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Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1988
Renal amyloidosis. Correlations between morphology, chemical types of amyloid protein and clinical features
H Shiiki, T Shimokama, Y Yoshikawa, et al.
Annals of Neurology
|
June 9, 1999
A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein
J A Hainfellner, P Parchi, T Kitamoto, et al.
Neuroscience
|
August 25, 2009
Changes in expression of sensory organ-specific microRNAs in rat dorsal root ganglia in association with mechanical hypersensitivity induced by spinal nerve ligation
B T Aldrich, E P Frakes, J Kasuya, et al.
Acta Neuropathologica
|
January 1, 1993
Widespread distribution of tau in the astrocytic elements of glial tumors
M Miyazono, T Iwaki, T Kitamoto, et al.
Clinical Molecular Pathology
|
June 1, 1996
Differential expression of CD44 variants among meningioma subtypes
S O Suzuki, T Iwaki, T Kitamoto, et al.
Acta Neuropathologica
|
January 1, 1991
Increased senile plaques without microglia in Alzheimer's disease
T Ohgami, T Kitamoto, R W Shin, et al.
The American Journal of Pathology
|
September 1, 1991
A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation
M Miyazono, T Iwaki, T Kitamoto, et al.
Biochemical and Biophysical Research Communications
|
March 15, 1993
Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome
T Kitamoto, M Ohta, K Doh-ura, et al.
The American Journal of Pathology
|
September 17, 1999
Interaction of aluminum with PHFtau in Alzheimer's disease neurofibrillary degeneration evidenced by desferrioxamine-assisted chelating autoclave method
H Murayama, R W Shin, J Higuchi, et al.
Neurology
|
February 1, 1994
Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene
I Inoue, T Kitamoto, K Doh-ura, et al.
Page
of 19
Search research articles
Search
Showing results (121-130 of 183) with videos related to
Sort By:
Page
of 19
Virchows Archiv. A, Pathological Anatomy and Histopathology
|
January 1, 1988
Renal amyloidosis. Correlations between morphology, chemical types of amyloid protein and clinical features
H Shiiki, T Shimokama, Y Yoshikawa, et al.
Annals of Neurology
|
June 9, 1999
A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein
J A Hainfellner, P Parchi, T Kitamoto, et al.
Neuroscience
|
August 25, 2009
Changes in expression of sensory organ-specific microRNAs in rat dorsal root ganglia in association with mechanical hypersensitivity induced by spinal nerve ligation
B T Aldrich, E P Frakes, J Kasuya, et al.
Acta Neuropathologica
|
January 1, 1993
Widespread distribution of tau in the astrocytic elements of glial tumors
M Miyazono, T Iwaki, T Kitamoto, et al.
Clinical Molecular Pathology
|
June 1, 1996
Differential expression of CD44 variants among meningioma subtypes
S O Suzuki, T Iwaki, T Kitamoto, et al.
Acta Neuropathologica
|
January 1, 1991
Increased senile plaques without microglia in Alzheimer's disease
T Ohgami, T Kitamoto, R W Shin, et al.
The American Journal of Pathology
|
September 1, 1991
A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation
M Miyazono, T Iwaki, T Kitamoto, et al.
Biochemical and Biophysical Research Communications
|
March 15, 1993
Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome
T Kitamoto, M Ohta, K Doh-ura, et al.
The American Journal of Pathology
|
September 17, 1999
Interaction of aluminum with PHFtau in Alzheimer's disease neurofibrillary degeneration evidenced by desferrioxamine-assisted chelating autoclave method
H Murayama, R W Shin, J Higuchi, et al.
Neurology
|
February 1, 1994
Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene
I Inoue, T Kitamoto, K Doh-ura, et al.
Page
of 19