藤田医科大学病院

研究成果 1994 2019

  • 3357 引用
  • 22 h指数
  • 106 Article
  • 8 Review article
  • 5 Letter
フィルター
Review article
2017
4 引用 (Scopus)

IQ·SPECT technology and its clinical applications using multicenter normal databases

Nakajima, K., Okuda, K., Momose, M., Matsuo, S., Kondo, C., Sarai, M., Shibutani, T., Onoguchi, M., Shimizu, T. & Vija, A. H., 01-11-2017, : : Annals of Nuclear Medicine. 31, 9, p. 649-659 11 p.

研究成果: Review article

Orbit
Databases
Technology
Perfusion
Gamma Cameras
2016
21 引用 (Scopus)
Dystroglycans
Therapeutic Human Experimentation
Glycosylation
Muscular Dystrophies
Walker-Warburg Syndrome
2013

[Fukuyama muscular dystrophy: elucidation of the gene and pathogenesis and approaches toward molecular targeting therapy].

Toda, T., Ikeda, M., Kanagawa, M. & Kobayashi, K., 01-01-2013, : : Unknown Journal. 85, 4, p. 253-260 8 p.

研究成果: Review article

Walker-Warburg Syndrome
Molecular Targeted Therapy
RNA Splicing
Genetic Testing
Genetic Predisposition to Disease
34 引用 (Scopus)

Coronary CT angiography and high-risk plaque morphology

Motoyama, S., Sarai, M., Narula, J. & Ozaki, Y., 18-02-2013, : : Cardiovascular Intervention and Therapeutics. 28, 1, p. 1-8 8 p.

研究成果: Review article

Acute Coronary Syndrome
Coronary Angiography
Angina Pectoris
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Blood Vessels
2009
4 引用 (Scopus)
Fatty Acids
Myocardial Infarction
Myocardial Ischemia
Single-Photon Emission-Computed Tomography
Perfusion
2007

The role of SPECT and MRI for pre and postoperative evaluation of childhood moyamoya disease: Case report and review of literature

Biswas, S. K., Toyama, H., Imizu, S., Odebode, T. O., Hattori, H., Kanamori, A., Sarai, M., Katada, K., Sano, H. & Hishida, H., 01-11-2007, : : Current Medical Imaging Reviews. 3, 4, p. 225-232 8 p.

研究成果: Review article

Moyamoya Disease
Single-Photon Emission-Computed Tomography
Angiography
Perfusion
Cerebrovascular Circulation
2005

Single gene disorder

Ikeda, M. & Kurahashi, H., 01-01-2005, : : Nippon rinsho. Japanese journal of clinical medicine. 63 Suppl 12, p. 57-63 7 p.

研究成果: Review article

Recessive Genes
Dominant Genes
X-Linked Genes
Inborn Genetic Diseases
Pedigree
2003
54 引用 (Scopus)

Fukuyama-type congenital muscular dystrophy (FCMD) and alpha-dystroglycanopathy.

Toda, T., Kobayashi, K., Takeda, S., Sasaki, J., Kurahashi, H., Kano, H., Tachikawa, M., Wang, F., Nagai, Y., Taniguchi, K., Ikeda, M., Sunada, Y., Terashima, T., Endo, T. & Matsumura, K., 01-01-2003, : : Congenital anomalies. 43, 2, p. 97-104 8 p.

研究成果: Review article

Walker-Warburg Syndrome
Dystroglycans
Muscular Dystrophies
Brain
Lissencephaly