Wolfgang Mueller‐Felber

Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation

Monika Hartig, Arcangela Iuso, Tobias B. Haack et al. · The American Journal of Human Genetics · 2011 · 266 citations · Full text

Life Sciences, Genetics, Neuroscience +12

Consensus Statement on Standard of Care for Congenital Muscular Dystrophies

Ching H. Wang, Carsten G. Bönnemann, A. Rutkowski et al. · Journal of Child Neurology · 2010 · 215 citations · Full text

Medicine, Neurology, Neuromuscular Disorders +9

A randomized placebo-controlled phase 3 trial of an antisense oligonucleotide, drisapersen, in Duchenne muscular dystrophy

Nathalie Goemans, Eugenio Mercuri, Hirofumi Komaki et al. · Neuromuscular Disorders · 2017 · 128 citations · Full text

Medicine, Molecular Medicine, Neuromuscular Disorders +7

Myogenic changes of the levator ani muscle in premenopausal women: The impact of vaginal delivery and age

Th. Dimpfl, Ch. Jaeger, Wolfgang Mueller‐Felber et al. · Neurourology and Urodynamics · 1998 · 114 citations

Medicine, Anatomy, Pathology +17

A phase 3 randomized placebo-controlled trial of tadalafil for Duchenne muscular dystrophy

Ronald G. Victor, H. Lee Sweeney, Richard S. Finkel et al. · Neurology · 2017 · 73 citations · Full text

Pharmacy, Pharmacotherapy, Exercise Testing +12