Takeshi Sato

发表

Association of an 11-12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases.

Tomoyuki N. Tanaka, S. Mohri, J. Ironside, 2003, The Journal of general virology.

Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment

L. Schonberger, P. Brown, R. Will, 2012, Emerging infectious diseases.

Mitochondrial encephalomyopathy (MELAS): Pathological study and successful therapy with coenzyme Q10 and idebenone

S. Kuroda, T. Shirabe, R. Namba, 1989, Journal of the Neurological Sciences.

The risk of iatrogenic Creutzfeldt‐Jakob disease through medical and surgical procedures

H. Mizusawa, Yosikazu Nakamura, M. Noguchi-Shinohara, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

Suppression of experimental autoimmune myasthenia gravis with new immunosuppressants: 15-deoxyspergualin and actinobolin

T. Aoyagi, K. Hayashi, Takeshi Sato, 1992, Journal of the Neurological Sciences.

M. Masuda, Takeshi Sato, 2007, Nihon rinsho. Japanese journal of clinical medicine.

Ophthalmic Surgery in Prion Diseases

H. Mizusawa, Yosikazu Nakamura, M. Noguchi-Shinohara, 2007, Emerging infectious diseases.

Extensive hemispheric lesions with radiological evidence of blood–brain barrier integrity in a patient with neuromyelitis optica

N. Hattori, S. Kawajiri, S. Saiki, 2009, Journal of the Neurological Sciences.

Mitochondrial Myopathies: Morphological Approach to Molecular Abnormalities

S. Horai, T. Ozawa, Shinji Nakamura, 1990 .

Iatrogenic Creutzfeldt–Jakob disease

P. Brown, J. Brandel, Takeshi Sato, 2006, Neurology.

Medical Procedures and Risk for Sporadic Creutzfeldt-Jakob Disease, Japan, 1999–2008

H. Mizusawa, Yosikazu Nakamura, M. Noguchi-Shinohara, 2009, Emerging infectious diseases.

Treatment of Experimental Allergic Myasthenia Gravis with a New Immunosuppressant: 15‐Deoxyspergualin a

K. Hayashi, Takeshi Sato, Y. Ishigaki, 1988 .

Neuropathology of Methylmercury Intoxication

Yasunori Nakamura, Takeshi Sato, 1991 .

Prospective 10-year surveillance of human prion diseases in Japan.

Y. Kuroiwa, M. Takeda, Y. Shiga, 2010, Brain : a journal of neurology.

Antifilamin, antivinculin, and antitropomyosin antibodies in myasthenia gravis

H. Sugita, Takeshi Sato, Takeshi Yamamoto, 1987, Neurology.

Angiographic Appearance of Glionlas of the Lateral Ventricle

J. Ito, K. Ueki, Takeshi Sato, 1976 .

Dura mater graft‐associated Creutzfeldt‐Jakob disease in Japan: Clinicopathological and molecular characterization of the two distinct subtypes

H. Mizusawa, Yosikazu Nakamura, M. Noguchi-Shinohara, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

[Prion disease surveillance in Japan: analysis of 1,241 patients].

H. Mizusawa, Yosikazu Nakamura, M. Noguchi-Shinohara, 2009, Rinsho shinkeigaku = Clinical neurology.

MELAS without Ragged Red Fibers or Lactic Acidosis Diagnosed by Mitochondrial DNA Testing

H. Ujike, S. Otsuki, I. Kohira, 1993, The Japanese journal of psychiatry and neurology.

Tau aggregation and seeding analyses of two novel MAPT variants found in patients with motor neuron disease and progressive parkinsonism

N. Hattori, T. Hatano, N. Ito, 2019, Neurobiology of Aging.

Survey of parasite helminths in the mongoose on Okinawajima Island.

O. Ishibashi, M. Asakawa, G. Ogura, 2010 .

Hirano bodies in the axon of peripheral nerves in a case with progressive external ophthalmoplegia with multisystemic involvements

Y. Yamamura, F. Ikuta, T. Atsumi, 2004, Acta Neuropathologica.

Clinical effects of MND-19 (Inosiplex) on subacute sclerosing panencephalitis — A multi-institutional collaborative study—

K. Takeshita, S. Matsumoto, K. Nihei, 1987, Brain and Development.

Creutzfeldt–Jakob disease associated with cadaveric dura mater grafts in Japan

T. Sato, H. Yanagawa, H. Yoshino, 2000, Neurology.

Clinical features and diagnosis of dura mater graft–associated Creutzfeldt–Jakob disease

T. Sato, H. Mizusawa, M. Noguchi-Shinohara, 2007, Neurology.

Iatrogenic Creutzfeldt–Jakob disease at the millennium

L. McShane, I. Zerr, T. Sato, 2000, Neurology.

Chronic polymyositis and myxovirus-like inclusions. Electron microscopic and viral studies.

D. Walker, D. Walker, T. Sato, 1971, Archives of neurology.

Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease

T. Sato, Y. Shiga, H. Mizusawa, 2005, Neurology.

Immunoadsorption therapy for myasthenia gravis.

M. Osame, N. Shibuya, T. Sato, 1994, Journal of neurology, neurosurgery, and psychiatry.

[Infectious prion disease: CJD with dura mater transplantation].

Takeshi Sato, 2003, Rinsho shinkeigaku = Clinical neurology.

Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting.

T. Sato, S. Shimizu, J. Ironside, 1999, Archives of neurology.