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21. Familial amyotrophic lateral sclerosis with novel A4D SOD1 mutation with late age at onset and rapid progressive course. Issue 1 (31st January 2013)

22. HECT (Homologous to the E6-AP Carboxyl Terminus)-Type Ubiquitin E3 Ligase ITCH Attenuates Cardiac Hypertrophy by Suppressing the Wnt/β-Catenin Signaling Pathway. Issue 6 (December 2020)

23. Impact of activities of daily living on percutaneous coronary intervention and acute and long-term mortality in patients with acute myocardial infarction: Yamagata AMI registry. Issue 4 (October 2022)

26. Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis. Issue 3 (11th February 2022)

27. Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletion. (April 2019)

28. Novel mutation in the membrane metalloendopeptidase gene in a patient with the autosomal recessive form of Charcot–Marie–Tooth disease. Issue 4 (20th June 2017)

29. Novel mutation in the SOD1 gene in a patient with early‐onset, rapidly progressive amyotrophic lateral sclerosis. Issue 6 (5th September 2017)

30. Partial duplication of DHH causes minifascicular neuropathy: A novel mutation detection of DHH. Issue 6 (22nd May 2017)