J. Tateishi

发表

Immunohistochemical distribution of amyloid precursor protein during normal rat development.

M. Fukui, T. Iwaki, M. Ohta, 1993, Brain research. Developmental brain research.

Formalin fixed brains are useful for magnetic resonance imaging (MRI) study

T. Inoue, J. Tateishi, H. Nagara, 1987, Journal of the Neurological Sciences.

Morphometric Comparison of the Vulnerability of Peripheral Motor and Sensory Neurons in Amyotrophic Lateral Sclerosis

P. Dyck, J. Tateishi, Y. Kawamura, 1981, Journal of neuropathology and experimental neurology.

A morphometric study of myelinated fibers in the fifth lumbar ventral roots in patients with cerebrovascular diseases.

J. Tateishi, H. Nagara, A. Kondo, 1987, Clinical neuropathology.

Scrapie removal using Planova virus removal filters.

S. Mohri, M. R. Macnaughton, T. Kitamoto, 2001, Biologicals : journal of the International Association of Biological Standardization.

Radial component of central myelin in shiverer mouse

J. Tateishi, Kinuko Suzuki, H. Nagara, 1983, Brain Research.

Sense and antisense modification of glial alpha B-crystallin production results in alterations of stress fiber formation and thermoresistance

T. Iwaki, J. Goldman, J. Tateishi, 1994, The Journal of cell biology.

Neurotoxicity of adriamycin passed through the transiently disrupted blood-brain barrier by mannitol in the rat brain

M. Fukui, Tooru Inoue, J. Tateishi, 1987, Brain Research.

αB-Crystallin in C6 glioma cells supports their survival in elevated extracellular K+: the implication of a protective role of αB-crystallin accumulation in reactive glia

T. Iwaki, Y. Fukumaki, J. Tateishi, 1995, Brain Research.

Hydrated autoclave pretreatment enhances tau immunoreactivity in formalin-fixed normal and Alzheimer's disease brain tissues.

T. Iwaki, R. Shin, T. Kitamoto, 1991, Laboratory investigation; a journal of technical methods and pathology.

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

B. Ghetti, M. Goedert, M. Spillantini, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann‐Straussler‐Scheinker syndrome

Y. Sakaki, K. Doh-ura, J. Warter, 1990, Neurology.

Micro-anatomical study of the carotid cave

M. Fukui, T. Matsushima, Y. Natori, 2005, Acta Neurochirurgica.

Transient expression of glial fibrillary acidic protein in developing oligodendrocytes in vitro.

J. Tateishi, I. Takeshita, K. Kitamura, 1985, Brain research.

A comparative study of abnormal prion protein isoforms between Gerstmann-Sträussler-Scheinker syndrome and Creutzfeldt-Jakob disease

T. Iwaki, K. Doh-ura, J. Tateishi, 1998, Journal of the Neurological Sciences.

Creutzfeldt-Jakob disease with florid plaques after cadaveric dural graft in a Japanese woman

J. Tateishi, S. Takashima, Y. Taguchi, 1997, The Lancet.

Successful transmission of Creutzfeldt-Jakob disease from human to mouse verified by prion protein accumulation in mouse brains

T. Kitamoto, J. Tateishi, I. Goto, 1992, Brain Research.

Alzheimer's amyloid precursor protein-positive degenerative neurites exist even within kuru plaques not specific to Alzheimer's disease.

K. Beyreuther, T. Kitamoto, T. Ohgami, 1991, American Journal of Pathology.

N-terminal sequence of prion protein is also intergrated into kuru plaques in patients with Gerstmann-Stra¨ussler syndrome

K. Beyreuther, T. Kitamoto, J. Tateishi, 1991, Brain Research.

Organ distribution of proteinase-resistant prion protein in humans and mice with Creutzfeldt-Jakob disease.

S. Mohri, T. Kitamoto, J. Tateishi, 1989, The Journal of general virology.

Immunohistochemical verification of senile and kuru plaques in Creutzfeldt‐Jakob disease and the allied disease

Yuji Sato, T. Kitamoto, J. Tateishi, 1988, Annals of neurology.

Scrapie-associated fibrils (SAF) purification method yields amyloid proteins from systemic and cerebral amyloidosis

T. Kitamoto, J. Tateishi, Y. Sato, 1986, Bioscience reports.

Amyloid plaques in Creutzfeldt‐Jakob disease stain with prion protein antibodies

S. Prusiner, S. DeArmond, R. A. Barry, 1986, Annals of neurology.

The primary structure of the prion protein influences the distribution of abnormal prion protein in the central nervous system.

K. Doh-ura, M. Miyazono, T. Kitamoto, 1992, The American journal of pathology.

Distribution of prion protein in German patients with Creutzfeldt-Jakob disease is different from that in Japanese patients

K. Ogomori, T. Kitamoto, J. Tateishi, 1994, Acta Neuropathologica.

Serial MRI in early Creutzfeldt-Jacob disease with a point mutation of prion protein at codon 180

K. Shinoda, M. Sugino, T. Kitamoto, 1995, Neuroradiology.

Codon 219 lys allele of PRNP is not found in sporadic Creutzfeldt‐Jakob disease

R. Shin, T. Kitamoto, J. Tateishi, 1998, Annals of neurology.

New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome.

T. Kitamoto, J. Tateishi, H. Furukawa, 1995, Brain research. Molecular brain research.

Apolipoprotein E in Creutzfeldt-Jakob disease

M. Pericak-Vance, B. Hyman, I. Zerr, 1995, The Lancet.

The Original Gerstmann‐Sträussler‐Scheinker Family of Austria: Divergent Clinicopathological Phenotypes but Constant PrP Genotype

H. Budka, F. Seitelberger, P. Liberski, 1995, Brain pathology.

Inherited Prion Diseases and Transmission to Rodents

T. Kitamoto, J. Tateishi, 1995, Brain pathology.

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome.

Y. Sakaki, K. Doh-ura, T. Kitamoto, 1989, Biochemical and biophysical research communications.

Creutzfeldt-Jakob disease with amyloid angiopathy: diagnosis by immunological analyses and transmission experiments

K. Doh-ura, J. Peiffer, T. Kitamoto, 1992, Acta Neuropathologica.

Immunoreactivity of cerebral amyloidosis is enhanced by protein denaturation treatments

T. Kitamoto, J. Tateishi, R. Doi-Yi, 1991, Acta Neuropathologica.

Neuropathological features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann-Sträussler-Scheinker disease

T. Iwaki, K. Doh-ura, J. Tateishi, 2003, Acta Neuropathologica.

Human prion disease and human prion protein disease.

T. Kitamoto, J. Tateishi, Tetsuyuki Kitamoto, 1996, Current topics in microbiology and immunology.

Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study

M. Hoque, T. Kitamoto, J. Tateishi, 1996, Acta Neuropathologica.

A variant of Gerstmann-Sträussler-Scheinker disease carrying codon 105 mutation with codon 129 polymorphism of the prion protein gene: A clinicopathological study

E. Otomo, Y. Itoh, T. Kitamoto, 1994, Journal of the Neurological Sciences.

A new inherited prion disease (PrP‐P105L mutation) showing spastic paraparesis

T. Mizutani, T. Kitamoto, J. Tateishi, 1993, Annals of neurology.

EXPERIMENTAL TRANSMISSION OF CREUTZFELDT‐JAKOB DISEASE

J. Tateishi, M. Koga, R. Mori, 1981, Acta pathologica japonica.

Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies.

T. Kitamoto, J. Tateishi, 1988, The American journal of pathology.

Transmission of chronic spongiform encephalopathy with kuru plaques from humans to small rodents

M. Ohta, J. Tateishi, Y. Kuroiwa, 1979, Annals of neurology.

Gerstmann‐Sträussler‐Scheinker disease: Immunohistological and experimental studies

T. Kitamoto, J. Tateishi, Hirofumi Shii, 1988, Annals of neurology.

A three-sister sibship of Gerstmann-Sträussler-Scheinker disease with a CJD phenotype

P. Brown, P. Brown, L. Goldfarb, 2000, Neurology.

An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques.

T. Kitamoto, J. Tateishi, R. Iizuka, 1993, Biochemical and biophysical research communications.

Rosenthal fibers share epitopes with alpha B-crystallin, glial fibrillary acidic protein, and ubiquitin, but not with vimentin. Immunoelectron microscopy with colloidal gold.

T. Iwaki, J. Goldman, J. Tateishi, 1991, The American journal of pathology.

An immunohistochemical study of tissue transglutaminase in gliomas with reference to their cell dying processes.

T. Iwaki, M. Miyazono, J. Tateishi, 1994, The American journal of pathology.

Ferritin immunohistochemistry as a marker for microglia

T. Kitamoto, J. Tateishi, K. Yamaguchi, 2004, Acta Neuropathologica.

Adrenoleukodystrophy Progressed from Frontal Lobes –Clinico‐pathological, Electron Microscopic and Chemical Study of a Case–

M. Igarashi, J. Tateishi, C. Nakayama, 1980, Folia psychiatrica et neurologica japonica.

Increased tau accumulation in senile plaques as a hallmark in Alzheimer's disease.

R. Shin, K. Ogomori, T. Kitamoto, 1989, The American journal of pathology.

Massive accumulation of modified tau and severe depletion of normal tau characterize the cerebral cortex and white matter of Alzheimer's disease. Demonstration using the hydrated autoclaving method.

T. Iwaki, R. Shin, T. Kitamoto, 1992, The American journal of pathology.

Alpha B-crystallin in C6 glioma cells supports their survival in elevated extracellular K+: the implication of a protective role of alpha B-crystallin accumulation in reactive glia.

Y. Fukumaki, J. Tateishi, A. Iwaki, 1995, Brain research.

MIB1 staining index and scoring of histologic features in meningioma. Indicators for the prediction of biologic potential and postoperative management

M. Fukui, T. Kitamoto, J. Tateishi, 1994, Cancer.

Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease

K. Doh-ura, S. Mohri, T. Kitamoto, 1991, Journal of virology.

Alpha B-crystallin and 27-kd heat shock protein are regulated by stress conditions in the central nervous system and accumulate in Rosenthal fibers.

Y. Sakaki, T. Iwaki, J. Goldman, 1993, The American journal of pathology.

Mitochondrial encenhdomyopathy with lachte‐pyruvate elevation and brain infarctions

M. Osame, J. Tateishi, M. Kuriyama, 1984, Neurology.

Accumulation of αB-crystallin in brains of patients with Alexander's disease is not due to an abnormality of the 5′-flanking and coding sequence of the genomic DNA

Y. Sakaki, T. Iwaki, J. Goldman, 1992, Neuroscience Letters.

Proliferative activity and apoptosis of Langerhans histiocytes in eosinophilic granulomas as evaluated by MIB-1 and TUNEL methods

M. Fukui, T. Iwaki, Y. Hamada, 1995, Clinical molecular pathology.

Neuropathological Diagnostic Criteria for Creutzfeldt‐Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)

K. Jellinger, W. Schlote, P. Lantos, 1995, Brain pathology.

The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease.

T. Kitamoto, J. Tateishi, I. Goto, 1992, The American journal of pathology.

Neurofibrillary degeneration in a case of quadriplegia and myoclonic movement

A. Hirano, S. Otsuki, J. Tateishi, 1979, Acta Neuropathologica.

Subacute myelo‐optico‐neuropathy: Clioquinol intoxication in humans and animals

J. Tateishi, Jun Tateishi, 2000, Neuropathology : official journal of the Japanese Society of Neuropathology.

Accumulation of alpha B-crystallin in central nervous system glia and neurons in pathologic conditions.

T. Wisniewski, T. Iwaki, J. Goldman, 1992, The American journal of pathology.

Toxic myocardial damage due to intravenous phenytoin administration

M. Fukui, T. Iwaki, J. Tateishi, 1995, Histopathology.

TRANSMISSION OF CREUTZFELDT-JAKOB DISEASE FROM HUMAN BLOOD AND URINE INTO MICE

J. Tateishi, 1985, The Lancet.

Accumulation of abnormal prion protein in mice infected with Creutzfeldt-Jakob disease via intraperitoneal route: a sequential study.

T. Kitamoto, J. Tateishi, I. Goto, 1993, The American journal of pathology.

Transmission of human prion diseases to rodents

J. Tateishi, 1996 .

Short Communication The Primary Structure of the Prion Protein Influences the Distribution of Abnormal Prion Protein in the Central Nervous System

K. Doh-ura, M. Miyazono, T. Kitamoto, 2007 .

Diffuse deposition of immunohistochemically labeled prion protein in the granular layer of the cerebellum in a patient with Creutzfeldt-Jakob disease

H. Kretzschmar, T. Kitamoto, J. Tateishi, 1991, Acta Neuropathologica.

Morphogenesis of amyloid plaques in mice with Creutzfeldt-Jakob disease

J. Tateishi, H. Nagara, K. Hikita, 2004, Acta Neuropathologica.

A new method to classify amyloid fibril proteins

T. Kitamoto, J. Tateishi, H. Nagara, 2004, Acta Neuropathologica.

A Japanese case of Creutzfeldt-Jakob disease with a point mutation in the prion protein gene at codon 210

T. Kitamoto, J. Tateishi, H. Furukawa, 1996, Journal of the Neurological Sciences.

Filtration of PrP

T. Kitamoto, J. Tateishi, K. Yamaguchi, 1995 .

Species Barrier Prevents an Abnormal Isoform of Prion Protein from Accumulating in Follicular Dendritic Cells of Mice with Creutzfeldt-Jakob Disease

M. Hoque, T. Kitamoto, J. Tateishi, 1993, Journal of virology.

Host genetic control of incubation periods of Creutzfeldt-Jakob disease in mice.

S. Mohri, J. Tateishi, 1989, The Journal of general virology.

Subcellular Distribution of the Transmissible Agent in Creutzfeldt‐Jakob Disease Mouse Brain

K. Uchida, F. Taguchi, Y. Ohtani, 1989, Microbiology and immunology.

Congophilia in cerebral amyloidosis is modified by inactivation procedures on slow transmissible pathogens

Yuji Sato, T. Kitamoto, J. Tateishi, 1986, Brain Research.

Unconventional pathogens causing spongiform encephalopathies absent in blood products

J. Tateishi, S. Tsuji, S. Tsuji, 1985, Journal of medical virology.

Amyloid plaques in the brains of mice with Creutzfeldt–Jakob disease

J. Tateishi, H. Nagara, Y. Sato, 1984, Annals of neurology.

A missense mutation at codon 105 with codon 129 polymorphism of the prison protein gene in a new variant of Gerstmann‐Strässler‐Scheinker disease

T. Miyatake, K. Kaneko, E. Otomo, 1993, Neurology.

Tissue Handling in Suspected Creutzfeldt‐Jakob Disease (CJD) and Other Human Spongiform Encephalopathies (Prion Diseases)

W. Schlote, P. Lantos, J. Hauw, 1995, Brain pathology.

Experimental transmission of human subacute spongiform encephalopathy to small rodents

M. Ohta, J. Tateishi, H. Doi, 2004, Acta Neuropathologica.

Experimental transmission of human subacute spongiform encephalopathy to small rodents

J. Tateishi, H. Doi, Y. Kuroiwa, 2004, Acta Neuropathologica.

Cytoplasmic inclusions of astrocytic elements of glial tumors: special reference to round granulated body and eosinophilic hyaline droplets

M. Fukui, T. Iwaki, J. Tateishi, 2004, Acta Neuropathologica.

Rosenthal fibers and glial filaments associated with hemidesmosome‐like structures in perivascular astrocytes in a juvenile form of Alexander's disease

T. Iwaki, K. Ogomori, J. Tateishi, 1997 .

Immunohistochemical demonstration of alphaB-crystallin in hamartomas of tuberous sclerosis.

T. Iwaki, J. Tateishi, 1991, The American journal of pathology.

RETROGRADE AXOPLASMIC TRANSPORT I N RATS

A. Ohnishi, J. Tateishi, H. Nagara, 2002 .

NEUROTOXICITY IN PRIMARY SENSORY NEURONS OF ADRIAMYCIN ADMINISTERED THROUGH RETROGRADE AXOPLASMIC TRANSPORT IN RATS

A. Ohnishi, J. Tateishi, H. Nagara, 1987, Neuropathology and applied neurobiology.

Accumulation of Neurofilaments in a Sporadic Case of Amyotrophic Lateral Sclerosis

T. Iwaki, J. Tateishi, A. Kondo, 1986, The Japanese journal of psychiatry and neurology.

Anaplastic large cell ki-1 lymphoma in the central nervous system: Report of an autopsy case

M. Fukui, T. Iwaki, M. Miyazono, 2004, Acta Neuropathologica.

Multiple ring enhancement in a case of acute reversible demyelinating disease in childhood suggestive of acute multiple sclerosis

T. Matsuishi, J. Tateishi, F. Yamashita, 1984, Brain and Development.

Alzheimer's amyloid precursor protein mRNA without exon 15 is ubiquitously expressed except in the rat central nervous system.

T. Kitamoto, T. Ohgami, J. Tateishi, 1993, Brain research. Molecular brain research.

The Rat Central Nervous System Expresses Alzheimer's Amyloid Precursor Protein APP695, but Not APP677 (L‐APP Form)

T. Kitamoto, T. Ohgami, J. Tateishi, 1993, Journal of neurochemistry.

MRI WITH AUTOPSIED BRAINS IN DEMYELINATING DISEASES: 98

Tooru Inoue, J. Tateishi, H. Nagara, 1987 .

Presence of HTLV‐I proviral DNA in central nervous system of patients with HTLV‐I–associated myelopathy

Y. Sakaki, Y. Itoyama, J. Kira, 1992, Annals of neurology.

Experimental transmission of human subacute spongiform encephalopathy to small rodents

J. Tateishi, H. Nagara, Y. Sato, 2004, Acta Neuropathologica.

Clustering of three cases of Creutzfeldt‐Jakob disease near Fukuoka City, Japan

Y. Itoyama, K. Doh-ura, J. Tateishi, 1991, Acta neurologica Scandinavica.

Unique distributions of natriuretic hormones in dog brain

H. Nawata, H. Matsuo, J. Tateishi, 1987, Regulatory Peptides.

Neuronal autophagy in experimental Creutzfeldt-Jakob's disease

W. Schlote, J. Tateishi, J. Boellaard, 2004, Acta Neuropathologica.

Focal intracerebral accumulation of a novel type of amyloid protein

R. Friede, T. Kitamoto, J. Tateishi, 1988, Acta Neuropathologica.

Aging and cerebral amyloid: early detection of amyloid in the human brain using biochemical extraction and immunostain.

K. Ogomori, T. Kitamoto, J. Tateishi, 1988, Journal of gerontology.

Brain stem gliomas: a clinicopathological analysis of 23 histologically proven cases

S. Nishio, M. Fukui, J. Tateishi, 1988, Journal of Neuro-Oncology.

Experimental transmission of human subacute spongiform encephalopathy to small rodents

M. Ohta, J. Tateishi, Y. Sato, 2004, Acta Neuropathologica.

Sequence heterogeneity of HTLV‐I proviral DNA in the central nervous system of patients with HTLV‐I–associated myelopathy

Y. Itoyama, E. Baba, J. Kira, 1994, Annals of neurology.

Atypical multiple sclerosis with concentric of lamellar demyelinated lesions: Two Japanese patients studied post mortem

Y. Itoyama, J. Tateishi, Y. Kuroiwa, 1985, Annals of neurology.

Immunhistological evaluation of Creutzfeldt-Jakob disease with reference to the type PrPres deposition.

H. Kretzschmar, T. Kitamoto, J. Tateishi, 1996, Clinical neuropathology.

Incidence and characterization of age related amyloid deposits in the human anterior pituitary gland

K. Ogomori, T. Kitamoto, J. Tateishi, 2004, Virchows Archiv A.

Proliferating potential of folliculo-stellate cells in human pituitary adenomas

T. Iwaki, J. Tateishi, I. Takeshita, 2004, Acta Neuropathologica.

Experimental reproduction of SMON in animals by prolonged administration of clioquinol: clinico-pathological findings.

S. Otsuki, J. Tateishi, 1975, Japanese journal of medical science & biology.

Practical Methods for Chemical Inactivation of Creutzfeldt‐Jakob Disease Pathogen

T. Kitamoto, J. Tateishi, T. Tashima, 1991, Microbiology and immunology.

Thiamine-deficient encephalopathy in rats: Effects of deficiencies of thiamine and magnesium

J. Tateishi, H. Nagara, I. Goto, 1986, Brain Research.

Advanced glycosylation end‐products and heat shock proteins accumulate in the basophilic degeneration of the myocardium and the corpora amylacea of the glia

J. Tateishi, T. Iwaki, Yasuhiro Harnada, 1996, Pathology international.

The coexistence of Alzheimer's disease and Creutzfeldt-Jakob disease in a patient with dementia of long duration

T. Kitamoto, J. Tateishi, T. Muramoto, 1992, Acta Neuropathologica.

Chordoma in early childhood: a clinicopathological study.

M. Fukui, Y. Sato, T. Iwaki, 1991, Neurosurgery.

Prion disease with 144 base pair insertion in a Japanese family line

E. Oguni, H. Kashima, T. Kitamoto, 2004, Acta Neuropathologica.

Ventricular and subarachnoid seeding of intracranial tumors of neuroectodermal origin--a study of 26 consecutive autopsy cases with reference to focal ependymal defect.

S. Nishio, M. Fukui, J. Tateishi, 1982, Clinical neuropathology.

CNS pathology in the neurological mutant rats zitter, tremor and zitter-tremor double mutant (spontaneously epileptic rat, SER). Exaggeration of clinical and neuropathological phenotypes in SER.

T. Serikawa, J. Tateishi, H. Nagara, 1991, Brain : a journal of neurology.

The presence of complements in amyloid plaques of Creutzfeldt-Jakob disease and Gerstmann-Straussler-Scheinker disease.

J. Tateishi, S. Yagishita, S. Haga, 1984, Applied pathology.

Creutzfeldt-Jakob disease transmitted by a cadaveric dura mater graft.

M. Hara, T. Aiba, T. Kitamoto, 1994, Neurosurgery.

Creutzfeldt-Jakob disease transmitted by a cadaveric dura mater graft.

M. Hara, T. Aiba, T. Kitamoto, 1994, Neurosurgery.

Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodents

M. Hoque, T. Kitamoto, J. Tateishi, 1996, Neurology.

Immunohistochemical quantification of substance P in spinal dorsal horns of patients with multiple system atrophy.

T. Kitamoto, J. Tateishi, Y. Sato, 1991, Journal of neurology, neurosurgery, and psychiatry.

Effects of intracarotid hyperosmolar mannitol in triethyl tin (TET)-induced rat brain edema — preservation of blood-brain barrier (BBB) in TET edema

M. Fukui, Tooru Inoue, J. Tateishi, 1987, Brain Research.

Expression of neurofibromatosis 2 protein in human brain tumors: an immunohistochemical study

Satoshi O. Suzuki, M. Fukui, T. Iwaki, 1997, Acta Neuropathologica.

Alzheimer's amyloid precursor protein accumulates within axonal swellings in human brain lesions

T. Kitamoto, T. Ohgami, J. Tateishi, 1992, Neuroscience Letters.

Medicinal and other products and human and animal transmissible spongiform encephalopathies: memorandum from a WHO meeting.

A. Aguzzi, H. Budka, J. Wilesmith, 1997, Bulletin of the World Health Organization.

Myelo-optic neuropathy induced by clioquinol in animals.

S. Otsuki, J. Tateishi, S. Kuroda, 1971, Lancet.

Intranuclear inclusions in muscle, nervous tissue, and adrenal gland

M. Ohta, J. Tateishi, H. Nagara, 2004, Acta Neuropathologica.

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

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

A comparative study of embedded nerve tissue in six NF2-associated schwannomas and 17 nonassociated NF2 schwannomas.

M. Fukui, T. Iwaki, J. Tateishi, 1997, Surgical neurology.

[An autopsy case of chorea-acanthocytosis. Special reference to the histopathological and biochemical findings of basal ganglia].

I. Kanazawa, Y. Kuroiwa, A. Ohnishi, 1984, No to shinkei = Brain and nerve.

Immunoblotting of Creutzfeldt‐Jakob disease prion proteins: Host species—specific epitopes

S. Prusiner, D. Kingsbury, J. Tateishi, 1987, Annals of neurology.

Morphometric evaluation of degenerative and regenerative changes in isoniazid-induced neuropathy

Y. Kuroiwa, A. Ohnishi, J. Tateishi, 2004, Acta Neuropathologica.

Formic acid pretreatment enhances immunostaining of cerebral and systemic amyloids.

S. Prusiner, K. Ogomori, T. Kitamoto, 1987, Laboratory investigation; a journal of technical methods and pathology.

Beitrag zur „lymphocytären Encephalomeningitis“

J. Tateishi, M. Minauf, 1967, Archiv für Psychiatrie und Nervenkrankheiten.

Three cases of Acute Diffuse Lymphocytic Meningo‐encephalitis

T. Ōkuma, J. Tateishi, H. Ishino, 1969, Folia psychiatrica et neurologica japonica.

[Contribution to "lymphocytic encephalomeningitis].

J. Tateishi, M. Minauf, 1967, Archiv fur Psychiatrie und Nervenkrankheiten.

Diagnostic criteria for sporadic Creutzfeldt-Jakob disease.

S. DeArmond, H. Kretzschmar, J. Ironside, 1996, Archives of neurology.

Relationship between neurological symptoms and concentrations of clioquinol in serum and nervous systems of beagle dogs.

K. Hayakawa, J. Tateishi, T. Imanari, 1977, Chemical & pharmaceutical bulletin.

Capillary permeability and boron distribution in ethylnitrosourea-induced rat glioma.

M. Ohta, J. Tateishi, M. Abe, 1988, Neurosurgery.

Neurodegeneration in the limbic and paralimbic system in progressive supranuclear palsy

T. Iwaki, J. Tateishi, Y Higuchi, 1995, Neuropathology and applied neurobiology.

Response from Tateishi

J. Tateishi, 1996 .

Colocalization of prion protein and β protein in the same amyloid plaques in patients with Gerstmann-Sträussler Syndrome

T. Iwaki, M. Miyazono, T. Kitamoto, 2004, Acta Neuropathologica.

Increased senile plaques without microglia in Alzheimer's disease

R. Shin, K. Ogomori, T. Kitamoto, 2004, Acta Neuropathologica.

Amyloid β-Protein (Aβ) 1–40 But Not Aβ1–42 Contributes to the Experimental Formation of Alzheimer Disease Amyloid Fibrils in Rat Brain

J. Trojanowski, R. Shin, T. Saido, 1997, The Journal of Neuroscience.

Typing prion isoforms

R. B. Petersen, H. Kretzschmar, P. Brown, 1997, Nature.

Relationships between Clinicopathological Features and Cerebrospinal Fluid Biomarkers in Japanese Patients with Genetic Prion Diseases

Y. Shiga, H. Mizusawa, S. Murayama, 2013, PloS one.

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome.

K. Doh-ura, M. Ohta, T. Kitamoto, 1993, Biochemical and biophysical research communications.

Allelic variation of apolipoprotein E in Japanese sporadic Creutzfeldt-Jakob disease patients

K. Ogomori, T. Kitamoto, J. Tateishi, 1995, Neuroscience Letters.

Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease.

R. Shin, K. Doh-ura, M. Miyazono, 1992, The American journal of pathology.

Human prion diseases with variant prion protein.

T. Kitamoto, J. Tateishi, 1994, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

Developments in diagnosis for prion diseases.

T. Kitamoto, J. Tateishi, 1993, British medical bulletin.

CJD discrepancy

Y. Sakaki, K. Doh-ura, T. Kitamoto, 1991, Nature.

Creutzfeldt-Jakob disease with codon 129 polymorphism (Valine): a comparative study of patients with codon 102 point mutation or without mutations

T. Iwaki, K. Doh-ura, M. Miyazono, 1992, Acta Neuropathologica.

Prion Diseases

J. Tateishi, 1995, Microbiology and immunology.

Protective prion protein polymorphisms against sporadic Creutzfeldt-Jakob disease

R. Shin, T. Kitamoto, J. Tateishi, 1998, The Lancet.

Cerebellar medulloblastoma associated with lumbosacral syringomyelia

S. Nishio, M. Fukui, J. Tateishi, 2004, Journal of Neurology.

Spinal subarachnoid seeding from glioblastoma multiforme of the brain stem--report of three autopsy cases.

S. Nishio, M. Fukui, M. Ohta, 1983, Neurologia medico-chirurgica.

Japanese family with Creutzfeldt‐Jakob disease with codon 200 point mutation of the prion protein gene

K. Doh-ura, T. Kitamoto, J. Tateishi, 1994, Neurology.

[Recent advances in the research of Creutzfeldt-Jakob disease (CJD) and Gerstmann-Strüssler syndrome (GSS)].

J. Tateishi, 1991, Rinsho shinkeigaku = Clinical neurology.

SUBACUTE SPONGIFORM ENCEPHALOPATHY (SSE) WITH KURU PLAQUES AND ITS SUCCESSFUL TRANSMISSION TO THE SMALL RODENTS

M. Ohta, J. Tateishi, Y. Kuroiwa, 1978 .

Properties of the transmissible agent derived from chronic spongiform encephalopathy

J. Tateishi, Y. Sato, M. Koga, 1980, Annals of neurology.

[Creutzfeldt-Jakob disease with a widespread presence of kuru-type plaques after cadaveric dural graft replacement. An autopsy case].

J. Tateishi, S. Takashima, Y. Taguchi, 1997, Rinsho shinkeigaku = Clinical neurology.

Anaplastic evolution of childhood optico-hypothalamic pilocytic astrocytoma: report of an autopsy case.

S. Nishio, M. Fukui, J. Tateishi, 1988, Clinical neuropathology.

Gerstmann-Sträussler-Scheinker disease in an Alsatian family: clinical and genetic studies.

K. Doh-ura, J. Warter, C. Tranchant, 1992, Journal of neurology, neurosurgery, and psychiatry.

Creutzfeldt‐Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann‐Sträussler syndrome

K. Doh-ura, T. Kitamoto, J. Tateishi, 1990, Annals of neurology.

12 Infectious and Sporadic Prion Diseases

M. Alpers, L. Schonberger, D. Dormont, 1999 .

Cerebral amyloid in mice with Creutzfeldt-Jakob disease is influenced by the strain of the infectious agent

S. Mohri, T. Kitamoto, J. Tateishi, 1990, Brain Research.

A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann‐Sträussler syndrome

K. Doh-ura, T. Kitamoto, J. Tateishi, 1991, Neurology.

Apolipoprotein E mRNA in the brains of patients with Alzheimer's disease

J. Tateishi, I. Goto, J. Takamatsu, 1995, Journal of the Neurological Sciences.

First experimental transmission of fatal familial insomnia

P. Brown, D. Gajdusek, R. Roos, 1995, Nature.

Humanized prion protein knock-in by Cre-induced site-specific recombination in the mouse.

M. Katsuki, Y. Gondo, R. Shin, 1996, Biochemical and biophysical research communications.

Hemangiopericytoma of the meninges: a clinicopathologic and immunohistochemical study.

M. Fukui, T. Iwaki, M. Tsuneyoshi, 1988, Clinical neuropathology.

Experimental myelo-optic neuropathy induced by clioquinol

S. Otsuki, J. Tateishi, S. Kuroda, 2004, Acta Neuropathologica.

Neurotoxicity of clioquinol in laboratory animals.

S. Otsuki, J. Tateishi, S. Kuroda, 1972, Lancet.

Neurotoxic Effects of Clinoquinol, Mouse

Yuji Sato, J. Tateishi, M. Koga, 1988 .

Strain differences in dogs for neurotoxicity of clioquinol.

S. Otsuki, J. Tateishi, S. Kuroda, 1972, Lancet.

Comparative Study of Neurotoxicity of Clioquinol, Ethambutol, Isoniazid and Chloramphenicol in Dogs

J. Tateishi, 1974, Folia psychiatrica et neurologica japonica.

Distribution of clioquinol in rats with hepatic dysfunction.

S. Otsuki, J. Tateishi, M. Ogata, 1973, Lancet.

Small heat-shock protein is expressed in meningiomas and in granulofilamentous inclusion bodies

M. Fukui, T. Iwaki, J. Goldman, 2004, Acta Neuropathologica.

Modified tau is present in younger nondemented persons: a study of subcortical nuclei in Alzheimer's disease and progressive supranuclear palsy

R. Shin, T. Kitamoto, J. Tateishi, 1991, Acta Neuropathologica.

[Atypical Alzheimer's disease--an autopsy case].

J. Tateishi, S. Kuroda, A. Shomori, 1976, No to shinkei = Brain and nerve.

Beta-protein amyloid is widely distributed in the central nervous system of patients with Alzheimer's disease.

K. Ogomori, T. Kitamoto, J. Tateishi, 1989, The American journal of pathology.

Amyloid beta-protein (Abeta) 1-40 but not Abeta1-42 contributes to the experimental formation of Alzheimer disease amyloid fibrils in rat brain.

J. Trojanowski, R. Shin, T. Saido, 1997, The Journal of neuroscience : the official journal of the Society for Neuroscience.

Leser-Trélat sign with anaplastic ependymoma – an autopsy case

M. Fukui, T. Iwaki, J. Tateishi, 1997, Acta Neuropathologica.

Abnormal cytoarchitecture of cortical dysplasia verified by immunohistochemistry.

T. Morioka, M. Fukui, T. Iwaki, 1998, Clinical Neuropathology.

Inactivation of the creutzfeldt‐jakob disease agent

T. Kitamoto, J. Tateishi, T. Tashima, 1988, Annals of neurology.

Marchiafava-bignami disease, striatal degeneration, and other neurological complications of chronic alcoholism in a Japanese

T. Tabira, J. Tateishi, Y. Sato, 2004, Acta Neuropathologica.

Novel histochemical approaches to the prealbumin-related senile and familial forms of systemic amyloidosis.

T. Kitamoto, J. Tateishi, T. Tashima, 1986, American Journal of Pathology.

A missense mutation in the proteolipid protein gene responsible for Pelizaeus-Merzbacher disease in a Japanese family.

J. Tateishi, A. Iwaki, I. Iwaki, 1993, Human molecular genetics.

Positive transmission of Creutzfeldt-Jakob disease verified by murine kuru plaques.

K. Doh-ura, T. Kitamoto, J. Tateishi, 1989, Laboratory investigation; a journal of technical methods and pathology.

Spinal cord multiple sclerosis lesions in Japanese patients: Schwann cell remyelination occurs in areas that lack glial fibrillary acidic protein (GFAP)

Y. Itoyama, Y. Kuroiwa, A. Ohnishi, 2004, Acta Neuropathologica.

[Olivo-ponto-cerebellar atrophy with notable changes of the striato-nigral and pyramidal system].

S. Otsuki, J. Tateishi, S. Kuroda, 1977, Rinsho shinkeigaku = Clinical neurology.

A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation.

T. Iwaki, K. Doh-ura, M. Miyazono, 1991, The American journal of pathology.

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.

Widespread distribution of tau in the astrocytic elements of glial tumors

M. Fukui, T. Iwaki, R. Shin, 1993, Acta Neuropathologica.

[Consensus report: tissue handling in suspected Creutzfeldt-Jakob disease and other spongiform encephalopathies (prion diseases) in the human. European Union Biomed-1 Concerted Action].

W. Schlote, P. Lantos, A. Aguzzi, 1996, Der Pathologe.

Chronic Alcoholism: Report of an Autopsy Case and Comparison With Pseudoulegyric Type of Hepatocerebral Degeneration

J. Tateishi, F. Ikuta, M. Koga, 1978, Folia psychiatrica et neurologica japonica.

Horizontal saccadic palsy associated with gliosis of the brainstem midline.

J. Büttner-Ennever, T. Uemura, Y. Arai, 2008, Progress in brain research.

[Ependymal changes in the ventricular wall of the human brain. Comparative study in hydrocephalus].

S. Nishio, S. Matsumoto, J. Tateishi, 1984, Neurologia medico-chirurgica.

[A case of spongiform encephalopathy with ataxia and amyloid plaques].

S. Nagataki, M. Tsujihata, J. Tateishi, 1984, No to shinkei = Brain and nerve.

Antibiotics and antivirals do not modify experimentally-induced Creutzfeldt-Jakob disease in mice

J. Tateishi, Jun Tateishi, 1981, Journal of neurology, neurosurgery, and psychiatry.

Metabolism of 14 C-iodochlorohydroxyquinoline (chinoform) in mice.

J. Tateishi, M. Ogata, K. Tomokuni, 1971, Acta medicinae Okayama.

Segmental demyelination and remyelination in lumbar spinal root of patients dying with diabetes mellitus

A. Ohnishi, J. Ogata, J. Tateishi, 1983, Annals of neurology.

Myeloneuropathy in dogs induced by iodoxyquinoline

S. Otsuki, J. Tateishi, S. Kuroda, 1972, Neurology.

Autoradiographic Distribution of 131I‐Clioquinol in Beagle Dogs

S. Otsuki, Shôsuke Watanabe, J. Tateishi, 1974, Folia psychiatrica et neurologica japonica.

Autoradiographic Distribution of 131I‐Clioquinol in Canine and Feline

S. Otsuki, Shôsuke Watanabe, J. Tateishi, 1972, Folia psychiatrica et neurologica japonica.

Boron distribution analysis by alpha-autoradiography.

J. Tateishi, M. Abe, H. Hatanaka, 1986, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

Distinctive immunohistochemical profiles of small heat shock proteins (Heat shock protein 27 and αB‐crystallin) in human brain tumors

M. Fukui, T. Iwaki, J. Tateishi, 1996, Cancer.

Histochemical classification of systemic amyloid fibril proteins. Alkaline guanidine method.

T. Kitamoto, J. Tateishi, T. Tashima, 1986, Archives of Pathology & Laboratory Medicine.

[Genetic aspects of Alzheimer's disease].

J. Tateishi, 1988, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

[Central pontine and extrapontine myelinolysis following rapid correction of hyponatremia--report of an autopsy case].

S. Ibayashi, M. Fujishima, J. Ogata, 1984, No to shinkei = Brain and nerve.

Parvalbumin-immunoreactive neurons in the human central nervous system are decreased in Alzheimer's disease

J. Satoh, T. Tabira, M. Sano, 2004, Acta Neuropathologica.

Accumulation of clioquinol in mice.

S. Otsuki, J. Tateishi, M. Ogata, 1973, Lancet.

Distribution of radioactive clioquinol in animals.

S. Otsuki, J. Tateishi, M. Ogata, 1973, Lancet.

Differential expression of CD44 variants among meningioma subtypes

M. Mizoguchi, T. Kitamoto, J. Tateishi, 1996, Clinical molecular pathology.

Gerstmann-Sträussler-Scheinker disease- the dilemma of molecular and clinical correlations.

P. Brown, J. Tateishi, J. Boellaard, 1999, Clinical neuropathology.

[An autopsy case of presenile dementia with numerous Lewy bodies in the cerebral cortex (author's transl)].

J. Tateishi, K. Iguchi, S. Kuroda, 1978, Rinsho shinkeigaku = Clinical neurology.

Adrenoleukodystrophy with olivopontocerebellar atrophy-like lesions.

J. Tateishi, Y. Sato, M. Suetsugu, 1986, Clinical neuropathology.

N-terminal sequence of prion protein is also integrated into kuru plaques in patients with Gerstmann-Sträussler syndrome.

K. Beyreuther, T. Kitamoto, J. Tateishi, 1991, Brain research.

[Slow virus, prion and nervous system].

J. Tateishi, 1990, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

Lack of effect of thymus and spleen on the incubation period of Creutzfeldt-Jakob disease in mice.

S. Mohri, J. Tateishi, S. Handa, 1987, The Journal of general virology.

Neuropathological Features of MS in Japan

T. Tabira, J. Tateishi, 1982 .

Immunohistochemistry with anti-prion protein 27–30 gives reactions with fungi

J. Peiffer, J. Tateishi, J. Doerr-Schott, 2004, Acta Neuropathologica.

Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions.

M. Osame, J. Tateishi, A. Igata, 1984, Neurology.

Experimental Myelo‐Optico‐Neuropathy due to Ethambutol

S. Otsuki, J. Tateishi, S. Kuroda, 1974, Folia psychiatrica et neurologica japonica.