M. Muglia
Institute for Biomedical Research and Innovation(IT)National Research Council(IT)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Neurological diseases and metabolism, Neurogenetic and Muscular Disorders Research, Genetic Neurodegenerative Diseases, Cerebrovascular and genetic disorders
Most-Cited Works
- → Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A(2004)1,546 cited
- → Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2(2000)457 cited
- → Monoamine Oxidase-A Genetic Variations Influence Brain Activity Associated with Inhibitory Control: New Insight into the Neural Correlates of Impulsivity(2005)168 cited
- → Loss-of-function mutations in theSIGMAR1gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+signalling(2016)93 cited
- → The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features(2014)92 cited
- → Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis(2012)85 cited