S. Kato

K. Nakashima, Y. Adachi, S. Kato, 2000, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.

Ultrastructure of spinal anterior horn cells in human Niemann‐Pick type C (NPC) patient and mouse model of NPC with retroposon insertion in NPC1 genes

Masako Kato, S. Kato, H. Ninomiya, 2020, Pathology international.

Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions: an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation

S. Sakoda, Masako Kato, H. Fujimura, 2001, Acta Neuropathologica.

Neuropathological study on 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine of the crab-eating monkey

S. Kato, K. Takada, H. Nakamura, 2004, Acta Neuropathologica.

Altered Expression of Cardiac Ankyrin Repeat Protein and Its Homologue, Ankyrin Repeat Protein with PEST and Proline-Rich Region, in Atrophic Muscles in Amyotrophic Lateral Sclerosis

M. Fukayama, S. Mori, M. Osaki, 2003, Pathobiology.

The immunohistochemical expression of stress-response protein (srp) 60 in human brain tumours: relationship of srp 60 to the other five srps, proliferating cell nuclear antigen and p53 protein.

E. Ohama, A. Hirano, S. Kato, 2001, Histology and histopathology.

Localization of a mutant SOD1 protein in E40K-heterozygous dogs: Implications for non-cell-autonomous pathogenesis of degenerative myelopathy

H. Sakai, Y. Kobatake, S. Kato, 2017, Journal of the Neurological Sciences.

Pathological characterization of astrocytic hyaline inclusions in familial amyotrophic lateral sclerosis.

K. Nakashima, Masako Kato, E. Nanba, 1997, The American journal of pathology.

New Strategy That Delays Progression of Amyotrophic Lateral Sclerosis in G1H-G93A Transgenic Mice: Oral Administration of Xanthine Oxidoreductase Inhibitors That Are Not Substrates for the Purine Salvage Pathway

Masako Kato, S. Kato, T. Nishino, 2016, Journal of neuropathology and experimental neurology.

Formation of advanced glycation end‐product‐modified superoxide dismutase‐1 (SOD1) is one of the mechanisms responsible for inclusions common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutation, and transgenic mice expressing human SOD1 gene mutation

K. Nakashima, S. Sakoda, Masako Kato, 2001 .

Familial amyotrophic lateral sclerosis with His46Arg mutation in Cu/Zn superoxide dismutase presenting characteristic clinical features and Lewy body-like hyaline inclusions

S. Yazawa, K. Nabeshima, S. Kato, 2004, Journal of the Neurological Sciences.

Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1.

L. Bruijn, S. D. Anderson, D. Cleveland, 1998, Science.

Immunohistochemical analysis of copper chaperone for superoxide dismutase in mouse central nervous system; a comparative study with paraffin and frozen section

S. Sakoda, H. Fujimura, E. Ohama, 2002 .

Familial amyotrophic lateral sclerosis with a two base pair deletion in superoxide dismutase 1: gene multisystem degeneration with intracytoplasmic hyaline inclusions in astrocytes.

K. Nakashima, E. Ohama, S. Kato, 1996, Journal of neuropathology and experimental neurology.

Immunohistochemical studies on the new type of astrocytic inclusions identified in a patient with brain malformation

T. Umahara, F. Herz, A. Hirano, 2004, Acta Neuropathologica.

Involvement of the brain stem reticular formation in familial amyotrophic lateral sclerosis.

A. Hirano, S. Kato, 1992, Clinical neuropathology.

Astrocytic hyaline inclusions contain advanced glycation endproducts in familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutation: immunohistochemical and immunoelectron microscopical analyses

K. Nakashima, Masako Kato, N. Shibata, 1999, Acta Neuropathologica.

Development of a rat model of amyotrophic lateral sclerosis expressing a human SOD1 transgene

Y. Itoyama, M. Aoki, S. Kato, 2005, Neuropathology : official journal of the Japanese Society of Neuropathology.

Motoneuron degeneration after facial nerve avulsion is exacerbated in presymptomatic transgenic rats expressing human mutant Cu/Zn superoxide dismutase

Y. Itoyama, Y. Hayashi, M. Aoki, 2005, Journal of neuroscience research.

Ultrastructural and ultracytochemical studies on the blood-brain barrier in chronic relapsing experimental allergic encephalomyelitis

S. Kato, H. Nakamura, 2004, Acta Neuropathologica.

Ultracytochemical localization of alkaline phosphatase activity in endothelial cells in chronic relapsing experimental allergic encephalomyelitis

S. Kato, H. Nakamura, 2004, Acta Neuropathologica.

Suppression of relapsing experimental allergic encephalomyelitis by mizoribine: Clinical, histological and immunohistochemical studies

E. Ohama, S. Kato, Y. Hosoda, 1996 .

Ubiquitin and phosphorylated neurofilament epitopes in ballooned neurons of the extraocular muscle nuclei in a case of Werdnig-Hoffmann disease

A. Hirano, S. Kato, 1990, Acta Neuropathologica.

Non‐neoplastic glandular structures in a benign peripheral nerve sheath tumor

T. Kusumi, T. Kurita, S. Kato, 2001, Pathology international.

Suppression of acute experimental allergic encephalomyelitis by neurotropin: clinical, histopathologic, immunologic and immunohistochemical studies

S. Kato, Haruomi Nakamura, M. Naiki, 1991, Journal of Neuroimmunology.

Systemic administration of lipopolysaccharide upregulates angiotensin II expression in rat renal tubules: Immunohistochemical and ELISA studies

Mika Fukada, K. Yamaguchi, S. Kato, 2005, Peptides.

Expression of stress-response protein 60 in iritis associated with experimental autoimmune encephalomyelitis.

E. Ohama, S. Kato, T. Kumagami, 1999, Japanese journal of ophthalmology.

Ossified Metaplastic Spinal Meningioma Without Psammomatous Calcification: A Case Report.

S. Tanishima, H. Nagashima, S. Kato, 2019, Yonago acta medica.

Familiar amyotrophic lateral sclerosis (FALS)-linked SOD1 mutation accelerates neuronal cell death by activating cleavage of caspase-4 under ER stress in an in vitro model of FALS

M. Tohyama, Y. Koyama, T. Katayama, 2010, Neurochemistry International.

Endosomal Accumulation of Toll-Like Receptor 4 Causes Constitutive Secretion of Cytokines and Activation of Signal Transducers and Activators of Transcription in Niemann–Pick Disease Type C (NPC) Fibroblasts: A Potential Basis for Glial Cell Activation in the NPC Brain

Y. Ioannou, Y. Ohsaki, Michitaka Suzuki, 2007, The Journal of Neuroscience.

Stress-response (heat-shock) protein 90 expression in tumors of the central nervous system: an immunohistochemical study

T. Takenaka, E. Ohama, F. Herz, 2004, Acta Neuropathologica.

Suppression of acute experimental allergic encephalomyelitis by synthetic serum thymic factor

S. Kato, H. Nakamura, 1988, Acta Neuropathologica.

Localization of adenosine triphosphatase activity of the endothelia in chronic relapsing experimental allergic encephalomyelitis

S. Kato, Haruomi Nakamura, 1987, Journal of Neuroimmunology.

Neuroaxonal Dystrophy in Calcium-Independent Phospholipase A2β Deficiency Results from Insufficient Remodeling and Degeneration of Mitochondrial and Presynaptic Membranes

S. Sakoda, M. Setou, Y. Tsujimoto, 2011, The Journal of Neuroscience.

Stress-response (heat-shock) protein 72 expression in tumors of the central nervous system: an immunohistochemical investigation

E. Ohama, F. Herz, A. Hirano, 1992, Acta Neuropathologica.

Immunohistochemical localization of truncated midkine in developing human bile ducts.

T. Terada, T. Shinozawa, S. Kato, 2003, Histology and histopathology.

Immunohistochemical and In Situ Hybridization Analyses of Midkine Expression in Thyroid Papillary Carcinoma

T. Terada, Masako Kato, T. Shinozawa, 2000, Modern Pathology.

Increased midkine expression in hepatocellular carcinoma.

T. Terada, T. Shinozawa, A. Awaya, 2000, Archives of pathology & laboratory medicine.

Monoclonal antibody to stage-specific fetal brain 68-kDa glycoprotein (FGP68) revealed increased FGP68 expression in human primary brain tumors

Masako Kato, T. Shinozawa, A. Awaya, 2002, Acta Neuropathologica.

Inverse correlation between the formation of mitochondria-derived vacuoles and Lewy-body-like hyaline inclusions in G93A superoxide-dismutase-transgenic mice

S. Sakoda, H. Fujimura, S. Kato, 2006, Acta Neuropathologica.

NEDL1, a Novel Ubiquitin-protein Isopeptide Ligase for Dishevelled-1, Targets Mutant Superoxide Dismutase-1*

Y. Itoyama, T. Goto, A. Nakagawara, 2004, Journal of Biological Chemistry.

Prognostic significance of sirtuin 2 protein nuclear localization in glioma: an immunohistochemical study.

M. Oshimura, M. Osaki, H. Kamitani, 2012, Oncology reports.

Massive Lung Metastasis from Cerebellar Medulloblastoma: a Report on One Case and Review of Literature

H. Hayashi, E. Ohama, S. Kato, 1997 .

Presence of two different fibril subtypes in the Pick body: an immunoelectron microscopic study

S. Kato, H. Nakamura, 2004, Acta Neuropathologica.

Cerebellar Ganglioglioma in Childhood: Histopathologic Implications for Management During Long-term Survival: A Case Report.

Y. Maegaki, S. Kato, Yoshiaki Saito, 2017, Yonago acta medica.

Divergent effects of hyperosmolality on stress-response (heat shock) protein expression in cultured human tumor cells: an immunocytochemical study

F. Herz, S. Kato, M. Kato, 1994, Experientia.

Nonoxidative protein glycation is implicated in familial amyotrophic lateral sclerosis with superoxide dismutase-1 mutation

N. Shibata, S. Horiuchi, R. Nagai, 2000, Acta Neuropathologica.

New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: Inclusions containing SOD1 in neurons and astrocytes

Kenji Nakashima, Eisaku Ohama, Shinsuke Kato, 2000, Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases.

Immunohistochemical and ultrastructural evidence for the pathogenesis of white matter degeneration in patients with panencephalopathic‐type Creutzfeldt–Jakob disease: Inducible nitric oxide synthase overexpression in bizarre astrocytes

Masako Kato, S. Kato, Kiyota Kato, 2020, Neuropathology : official journal of the Japanese Society of Neuropathology.

Ultrastructural and immunohistochemical studies on ballooned cortical neurons in Creutzfeldt-Jakob disease: expression of αB-crystallin, ubiquitin and stress-response protein 27

T. Umahara, E. Ohama, F. Herz, 2004, Acta Neuropathologica.

Pathologic Reappraisal of Wallenberg Syndrome: A Pathologic Distribution Study and Analysis of Literature

Masako Kato, S. Ishihara, S. Kato, 2014, Yonago acta medica.

Amyotrophic Lateral Sclerosis, Primary Lateral Sclerosis and Spinal Muscular Atrophy

T. Hortobágyi, M. Strong, K. Okamoto, 2011 .

Divergent expression of midkine in the human fetal liver and kidney: immunohistochemical analysis of developmental changes in hilar primitive bile ducts and hepatocytes.

T. Terada, T. Shinozawa, S. Kato, 2000, Liver.

Nuclear TAR DNA Binding Protein 43 Expression in Spinal Cord Neurons Correlates With the Clinical Course in Amyotrophic Lateral Sclerosis

S. Sakoda, H. Fujimura, S. Kato, 2009, Journal of neuropathology and experimental neurology.

Amyotrophic lateral sclerosis models and human neuropathology: similarities and differences

S. Kato, 2007, Acta Neuropathologica.

Reappraisal of neurofibrillary tangles

E. Otomo, S. Kato, H. Nakamura, 1989, Acta Neuropathologica.

Alterations in renal iron metabolism caused by a copper/zinc-superoxide dismutase deficiency

Keiichiro Suzuki, N. Fujiwara, Haruhiko Sakiyama, 2012, Free radical research.

Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutation

K. Nakashima, Masako Kato, N. Shibata, 2000, Acta Neuropathologica.

High expression of α-synuclein in damaged mitochondria with PLA2G6 dysfunction

S. Sakoda, Y. Tsujimoto, H. Fujimura, 2016, Acta neuropathologica communications.

Autopsy case of spinocerebellar ataxia type 31 with severe dementia at the terminal stage

K. Nakashima, Y. Adachi, S. Kato, 2015, Neuropathology : official journal of the Japanese Society of Neuropathology.

Cerebellar Expression of Copper Chaperone for Superoxide, Cytosolic Cu/Zn-Superoxide Dismutase, 4-Hydroxy-2-Nonenal, Acrolein and Heat Shock Protein 32 in Patients with Menkes Kinky Hair Disease: Immunohistochemical Study

K. Hayashi, Masako Kato, A. Hirano, 2014, Yonago acta medica.

High expression of α-synuclein in damaged mitochondria with PLA2G6 dysfunction

S. Sakoda, Y. Tsujimoto, Mari Yoshida, 2016, Acta Neuropathologica Communications.

Mutant SOD1 impairs axonal transport of choline acetyltransferase and acetylcholine release by sequestering KAP3

R. Takahashi, N. Nukina, T. Araki, 2008, Neuroscience Research.

Demonstration of β amyloid protein‐containing neurofibrillary tangles in parkinsonism‐dementia complex on Guam

H. Ito, S. Yen, A. Hirano, 1991, Neuropathology and applied neurobiology.

Expression of stress-response protein 60 in lens epithelial cells in atopic cataract.

E. Ohama, S. Kato, A. Tamai, 1999, Japanese journal of ophthalmology.

Comparative immunohistochemical study on the expression of αB crystallin, ubiquitin and stress‐response protein 27 in ballooned neurons in various disorders

T. Umahara, E. Ohama, F. Herz, 1992, Neuropathology and applied neurobiology.

Cytoplasmic argyrophilic inclusions in neurons of pontine nuclei in patients with olivopontocerebellar atrophy: immunohistochemical and ultrastructural studies

S. Kato, H. Nakamura, Shinsuke Kato, 2004, Acta Neuropathologica.

Purkinje cells in olivopontocerebellar atrophy and granule cell-type cerebellar degeneration: an immunohistochemical study

K. Mikoshiba, S. Yen, E. Ohama, 1998, Acta Neuropathologica.

Immunohistochemical Studies on Cerebellar Purkinje Cells of Patients with Menkes' Kinky Hair Disease

K. Mikoshiba, S. Yen, E. Ohama, 1993 .

Demonstration of neurofibrillary tangles and neuropil thread-like structures in spinal cord white matter in parkinsonism-dementia complex on Guam and in Guamanian amyotrophic lateral sclerosis

T. Umahara, N. Shibata, S. Yen, 2004, Acta Neuropathologica.

Oxidative Modification to Cysteine Sulfonic Acid of Cys111 in Human Copper-Zinc Superoxide Dismutase*

Keiichiro Suzuki, N. Taniguchi, M. Nakano, 2007, Journal of Biological Chemistry.

Mutant SOD1 impairs axonal transport of choline acetyltransferase and acetylcholine release by sequestering KAP3

R. Takahashi, N. Nukina, T. Araki, 2008, Neuroscience Research.

Aberrant expression of a fetal glycoprotein 68 in hepatocellular carcinoma: a comparative study on the expression of alpha-fetoprotein and carcinoembryonic antigen.

T. Terada, T. Shinozawa, S. Kato, 2004, Histology and histopathology.

Individuals Exhibiting Conspicuous Nevi (Lentigo Simplex) Are Resistant to Allergic Rhinitis/Conjunctivitis (Pollinosis), but Those Who Do Not Show Increased Susceptibility to Pollinosis

Ken-ichi Watanabe, A. Awaya, S. Kato, 2003, Microbiology and immunology.

Mitochondria covered with a net of parallel and latticed filaments in nigral neurons of monkeys with experimental parkinsonism

S. Kato, H. Nakamura, J. Tanaka, 2004, Acta Neuropathologica.

Increased midkine expression in intrahepatic cholangiocarcinoma: immunohistochemical and in situ hybridization analyses.

K. Endo, T. Terada, T. Shinozawa, 2000, Liver.

Experimental Acute Dorsal Compression of Cat Spinal Cord: Correlation of Magnetic Resonance Signal Intensity With Spinal Cord Evoked Potentials and Morphology

E. Ohama, S. Kato, S. Kato, 1996, Spine.

FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS WITH A MUTATION IN THE Cu/Zn SUPEROXIDE DISMUTASE (SOD1) GENE: SIBLINGS HAVING ONE AND A HALF-YEAR and ELEVEN-YEAR CLINICAL COURSES

K. Nakashima, E. Ohama, S. Kato, 1995 .

Recent advances in research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 gene mutations: neuronal Lewy body-like hyaline inclusions and astrocytic hyaline inclusions.

E. Ohama, A. Hirano, S. Kato, 1999, Histology and histopathology.

Immunohistochemical Investigations on Cerebellar Purkinje Cells of Menkes' Kinky Hair Disease: Disappearance of Inositol 1, 4, 5‐Triphosphate Receptor Protein, and Expression of Phosphorylated Neurofilament Proteins, αB‐Crystallin and Stress‐response Proteins

K. Mikoshiba, E. Ohama, A. Hirano, 1993 .

Immunohistochemical and Ultrastructural Comparison between Neuronal and Oligodendroglial Inclusions in Olivopontocerebellar Atrophy

E. Ohama, S. Kato, 1993 .

Demonstration and distribution of tau‐positive glial coiled body‐like structures in white matter and white matter threads in early onset Alzheimer’s disease

T. Iwamoto, T. Umahara, N. Shibata, 2002, Neuropathology : official journal of the Japanese Society of Neuropathology.

Demonstration of neurofibrillary tangles in the indusium griseum and of axonal disturbances in sagittal sulcal lesions of the corpus callosum: An immunohistochemical investigation

T. Kawanami, T. Umahara, N. Shibata, 1996 .

Autopsy case of spinocerebellar ataxia type 31 with severe dementia at the terminal stage

K. Nakashima, Y. Adachi, S. Kato, 2015, Neuropathology : official journal of the Japanese Society of Neuropathology.

Colocalization of 14-3-3 Proteins with SOD1 in Lewy Body-Like Hyaline Inclusions in Familial Amyotrophic Lateral Sclerosis Cases and the Animal Model

S. Shimohama, R. Takahashi, Hidefumi Ito, 2011, PloS one.

Protective role of glutathione S-transferase A4 induced in copper/zinc-superoxide dismutase knockout mice.

Keiichiro Suzuki, N. Fujiwara, Haruhiko Sakiyama, 2009, Free radical biology & medicine.

S. Sakoda, Masako Kato, S. Horiuchi, 2001, Neuropathology : official journal of the Japanese Society of Neuropathology.

Cerebellar Ganglioglioma in Childhood: Histopathologic Implications for Management During Long-term Survival: A Case Report.

Y. Maegaki, S. Kato, Yoshiaki Saito, 2017, Yonago acta medica.

K. Hayashi, Masako Kato, A. Hirano, 2014, Yonago acta medica.

Ubiquitinated eosinophilic granules in the inferior olivary nucleus

A. Hirano, S. Kato, T. Suenaga, 1990, Neuropathology and applied neurobiology.

A pediatric intramedullary spinal cord tumor with unusual solid‐cystic and papillary features: A case report

K. Hayashi, Takashi Watanabe, S. Kuwamoto, 2011, Neuropathology : official journal of the Japanese Society of Neuropathology.