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Multiple System Atrophy Showing Portomesenteric Venous Gas with Pneumatosis Intestinalis on Abdominal Computed Tomography Associated with a Cause of Death

Internal Medicine, 2019/10/01, Vol.58(19), pp.2857-2859

2019

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Antibodies to N-methyl-D-aspartate glutamate receptors in Creutzfeldt–Jakob disease patients

Journal of neuroimmunology, 2012-10, Vol.251 (1), p.90-93

2012

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A case of probable cerebral amyloid angiopathy preceded by symmetrical diffusion‐weighted imaging lesions

Neurology and clinical neuroscience, 2019-09, Vol.7 (5), p.285-287

2019

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Narrow CSF space at high convexity and high midline areas in idiopathic normal pressure hydrocephalus detected by axial and coronal MRI

Neuroradiology, 2008-02, Vol.50 (2), p.117-122

2008

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Voltage-gated potassium channel complex antibodies in Creutzfeldt-Jakob disease

Journal of neurology, 2012-10, Vol.259 (10), p.2249-2250

2012

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Correlation of right frontal hypoperfusion and urinary dysfunction in iNPH: A SPECT study

Neurourology and urodynamics, 2012-01, Vol.31 (1), p.50-55

2012

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Increased interleukin-17 in the cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease: a case-control study of rapidly progressive dementia

Journal of neuroinflammation, 2013-11, Vol.10 (1), p.135-135, Article 903

2013

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Mechanism of bladder dysfunction in idiopathic normal pressure hydrocephalus

Neurourology and urodynamics, 2008-01, Vol.27 (6), p.507-510

2008

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A Case of Multiple System Atrophy Showing Portomesenteric Venous Gas with Pneumatosis Intestinalis on Abdominal Computed Tomography Associated with a Cause of Death

Internal Medicine, 2019, pp.2949-19

2019

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A Case of Anti-aquaporin-4 and Anti-glutamate Receptor Antibodies Positive Myelitis Presented with Modest Clinical Signs

Magnetic Resonance in Medical Sciences, 2008, Vol.7(1), pp.55-58

2008

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Correlation of callosal angle at the splenium with gait and cognition in normal pressure hydrocephalus

Journal of neurosurgery, 2023-08, Vol.139 (2), p.481-491

2023

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Multicentre multiobserver study of diffusion-weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt–Jakob disease: a reliability and agreement study

BMJ open, 2012-01, Vol.2 (1), p.e000649-e000649

2012

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High Throughput ELISAs to Measure a Unique Glycan on Transferrin in Cerebrospinal Fluid : A Possible Extension toward Alzheimer's Disease Biomarker Development

International journal of alzheimer's disease, 2011, Vol.2011 (2011), p.1-5

2011

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Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy

The New England journal of medicine, 2013-07, Vol.369 (3), p.233-244

The Multiple-System Atrophy Research Collaboration

2013

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Next-generation sequencing of 28 ALS-related genes in a Japanese ALS cohort

Neurobiology of aging, 2016-03, Vol.39, p.219.e1-219.e8

2016

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Bilevel Nasal Positive Airway Pressure and Ballooning of the Stomach

Chest, 2001-06, Vol.119 (6), p.1965-1966

2001

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Transient Splenial Lesion of the Corpus Callosum after Acute Withdrawal of Antiepileptic Drug: A Case Report

Magnetic Resonance in Medical Sciences, 2006, Vol.5(4), pp.211-215

2006

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Efficacy and Safety of BIIB092 in Patients with Progressive Supranuclear Palsy: PASSPORT Phase 2 Study Design (P6.073)

Neurology, 2018-04, Vol.90 (15_supplement)

2018

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A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTN

Journal of neurology, neurosurgery and psychiatry, 2016-08, Vol.87 (8), p.851-858

2016

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Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expanded CAG repeats in the MJD1 gene in Machado-Joseph disease

Annals of neurology, 1998-03, Vol.43 (3), p.288-296

1998

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Age at onset influences on wide-ranged clinical features of sporadic amyotrophic lateral sclerosis

Journal of the neurological sciences, 2009-01, Vol.276 (1), p.163-169

2009

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A unique N-glycan on human transferrin in CSF: a possible biomarker for iNPH

Neurobiology of aging, 2012-08, Vol.33 (8), p.1807-1815

2012

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Increased Interleukin-17 In The Cerebrospinal Fluid In Sporadic Creutzfeldt-Jakob Disease (P5.234)

Neurology, 2014-04, Vol.82 (10_supplement)

2014

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Limbic encephalitis--history,symptoms,and the latest classification

Brain and nerve = Shinkei kenkyū no shinpo, 2010-08, Vol.62 (8), p.817

2010

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Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

Nature genetics, 2001-10, Vol.29 (2), p.184-188

2001

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Multiple System Atrophy Showing Portomesenteric Venous Gas with Pneumatosis Intestinalis on Abdominal Computed Tomography Associated with a Cause of Death

Antibodies to N-methyl-D-aspartate glutamate receptors in Creutzfeldt–Jakob disease patients

A case of probable cerebral amyloid angiopathy preceded by symmetrical diffusion‐weighted imaging lesions

Narrow CSF space at high convexity and high midline areas in idiopathic normal pressure hydrocephalus detected by axial and coronal MRI

Voltage-gated potassium channel complex antibodies in Creutzfeldt-Jakob disease

Correlation of right frontal hypoperfusion and urinary dysfunction in iNPH: A SPECT study

Increased interleukin-17 in the cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease: a case-control study of rapidly progressive dementia

Mechanism of bladder dysfunction in idiopathic normal pressure hydrocephalus

A Case of Multiple System Atrophy Showing Portomesenteric Venous Gas with Pneumatosis Intestinalis on Abdominal Computed Tomography Associated with a Cause of Death

A Case of Anti-aquaporin-4 and Anti-glutamate Receptor Antibodies Positive Myelitis Presented with Modest Clinical Signs

Correlation of callosal angle at the splenium with gait and cognition in normal pressure hydrocephalus

Multicentre multiobserver study of diffusion-weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt–Jakob disease: a reliability and agreement study

High Throughput ELISAs to Measure a Unique Glycan on Transferrin in Cerebrospinal Fluid : A Possible Extension toward Alzheimer's Disease Biomarker Development

Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy

Next-generation sequencing of 28 ALS-related genes in a Japanese ALS cohort

Bilevel Nasal Positive Airway Pressure and Ballooning of the Stomach

Transient Splenial Lesion of the Corpus Callosum after Acute Withdrawal of Antiepileptic Drug: A Case Report

Efficacy and Safety of BIIB092 in Patients with Progressive Supranuclear Palsy: PASSPORT Phase 2 Study Design (P6.073)

A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTN

Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expanded CAG repeats in the MJD1 gene in Machado-Joseph disease

Age at onset influences on wide-ranged clinical features of sporadic amyotrophic lateral sclerosis

A unique N-glycan on human transferrin in CSF: a possible biomarker for iNPH

Increased Interleukin-17 In The Cerebrospinal Fluid In Sporadic Creutzfeldt-Jakob Disease (P5.234)

Limbic encephalitis--history,symptoms,and the latest classification

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

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