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Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosis.
Zu JS, Deng HX, Lo TP, Mitsumoto H, Ahmed MS, Hung WY, Cai ZJ, Tainer JA, Siddique T. Zu JS, et al. Among authors: mitsumoto h. Neurogenetics. 1997 May;1(1):65-71. doi: 10.1007/s100480050010. Neurogenetics. 1997. PMID: 10735277
Novel mutations in spastin gene and absence of correlation with age at onset of symptoms.
Hentati A, Deng HX, Zhai H, Chen W, Yang Y, Hung WY, Azim AC, Bohlega S, Tandan R, Warner C, Laing NG, Cambi F, Mitsumoto H, Roos RP, Boustany RM, Ben Hamida M, Hentati F, Siddique T. Hentati A, et al. Among authors: mitsumoto h. Neurology. 2000 Nov 14;55(9):1388-90. doi: 10.1212/wnl.55.9.1388. Neurology. 2000. PMID: 11087788
Phase II trial of CoQ10 for ALS finds insufficient evidence to justify phase III.
Kaufmann P, Thompson JL, Levy G, Buchsbaum R, Shefner J, Krivickas LS, Katz J, Rollins Y, Barohn RJ, Jackson CE, Tiryaki E, Lomen-Hoerth C, Armon C, Tandan R, Rudnicki SA, Rezania K, Sufit R, Pestronk A, Novella SP, Heiman-Patterson T, Kasarskis EJ, Pioro EP, Montes J, Arbing R, Vecchio D, Barsdorf A, Mitsumoto H, Levin B; QALS Study Group. Kaufmann P, et al. Among authors: mitsumoto h. Ann Neurol. 2009 Aug;66(2):235-44. doi: 10.1002/ana.21743. Ann Neurol. 2009. PMID: 19743457 Free PMC article. Clinical Trial.
Treatment of myasthenia gravis by immunoadsorption of plasma.
Grob D, Simpson D, Mitsumoto H, Hoch B, Mokhtarian F, Bender A, Greenberg M, Koo A, Nakayama S. Grob D, et al. Among authors: mitsumoto h. Neurology. 1995 Feb;45(2):338-44. doi: 10.1212/wnl.45.2.338. Neurology. 1995. PMID: 7854536 Clinical Trial.
303 results