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Journal of Neurology
|
March 30, 2019
Prognostic factors in ALS: a comparison between Germany and China
Johannes Dorst, Lu Chen, Angela Rosenbohm, et al.
The Lancet. Neurology
|
October 18, 2024
Safety, tolerability, and efficacy of fasudil in amyotrophic lateral sclerosis (ROCK-ALS): a phase 2, randomised, double-blind, placebo-controlled trial
Jan C Koch, Andreas Leha, Helen Bidner, et al.
Brain Communications
|
May 24, 2023
Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis
Wolfgang P Ruf, Matej Boros, Axel Freischmidt, et al.
Brain : a Journal of Neurology
|
January 18, 2018
Hot-spot KIF5A mutations cause familial ALS
David Brenner, Rüstem Yilmaz, Kathrin Müller, et al.
Neurological Research and Practice
|
July 3, 2024
Patients' and caregivers' perception of multidimensional and palliative care in amyotrophic lateral sclerosis - protocol of a German multicentre study
Katharina Linse, Constanze Weber, Peter Reilich, et al.
Journal of Neuromuscular Diseases
|
December 24, 2022
Improvements in Walking Distance during Nusinersen Treatment - A Prospective 3-year SMArtCARE Registry Study
Astrid Pechmann, Max Behrens, Katharina Dörnbrack, et al.
Parkinsonism & Related Disorders
|
August 1, 2025
Validation of clinical ratings of cervical dystonia using computer-generated avatars
Sebastian Loens, Roland Stenger, Feline Hamami, et al.
Journal of Neurology
|
February 27, 2024
5qSMA: standardised retrospective natural history assessment in 268 patients with four copies of SMN2
Katharina Vill, Moritz Tacke, Anna König, et al.
The Lancet Regional Health. Europe
|
February 16, 2024
Long-term efficacy and safety of nusinersen in adults with 5q spinal muscular atrophy: a prospective European multinational observational study
René Günther, Claudia Diana Wurster, Svenja Brakemeier, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 69) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 69 results.
Journal of Neurology
|
March 30, 2019
Prognostic factors in ALS: a comparison between Germany and China
Johannes Dorst, Lu Chen, Angela Rosenbohm, et al.
The Lancet. Neurology
|
October 18, 2024
Safety, tolerability, and efficacy of fasudil in amyotrophic lateral sclerosis (ROCK-ALS): a phase 2, randomised, double-blind, placebo-controlled trial
Jan C Koch, Andreas Leha, Helen Bidner, et al.
Brain Communications
|
May 24, 2023
Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis
Wolfgang P Ruf, Matej Boros, Axel Freischmidt, et al.
Brain : a Journal of Neurology
|
January 18, 2018
Hot-spot KIF5A mutations cause familial ALS
David Brenner, Rüstem Yilmaz, Kathrin Müller, et al.
Neurological Research and Practice
|
July 3, 2024
Patients' and caregivers' perception of multidimensional and palliative care in amyotrophic lateral sclerosis - protocol of a German multicentre study
Katharina Linse, Constanze Weber, Peter Reilich, et al.
Journal of Neuromuscular Diseases
|
December 24, 2022
Improvements in Walking Distance during Nusinersen Treatment - A Prospective 3-year SMArtCARE Registry Study
Astrid Pechmann, Max Behrens, Katharina Dörnbrack, et al.
Parkinsonism & Related Disorders
|
August 1, 2025
Validation of clinical ratings of cervical dystonia using computer-generated avatars
Sebastian Loens, Roland Stenger, Feline Hamami, et al.
Journal of Neurology
|
February 27, 2024
5qSMA: standardised retrospective natural history assessment in 268 patients with four copies of SMN2
Katharina Vill, Moritz Tacke, Anna König, et al.
The Lancet Regional Health. Europe
|
February 16, 2024
Long-term efficacy and safety of nusinersen in adults with 5q spinal muscular atrophy: a prospective European multinational observational study
René Günther, Claudia Diana Wurster, Svenja Brakemeier, et al.
Page
of 7