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T Kitamoto

Showing results (111-120 of 183) with videos related to

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Gut|October 1, 1993
Intestinal pseudo-obstruction in patients with amyloidosis: clinicopathologic differences between chemical types of amyloid proteinS Tada, M Iida, T Yao, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|June 9, 2001
Severe brain atrophy in a case of thalamic variant of sporadic CJD with plaque-like PrP depositionM Yamashita, T Yamamoto, K Nishinaka, et al.
Cancer|December 15, 1994
MIB1 staining index and scoring of histologic features in meningioma. Indicators for the prediction of biologic potential and postoperative managementM Ohta, T Iwaki, T Kitamoto, et al.
FEMS Immunology and Medical Microbiology|April 29, 1999
A chicken monoclonal antibody with specificity for the N-terminal of human prion proteinH Matsuda, H Mitsuda, N Nakamura, et al.
Neurology|November 24, 2004
Creutzfeldt-Jakob disease with a novel insertion and codon 219 Lys/Lys polymorphism in PRNPY Nishida, N Sodeyama, Y Toru, et al.
Acta Neuropathologica|January 1, 1992
Creutzfeldt-Jakob disease with amyloid angiopathy: diagnosis by immunological analyses and transmission experimentsJ Tateishi, T Kitamoto, K Doh-ura, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1984
Neck-abdominal reflexH Shibasaki, M Nakashima, R Neshige, et al.
Neurosurgery|September 1, 1988
Choroid plexus papillomas: an immunohistochemical study with particular reference to the coexpression of prealbuminT Matsushima, T Inoue, I Takeshita, et al.
Neurosurgery|April 1, 1994
Creutzfeldt-Jakob disease transmitted by a cadaveric dura mater graftS Yamada, T Aiba, Y Endo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2004
MRI characteristics of sporadic CJD with valine homozygosity at codon 129 of the prion protein gene and PrPSc type 2 in JapanR Fukushima, Y Shiga, M Nakamura, et al.
Pageof 19

Showing results (111-120 of 183) with videos related to

Sort By:
Pageof 19
Gut|October 1, 1993
Intestinal pseudo-obstruction in patients with amyloidosis: clinicopathologic differences between chemical types of amyloid proteinS Tada, M Iida, T Yao, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|June 9, 2001
Severe brain atrophy in a case of thalamic variant of sporadic CJD with plaque-like PrP depositionM Yamashita, T Yamamoto, K Nishinaka, et al.
Cancer|December 15, 1994
MIB1 staining index and scoring of histologic features in meningioma. Indicators for the prediction of biologic potential and postoperative managementM Ohta, T Iwaki, T Kitamoto, et al.
FEMS Immunology and Medical Microbiology|April 29, 1999
A chicken monoclonal antibody with specificity for the N-terminal of human prion proteinH Matsuda, H Mitsuda, N Nakamura, et al.
Neurology|November 24, 2004
Creutzfeldt-Jakob disease with a novel insertion and codon 219 Lys/Lys polymorphism in PRNPY Nishida, N Sodeyama, Y Toru, et al.
Acta Neuropathologica|January 1, 1992
Creutzfeldt-Jakob disease with amyloid angiopathy: diagnosis by immunological analyses and transmission experimentsJ Tateishi, T Kitamoto, K Doh-ura, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1984
Neck-abdominal reflexH Shibasaki, M Nakashima, R Neshige, et al.
Neurosurgery|September 1, 1988
Choroid plexus papillomas: an immunohistochemical study with particular reference to the coexpression of prealbuminT Matsushima, T Inoue, I Takeshita, et al.
Neurosurgery|April 1, 1994
Creutzfeldt-Jakob disease transmitted by a cadaveric dura mater graftS Yamada, T Aiba, Y Endo, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2004
MRI characteristics of sporadic CJD with valine homozygosity at codon 129 of the prion protein gene and PrPSc type 2 in JapanR Fukushima, Y Shiga, M Nakamura, et al.
Pageof 19