Claudia Stendel
German Center for Neurodegenerative Diseases(DE)Friedrich Baur Stiftung(DE)Ludwig-Maximilians-Universität München(DE)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Hereditary Neurological Disorders, Parkinson's Disease Mechanisms and Treatments, Metabolism and Genetic Disorders
Most-Cited Works
- → Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy(2005)249 cited
- → Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy(2003)210 cited
- → Autosomal-Dominant Distal Myopathy Associated with a Recurrent Missense Mutation in the Gene Encoding the Nuclear Matrix Protein, Matrin 3(2009)176 cited
- → Transcriptional regulator PRDM12 is essential for human pain perception(2015)171 cited
- → Progression characteristics of the European Friedreich’s Ataxia Consortium for Translational Studies (EFACTS): a 2 year cohort study(2016)151 cited
- → Peripheral Nerve Demyelination Caused by a Mutant Rho GTPase Guanine Nucleotide Exchange Factor, Frabin/FGD4(2007)132 cited