R. Koide

发表

A novel WDR45 mutation in a patient with static encephalopathy of childhood with neurodegeneration in adulthood (SENDA)

N. Matsumoto, S. Orimo, H. Saitsu, 2014, American journal of medical genetics. Part A.

Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)

O. Onodera, S. Tsuji, Hitoshi Takahashi, 1994, Nature Genetics.

Complex Aortic Arch Atherosclerosis in Acute Ischemic Stroke Patients with Non-Valvular Atrial Fibrillation

T. Ozawa, R. Koide, Masayuki Suzuki, 2020, Journal of atherosclerosis and thrombosis.

Clinical and genetic characterizations of 16q‐linked autosomal dominant spinocerebellar ataxia (AD‐SCA) and frequency analysis of AD‐SCA in the Japanese population

M. Nishizawa, T. Ikeuchi, O. Onodera, 2007, Movement disorders : official journal of the Movement Disorder Society.

Characteristics of aged ischemic stroke patients indicative of cardioembolism

H. Shimazaki, T. Ozawa, R. Koide, 2020, Journal of Thrombosis and Thrombolysis.

Tissue Plasminogen Activator to Treat a Stroke after Foam Sclerotherapy in a Woman with a Patent Foramen Ovale.

H. Shimazaki, T. Ozawa, R. Koide, 2018, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Successful endovascular coiling of infectious cerebral aneurysm following Staphylococcus haemolyticus endocarditis

K. Kario, K. Kawai, K. Harada, 2021, The Journal of international medical research.

Clinical and neuroradiological improvement in chronic acquired hepatocerebral degeneration after branched‐chain amino acid therapy

Toshio Shimizu, S. Hirai, T. Shimizu, 2002, Acta neurologica Scandinavica.

Successful Tissue Plasminogen Activator for a Patient with Stroke After Stanford Type A Aortic Dissection Treatment.

H. Shimazaki, T. Ozawa, R. Koide, 2018, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

No mutation in the entire coding region of the α-synuclein gene in pathologically confirmed cases of multiple system atrophy

S. Tsuji, Hitoshi Takahashi, T. Shimohata, 1999, Neuroscience Letters.

Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosis.

S. Tsuji, Y. Takiyama, T. Ikeuchi, 1996, American journal of human genetics.

Left thalamus infarction in the thalamotuberal artery perfusion area causing subcortical diaschisis and transcortical sensory aphasia

H. Shimazaki, T. Ozawa, R. Koide, 2020, Journal of the Neurological Sciences.

MRI Findings in Spinocerebellar Ataxias

K. Oyanagi, I. Nakano, A. Kawata, 2014 .

A change in Broadmann area 10 activity precedes a decrease in cerebral blood flow in the left posterior perisylvian part during logopenic progressive aphasia

K. Kawai, T. Ozawa, R. Koide, 2022, Journal of the Neurological Sciences.

Mitophagy in three cases of immune-mediated necrotizing myopathy associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase autoantibodies: ultrastructural and immunohistochemical studies

I. Nishino, Shigeaki Suzuki, T. Komori, 2018, Neuromuscular Disorders.

A case of primary torsion dystonia in Japan with the 3-bp (GAG) deletion in the DYT1 gene with a unique clinical presentation

S. Tsuji, T. Shimohata, T. Ikeuchi, 1999, Neurogenetics.

Higher incidence of cervical spinal cord compression in amyotrophic lateral sclerosis: a single-institute cohort study

T. Ozawa, R. Koide, Masayuki Suzuki, 2021, Neurological Sciences.

A new simple method using carotid duplex ultrasonography to assess intracranial vertebrobasilar arterial stenosis

H. Shimazaki, T. Ozawa, R. Koide, 2020, Journal of the Neurological Sciences.

Widespread occurrence of alpha-synuclein/NACP-immunoreactive neuronal inclusions in juvenile and adult-onset Hallervorden-Spatz disease with Lewy bodies.

K. Wakabayashi, M. Yoshimoto, H. Takahashi, 1999, Neuropathology and applied neurobiology.

Unusual Presentation of Sarcoidosis: Solitary Intracranial Mass Lesion Mimicking a Glioma

M. Taniguchi, R. Koide, A. Uruha, 2011, Journal of neuroimaging : official journal of the American Society of Neuroimaging.

A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?

S Kobayashi, S. Tsuji, M. Yamada, 1999, Human molecular genetics.

Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch

S. Tsuji, Hitoshi Takahashi, T. Inuzuka, 1998, Nature Genetics.

A sporadic case of dentatorubral pallidoluysian atrophy (DRPLA) with CAG repeat expansion but no clinical abnormalities in the father.

S. Tsuji, T. Ikeuchi, R. Koide, 1996, Journal of neurology, neurosurgery, and psychiatry.

Real-time data on the prognosis of acute ischemic stroke patients in the Tochigi Clinical ObservatioNal registry for 1-year mortality of aCute ischEmic stRoke patieNt (T-CONCERN) study

T. Ozawa, R. Koide, Masayuki Suzuki, 2022, Neurological Sciences.

Cerebral venous sinus thrombosis associated with protein S deficiency during pregnancy: a case report

K. Kokame, T. Ozawa, R. Koide, 2019, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Callosal disconnection syndrome in symptomatic female carrier of Pelizaeus–Merzbacher disease

N. Matsumoto, H. Saitsu, R. Koide, 2015, Journal of the Neurological Sciences.

Catastrophic Secondary Infarctions with Onset Seizure Following Tissue Plasminogen Activator Therapy.

H. Shimazaki, T. Ozawa, R. Koide, 2019, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

A case of reversible cerebral vasoconstriction syndrome presenting with recurrent neurological deficits: Evaluation using noninvasive arterial spin labeling MRI

R. Koide, Kazushi Takahashi, T. Komatsu, 2014, Clinical Neurology and Neurosurgery.

Real-time data on the prognosis of acute ischemic stroke patients in the Tochigi Clinical ObservatioNal registry for 1-year mortality of aCute ischEmic stRoke patieNt (T-CONCERN) study

T. Ozawa, R. Koide, Masayuki Suzuki, 2022, Neurological Sciences.

Case report of an elderly woman with atypical imaging for primary central nervous system lymphoma who needed a brain biopsy for diagnosis

K. Kawai, Yohei Ishishita, T. Ozawa, 2021, The Journal of international medical research.

Neurosarcoidosis: a treatable cause of vestibular dysfunction

R. Koide, R. Naito, H. Yoshida, 2007, The Lancet.

[A case of lumbar intradural and epidural abscesses presenting with elevated serum carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9 (CA19-9)].

M. Taniguchi, R. Koide, H. Hayashi, 2003, No to shinkei = Brain and nerve.

EFA6A-like antibodies in paraneoplastic encephalitis associated with immature ovarian teratoma: a case report

Toshio Shimizu, J. Dalmau, R. Koide, 2006, Journal of Neuro-Oncology.

Relapse of herpes simplex virus encephalitis after surgical treatment for temporal lobe epilepsy: rare complication of epilepsy surgery

M. Morino, T. Uda, Hirotaka Ito, 2012, Journal of Neurology.

Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.

S. Tsuji, M. Pandolfo, R. Margolis, 2002, Archives of neurology.

Trinucleotide Repeats in 202 Families With Ataxia

J. Vale, J. Sequeiros, S. Tsuji, 2002 .

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT

S. Tsuji, Hitoshi Takahashi, H. Takahashi, 1996, Nature Genetics.

Paraneoplastic anti–N‐methyl‐D‐aspartate receptor encephalitis associated with ovarian teratoma

Josep Dalmau, W. Mason, M. Dichter, 2007, Annals of neurology.

[Clinical usefulness of thallium-201 single-photon emission CT in the patient with hypertrophic cranial pachymeningitis].

Y. Kagamihara, R. Koide, H. Hayashi, 2004, No to shinkei = Brain and nerve.

Neuro-Ophthalmic Manifestations of Hypertrophic Cranial Pachymeningitis Associated With Antineutrophil Cytoplasmic Antibody for Myeloperoxidase

R. Koide, H. Yoshida, E. Isozaki, 2010 .

Recurrent pneumococcal meningitis due to occult middle fossa encephalocele

K. Kawai, T. Ozawa, R. Koide, 2021 .

H. Mori, Risa Suzuki, T. Ozawa, 2021, Internal medicine.

Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patients.

I. Kanazawa, G. Sobue, T. Shimohata, 1999, Human molecular genetics.

Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations.

H. Zoghbi, S. Tsuji, A. Durr, 1998, American journal of human genetics.

Pseudomyopathic Changes in Needle Electromyography in Lambert-Eaton Myasthenic Syndrome

Toshio Shimizu, T. Komori, R. Koide, 2013, Case reports in neurological medicine.

Somatic mosaicism of expanded CAG repeats in brains of patients with dentatorubral-pallidoluysian atrophy: cellular population-dependent dynamics of mitotic instability.

S. Tsuji, M. Yamada, H. Takahashi, 1996, American journal of human genetics.

Diffuse idiopathic skeletal hyperostosis: A rare cause of dysphagia in the elderly

I. Nakano, R. Koide, Kazushi Takahashi, 2013 .

A Japanese familial ALS patient with autonomic failure and a p.Cys146Arg mutation in the gene for SOD1 (SOD1)

Toshio Shimizu, A. Kawata, T. Komori, 2016, Neuropathology : official journal of the Japanese Society of Neuropathology.

Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription

I. Kanazawa, S. Tsuji, Hitoshi Takahashi, 2000, Nature Genetics.

Dentatorubral-pallidoluysian atrophy (DRPLA): close correlation of CAG repeat expansions with the wide spectrum of clinical presentations and prominent anticipation.

S. Tsuji, T. Ikeuchi, Hajime Tanaka, 1995, Seminars in cell biology.

A case of Andersen–Tawil syndrome presenting periodic paralysis exacerbated by acetazolamide

I. Nakano, A. Kawata, H. Takashima, 2014, Journal of the Neurological Sciences.

Akinesis of the apex similar to takotsubo cardiomyopathy following tetanus

H. Shimazaki, T. Ozawa, R. Koide, 2019, Journal of the Neurological Sciences.

Spinocerebellar ataxia type 6: CAG repeat expansion in α1a voltage‐dependent calcium channel gene and clinical variations in japanese population

S. Tsuji, Hitoshi Takahashi, H. Tsukagoshi, 1997 .

Anti-NMDAR encephalitis in small-cell lung cancer: A case report

R. Koide, Keiko Tanaka, A. Uruha, 2012, Clinical Neurology and Neurosurgery.

Spontaneous Echo Contrast in the Left Atrium and Aortic-Arch Atheroma, Detected by Transesophageal Echocardiography, Was Negatively Correlated with Cognitive Function.

T. Ozawa, R. Koide, Masayuki Suzuki, 2022, Journal of Alzheimer's disease : JAD.

Coexisting of aortic arch atheroma and atrial fibrillation for short-term recurrence and poor functional outcome in acute stroke

T. Ozawa, R. Koide, Masayuki Suzuki, 2021, Neurological Sciences.

Internal Jugular Vein Velocity and Spontaneous Echo Contrast Correlate with Alzheimer's Disease and Cognitive Function.

T. Ozawa, R. Koide, Masayuki Suzuki, 2021, Journal of Alzheimer's disease : JAD.

Hereditary dentatorubral-pallidoluysian atrophy: detection of widespread ubiquitinated neuronal and glial intranuclear inclusions in the brain

Yasuko Hayashi, Takeshi Ikeuchi, Akiyoshi Kakita, 1998, Acta Neuropathologica.

Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy

O. Onodera, H. Beppu, S. Tsuji, 1997, Neurology.

Relapsing polychondritis coupling with cerebral amyloid deposit inducing cerebral amyloid angiopathy-related inflammation

H. Shimazaki, T. Ozawa, R. Koide, 2020, Journal of Thrombosis and Thrombolysis.

Adenovirus-mediated expression of mutant DRPLA proteins with expanded polyglutamine stretches in neuronally differentiated PC12 cells. Preferential intranuclear aggregate formation and apoptosis.

S. Tsuji, T. Inuzuka, T. Shimohata, 1999, Human molecular genetics.

Time course of polyglutamine aggregate body formation and cell death: Enhanced growth in nucleus and an interval for cell death

S. Tsuji, T. Shimohata, O. Onodera, 2002, Journal of neuroscience research.

Dentatorubral‐pallidoluysian atrophy: Clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat

Osamu Onodera, Hitoshi Takahashi, Takeshi Ikeuchi, 1995, Annals of neurology.

Opsoclonus-myoclonus syndrome during pregnancy.

R. Koide, H. Hayashi, Kozue Tanaka, 2004, Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.

Juvenile-onset generalized neuroaxonal dystrophy (Hallervorden-Spatz disease) with diffuse neurofibrillary and Lewy body pathology

T. Iwatsubo, M. Hasegawa, K. Wakabayashi, 2000, Acta Neuropathologica.

Noteworthy Cardiovascular Involvement with Sporadic Late-onset Nemaline Myopathy

K. Kario, I. Nishino, H. Shimazaki, 2021, Internal medicine.

Dentatorubral-pallidoluysian atrophy (DRPLA). Molecular basis for wide clinical features of DRPLA.

S. Tsuji, T. Ikeuchi, O. Onodera, 1995, Clinical neuroscience.

Vertical Gaze Palsy Caused by Selective Unilateral Rostral Midbrain Infarction

H. Shimazaki, T. Ozawa, R. Koide, 2018, Neuro-ophthalmology.

[A case of NARP (neurogenic muscle weakness, ataxia, and retinitis pigmentosa) with a T-to-C point mutation at nt 8993 of mitochondrial DNA].

S. Tsuji, R. Koide, K. Jinnai, 2000, Rinshō shinkeigaku Clinical neurology.

A Novel Double Mutation in the ABCD1 Gene in a Patient with X-linked Adrenoleukodystrophy: Analysis of the Stability and Function of the Mutant ABCD1 Protein.

N. Shimozawa, M. Morita, R. Koide, 2013, JIMD reports.

[Recent topics on paraneoplastic neurological syndromes: anti-NMDA antibody].

R. Koide, 2008, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

Radiologic and Neuropathologic Findings in Patients in a Family with Dentatorubral-Pallidoluysian Atrophy

T. Mizutani, K. Oyanagi, R. Koide, 2010, American Journal of Neuroradiology.

Magnetic resonance imaging findings in Leigh syndrome with a novel compound heterozygous SURF1 gene mutation

R. Koide, E. Isozaki, Younhee Kim, 2016 .

Dentatorubral-pallidoluysian atrophy and Haw River syndrome

M. Pericak-Vance, S. Tsuji, M. Yamada, 1994, The Lancet.

Rheumatoid leptomeningitis: rare complication of rheumatoid arthritis

R. Koide, A. Uruha, K. Ishii, 2009, Clinical Rheumatology.

Widespread occurrence of α‐synuclein/NACP‐immunoreactive neuronal inclusions in juvenileand adult‐onset Hallervorden–Spatz diseasewith Lewy bodies

K. Wakabayashi, M. Yoshimoto, T. Morita, 1999 .

Dentatorubral‐pallidoluysian atrophy: Clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat

A. Tomoda, T. Miike, T. Ikeuchi, 1995, Annals of neurology.

[A sporadic dentatorubral-pallidoluysian atrophy (DRPLA) diagnosed by gene analysis].

S. Tsuji, H. Yoshimoto, T. Ikeuchi, 1995, Rinshō shinkeigaku Clinical neurology.

Management Effort for Delirium and Insomnia in Patients with Acute Ischemic Stroke (MEDIAS) Study

H. Shimazaki, T. Ozawa, R. Koide, 2020, Psychiatry and Clinical Neurosciences.

A Case of Long-Term Exposure to Valproic Acid Mimicking Tremor-Dominant Parkinson’s Disease

K. Kawai, T. Mashiko, R. Koide, 2023, Tremor and other hyperkinetic movements.

Unilateral posterior reversible encephalopathy syndrome: A case report

K. Kawai, H. Shimazaki, T. Ozawa, 2019, Clinical Neurology and Neurosurgery.

Dentatorubral-Pallidoluysian Atrophy Patients in a Family with Radiologic and Neuropathologic Findings in

K. Oyanagi, R. Koide, Y. Sunami, 2022 .