355 results on '"MOTOR NEURON DISEASE"'
Search Results
2. Narrative review of diagnosis, management and treatment of dysphagia and sialorrhea in amyotrophic lateral sclerosis
3. Clinical characterization of common pathogenic variants of SOD1-ALS in Germany
4. Analysis and occurrence of biallelic pathogenic repeat expansions in RFC1 in a German cohort of patients with a main clinical phenotype of motor neuron disease
5. Rare association between spinocerebellar ataxia and amyotrophic lateral sclerosis: a case series
6. Prognostic communication in amyotrophic lateral sclerosis: findings from a Nationwide Italian survey
7. Lifestyle and medical conditions in relation to ALS risk and progression—an introduction to the Swedish ALSrisc Study
8. Genotypes and phenotypes of motor neuron disease: an update of the genetic landscape in Scotland
9. Exploratory study to evaluate the acceptability of a wearable accelerometer to assess motor progression in motor neuron disease
10. Non-motor symptoms in patients with amyotrophic lateral sclerosis: current state and future directions
11. Update on recent advances in amyotrophic lateral sclerosis
12. Diagnostic value of neurofilaments in differentiating motor neuron disease from multifocal motor neuropathy
13. Corneal nerves and amyotrophic lateral sclerosis: an in vivo corneal confocal imaging study
14. Quality of life, cognitive and behavioural impairment in people with motor neuron disease: a systematic review
15. Distinct Longitudinal Changes in EEG Measures Reflecting Functional Network Disruption in ALS Cognitive Phenotypes
16. Neuropathological spectrum of anti-IgLON5 disease and stages of brainstem tau pathology: updated neuropathological research criteria of the disease-related tauopathy
17. Clinical and Ultrasonographic Bilateral Split Elbow Sign as the Initial and Sole Presentation of Suspected Motor Neuron Disease in a Young Filipino Male: a Case Report
18. Amyotrophic lateral sclerosis associated with Sjögren’s syndrome: a case report
19. User expectations and experiences of an assistive robotic arm in amyotrophic lateral sclerosis: a multicenter observational study
20. Patients’ and caregivers’ perception of multidimensional and palliative care in amyotrophic lateral sclerosis – protocol of a German multicentre study
21. Ebselen analogues delay disease onset and its course in fALS by on-target SOD-1 engagement
22. Molecular mechanisms and therapeutic strategies for neuromuscular diseases
23. Optimizing breathlessness management in amyotrophic lateral sclerosis: insights from a comprehensive systematic review
24. Administration of adipose-derived stem cells extracellular vesicles in a murine model of spinal muscular atrophy: effects of a new potential therapeutic strategy
25. Psychosocial interventions for people with amyotrophic lateral sclerosis and motor neuron disease and their caregivers: a scoping review
26. Increased incidence of motor neuron disease in Sweden: a population-based study during 2002–2021
27. Potential of neuroimaging as a biomarker in amyotrophic lateral sclerosis: from structure to metabolism
28. Dysphagia Assessments as Criteria in the ‘Decision-Making Process’ for Percutaneous Endoscopic Gastrostomy Placement in People with Amyotrophic Lateral Sclerosis: A Systematic Review
29. Unveiling the SOD1-mediated ALS phenotype: insights from a comprehensive meta-analysis
30. Neuronal STING activation in amyotrophic lateral sclerosis and frontotemporal dementia
31. Prevalence and correlates of fatigue in amyotrophic lateral sclerosis: A systematic review and meta-analysis
32. Selective vulnerability of motor neuron types and functional groups to degeneration in amyotrophic lateral sclerosis: review of the neurobiological mechanisms and functional correlates
33. Factors impacting trial participation in people with motor neuron disease
34. Impact of the metabolic syndrome on prevalence and survival in motor neuron disease: a retrospective case series
35. Clinical characteristics, course, and outcomes of amyotrophic lateral sclerosis overlapping with pregnancy: a systematic review of 38 published cases
36. Amyotrophic lateral sclerosis with upper motor neuron predominance: diagnostic accuracy of qualitative and quantitative susceptibility metrics in the precentral gyrus
37. The Molecular Link Between TDP-43, Endogenous Retroviruses and Inflammatory Neurodegeneration in Amyotrophic Lateral Sclerosis: a Potential Target for Triumeq, an Antiretroviral Therapy
38. Autonomic dysfunction is associated with disease progression and survival in amyotrophic lateral sclerosis: a prospective longitudinal cohort study
39. Safety and efficacy of lithium in patients with amyotrophic lateral sclerosis: a systematic review and meta-analysis of randomized controlled trials
40. Chlamydia psittaci Pneumonia in a patient with motor neuron disease: a case report
41. Statistical analysis plan for the motor neuron disease systematic multi-arm adaptive randomised trial (MND-SMART)
42. The era of cryptic exons: implications for ALS-FTD
43. Digital peer-to-peer support programme for informal caregivers of people living with motor neuron disease: study protocol for a multi-centre parallel group, single-blinded (outcome assessor) randomised controlled superiority trial
44. Opinion: more mouse models and more translation needed for ALS
45. Memory-guided navigation in amyotrophic lateral sclerosis
46. Increasing prevalence 2015–2019 of amyotrophic lateral sclerosis in Sardinia, Italy
47. Spectrum of SPTLC1-related disorders: a novel case of ‘Ser331 syndrome’ that expand the phenotype of hereditary sensory and autonomic neuropathy type 1A and motor neuron diseases
48. Spinal astrocyte dysfunction drives motor neuron loss in late-onset spinal muscular atrophy
49. Use of hip- versus wrist-based actigraphy for assessing functional decline and disease progression in patients with motor neuron disease
50. Brainstem–cortex disconnection in amyotrophic lateral sclerosis: bulbar impairment, genotype associations, asymptomatic changes and biomarker opportunities
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