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Publications by Hanns Lochmüller
Identification of Novel, Therapy-Responsive Protein Biomarkers in a Mouse Model of Duchenne Muscular Dystrophy by Aptamer-Based Serum Proteomics
Scientific Reports
Multidisciplinary
Correction To: Eight Years After an International Workshop on Myotonic Dystrophy Patient Registries: Case Study of a Global Collaboration for a Rare Disease
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Transition From Childhood to Adulthood in Duchenne Muscular Dystrophy (DMD)
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Facilitating Orphan Drug Development: Proceedings of the TREAT-NMD International Conference, December 2015, Washington, DC, USA
Neuromuscular Disorders
Child Health
Neurology
Pediatrics
Perinatology
Genetics
European Cross-Sectional Survey of Current Care Practices for Duchenne Muscular Dystrophy Reveals Regional and Age-Dependent Differences
Journal of Neuromuscular Diseases
Neurology
Drosophila Studies Support a Role for a Presynaptic Synaptotagmin Mutation in a Human Congenital Myasthenic Syndrome
PLoS ONE
Multidisciplinary
A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy
American Journal of Human Genetics
Genetics
Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal Γ Subunit
American Journal of Human Genetics
Genetics
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