Benedikt Schoser

No ORCID on file · 2 papers in corpus
review 2019
Neurology. Clinical practice ·doi:10.1212/cpj.0000000000000645

PURPOSE OF REVIEW: Myotonic dystrophy type 2 (DM2) is a rare, progressive multisystem disease particularly affecting the skeletal muscle. A causal therapy is not yet available; however, prompt, appropriate symptomatic treatments are essenti…

review 2018
Neurology. Clinical practice ·doi:10.1212/cpj.0000000000000531

PURPOSE OF REVIEW: Myotonic dystrophy type 1 (DM1) is a severe, progressive genetic disease that affects between 1 in 3,000 and 8,000 individuals globally. No evidence-based guideline exists to inform the care of these patients, and most do…