Spastic Paraplegia Type 7 Latest Advances

Correction to "Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia".

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: April 13, 2026

ER discontinuities are common in C. elegans neurons, revealing a genetically tractable model for ER network maintenance.

Journal: bioRxiv : the preprint server for biology

Published: April 10, 2026

Epidural spinal cord stimulation in hereditary spastic paraplegia: preliminary results

Journal: Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko

Published: April 03, 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

Fetal and Perinatal Brain MRI Findings in Adaptor Protein Complex 4-Associated Hereditary Spastic Paraplegia.

Journal: Annals of the Child Neurology Society

Published: March 12, 2026

Beyond motor impairment: investigating cognitive aspects of hereditary spastic paraplegia in a Greek case series.

Journal: Neurocase

Published: March 03, 2026

MK4 Repositioning for IAHSP: Overcoming In Vivo Data Gaps through In Silico Refinement and In Vitro Validation.

Journal: ACS chemical neuroscience

Published: February 09, 2026

Analysis of a three-generation Chinese pedigree affected with Hereditary spastic paraplegia type 3A due to variant of ATL1 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: February 09, 2026

Expanding the clinical and mutational spectrum of hereditary spastic paraplegia type 4 in a cohort of patients from central China.

Journal: Frontiers in genetics

Published: January 31, 2026

Selective Dorsal Rhizotomy in Children with Hereditary Spastic Paraplegia.

Journal: Pediatric neurosurgery

Published: January 29, 2026

The genetics of autosomal recessive ALS: a review of the common forms and their phenotypes.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: January 27, 2026

Repetitive Transcranial Magnetic Stimulation for Spasticity in Stroke and Other Neuromotor Disorders: A Systematic Review of Randomized Clinical Trials.

Journal: Journal of clinical medicine

Published: January 25, 2026

Spastic Paraplegia Type 7 Latest Advances

Find the Latest Research About Spastic Paraplegia Type 7

Correction to "Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia".

Correction to "Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia".

ER discontinuities are common in C. elegans neurons, revealing a genetically tractable model for ER network maintenance.

ER discontinuities are common in C. elegans neurons, revealing a genetically tractable model for ER network maintenance.

Epidural spinal cord stimulation in hereditary spastic paraplegia: preliminary results

Epidural spinal cord stimulation in hereditary spastic paraplegia: preliminary results

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.

Fetal and Perinatal Brain MRI Findings in Adaptor Protein Complex 4-Associated Hereditary Spastic Paraplegia.

Fetal and Perinatal Brain MRI Findings in Adaptor Protein Complex 4-Associated Hereditary Spastic Paraplegia.

Beyond motor impairment: investigating cognitive aspects of hereditary spastic paraplegia in a Greek case series.

Beyond motor impairment: investigating cognitive aspects of hereditary spastic paraplegia in a Greek case series.

MK4 Repositioning for IAHSP: Overcoming In Vivo Data Gaps through In Silico Refinement and In Vitro Validation.

MK4 Repositioning for IAHSP: Overcoming In Vivo Data Gaps through In Silico Refinement and In Vitro Validation.

Analysis of a three-generation Chinese pedigree affected with Hereditary spastic paraplegia type 3A due to variant of ATL1 gene

Analysis of a three-generation Chinese pedigree affected with Hereditary spastic paraplegia type 3A due to variant of ATL1 gene

Expanding the clinical and mutational spectrum of hereditary spastic paraplegia type 4 in a cohort of patients from central China.

Expanding the clinical and mutational spectrum of hereditary spastic paraplegia type 4 in a cohort of patients from central China.

Selective Dorsal Rhizotomy in Children with Hereditary Spastic Paraplegia.

Selective Dorsal Rhizotomy in Children with Hereditary Spastic Paraplegia.

The genetics of autosomal recessive ALS: a review of the common forms and their phenotypes.

The genetics of autosomal recessive ALS: a review of the common forms and their phenotypes.

Repetitive Transcranial Magnetic Stimulation for Spasticity in Stroke and Other Neuromotor Disorders: A Systematic Review of Randomized Clinical Trials.

Repetitive Transcranial Magnetic Stimulation for Spasticity in Stroke and Other Neuromotor Disorders: A Systematic Review of Randomized Clinical Trials.