Suchergebnisse - "Neuromuscular disease"

PubPharm (3.219)

1

A review on mechanistic insights into structure and function of dystrophin protein in pathophysiology and therapeutic targeting of Duchenne muscular dystrophy

enthalten in: International journal of biological macromolecules | 2024

von Elasbali, A. | Al-Soud, W. | Anwar, S. | +3

2

Dysregulation of innate immune signaling in animal models of spinal muscular atrophy

enthalten in: BMC biology | 2024

von Garcia, E. | Steiner, R. | Raimer, A. | +3

3

Dysregulation of innate immune signaling in animal models of spinal muscular atrophy

enthalten in: BMC biology | 2024

von Garcia, E. | Steiner, R. | Raimer, A. | +3

4

Pain and Muscle Biopsy : Exploring Pain: Prospective Observational Study on Pain Perception During and After Muscle Biopsy

enthalten in: ClinicalTrials.gov | 2024

5

Prevention of axonal loss after immediate dosage titration of immunoglobulin in multifocal motor neuropathy

enthalten in: European journal of neurology | 2024

von Al-Zuhairy, A. | Jakobsen, J. | Krarup, C.

6

COVID-19 in patients with myasthenia gravis : a single-center retrospective study in China

enthalten in: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2024

von Li, J. | Zheng, Y. | Zhao, Y. | +7

7

The value of knowing : preferences for genetic testing to diagnose rare muscle diseases

enthalten in: Orphanet journal of rare diseases | 2024

von Mansfield, C. | Boeri, M. | Coulter, J. | +4

8

Improved therapeutic approach for spinal muscular atrophy via ubiquitination-resistant survival motor neuron variant

enthalten in: Journal of cachexia, sarcopenia and muscle | 2024

von Rhee, J. | Kang, J. | Jo, Y. | +7

9

Predictors of Loss of Ambulation in Duchenne Muscular Dystrophy : A Systematic Review and Meta-Analysis

enthalten in: Journal of neuromuscular diseases | 2024

von Landfeldt, E. | Alemán, A. | Abner, S. | +6

10

The value of knowing: preferences for genetic testing to diagnose rare muscle diseases

enthalten in: Orphanet journal of rare diseases | 2024

von Mansfield, C. | Boeri, M. | Coulter, J. | +4

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