Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis

Progress towards a biotypic biomarker profile for amyotrophic lateral sclerosis-frontotemporal spectrum disorders.

Brain : a journal of neurology·2026

TDP-43-Associated Neurodegenerative Disease Conceptualization and Integrated Staging: A Review.

JAMA neurology·2026

The EQ-5D-5L in amyotrophic lateral sclerosis: an international longitudinal exploration as part of ALS-CarE.

Amyotrophic lateral sclerosis & frontotemporal degeneration·2026

Strenuous physical activity is associated with a younger age of amyotrophic lateral sclerosis onset in two independent cohorts.

Brain communications·2026

Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.

medRxiv : the preprint server for health sciences·2026

Plasma exosomal HERV-K transcripts are increased in amyotrophic lateral sclerosis.

BMC neuroscience·2026

Clinical and genetic findings in Parkinson's disease in a Turkish cohort: a retrospective exome sequencing study.

Neurogenetics·2026

Further delineation of 2p13.2-p11.2 deletion syndrome by optical genome mapping.

Neurogenetics·2026

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

Neurogenetics·2026

Glutaric aciduria type 1 presenting with Parkinsonism with presynaptic dopaminergic dysfunction in an adult female: a case report.

Neurogenetics·2026

Expansion of the allelic and phenotypic spectrum of MED25-related developmental disorder: novel compound heterozygous variants with structural domain implications.

Neurogenetics·2026

Downbeat nystagmus without ataxia as an early manifestation of spinocerebellar ataxia, autosomal recessive type 10 (SCAR10): a case report.

Neurogenetics·2026

A new species of Heremites Gray, 1845 (Squamata, Scincidae) from the transboundary Hindu Kush foothills.

ZooKeys·2026

Exploratory imaging in SWEDD: Insights from dopaminergic PET, synaptic density PET, and volumetric MRI.

Parkinsonism & related disorders·2026

Viscous remanent magnetization authentication method for archaeological artifacts.

Proceedings of the National Academy of Sciences of the United States of America·2026

Solitary benign thyroid nodule in an elderly female cadaver.

Folia medica·2026

Hallux Valgus, Not Hallux Abductus Valgus: A Short Report on Historical and Anatomical Terminology.

Foot & ankle international·2026

The Dentition of the Aurignacian Mandible Les Rois 2, France: New Data and Taxonomic Reassessment.

American journal of biological anthropology·2026

Related Experiment Videos

Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis

Related Concept Videos

Progress towards a biotypic biomarker profile for amyotrophic lateral sclerosis-frontotemporal spectrum disorders.

TDP-43-Associated Neurodegenerative Disease Conceptualization and Integrated Staging: A Review.

The EQ-5D-5L in amyotrophic lateral sclerosis: an international longitudinal exploration as part of ALS-CarE.

Strenuous physical activity is associated with a younger age of amyotrophic lateral sclerosis onset in two independent cohorts.

Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.

Plasma exosomal HERV-K transcripts are increased in amyotrophic lateral sclerosis.

Clinical and genetic findings in Parkinson's disease in a Turkish cohort: a retrospective exome sequencing study.

Further delineation of 2p13.2-p11.2 deletion syndrome by optical genome mapping.

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

Glutaric aciduria type 1 presenting with Parkinsonism with presynaptic dopaminergic dysfunction in an adult female: a case report.

Expansion of the allelic and phenotypic spectrum of MED25-related developmental disorder: novel compound heterozygous variants with structural domain implications.

Downbeat nystagmus without ataxia as an early manifestation of spinocerebellar ataxia, autosomal recessive type 10 (SCAR10): a case report.

A new species of Heremites Gray, 1845 (Squamata, Scincidae) from the transboundary Hindu Kush foothills.

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Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis

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