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Williams L, Olszewska DA, Fearon C, et al. (2021) Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by Variants. Movement Disorders Clinical Practice. 8: 954-958
McCarthy A, Lonergan R, Olszewska DA, et al. (2015) Closing the tau loop: the missing tau mutation. Brain : a Journal of Neurology
Hirano M, Quinzii CM, Mitsumoto H, et al. (2011) Senataxin mutations and amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 12: 223-7
Traub R, Mitsumoto H, Rowland LP. (2011) Research advances in amyotrophic lateral sclerosis, 2009 to 2010. Current Neurology and Neuroscience Reports. 11: 67-77
Gilbert RM, Fahn S, Mitsumoto H, et al. (2010) Parkinsonism and motor neuron diseases: twenty-seven patients with diverse overlap syndromes. Movement Disorders : Official Journal of the Movement Disorder Society. 25: 1868-75
Rowland LP, Bird TD. (2008) Silver syndrome: The complexity of complicated hereditary spastic paraplegia. Neurology. 70: 1948-9
Quinzii CM, Vu TH, Min KC, et al. (2008) X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1. American Journal of Human Genetics. 82: 208-13
Rosenberg RN, Pedley TA, Baringer JR, et al. (2003) At jeopardy: the NIH as we know it. Neurorehabilitation and Neural Repair. 17: 203-5
Rosenberg RN, Pedley TA, Baringer JR, et al. (2003) At jeopardy: the NIH as we know it. Archives of Neurology. 60: 1191-2
Lynch T, Sano M, Marder KS, et al. (2001) Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994. Neurology. 57: S39-45
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