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You searched for: Author/Creator Maruyama, Hirofumi

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3. A Japanese patient with familial ALS and a p.K510M mutation in the gene for FUS (FUS) resulting in the totally locked‐in state. Issue 5 (19th May 2014)

4. A mutant MATR3 mouse model to explain multisystem proteinopathy. Issue 2 (18th June 2019)

5. A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia. Issue 1 (December 2015)

6. A rational, multispectral mapping algorithm for primary motor cortex: A primary step before cortical stimulation. (20th February 2019)

7. A Role of Aging in the Progression of Cortical Excitability in Benign Adult Familial Myoclonus Epilepsy type 1 Patients. Issue 10 (24th July 2021)

8. A score to map the lateral nonprimary motor area: Multispectrum intrinsic brain activity versus cortical stimulation. (15th October 2019)

9. Amyotrophic lateral sclerosis of long clinical course clinically presenting with progressive muscular atrophy. Issue 1 (3rd December 2018)

10. An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1 mutation. Issue 1 (17th June 2013)