Spastic Paraplegia Type 2 Latest Advances

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

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

Novel KIF5A variant in a patient with early-onset levodopa-responsive Parkinson's syndrome.

Journal: BMJ case reports

Published: February 02, 2026

Pearls & Oy-sters: Hereditary Spastic Paraplegia Type 15 Presenting as Juvenile Onset Levodopa-Responsive Parkinsonism.

Journal: Neurology

Published: January 08, 2026

Fampridine in Hereditary Spastic Paraplegia Type 4 With SPAST Variant c.683-2A>C: A Case Report.

Journal: The American journal of case reports

Published: January 07, 2026

Clinical, Radiological, and Genetic Profile of Patients with FA2H-Associated Neurodegeneration: Eight Cases from India and a Review of the Literature.

Journal: Tremor and other hyperkinetic movements (New York, N.Y.)

Published: December 31, 2025

Apoptosis and motor deficits in SPG76 hereditary spastic paraplegia: Calpain 2 inhibition as therapeutic strategy.

Journal: Pharmacological research

Published: December 18, 2025

DDHD2 possesses both lipase and transacylase capacities that remodel triglyceride acyl chains.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: November 20, 2025

Novel MTHFR variants manifesting with hereditary spastic paraplegia and recurrent pulmonary embolism: a case report and literature review of adult-onset severe MTHFR deficiency.

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

Published: November 13, 2025

Clinical characteristics and genetic study of a child with Spastic paraplegia 52 due to variant of AP4S1 gene and a literature review

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

Published: November 13, 2025

Spastic Paraplegia Type 2 Latest Advances

Find the Latest Research About Spastic Paraplegia Type 2

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.

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

Novel KIF5A variant in a patient with early-onset levodopa-responsive Parkinson's syndrome.

Novel KIF5A variant in a patient with early-onset levodopa-responsive Parkinson's syndrome.

Pearls & Oy-sters: Hereditary Spastic Paraplegia Type 15 Presenting as Juvenile Onset Levodopa-Responsive Parkinsonism.

Pearls & Oy-sters: Hereditary Spastic Paraplegia Type 15 Presenting as Juvenile Onset Levodopa-Responsive Parkinsonism.

Fampridine in Hereditary Spastic Paraplegia Type 4 With SPAST Variant c.683-2A>C: A Case Report.

Fampridine in Hereditary Spastic Paraplegia Type 4 With SPAST Variant c.683-2A>C: A Case Report.

Clinical, Radiological, and Genetic Profile of Patients with FA2H-Associated Neurodegeneration: Eight Cases from India and a Review of the Literature.

Clinical, Radiological, and Genetic Profile of Patients with FA2H-Associated Neurodegeneration: Eight Cases from India and a Review of the Literature.

Apoptosis and motor deficits in SPG76 hereditary spastic paraplegia: Calpain 2 inhibition as therapeutic strategy.

Apoptosis and motor deficits in SPG76 hereditary spastic paraplegia: Calpain 2 inhibition as therapeutic strategy.

DDHD2 possesses both lipase and transacylase capacities that remodel triglyceride acyl chains.

DDHD2 possesses both lipase and transacylase capacities that remodel triglyceride acyl chains.

Novel MTHFR variants manifesting with hereditary spastic paraplegia and recurrent pulmonary embolism: a case report and literature review of adult-onset severe MTHFR deficiency.

Novel MTHFR variants manifesting with hereditary spastic paraplegia and recurrent pulmonary embolism: a case report and literature review of adult-onset severe MTHFR deficiency.

Clinical characteristics and genetic study of a child with Spastic paraplegia 52 due to variant of AP4S1 gene and a literature review

Clinical characteristics and genetic study of a child with Spastic paraplegia 52 due to variant of AP4S1 gene and a literature review