• 4246 Citations
  • 38 h-Index
1987 …2020

Research output per year

If you made any changes in Pure these will be visible here soon.

Research Output

Filter
Letter
2020

Specific aspects of operating an unfamiliar touchscreen for individuals with autism spectrum disorders

Watanabe, T., Kumazaki, H., Muramatsu, T. & Mimura, M., 2020 Feb 1, In : Psychiatry and Clinical Neurosciences. 74, 2, p. 157-158 2 p.

Research output: Contribution to journalLetter

2019

Comedic experience with two robots aided a child with autism spectrum disorder to realize the importance of nonverbal communication

Kumazaki, H., Muramatsu, T., Yoshikawa, Y., Matsumoto, Y., Ishiguro, H., Sumiyoshi, T., Mimura, M. & Kikuchi, M., 2019 Jan 1, In : Psychiatry and Clinical Neurosciences.

Research output: Contribution to journalLetter

1 Citation (Scopus)
2017

Tele-operating an android robot to promote the understanding of facial expressions and to increase facial expressivity in individuals with autism spectrum disorder

Kumazaki, H., Muramatsu, T., Yoshikawa, Y., Matsumoto, Y., Miyao, M., Ishiguro, H., Mimura, M., Minabe, Y. & Kikuchi, M., 2017 Sep 1, In : American Journal of Psychiatry. 174, 9, p. 904-905 2 p.

Research output: Contribution to journalLetter

7 Citations (Scopus)
2005

Mitochondrial tRNA Leu(UUR) mutation at position 3243 detected in patients with type 1 diabetes

Suzuki, Y., Atsumi, Y., Matsuoka, K., Nishimaki, K., Ohta, S., Taniyama, M. & Muramatsu, T., 2005 Jan 1, In : Diabetes Research and Clinical Practice. 67, 1, p. 92-94 3 p.

Research output: Contribution to journalLetter

4 Citations (Scopus)
2004

Acute metabolic cataract as a first manifestation of diabetes mellitus in a 12-year-old girl [2]

Suzuki, Y., Atsumi, Y., Matsuoka, K., Nishimaki, Ohta, S., Taniyama, M. & Muramatsu, T., 2004 Mar 1, In : Diabetologia. 47, 3, p. 592-593 2 p.

Research output: Contribution to journalLetter

11 Citations (Scopus)

Lipoma and opthalmoplegia in mitochondrial diabetes associated with small heteroplasmy level of 3243 tRNALeu(UUR) mutation

Suzuki, Y., Nishimaki, K., Taniyama, M., Muramatsu, T., Atsumi, Y., Matsuoka, K. & Ohta, S., 2004 Mar, In : Diabetes Research and Clinical Practice. 63, 3, p. 225-229 5 p.

Research output: Contribution to journalLetter

17 Citations (Scopus)

Repeated clinical episodes of Wernicke-Korsakoff syndrome [3]

Moriyama, Y., Muramatsu, T., Kato, M., Kashima, H. & Mimura, M., 2004 Aug 1, In : Australian and New Zealand Journal of Psychiatry. 38, 8, 1 p.

Research output: Contribution to journalLetter

3 Citations (Scopus)
2003

Aldehyde dehydrogenase 2 genotype in type 1 diabetes mellitus [1]

Suzuki, Y., Matsuura, N., Suzuki, S., Muramatsu, T., Taniyama, M., Ohta, S., Higuchi, S., Tsukahara, M., Atusmi, Y. & Matsuoka, K., 2003 May 1, In : Diabetes Research and Clinical Practice. 60, 2, p. 139-141 3 p.

Research output: Contribution to journalLetter

3 Citations (Scopus)

Maternal inheritance of diabetes is associated with inactive ALDH2 genotype in diabetics with renal failure in Japanese [2]

Suzuki, Y., Kuriyama, S., Atsumi, Y., Murata, C., Matsuoka, K., Taniyama, M., Muramatsu, T. & Ohta, S., 2003 May 1, In : Diabetes Research and Clinical Practice. 60, 2, p. 143-145 3 p.

Research output: Contribution to journalLetter

5 Citations (Scopus)

Mitochondrial tRNALeu(UUR) mutation at position 3243 and symptomatic polyneuropathy in type 2 diabetes [4]

Suzuki, Y., Taniyama, M., Muramatsu, T., Ohta, S., Murata, C., Atsumi, Y. & Matsuoka, K., 2003 Apr 1, In : Diabetes care. 26, 4, p. 1315-1316 2 p.

Research output: Contribution to journalLetter

8 Citations (Scopus)

Multiple cranial mononeuropathies with acetylcholine receptor antibody in mitochondrial diabetes [6]

Suzuki, Y., Suzuki, S., Taniyama, M., Muramatsu, T., Ohta, S., Oka, Y., Atsumi, Y. & Matsuoka, K., 2003 Apr 1, In : Diabetes care. 26, 4, 1 p.

Research output: Contribution to journalLetter

2 Citations (Scopus)

Multiple tumors in mitochondrial diabetes associated with tRNAleu(UUR) mutation at position 3264 [4]

Suzuki, Y., Suzuki, S., Taniyama, M., Muramatsu, T., Ohta, S., Oka, Y., Atsumi, Y. & Matsuoka, K., 2003 Jun 1, In : Diabetes care. 26, 6, p. 1942-1943 2 p.

Research output: Contribution to journalLetter

4 Citations (Scopus)

Vasculopathy and alcohol tolerance trait in type 2 diabetes [2]

Suzuki, Y., Taniyama, M., Muramatsu, T., Higuchi, S., Ohta, S., Atsumi, Y. & Matsuoka, K., 2003 Jan 1, In : Diabetes care. 26, 1, p. 246-247 2 p.

Research output: Contribution to journalLetter

2 Citations (Scopus)
1997

No association of ALDH2 genotype in MELAS

Suzuki, Y., Muramatsu, T., Taniyama, M., Goto, Y. I., Oka, Y., Suzuki, S., Tsukuda, K., Atsumi, Y., Nonaka, I., Hosokawa, K., Shimada, A., Asahima, T., Matsuoka, K. & Maassen, J. A., 1997 Oct 14, In : Diabetologia. 40, 10, p. 1241-1242 2 p.

Research output: Contribution to journalLetter

2 Citations (Scopus)

The frequency of the methylenetetrahydrofolate reductase-gene mutation varies with age in the normal population [6]

Matsushita, S., Muramatsu, T., Arai, H., Matsui, T. & Higuchi, S., 1997 Jan 1, In : American Journal of Human Genetics. 61, 6, p. 1459-1460 2 p.

Research output: Contribution to journalLetter

43 Citations (Scopus)
1996

Lack of association of apolipoprotein E epsilon 4 allele with progressive supranuclear palsy.

Arai, H., Higuchi, S., Muramatsu, T., Matsushita, S., Itabashi, S. & Sasaki, H., 1996 Jun 1, In : Neurodegeneration : a journal for neurodegenerative disorders, neuroprotection, and neuroregeneration. 5, 2, p. 194-195 2 p.

Research output: Contribution to journalLetter

8 Citations (Scopus)

Presenilin-1 polymorphism and Alzheimer's disease [6]

Kehoe, P., Williams, J., Lovestone, S., Wilcock, G., Owen, M. J., Holmans, P., Liddell, M., Holmes, C., Powall, J., Neal, J., Bouras, C., Giannakopoulos, P., Schioi, J., Tezapsidis, N., Robakis, N. K., Higuchi, S., Muramatsu, T., Matsushita, S. & Arai, H., 1996 Jan 1, In : Lancet. 347, 9009, p. 185-187 3 p.

Research output: Contribution to journalLetter

S182 and STM2 gene missense mutations in sporadic Alzheimer disease.

Higuchi, S., Matsushita, S., Hasegawa, Y., Muramatsu, T., Itabashi, S. & Arai, H., 1996 Jul 26, In : American journal of medical genetics. 67, 4, 1 p.

Research output: Contribution to journalLetter

6 Citations (Scopus)
1994

Apolipoprotein E gene in diffuse Lewy body disease with or without co-existing Alzheimer's disease

Arai, H., Higuchi, S., Muramatsu, T., Iwatsubo, T., Sasaki, H. & Trojanowski, J. Q., 1994 Nov 5, In : The Lancet. 344, 8932, 1 p.

Research output: Contribution to journalLetter

52 Citations (Scopus)

Apolipoprotein E gene in Parkinson's disease with or without dementia

Arai, H., Muramatsu, T., Higuchi, S., Sasaki, H. & Trojanowski, J. Q., 1994 Sep 24, In : The Lancet. 344, 8926, 1 p.

Research output: Contribution to journalLetter

51 Citations (Scopus)
1987

ETHANOL PATCH TEST FOR LOW Km ALDEHYDE DEHYDROGENASE DEFICIENCY

Higuchi, S., Muramatsu, T., Saito, M., Sasao, M., Maruyama, K., Kono, H. & Niimi, Y., 1987 Mar 14, In : The Lancet. 329, 8533, 1 p.

Research output: Contribution to journalLetter

26 Citations (Scopus)