486 results on '"Lulé, Dorothée"'
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2. Presymptomatic grey matter alterations in ALS kindreds: a computational neuroimaging study of asymptomatic C9orf72 and SOD1 mutation carriers
3. Quality of life and depression in patients with amyotrophic lateral sclerosis – does the country of origin matter?
4. Religiosity in patients with amyotrophic lateral sclerosis, a cross-country comparison
5. Structural and microstructural neuroimaging signature of C9orf72-associated ALS: A multiparametric MRI study
6. Neuropsychological deficits have only limited impact on psychological well-being in amyotrophic lateral sclerosis
7. Brain Function, Learning, and Role of Feedback in Complete Paralysis.
8. Primary lateral sclerosis: application and validation of the 2020 consensus diagnostic criteria in an expert opinion-based PLS cohort.
9. Clinicoanatomical substrates of selfish behaviour in amyotrophic lateral sclerosis – An observational cohort study
10. A multivariate Bayesian classification algorithm for cerebral stage prediction by diffusion tensor imaging in amyotrophic lateral sclerosis
11. Lebensqualität
12. Eye movement alterations in presymptomatic C9orf72 expansion gene carriers
13. Functional and structural impairment of transcallosal motor fibres in ALS: a study using transcranial magnetic stimulation, diffusion tensor imaging, and diffusion weighted spectroscopy
14. Neural substrates of anorexia nervosa patient’s deficits to decode emotional information
15. Screening instruments of cognition: The relation of the mini-mental state examination to the Edinburgh cognitive and behavioural ALS screen in amyotrophic lateral sclerosis.
16. One third of physicians discuss exit strategies with patients with amyotrophic lateral sclerosis: Results from nationwide surveys among German and Polish neurologists
17. Disease progression but not physical state per se determines mental wellbeing in ALS
18. Executive function is inversely correlated with physical function: the cognitive profile of adult Spinal Muscular Atrophy (SMA)
19. Coping as a resource to allow for psychosocial adjustment in fatal disease: results from patients with amyotrophic lateral sclerosis.
20. Cognitive phenotypes of sequential staging in amyotrophic lateral sclerosis
21. Bevacizumab is associated with cerebral microstructural alterations: a DTI study in high-grade glioma
22. Author response: An observational study on quality of life and preferences to sustain life in locked-in state
23. Therapeutic decisions in ALS patients: cross-cultural differences and clinical implications
24. Functional reorganization during cognitive function tasks in patients with amyotrophic lateral sclerosis
25. Phenotypic differences of amyotrophic lateral sclerosis (ALS) in China and Germany
26. Determining impairment in the Swedish, Polish and German ECAS: the importance of adjusting for age and education
27. Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations
28. Synapse loss in the prefrontal cortex is associated with cognitive decline in amyotrophic lateral sclerosis
29. Determining impairment in the Swedish, Polish and German ECAS : the importance of adjusting for age and education
30. Altered Gaze Control During Emotional Face Exploration in Patients With Amyotrophic Lateral Sclerosis
31. An observational study on quality of life and preferences to sustain life in locked-in state
32. Psychological morbidity in amyotrophic lateral sclerosis: Depression, anxiety, hopelessness
33. Attitudes of caregivers towards prolonging and shortening life in advanced stages of amyotrophic lateral sclerosis.
34. Health-Related Quality of Life in Spinal Muscular Atrophy Patients and Their Caregivers—A Prospective, Cross-Sectional, Multi-Center Analysis
35. To rise and to fall: functional connectivity in cognitively normal and cognitively impaired patients with Parkinson's disease
36. The quality of life and depression in primary caregivers of patients with amyotrophic lateral sclerosis is affected by patient-related and culture-specific conditions
37. Well‐being on supportive techniques in amyotrophic lateral sclerosis: from neurologists' perspective
38. An eye-tracker controlled cognitive battery: overcoming verbal-motor limitations in ALS
39. Attitudes of Patients and Relatives Toward Disability and Treatment in Malignant MCA Infarction
40. Epidemiology of amyotrophic lateral sclerosis in Southern Germany
41. Experience matters: neurologists’ perspectives on ALS patients’ well-being
42. An eye-tracking controlled neuropsychological battery for cognitive assessment in neurological diseases
43. Brain-Computer Interface: A Communication Aid?
44. Longitudinal monitoring of amyotrophic lateral sclerosis by diffusion tensor imaging: Power calculations for group studies
45. The quality of life and depression in primary caregivers of patients with amyotrophic lateral sclerosis is affected by patient-related and culture-specific conditions.
46. Pathological laughing and crying in amyotrophic lateral sclerosis is related to frontal cortex function
47. The association between alterations of eye movement control and cerebral intrinsic functional connectivity in Parkinson’s disease
48. Cognition in the course of ALS—a meta-analysis
49. Multimodal in vivo staging in amyotrophic lateral sclerosis using artificial intelligence
50. Probing command following in patients with disorders of consciousness using a brain–computer interface
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