Friedrich Asmus
Oxford BioMedica (United Kingdom)(GB)
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Neurological disorders and treatments, Glycogen Storage Diseases and Myoclonus, Genetic Neurodegenerative Diseases, Neurological and metabolic disorders
Most-Cited Works
- → Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology(2004)3,022 cited
- → Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome(2001)475 cited
- → EFNS guidelines on diagnosis and treatment of primary dystonias(2010)429 cited
- → Variant in the sequence of the LINGO1 gene confers risk of essential tremor(2009)226 cited
- → The PARK8 Locus in Autosomal Dominant Parkinsonism: Confirmation of Linkage and Further Delineation of the Disease-Containing Interval(2004)223 cited
- → Intravitreal Aflibercept Injection in Patients with Myopic Choroidal Neovascularization(2015)211 cited
- → The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted(2003)159 cited
- → Myoclonus–dystonia syndrome: ε‐sarcoglycan mutations and phenotype(2002)155 cited
- → A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia(2015)140 cited
- → Pallidal and thalamic deep brain stimulation in myoclonus‐dystonia(2010)137 cited