Koh K, Ichinose Y, Ishiura H, Nan H, Mitsui J, Takahashi J, Sato W, Itoh Y, Hoshino K, Tsuji S, Takiyama Y, Japan Spastic Paraplegia Research Consotium.
Yamaguchi N, Mano T, Ohtomo R, Ishiura H, Almansour MA, Mori H, Kanda J, Shirota Y, Taira K, Morikawa T, Ikemura M, Yanagi Y, Murayama S, Shimizu J, Sakurai Y, Tsuji S, Iwata A
Internal medicine (Tokyo, Japan) Aug 2018 [Refereed]
Misawa S, Kuwabara S, Sato Y, Yamaguchi N, Nagashima K, Katayama K, Sekiguchi Y, Iwai Y, Amino H, Suichi T, Yokota T, Nishida Y, Kanouchi T, Kohara N, Kawamoto M, Ishii J, Kuwahara M, Suzuki H, Hirata K, Kokubun N, Masuda R, Kaneko J, Yabe I, Sasaki H, Kaida KI, Takazaki H, Suzuki N, Suzuki S, Nodera H, Matsui N, Tsuji S, Koike H, Yamasaki R, Kusunoki S, Japanese Eculizumab Trial for GBS (JET-GBS) Study Group.
The Lancet. Neurology 17(6) 519-529 Jun 2018 [Refereed]
Higuchi Y, Okunushi R, Hara T, Hashiguchi A, Yuan J, Yoshimura A, Murayama K, Ohtake A, Ando M, Hiramatsu Y, Ishihara S, Tanabe H, Okamoto Y, Matsuura E, Ueda T, Toda T, Yamashita S, Yamada K, Koide T, Yaguchi H, Mitsui J, Ishiura H, Yoshimura J, Doi K, Morishita S, Sato K, Nakagawa M, Yamaguchi M, Tsuji S, Takashima H
Brain : a journal of neurology 141(6) 1622-1636 Jun 2018 [Refereed]
Cen Z, Jiang Z, Chen Y, Zheng X, Xie F, Yang X, Lu X, Ouyang Z, Wu H, Chen S, Yin H, Qiu X, Wang S, Ding M, Tang Y, Yu F, Li C, Wang T, Ishiura H, Tsuji S, Jiao C, Liu C, Xiao J, Luo W
Brain : a journal of neurology Jun 2018 [Refereed]
Tohnai G, Nakamura R, Sone J, Nakatochi M, Yokoi D, Katsuno M, Watanabe H, Watanabe H, Ito M, Li Y, Izumi Y, Morita M, Taniguchi A, Kano O, Oda M, Kuwabara S, Abe K, Aiba I, Okamoto K, Mizoguchi K, Hasegawa K, Aoki M, Hattori N, Onodera O, Naruse H, Mitsui J, Takahashi Y, Goto J, Ishiura H, Morishita S, Yoshimura J, Doi K, Tsuji S, Nakashima K, Kaji R, Atsuta N, Sobue G, Japanese Consortium for Amyotrophic Lateral Sclerosis Research (JaCALS).
Neurobiology of aging 64 158.e15-158.e19 Apr 2018 [Refereed]
Ishiura H, Doi K, Mitsui J, Yoshimura J, Matsukawa MK, Fujiyama A, Toyoshima Y, Kakita A, Takahashi H, Suzuki Y, Sugano S, Qu W, Ichikawa K, Yurino H, Higasa K, Shibata S, Mitsue A, Tanaka M, Ichikawa Y, Takahashi Y, Date H, Matsukawa T, Kanda J, Nakamoto FK, Higashihara M, Abe K, Koike R, Sasagawa M, Kuroha Y, Hasegawa N, Kanesawa N, Kondo T, Hitomi T, Tada M, Takano H, Saito Y, Sanpei K, Onodera O, Nishizawa M, Nakamura M, Yasuda T, Sakiyama Y, Otsuka M, Ueki A, Kaida KI, Shimizu J, Hanajima R, Hayashi T, Terao Y, Inomata-Terada S, Hamada M, Shirota Y, Kubota A, Ugawa Y, Koh K, Takiyama Y, Ohsawa-Yoshida N, Ishiura S, Yamasaki R, Tamaoka A, Akiyama H, Otsuki T, Sano A, Ikeda A, Goto J, Morishita S, Tsuji S
Tanabe H, Higuchi Y, Yuan JH, Hashiguchi A, Yoshimura A, Ishihara S, Nozuma S, Okamoto Y, Matsuura E, Ishiura H, Mitsui J, Takashima R, Kokubun N, Maeda K, Asano Y, Sunami Y, Kono Y, Ishigaki Y, Yanamoto S, Fukae J, Kida H, Morita M, Tsuji S, Takashima H
Journal of the peripheral nervous system : JPNS 23(1) 40-48 Mar 2018 [Refereed]
Naruse H, Ishiura H, Mitsui J, Date H, Takahashi Y, Matsukawa T, Tanaka M, Ishii A, Tamaoka A, Hokkoku K, Sonoo M, Segawa M, Ugawa Y, Doi K, Yoshimura J, Morishita S, Goto J, Tsuji S
Neurobiology of aging 61 255.e9-255.e16 Jan 2018 [Refereed]
Eriguchi Y, Kuwabara H, Inai A, Kawakubo Y, Nishimura F, Kakiuchi C, Tochigi M, Ohashi J, Aoki N, Kato K, Ishiura H, Mitsui J, Tsuji S, Doi K, Yoshimura J, Morishita S, Shimada T, Furukawa M, Umekage T, Sasaki T, Kasai K, KanoMD PhD Y
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 174(7) 712-723 Oct 2017 [Refereed]
Ando M, Hashiguchi A, Okamoto Y, Yoshimura A, Hiramatsu Y, Yuan J, Higuchi Y, Mitsui J, Ishiura H, Umemura A, Maruyama K, Matsushige T, Morishita S, Nakagawa M, Tsuji S, Takashima H
Journal of the peripheral nervous system : JPNS 22(3) 191-199 Sep 2017 [Refereed]
Ikeda T, Nakahara A, Nagano R, Utoyama M, Obara M, Moritake H, Uechi T, Mitsui J, Ishiura H, Yoshimura J, Doi K, Kenmochi N, Morishita S, Nishino I, Tsuji S, Nunoi H
Journal of human genetics 62(4) 473-480 Apr 2017 [Refereed]
Yamashita T, Mitsui J, Shimozawa N, Takashima S, Umemura H, Sato K, Takemoto M, Hishikawa N, Ohta Y, Matsukawa T, Ishiura H, Yoshimura J, Doi K, Morishita S, Tsuji S, Abe K
Journal of the neurological sciences 375 424-429 Apr 2017 [Refereed]
Kadoya M, Hida A, Hashimoto Maeda M, Taira K, Ikenaga C, Uchio N, Kubota A, Kaida K, Miwa Y, Kurasawa K, Shimada H, Sonoo M, Chiba A, Shiio Y, Uesaka Y, Sakurai Y, Izumi T, Inoue M, Kwak S, Tsuji S, Shimizu J
Neurology(R) neuroimmunology & neuroinflammation 3(6) e290 Dec 2016 [Refereed]
Amiya E, Morita H, Hatano M, Nitta D, Hosoya Y, Maki H, Motozawa Y, Sato N, Ishiura H, Numakura S, Shintani Y, Kinugawa K, Takeda N, Shimizu J, Tsuji S, Komuro I
International journal of cardiology 222 727-729 Nov 2016 [Refereed]
Yamaguchi N, Misawa S, Sato Y, Nagashima K, Katayama K, Sekiguchi Y, Iwai Y, Amino H, Suichi T, Yokota T, Nishida Y, Kohara N, Hirata K, Nishiyama K, Yabe I, Kaida KI, Suzuki N, Nodera H, Tsuji S, Koike H, Kira JI, Hanaoka H, Kusunoki S, Kuwabara S, JET-GBS Group.
JMIR research protocols 5(4) e210 Nov 2016 [Refereed]
Watanabe H, Atsuta N, Hirakawa A, Nakamura R, Nakatochi M, Ishigaki S, Iida A, Ikegawa S, Kubo M, Yokoi D, Watanabe H, Ito M, Katsuno M, Izumi Y, Morita M, Kanai K, Taniguchi A, Aiba I, Abe K, Mizoguchi K, Oda M, Kano O, Okamoto K, Kuwabara S, Hasegawa K, Imai T, Kawata A, Aoki M, Tsuji S, Nakashima K, Kaji R, Sobue G
Journal of neurology, neurosurgery, and psychiatry 87(8) 851-858 Aug 2016 [Refereed]
Miyagawa T, Ebinuma I, Morohashi Y, Hori Y, Young Chang M, Hattori H, Maehara T, Yokoshima S, Fukuyama T, Tsuji S, Iwatsubo T, Prendergast GC, Tomita T
Human molecular genetics 25(14) 2948-2958 Jul 2016 [Refereed]
Hida A, Yamashita T, Hosono Y, Inoue M, Kaida K, Kadoya M, Miwa Y, Yajima N, Maezawa R, Arai S, Kurasawa K, Ito K, Shimada H, Iwanami T, Sonoo M, Hatanaka Y, Murayama S, Uchibori A, Chiba A, Aizawa H, Momoo T, Nakae Y, Sakurai Y, Shiio Y, Hashida H, Yoshizawa T, Sakiyama Y, Oda A, Inoue K, Takeuchi S, Iwata NK, Date H, Masuda N, Mikata T, Motoyoshi Y, Uesaka Y, Maeda MH, Nakashima R, Tsuji S, Kwak S, Mimori T, Shimizu J
Higasa K, Miyake N, Yoshimura J, Okamura K, Niihori T, Saitsu H, Doi K, Shimizu M, Nakabayashi K, Aoki Y, Tsurusaki Y, Morishita S, Kawaguchi T, Migita O, Nakayama K, Nakashima M, Mitsui J, Narahara M, Hayashi K, Funayama R, Yamaguchi D, Ishiura H, Ko WY, Hata K, Nagashima T, Yamada R, Matsubara Y, Umezawa A, Tsuji S, Matsumoto N, Matsuda F
Journal of human genetics 61(6) 547-553 Jun 2016 [Refereed]
Higuchi Y, Hashiguchi A, Yuan J, Yoshimura A, Mitsui J, Ishiura H, Tanaka M, Ishihara S, Tanabe H, Nozuma S, Okamoto Y, Matsuura E, Ohkubo R, Inamizu S, Shiraishi W, Yamasaki R, Ohyagi Y, Kira J, Oya Y, Yabe H, Nishikawa N, Tobisawa S, Matsuda N, Masuda M, Kugimoto C, Fukushima K, Yano S, Yoshimura J, Doi K, Nakagawa M, Morishita S, Tsuji S, Takashima H
Annals of neurology 79(4) 659-672 Apr 2016 [Refereed]
Ishiura H, Takahashi Y, Hayashi T, Saito K, Furuya H, Watanabe M, Murata M, Suzuki M, Sugiura A, Sawai S, Shibuya K, Ueda N, Ichikawa Y, Kanazawa I, Goto J, Tsuji S
Journal of human genetics 61(4) 363-364 Apr 2016 [Refereed]
Nakamura R, Sone J, Atsuta N, Tohnai G, Watanabe H, Yokoi D, Nakatochi M, Watanabe H, Ito M, Senda J, Katsuno M, Tanaka F, Li Y, Izumi Y, Morita M, Taniguchi A, Kano O, Oda M, Kuwabara S, Abe K, Aiba I, Okamoto K, Mizoguchi K, Hasegawa K, Aoki M, Hattori N, Tsuji S, Nakashima K, Kaji R, Sobue G, Japanese Consortium for Amyotrophic Lateral Sclerosis Research (JaCALS).
Neurobiology of aging 39 219.e1-8 Mar 2016 [Refereed]
Mano KK, Matsukawa T, Mitsui J, Ishiura H, Tokushige S, Takahashi Y, Sato NS, Nakamoto FK, Ichikawa Y, Nagashima Y, Terao Y, Shimizu J, Hamada M, Uesaka Y, Oyama G, Ogawa G, Yoshimura J, Doi K, Morishita S, Tsuji S, Goto J
Fujisawa T, Yamaguchi N, Kadowaki H, Tsukamoto Y, Tsuburaya N, Tsubota A, Takahashi H, Naguro I, Takahashi Y, Goto J, Tsuji S, Nishitoh H, Homma K, Ichijo H
Neurobiology of disease 82 478-486 Oct 2015 [Refereed]
Hanajima R, Shadmehr R, Ohminami S, Tsutsumi R, Shirota Y, Shimizu T, Tanaka N, Terao Y, Tsuji S, Ugawa Y, Uchimura M, Inoue M, Kitazawa S
Journal of neurophysiology 114(4) 2460-2471 Oct 2015 [Refereed]
[112th Scientific Meeting of the Japanese Society of Internal Medicine: Educational Lecture: Elucidation of Molecular Bases of Brain Diseases Based on Personal Genome Analyses].
Tsuji S
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine 104(9) 1924-1929 Sep 2015 [Refereed]
Ozaki K, Doi H, Mitsui J, Sato N, Iikuni Y, Majima T, Yamane K, Irioka T, Ishiura H, Doi K, Morishita S, Higashi M, Sekiguchi T, Koyama K, Ueda N, Miura Y, Miyatake S, Matsumoto N, Yokota T, Tanaka F, Tsuji S, Mizusawa H, Ishikawa K
Watanabe H, Atsuta N, Nakamura R, Hirakawa A, Watanabe H, Ito M, Senda J, Katsuno M, Izumi Y, Morita M, Tomiyama H, Taniguchi A, Aiba I, Abe K, Mizoguchi K, Oda M, Kano O, Okamoto K, Kuwabara S, Hasegawa K, Imai T, Aoki M, Tsuji S, Nakano I, Kaji R, Sobue G
Yamashita S, Mori A, Nishida Y, Kurisaki R, Tawara N, Nishikami T, Misumi Y, Ueyama H, Imamura S, Higuchi Y, Hashiguchi A, Higuchi I, Morishita S, Yoshimura J, Uchino M, Takashima H, Tsuji S, Ando Y
Neuropathology and applied neurobiology 41(3) 391-398 Apr 2015 [Refereed]
Mitsui J, Matsukawa T, Sasaki H, Yabe I, Matsushima M, Dürr A, Brice A, Takashima H, Kikuchi A, Aoki M, Ishiura H, Yasuda T, Date H, Ahsan B, Iwata A, Goto J, Ichikawa Y, Nakahara Y, Momose Y, Takahashi Y, Hara K, Kakita A, Yamada M, Takahashi H, Onodera O, Nishizawa M, Watanabe H, Ito M, Sobue G, Ishikawa K, Mizusawa H, Kanai K, Hattori T, Kuwabara S, Arai K, Koyano S, Kuroiwa Y, Hasegawa K, Yuasa T, Yasui K, Nakashima K, Ito H, Izumi Y, Kaji R, Kato T, Kusunoki S, Osaki Y, Horiuchi M, Kondo T, Murayama S, Hattori N, Yamamoto M, Murata M, Satake W, Toda T, Filla A, Klockgether T, Wüllner U, Nicholson G, Gilman S, Tanner CM, Kukull WA, Stern MB, Lee VM, Trojanowski JQ, Masliah E, Low PA, Sandroni P, Ozelius LJ, Foroud T, Tsuji S
Annals of clinical and translational neurology 2(4) 417-426 Apr 2015 [Refereed]
Journal of neurogenetics 29(2-3) 85-94 2015 [Refereed]
Recurrent cerebral aneurysm formation and rupture within a short period due to invasive aspergillosis of the nasal sinus; pathological analysis of the catastrophic clinical course.
Shinya Y, Miyawaki S, Nakatomi H, Okano A, Imai H, Shin M, Sato K, Tsuchida T, Hayashi T, Terao Y, Numakura S, Morikawa T, Shibahara J, Kikuta S, Kondo K, Tatsuno K, Mori H, Kunimatsu A, Tsuji S, Saito N
International journal of clinical and experimental pathology 8(10) 13510-13522 2015 [Refereed]
Doi H, Ushiyama M, Baba T, Tani K, Shiina M, Ogata K, Miyatake S, Fukuda-Yuzawa Y, Tsuji S, Nakashima M, Tsurusaki Y, Miyake N, Saitsu H, Ikeda S, Tanaka F, Matsumoto N, Yoshida K
Shimazaki H, Honda J, Naoi T, Namekawa M, Nakano I, Yazaki M, Nakamura K, Yoshida K, Ikeda S, Ishiura H, Fukuda Y, Takahashi Y, Goto J, Tsuji S, Takiyama Y
Journal of neurology, neurosurgery, and psychiatry 85(9) 1024-1028 Sep 2014 [Refereed]
Tezenas du Montcel S, Durr A, Bauer P, Figueroa KP, Ichikawa Y, Brussino A, Forlani S, Rakowicz M, Schöls L, Mariotti C, van de Warrenburg BP, Orsi L, Giunti P, Filla A, Szymanski S, Klockgether T, Berciano J, Pandolfo M, Boesch S, Melegh B, Timmann D, Mandich P, Camuzat A, Clinical Research Consortium for Spinocerebellar Ataxia (CRC-SCA)., EUROSCA network., Goto J, Ashizawa T, Cazeneuve C, Tsuji S, Pulst SM, Brusco A, Riess O, Brice A, Stevanin G
Brain : a journal of neurology 137(Pt 9) 2444-2455 Sep 2014 [Refereed]
Yasui K, Yabe I, Yoshida K, Kanai K, Arai K, Ito M, Onodera O, Koyano S, Isozaki E, Sawai S, Adachi Y, Sasaki H, Kuwabara S, Hattori T, Sobue G, Mizusawa H, Tsuji S, Nishizawa M, Nakashima K
Orphanet journal of rare diseases 9 118 Jul 2014 [Refereed]
Biochemical and Biophysical Research Communications 177(3) 1211-1216 1991
Adult-form galactosialidosis : ocular findings in three cases. (共著)
Ophthalmologica 203(4) 176-179 1991
Indentification of a mutation in the arylsulfatase A gene of a patient with adult-type metachromatic leukodystrophy. (共著)
The American Journal of Human Genetics 48(5) 971-978 1991
Linkage analysis of juvenile parkinsonism to tyrosine hydroxylase gene locus on chromosome 11. (共著)
Neurology 41(5) 719-722 1991
Physiological significance of fatty acid elongation system in adrenoleukodystrophy. (共著)
Journal of the Neurological Sciences 103(2) 188-194 1991
Isolation and characterization of major urinary oligosaccharides excreted in a patient with type 3 GM1 gangliosidosis. (共著)
Journal of Biochemistry 109,722-727 1991
Two Japanese cases with aspartylglycosaminuria : clinical and morphological features. (共著)
Clinical Genetics 40,318-325 1991
Simple detection of tRNALys mutation in myoclonus epilepsy associated with ragged-red fibers(MERRF)by polymerase chain reaction with a mismatched primer. (共著)
Neurology 41(11) 1838-1840 1991
Stability of messenger RNA in postmortem human brains and construction of human brain cDNA libraries. (共著)
Journal of Molecular Neuroscience 2(1) 29-34 1990
Abnormal glycosphingolipid metabolism in the nervous system of galactosialidosis. (共著)
Journal of the Neurological Sciences 97(1) 53-65 1990
Rapid diagnosis of tuberculous meningitis by polymerase chain reaction(PCR). (共著)
Neurology 40(10) 1617-1618 1990
A common mitochondrial DNA mutation in the t-RNALys of patients with myoclonus epilepsy associated with ragged-red fibers. (共著)
Biochemical and Biophysical Research Communications 163(3) 1498-1504 1989
Gene mapping and leader polypeptide sequence of human glucocerebrosidase : Implications for Gaucher disease. (共著)
Proceedings of the National Academy of Sciences of the United States of America 82(20) 7101-7105 1985
Adult GM1-gangliosidosis : Clinical patterns and rectal biopsy. (共著)
Neurology 35(6) 875-880 1985
Metabolism of 〔17,18- 3H2〕hexacosanoic acid and 〔15,16- 3H2〕lignoceric acid in cultured skin fibroblasts from patients with adrenoleukodystrophy(ALD)and adrenomyeloneuropathy(AMN). (共著)
Journal of the Neurological Sciences 71,359-367 1985
Nucleotide sequence of cDNA containing the complete coding sequence for human lysosomal glucocerebrosidase. (共著)
The Journal of Biological Chemistry 261(1) 50-53 1986
Retroviral transfer of the human glucocerebrosidase gene to Gaucher fibroblasts. (共著)
Lysosomal sialidase deficiency in sialidosis with partial β-galactosidase deficiency. (共著)
Biochimica et Biophysica Acta 755,106-111 1983
Fatty acid elongation activity in fibroblasts from patients with adrenoleukodystrophy(ALD). (共著)
Journal of Biochemistry 96,1241-1247 1984
Carrier detection of sialidosis with partial β-galactosidase deficiency by the assay of lysosomal sialidase in lymphocytes. (共著)
Annals of Neurology 15(2) 181-182 1984
Adrenoleukodystrophy : a clinical variant presenting as olivopontocerebellar atrophy. (共著)
Journal of Neurology 231(4) 167-169 1984
Sialidosis with partial β-galactosidase deficiency (galactosialidosis). (共著)
International Journal of Neurology 18(1-2-3-4) 138-150 1984
Type 3(adult) GM1 gangliosidosis : Case report. (共著)
Neurology 35(10) 1490-1494 1985
Coenzyme Q10, iron, and vitamin B6 therapy in genetically-confirmed Alzheimer's disease. (共著)
Lancet 340(8820) 671 1992
Molecular cloning of human growth inhibitory factor cDNA and its down-regulation in Alzheimer's disease. (共著)
The EMBO Journal 11(13) 4843-4850 1992
Genomic organization of a cDNA(QM)demonstrating an altered mRNA level in nontumorigenic Wilms' microcell hybrid cells and its location to Xq28. (共著)
Human Molecular Genetics 1(7) 529-533 1992
Interferon γ but not tumor necrosis factor α decreases susceptibility of human renal cell cancer cell lines to lymphokine-activated killer cells. (共著)
Cancer Immunology Immunotherapy 35,381-387 1992
Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy. (共著)
Neurology 42(12) 2300-2302 1992
Lymphocyte subsets in amyotrophic lateral sclerosis with motor conduction block. (共著)
Muscle & Nerve 16(1) 116-117 1993
Treatment of multifocal motor neuropathy with a high dosage of intravenous immunoglobulin. (共著)
Muscle & Nerve 16(2) 220-221 1993
Frequent presence of anti-GQ1b antibody in Fisher's syndrome. (共著)
Neurology 43(2) 414-417 1993
Stereotyped hand clasping : An unusual tardive movement disorder. (共著)
Movement disorders 8(2) 230-231 1993
The gene for Machado-Joseph disease maps to human chromosome 14q. (共著)
Nature Genetics 4(4) 300-304 1993
Isolation of 353 NotI linking clones and 62 DNA markers(DXS607-DXS668)from human chromosome Xq24-qter. (共著)
Cytogenetics and Cell Genetics 64,5-8 1993
Human leukocyte antigens in Fisher's syndrome. (共著)
Biochemical and Biophysical Research Communications 200(2) 695-703 1994
ApoE-ε4 and early-onset Alzheimer's disease. (共著)
Nature Genetics 7(1) 10-11 1994
Effect of intravenous immunoglobulin in Lambert-Eaton myasthenic syndrome with small-cell lung cancer : Correlation with the titer of anti-voltage-gated calcium channel antibody. (共著)
Dentatorubral-pallidoluysian atrophy and Haw River syndrome. (共著)
Lancet 344(8938) 1711-1712 1994
Passive transfer and active immunization with the recombinant leucine-zipper (Yo) protein as an attempt to establish an animal model of paraneoplastic cerebellar degeneration. (共著)
Journal of the Neurological Sciences 127(2) 153-158 1994
HLA antigens in paraneoplastic cerebellar degeneration associated with anti-Yo antibody. (共著)
Trial to establish an animal model of paraneoplastic cerebellar degeneration with anto-Yo antibody. 1. Mouse strains bearing different MHC molecules produce antibodies on immunization with recombinant Yo protein, but do not case Purkinje cell loss. (共著)
Clinical Neurology and Neurosurgery 97,95-100 1995
Trial to establish an animal model of paraneoplastic cerebellar degeneration with anti-Yo antibody. 2. Passive transfer of murine mononuclear cells activated with recombinant Yo protein to paraneoplastic cerebellar degeneration lymphocytes in severe co・・・
Clinical Neurology and Neurosurgery 97,101-105 1995
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The gene for hereditary progressive dystonia with marked diurnal fluctuation maps to chromosome 14q. (共著)
Molecular biology of Gaucher disease : therapeutic strategies utilizing recombinant DNA technology. (共著)
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Genetic heterogeneity in Gaucher disease : Identification of multiple allelic mutations and implications for therapeutic approaches utilizing gene transfer. (共著)
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Linkage analysis of hereditary progressive dystonia to the tyrosine hydroxylase gene locus. (共著)
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Mo1ecu1ar c1oning of human growth inhiditory Factor cDNA and its down-regu1ation in A1zheimer,disease.
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