary spastic paraparesis: A case report and literature review.

Clinical and Electrodiagnostic Characterization of Pediatric Triple A Syndrome: A Cohort of 17 Patients.

Clinical and Electrodiagnostic Characterization of Pediatric Triple A Syndrome: A Cohort of 17 Patients.

Finite Element-Based Biomechanical Evaluation of Patient-Specific Insoles for a Pediatric Patient with Hereditary Spastic Paraplegia Using the Taguchi Method.

Finite Element-Based Biomechanical Evaluation of Patient-Specific Insoles for a Pediatric Patient with Hereditary Spastic Paraplegia Using the Taguchi Method.