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Adult GM1-gangliosidosis : Clinical patterns and rectal biopsy.Neurology 35:834-840,1985.
Nakano T, Ikeda S, Kondo K, Yanagisawa N, Tsuji S
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A point mutation in the coding sequence of the beta-hexosaminidase alpha gene results in defective processing of the enzyme protein in an unusual GM2-gangliosidosis variant. J Neurochem 51: 984-987,1988.
Nakano T, Muscillo M, Ohno K, Hoffman AJ, Suzuki K
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Structure of full-length cDNA coding for sulfatide activator, a co-beta-glucosidase and two other homologous proteins : two alternate forms of the sulfatide activator. J Biochem 195: 152-154,1989.
Nakano T, Sandhoff K, Stumper J, Chistomanou H, Suzuki K
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Genetic cause of a juvenile form of Sandhoff disease : abnormal splicing of beta-hexosaminidase beta chain gene transcript due to a point mutation within intron 12. J Biol Chem 264: 5155-5158,1989.
Nakano T, Suzuki K
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Point mutation within Exon 5 of beta-Hexosaminidase alpha Gene in a Japanese Infant with Tay-Sachs Disease. Ann Neurol 27:465-473,1990.
Nakano T, Nanba E, Tanaka A, Ohno K, Suzuki Y, Suzuki K
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Ultrastructual findings of rectal and skin biopsies in adult GM1-gangliosidosis. Acta Pathol Jpn 36: 1823-1831,1986.
Ikeda S, Ushiyama M, Nakano T, Kikkawa T, Kondo K, Yanagisawa N
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Blood-brain barrier permeability to horseradish peroxidase in twicher and cuprizone-intoxicated mice. Brain Research 425:186-190,1987.
Kondo A, Nakano T, Suzuki K
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Infantile and fetal globoid cell leukodystrophy : analysis of galactosylceramide and galactosylsphingosine. Ann Neurol 24:517-522,1988.
Kobayashi T, Goto I, Yamanaka T, Suzuki Y, Nakano T, Suzuki K
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Molecular genetics of beta-N-acetylhexosaminidase alpha subunit mutations. Salvayre R, Douste-Blazy L, Gatt S eds : Lipid storage disorders. pp215-223. Plenum Publishing Corporation, New York,1988.
Ohno K, Muscillo M, Nakano T, Suzuki K
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Isolation of a cDNA coding the human GM2 activator protein. FEBS LETTER 251:197-200,1989.
Scroder M, Klima H, Nakano T, Kwon H, Quintern LE、 Gartner S, Suzuki K, Sandhoff K
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Juvenile Sandhoff disease : a Japanese patient carrying a mutation identical to that found earlier in Canadian patient. J Neurol Sci 98: 277-286,1990.
Mitsuo K, Nakano T, Kobayashi T, Goto I, Taniike M, Suzuki K
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Sulfatide Activator Protein alternative splicing that generates three mRNA and a newly found mutation responsible for a clinical disease. J Biol Chem 266:7556-7560,1991.
Holtschmidt H, Sandhoff K, Kwon HY, Harzer K, Nakano T, Suzuki K
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Accumulation of Lysosphingolipids in Tissues from Patients with GM1 and GM2 Gangliosidoses. J Neurochem 59:1452-1458,1992.
Kobayashi T, Goto I, Okada S, Orii T, Ohno K, Nakano T
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GM1 Gangliosidosis in Adults : Clinical and Molecular Analysis of 16 Japanese Patients. Ann Neurol l31:328-332,1992.
Yoshida K, Oshima A, Sakuraba H, Nakano T, Yanagisawa N, Inui K, Okada S, Uyama E, Namba R, Kondo K, Iwasaki S, Takamiya K, Suzuki Y
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Altered sensitivities to potentials inhibitors of cholesterol biosynthesis in Niemann-Pick TypeC fibroblasts. Cell Structure and Function 18:231-240,1993.
Ohno K, Nanba E, Nakano T, Inui K, Okada S, Takeshita K
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Detection of immune complexes in experimental allergic neuritis. J Nurol Sci 63: 229-239,1984.
Koh CS, Nakano T, Tsukada N, Yanagisawa N, Okano T, Taketomi T
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Asymptomatic Homozygous Gene Carrier in a Family with Type1 Familial Amyloid Polyneuropathy. Eur Neurol l32: 308-313,1992.
Ikeda S, Nakano T, Yanagisawa N, Nakazato M, Tsukagoshi H
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Three Patients with Isolated Adrenocorticotropin Deficiency Presenting with Neuroleptic Malignant Syndrome-like Symptoms. Internal Medicine 40: 510-514,2001.
Sekijima Y, Hoshi K, Kasai H, Okada M, Namiki S, Ohta K, Nakano T, Hirayama J, Ikeda S
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Validity of a newly developed Japanese SS-QOL (Stroke-Specific Quality of Life) measure. Quality of life research 30: 285,2001.
Origasa H, Nakano T, Morioka T, Owa M
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Hypersomnia and Low CSF Hypocretin-1 (Orexin-A ) Concentration in a Patient with Multiple Sclerosis Showing Bilateral Hypothalamic Lesions. Internal medicine 42:743-745 2003.
Kato T, Kanbayashi T, Yamamoto K, Nakano T, Shimizu T, Hashimoto T, Ikeda S