Hallervorden-Spatz Disease Latest Advances

Find the Latest Research About Hallervorden-Spatz Disease

Last Updated: 09/26/2026

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Found 1864 publications

When Powerhouses Fail and Rust Takes Over: Primary Mitochondrial and Lipid Metabolism Failure with Secondary Iron Accumulation and Lipid Peroxidation in Neurodegeneration with Brain Iron Accumulation.

When Powerhouses Fail and Rust Takes Over: Primary Mitochondrial and Lipid Metabolism Failure with Secondary Iron Accumulation and Lipid Peroxidation in Neurodegeneration with Brain Iron Accumulation.

Journal: ASN neuro
Published: August 18, 2026

Supplementation via DAF-16 and pnk-1 driven pantothenate-coenzyme A flux improves disease related stress resistance in C. elegans.

Supplementation via DAF-16 and pnk-1 driven pantothenate-coenzyme A flux improves disease related stress resistance in C. elegans.

Journal: bioRxiv : the preprint server for biology
Published: July 29, 2026

Psychological impact of being a caregiver to children with infantile neuroaxonal dystrophy.

Psychological impact of being a caregiver to children with infantile neuroaxonal dystrophy.

Journal: Arquivos de neuro-psiquiatria
Published: July 21, 2026

Clinically Suspected Atypical Pantothenate Kinase-Associated Neurodegeneration Without the Eye-of-the-Tiger Sign: A Case Report.

Clinically Suspected Atypical Pantothenate Kinase-Associated Neurodegeneration Without the Eye-of-the-Tiger Sign: A Case Report.

Journal: Cureus
Published: July 14, 2026

Functional Homology of WIPI4 and Atg18 Enables WDR45 Variant Interpretation for BPAN Diagnosis.

Functional Homology of WIPI4 and Atg18 Enables WDR45 Variant Interpretation for BPAN Diagnosis.

Journal: International journal of molecular sciences
Published: July 09, 2026

Rare hereditary and acquired diseases with parkinson's syndrome

Rare hereditary and acquired diseases with parkinson's syndrome

Journal: Fortschritte der Neurologie-Psychiatrie
Published: July 02, 2026

Clinical and biochemical footprints of inherited disorders of autophagy.

Clinical and biochemical footprints of inherited disorders of autophagy.

Journal: Molecular genetics and metabolism
Published: June 30, 2026

From Common Pathway to Divergent Diseases: Metabolic Aspects of Inborn Errors of CoA Biosynthesis.

From Common Pathway to Divergent Diseases: Metabolic Aspects of Inborn Errors of CoA Biosynthesis.

Journal: Journal of inherited metabolic disease
Published: June 25, 2026

Pathophysiology, biological models and new therapeutic approaches in β-Propeller Associated Neurodegeneration.

Pathophysiology, biological models and new therapeutic approaches in β-Propeller Associated Neurodegeneration.

Journal: International review of cell and molecular biology
Published: June 16, 2026

Therapeutic Advances in Major NBIA Disorders: Current Strategies and Translational Challenges.

Therapeutic Advances in Major NBIA Disorders: Current Strategies and Translational Challenges.

Journal: Neurology international
Published: June 11, 2026

Regression, Ataxia, and Nystagmus in a Toddler: Unraveling a Rare Neurodegenerative Disorder.

Regression, Ataxia, and Nystagmus in a Toddler: Unraveling a Rare Neurodegenerative Disorder.

Journal: Clinical case reports
Published: May 24, 2026

Beta-propeller protein-associated neurodegeneration (BPAN) associated with heper-CKemia-case report

Beta-propeller protein-associated neurodegeneration (BPAN) associated with heper-CKemia-case report

Journal: Rinsho shinkeigaku = Clinical neurology
Published: May 24, 2026
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Last Updated: 09/26/2026