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What researchers published on ALS (motor neurone disease)

2,064 papers, newest first.

Showing 20 of 2,064

  • Not labelled yetCommunity awareness and knowledge of amyotrophic lateral sclerosis: a cross-sectional study in the Northern Border Region of Saudi Arabia.PeerJ
  • Not labelled yetCorrespondence- The Unfinished Breath: Caregiver Perceptions of Terminal Events and Gaps in Amyotrophic Lateral Sclerosis Care in India - Methodological Considerations.Annals of Indian Academy of Neurology
  • ReviewBeyond neurones: cardiac involvement in motor neurone disease.Neuroscience
  • Not labelled yetAmyotrophic lateral sclerosis treated with the modified Bu-Shen-Jian-Pi decoction (mBSJP): Multicenter study.International journal of clinical pharmacology and therapeutics
  • PreprintTemporal RNA splicing dysregulation in a human multicellular model of C9orf72 ALS.bioRxiv : the preprint server for biology
  • PreprintCerebrospinal fluid α-synuclein seed amplification assay positivity identifies a prognostically distinct subgroup in amyotrophic lateral sclerosis.medRxiv : the preprint server for health sciences
  • Not labelled yetThe decline of respiratory function in amyotrophic lateral sclerosis patients and the role of non-invasive ventilation.Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace
  • Not labelled yetEfficacy and tolerability of D-β-hydroxybutyrate ester in patients with amyotrophic lateral sclerosis (KETO-ALS)-a randomised, placebo-controlled, double-blind study.EClinicalMedicine
  • Not labelled yetTDP-43-related cryptic splicing reflects pathological heterogeneity in amyotrophic lateral sclerosis.Acta neuropathologica communications
  • Not labelled yetA revised motor unit number estimate detects presymptomatic motor neuron loss in amyotrophic lateral sclerosis.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
  • Not labelled yetProtein Isoaspartate Repair in Amyotrophic Lateral Sclerosis: An Integrative Bioinformatic Analysis of the PCMT Gene Family.ACS chemical neuroscience
  • Not labelled yetPersonalizing nutritional care in amyotrophic lateral sclerosis (ALS): a multi-perspective qualitative focus group study of experiences and challenges.Amyotrophic lateral sclerosis & frontotemporal degeneration
  • Not labelled yetSubtype and stage inference of tract-level diffusion abnormalities in amyotrophic lateral sclerosis.Journal of neurology
  • ReviewCurrent findings, application, and diagnosis of magnetic resonance imaging in amyotrophic lateral sclerosis.Reviews in the neurosciences
  • Not labelled yetA validated antibody toolbox for ALS research.eLife
  • Not labelled yetLack of NRF2 expression alters the dynamics of stress granules promoting the aggregation of ALS disease-associated proteins.Redox biology
  • Not labelled yetUrinary Dysfunction in ALS Patients: Assessment With the Overactive Bladder Awareness Tool.Neurourology and urodynamics
  • Not labelled yetVoxel-based texture similarity networks reveal abnormal brain network topology linked to molecular signatures in amyotrophic lateral sclerosis.BMC medicine
  • Not labelled yet[Mitochondria in sporadic amyotrophic lateral sclerosis: actor or initiator?].Medecine sciences : M/S
  • Not labelled yetThe impact of diagnostic criteria on the detection of nocturnal hypoventilation in adult amyotrophic lateral sclerosis patients.Sleep medicine