C. Müller‐Reible

Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial

Maggie C. Walter, Peter Reilich, Simone Thiele et al. · Orphanet Journal of Rare Diseases · 2013 · 102 citations · Full text

Medicine, Neurology, Pharmacotherapy +16

Current pharmacogenetic developments in oral anticoagulation therapy: The influence of variant VKORC1 and CYP2C9 alleles

Carville G. Bevans, Andreas Fregin, Christof Geisen et al. · Thrombosis and Haemostasis · 2007 · 69 citations

Medicine, Molecular Genetics, Pharmacology +11

Positive Malignant Hyperthermia Susceptibility In Vitro  Test in a Patient with Mitochondrial Myopathy and Myoadenylate Deaminase Deficiency

Ruth Fricker, Thomas Raffelsberger, Sigrid Rauch-Shorny et al. · Anesthesiology · 2002 · 44 citations · Full text

Life Sciences, Biochemistry, Neurology +17

De-duplicating patient records from three independent data sources reveals the incidence of rare neuromuscular disorders in Germany

Kirsten König, Astrid Pechmann, Simone Thiele et al. · Orphanet Journal of Rare Diseases · 2019 · 34 citations · Full text

Health Professions, Biomedical Informatics, Health Informatics +15

Facing the genetic heterogeneity in neuromuscular disorders: Linkage analysis as an economic diagnostic approach towards the molecular diagnosis

Maja von der Hagen, J. Schallner, Angela M. Kaindl et al. · Neuromuscular Disorders · 2005 · 26 citations

Life Sciences, Genetics, Molecular Genetics +10