134 results on '"De Carvalho, Mamede"'
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2. Proton pump inhibitors and amyotrophic lateral sclerosis: A case-control study
3. A neurophysiological approach to mirror movements in amyotrophic lateral sclerosis
4. Novel approaches to motoneuron disease/ALS treatment using non-invasive brain and spinal stimulation: IFCN Handbook Chapter
5. Diagnosis and differential diagnosis of MND/ALS: IFCN Handbook Chapter
6. Exploring the split hand phenomenon with the neurophysiological index
7. The cutaneous silent period as a measure of upper motor neuron dysfunction in amyotrophic lateral sclerosis
8. Artificial intelligence and statistical methods for stratification and prediction of progression in amyotrophic lateral sclerosis: A systematic review
9. Clinical characteristics in amyotrophic lateral sclerosis with Sub-Saharan Africa ancestry – A Portuguese hospital-based cohort study
10. Mirror movements – A simple algorithm for mirror activity signal processing and normative values
11. Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis
12. Advances in amyotrophic lateral sclerosis research in 2022
13. TMS-based neurophysiologic markers for ALS
14. Transcranial magnetic stimulation in amyotrophic lateral sclerosis: testing its predictive value for functional decline
15. Model-guided transcutaneous direct current stimulation of the brain and spinal cord to repair ALS-induced motor dysfunctions
16. A morphology-based feature set for automated Amyotrophic Lateral Sclerosis diagnosis on surface electromyography
17. Mild dysphagia does not influence survival in ventilated amyotrophic lateral sclerosis patients
18. Learning prognostic models using a mixture of biclustering and triclustering: Predicting the need for non-invasive ventilation in Amyotrophic Lateral Sclerosis
19. Imaging motor unit territory
20. WE-145. The cutaneous silent period in motor neuron disease
21. TH-183. Relevance of realistic human models to guide non-invasive spinal stimulation: A review of current findings
22. FOSMN: The facial expression of ALS
23. Exercise following immobility increases lower motor neuron excitability: F-wave and H-reflex studies
24. Respiratory function tests in amyotrophic lateral sclerosis: The role of maximal voluntary ventilation
25. Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
26. Prognostic Prediction in ALS: Triclustering-Based Classification of Longitudinal Data Targeting Relevant Clinical Endpoints
27. Gold Coast diagnostic criteria increase sensitivity in amyotrophic lateral sclerosis
28. Surface electromyography for testing motor dysfunction in amyotrophic lateral sclerosis
29. Electromyographic findings in primary lateral sclerosis during disease progression
30. Assessment of sympathetic sudomotor function in amyotrophic lateral sclerosis with electrochemical skin conductance
31. In the spiral of history: SARS-Cov-2 infection
32. Learning dynamic Bayesian networks from time-dependent and time-independent data: Unraveling disease progression in Amyotrophic Lateral Sclerosis
33. Cardiovascular comorbidities in amyotrophic lateral sclerosis
34. The cutaneous silent period in motor neuron disease
35. Explainable models of disease progression in ALS: Learning from longitudinal clinical data with recurrent neural networks and deep model explanation
36. Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene
37. Modulation of neuromuscular transmission using transcutaneous direct currents: An exploratory study
38. Needling the future in ALS
39. Measuring spinal presynaptic inhibition in human subjects
40. A proposal for new diagnostic criteria for ALS
41. Motor excitability measurements in early stage familial amyloid polyneuropathy: The influence of tafamidis treatment
42. AANEM – IFCN glossary of terms in neuromuscular electrodiagnostic medicine and ultrasound
43. A comparative study of South African and Portuguese amyotrophic lateral sclerosis cohorts
44. Authors’ reply: Differences between South African and Portuguese ALS cohorts from an environmental perspective
45. Transforming growth factor-β plasma levels and its role in amyotrophic lateral sclerosis
46. Motor unit estimation by MRI: Integrating old and new ideas
47. Reliability of phrenic nerve conduction study: In healthy controls and in patients with primary lateral sclerosis
48. Fasciculations: Opening Pandora’s box
49. Prognostic value of phrenic nerve conduction study in amyotrophic lateral sclerosis: Systematic review and meta-analysis
50. Standards of instrumentation of EMG
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