• 'A lightbulb moment': carers' experiences of behavioural symptoms in motor neurone disease before and after MiNDToolkit
• A novel <em>TBK1</em> loss-of-function variant associated with ALS and parkinsonism phenotypes
• A Peculiar Tau Accumulation Pattern Identified Via 18F-Florzolotau PET Imaging in a Patient With Frontotemporal Dementia Caused by a Mutation in the MAPT Gene
• Abnormal Splicing Events due to Loss of Nuclear Function of TDP-43: Pathophysiology and Perspectives
• Accuracy of clinical diagnosis of behavioural variant frontotemporal dementia: a protocol for a systematic review and meta-analysis
• Alzheimer's disease linked Aβ42 exerts product feedback inhibition on γ-secretase impairing downstream cell signaling
• Association of cortical morphology, white matter hyperintensity, and glymphatic function in frontotemporal dementia variants
• Association of Open-Angle Glaucoma with Dementia in California Medicare Beneficiaries
• Automatic Classification of Conclusions from Multi-Tracer Reports of PET Brain Imaging in Cognitive Impairment
• Basal parasympathetic deficits in C9orf72 hexanucleotide repeat expansion carriers relate to smaller frontoinsula and thalamus volume and lower empathy
• Behavioral variant of frontotemporal dementia in carriers of biallelic TREM2 variants: cases study
• Benzoxazole-derivatives enhance progranulin expression and reverse the aberrant lysosomal proteome caused by GRN haploinsufficiency
• Beta-to-Theta Entropy Ratio of EEG in Aging, Frontotemporal Dementia, and Alzheimer's Dementia
• Blood inflammation relates to neuroinflammation and survival in frontotemporal lobar degeneration
• Brain clocks capture diversity and disparity in aging and dementia
• Caregiving in the face of empathy loss in Frontotemporal Dementia: an integrative review
• Case report: Assessing criminal responsibility and recidivism risk in the behavioral variant of frontotemporal dementia
• Causal relationship between imaging-derived phenotypes and neurodegenerative diseases: a Mendelian randomization study
• Cellular and pathological functions of tau
• Cerebellum in Alzheimer's disease and other neurodegenerative diseases: an emerging research frontier
• Changes of brain functional network in Alzheimer's disease and frontotemporal dementia: a graph-theoretic analysis
• Characteristics of Patients With Amyotrophic Lateral Sclerosis Followed by a Home Palliative Care Team
• CHCHD2 P14L, found in amyotrophic lateral sclerosis, exhibits cytoplasmic mislocalization and alters Ca²⁺ homeostasis
• Clinical and morphologic characterization of Pick's dementia: case report and review of the literature
• Clinical application of whole genome sequencing in young onset dementia: challenges and opportunities
• Clinical Manifestations
• Clinical recognition of frontotemporal dementia with right anterior temporal predominance: A multicenter retrospective cohort study
• Cognitive and behavioural profile of patients with Amyotrophic Lateral Sclerosis spectrum in the Indian Context
• Cognitive and morphometric features of mild cognitive impairment reversion in early patients with Parkinson's disease
• Cognitive reserve as a modulator of cognitive decline and of behavioral symptoms in patients with amyotrophic lateral sclerosis
• Comprehensive Analysis of Dementia Types and Risk Factors: A Study From a Tertiary Care Center in India
• Contrastive Self-supervised Learning for Neurodegenerative Disorder Classification
• Conventional magnetic resonance imaging key features for distinguishing pathologically confirmed corticobasal degeneration from its mimics: a retrospective analysis of the J-VAC study
• Cytoarchitectonic gradients of laminar degeneration in behavioural variant frontotemporal dementia
• De Novo Rational Design of Peptide-Based Protein-Protein Inhibitors (Pep-PPIs) Approach by Mapping the Interaction Motifs of the PP Interface and Physicochemical Filtration: A Case on p25-Cdk5-Mediated Neurodegenerative Diseases
• Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing
• Dementia Can Unleash Creativity: Frontotemporal dementia can release the creative potential of the brain's visual areas
• Depletion of TDP-43 exacerbates tauopathy-dependent brain atrophy by sensitizing vulnerable neurons to caspase 3-mediated endoproteolysis of tau in a mouse model of Multiple Etiology Dementia
• Developing Topics
• Development of thresholds and a visualization tool for use of a blood test in routine clinical dementia practice
• Diagnostic Performance of ASL-MRI and FDG-PET in Frontotemporal Dementia: A Systematic Review and Meta-Analysis
• Diverse Phenotypic Presentation of the Welander Distal Myopathy Founder Mutation, With Myopathy and Amyotrophic Lateral Sclerosis in the Same Family
• Editorial: The role of glial cells in neurodegeneration
• Educational disparities in brain health and dementia across Latin America and the United States
• Fatty links between multisystem proteinopathy and small VCP-interacting protein
• FDG-PET in the diagnosis of primary progressive aphasia: a systematic review
• Focal epilepsy followed by rapidly progressive frontotemporal dementia: a rare manifestation of VCP mutation
• Genetic evidence for causal association between migraine and dementia: a mendelian randomization study
• Genetic Landscape of Amyotrophic Lateral Sclerosis in Czech Patients
• Genotype-phenotype correlation of <em>SQSTM1</em> variants in patients with amyotrophic lateral sclerosis
• Identification of retinal oligomeric, citrullinated, and other tau isoforms in early and advanced AD and relations to disease status
• Impaired glymphatic system in genetic frontotemporal dementia: a GENFI study
• Improved Accuracy of the Addenbrooke's Cognitive Examination-Revised in the Diagnosis of Mild Cognitive Impairment, Mild Dementia Due to Alzheimer's Disease and Behavioral Variant Frontotemporal Dementia Using Mokken Scale Analysis
• Incidence and Prevalence of Early-Onset Dementia in Finland
• Inflammasome-Inhibiting Nanoligomers Are Neuroprotective against Space-Induced Pathology in Healthy and Diseased Three-Dimensional Human Motor and Prefrontal Cortex Brain Organoids
• Inflammatory plasma profile in genetic symptomatic and presymptomatic Frontotemporal Dementia - A GENFI study
• Itching Frequency and Neuroanatomic Correlates in Frontotemporal Lobar Degeneration
• Long Non-Coding RNA Profile in Genetic Symptomatic and Presymptomatic Frontotemporal Dementia: A GENFI Study
• Loss of TDP-43 induces synaptic dysfunction that is rescued by <em>UNC13A</em> splice-switching ASOs
• Lysosomal TBK1 responds to amino acid availability to relieve Rab7-dependent mTORC1 inhibition
• Machine and deep learning algorithms for classifying different types of dementia: A literature review
• MAPT mutations associated with familial tauopathies lead to formation of conformationally distinct oligomers that have cross-seeding ability
• Mechanisms of autophagy-lysosome dysfunction in neurodegenerative diseases
• miR-92a-3p and miR-320a are Upregulated in Plasma Neuron-Derived Extracellular Vesicles of Patients with Frontotemporal Dementia
• Multiparameter cortical surface morphology in former amateur contact sport athletes
• Mutational Landscape of Alzheimer's Disease and Frontotemporal Dementia: Regional Variances in Northern, Central, and Southern Italy
• Neuropsychological and electrophysiological measurements for diagnosis and prediction of dementia: a review on Machine Learning approach
• Organ donation after euthanasia in a patient living with dementia: a landmark case report
• Overexpression of Toxic Poly(Glycine-Alanine) Aggregates in Primary Neuronal Cultures Induces Time-Dependent Autophagic and Synaptic Alterations but Subtle Activity Impairments
• Perceptual and semantic deficits in face recognition in semantic dementia
• Perivascular spaces, plasma GFAP, and speeded executive function in neurodegenerative diseases
• Plasma extracellular vesicle biomarkers for frontotemporal dementia and related disorders
• Plasma Phosphorylated Tau 217 and Aβ42/40 to Predict Early Brain Aβ Accumulation in People Without Cognitive Impairment
• Poly-GR Impairs PRMT1-Mediated Arginine Methylation of Disease-Linked RNA-Binding Proteins by Acting as a Substrate Sink
• Poly-GR repeats associated with ALS/FTD gene <em>C9ORF72</em> impair translation elongation and induce a ribotoxic stress response in neurons
• Psychiatric Manifestations of Neurological Diseases: A Narrative Review
• Research trends and hotspots for frontotemporal dementia from 2000 to 2022: a bibliometric analysis
• Reversal of cognitive deficits in FUS^R521G amyotrophic lateral sclerosis mice by arimoclomol and a class I histone deacetylase inhibitor independent of heat shock protein induction
• Reversible Frontotemporal Dementia in Spinal Cerebrospinal Fluid-Venous Fistula
• Safety, tolerability, and pharmacokinetics of antisense oligonucleotide BIIB078 in adults with C9orf72-associated amyotrophic lateral sclerosis: a phase 1, randomised, double blinded, placebo-controlled, multiple ascending dose study
• Serum Beta-Secretase 1 Activity Is a Potential Marker for the Differential Diagnosis between Alzheimer's Disease and Frontotemporal Dementia: A Pilot Study
• Socioemotional Dysfunction From Temporal Lobe Involvement in Frontotemporal Dementia: A Preliminary Report
• Sodium-glucose cotransporter 1/2 inhibition and risk of neurodegenerative disorders: A Mendelian randomization study
• SpectroCVT-Net: A convolutional vision transformer architecture and channel attention for classifying Alzheimer's disease using spectrograms
• Spinal dementia: Don't miss it, it's treatable
• Stress granule formation helps to mitigate neurodegeneration
• Structural basis for RNA recognition by the C-terminal RRM domain of human RBM45
• Synaptic gene expression changes in frontotemporal dementia due to the MAPT 10 + 16 mutation
• Systemic inflammatory markers in ageing, Alzheimer's disease and other dementias
• TBK1 p.Y153Qfs*9 variant may be associated with young-onset, rapidly progressive amyotrophic lateral sclerosis through a haploinsufficiency mechanism
• The emerging role of the cerebellum in the affective theory of mind in the behavioral variant of frontotemporal dementia
• The genetics of amyotrophic lateral sclerosis
• The graded multidimensional geometry of phenotypic variation and progression in neurodegenerative syndromes
• The HRD1-SEL1L ubiquitin ligase regulates stress granule homeostasis in couple with distinctive signaling branches of ER stress
• Trajectories of behavior and social cognition in behavioral variant frontotemporal dementia and primary psychiatric disorders: A call for better operationalization of socioemotional changes
• Valosin-Containing Protein (VCP)/p97 Oligomerization
• Visual Electroencephalography Assessment in the Diagnosis and Prognosis of Cognitive Disorders
• VPS35 or retromer as a potential target for neurodegenerative disorders: barriers to progress
• Zfp106 binds to G-quadruplex RNAs and inhibits RAN translation and formation of RNA foci caused by G4C2 repeats
• γ-Secretase activity, clinical features, and biomarkers of autosomal dominant Alzheimer's disease: cross-sectional and longitudinal analysis of the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS)