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"The Invisible Corset": A Rare Manifestation of Neurosarcoidosis

Internal Medicine, 2023/01/15, Vol.62(2), pp.317-318

2023

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Reversible cerebral vasoconstriction syndrome with cardiac involvement during treatment for iron deficiency anemia: caser report

BMC neurology, 2021-12, Vol.21 (1), p.479-479, Article 479

2021

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The effects of visual cues from optical stimulation devices on gait disturbance in patients with Parkinson’s disease

Journal of Physical Therapy Science, 2023, Vol.35(3), pp.230-236

2023

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Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers

Human molecular genetics, 2011-05, Vol.20 (9), p.1787-1799

2011

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Early Involvement of the Corpus Callosum in a Patient with Hereditary Diffuse Leukoencephalopathy with Spheroids Carrying the de novo K793T Mutation of CSF1R

Internal Medicine, 2013, Vol.52(4), pp.503-506

2013

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Differential roles of MMP-9 in early and late stages of dystrophic muscles in a mouse model of Duchenne muscular dystrophy

Biochimica et biophysica acta. Molecular basis of disease, 2015-10, Vol.1852 (10), p.2170-2182

2015

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Intravenous Immunoglobulin (IVIg) with Methylprednisolone Pulse Therapy for Motor Impairment of Neuralgic Amyotrophy: Clinical Observations in 10 Cases

Internal Medicine, 2012, Vol.51(12), pp.1493-1500

2012

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Improvement of Cu2ZnSnS4 thin film morphology using Cu–Zn–Sn–O precursor fabricated by sputtering

Current Applied Physics, 2013, 13(9), , pp.1861-1864

2013

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Genetic and reproductive characterization of distylous Primula reinii in the Hakone volcano, Japan: implications for conservation of the rare and endangered plant

Journal of threatened taxa, 2020-12, Vol.12 (17), p.17263-17275

2020

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Imbalanced expression of dysfunctional regulatory T cells and T-helper cells relates to immunopathogenesis in polyarteritis nodosa

Modern rheumatology, 2017-01, Vol.27 (1), p.102-109

2017

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Elderly-Onset Multiple System Atrophy with Lewy Body Pathology: A Case Report

Case reports in neurology, 2021-09, Vol.13 (3), p.613-619

2021

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Corpus Callosum Atrophy in Patients with Hereditary Diffuse Leukoencephalopathy with Neuroaxonal Spheroids: An MRI-based Study

Internal Medicine, 2014, Vol.53(1), pp.21-27

2014

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Crossed Cerebellar Diaschisis in Status Epilepticus

Internal Medicine, 2016/06/15, Vol.55(12), pp.1649-1651

2016

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Like a Rolling Stone: Year-Over-Year Growth of a Rectal Fecalith

Case reports in gastroenterology, 2022-05, Vol.16 (2), p.278-283

2022

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Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ)

BMC musculoskeletal disorders, 2007-06, Vol.8 (1), p.54-54, Article 54

2007

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Complete chaotic synchronization and exclusion of mutual Pyragas control in two delay-coupled Rössler-type oscillators

Physical review. E, Statistical, nonlinear, and soft matter physics, 2011-11, Vol.84 (5 Pt 2), p.056208-056208, Article 056208

2011

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Conventional Diet Therapy for Hyperammonemia is Risky in the Treatment of Hepatic Encephalopathy Associated with Citrin Deficiency

Internal Medicine, 2010, Vol.49(3), pp.243-247

2010

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Leukoencephalopathy Induced by Low-dose Methotrexate in a Patient with Rheumatoid Arthritis

Internal Medicine, 2011, Vol.50(19), pp.2219-2222

2011

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Polyarteritis nodosa with central nervous system involvement mimicking relapsing–remitting multiple sclerosis

Modern rheumatology, 2014-05, Vol.24 (3), p.525-528

2014

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Patient with adult‐onset type II citrullinemia beginning 2 years after operation for duodenal malignant somatostatinoma: Indication for liver transplantation

Hepatology research, 2013-05, Vol.43 (5), p.563-568

2013

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Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45-55 of the Duchenne muscular dystrophy (DMD) gene

Journal of human genetics, 2009-02, Vol.54 (2), p.127-130

2009

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First two cases of adult‐onset type II citrullinemia successfully treated by deceased‐donor liver transplantation in Japan

Hepatology research, 2012-09, Vol.42 (9), p.934-939

2012

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The Characteristics of Food Intake in Patients with Type II Citrullinemia

Journal of Nutritional Science and Vitaminology, 2011, Vol.57(3), pp.239-245

2011

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Gastro-protective action of lafutidine mediated by capsaicin-sensitive afferent neurons without interaction with TRPV1 and involvement of endogenous prostaglandins

World journal of gastroenterology : WJG, 2006-05, Vol.12 (19), p.3031

2006

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"The Invisible Corset": A Rare Manifestation of Neurosarcoidosis

Reversible cerebral vasoconstriction syndrome with cardiac involvement during treatment for iron deficiency anemia: caser report

Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2

The effects of visual cues from optical stimulation devices on gait disturbance in patients with Parkinson’s disease

Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers

Early Involvement of the Corpus Callosum in a Patient with Hereditary Diffuse Leukoencephalopathy with Spheroids Carrying the de novo K793T Mutation of CSF1R

Differential roles of MMP-9 in early and late stages of dystrophic muscles in a mouse model of Duchenne muscular dystrophy

Intravenous Immunoglobulin (IVIg) with Methylprednisolone Pulse Therapy for Motor Impairment of Neuralgic Amyotrophy: Clinical Observations in 10 Cases

Improvement of Cu2ZnSnS4 thin film morphology using Cu–Zn–Sn–O precursor fabricated by sputtering

Genetic and reproductive characterization of distylous Primula reinii in the Hakone volcano, Japan: implications for conservation of the rare and endangered plant

Imbalanced expression of dysfunctional regulatory T cells and T-helper cells relates to immunopathogenesis in polyarteritis nodosa

Elderly-Onset Multiple System Atrophy with Lewy Body Pathology: A Case Report

Corpus Callosum Atrophy in Patients with Hereditary Diffuse Leukoencephalopathy with Neuroaxonal Spheroids: An MRI-based Study

Crossed Cerebellar Diaschisis in Status Epilepticus

Like a Rolling Stone: Year-Over-Year Growth of a Rectal Fecalith

Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ)

Complete chaotic synchronization and exclusion of mutual Pyragas control in two delay-coupled Rössler-type oscillators

Conventional Diet Therapy for Hyperammonemia is Risky in the Treatment of Hepatic Encephalopathy Associated with Citrin Deficiency

Leukoencephalopathy Induced by Low-dose Methotrexate in a Patient with Rheumatoid Arthritis

Polyarteritis nodosa with central nervous system involvement mimicking relapsing–remitting multiple sclerosis

Patient with adult‐onset type II citrullinemia beginning 2 years after operation for duodenal malignant somatostatinoma: Indication for liver transplantation

Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45-55 of the Duchenne muscular dystrophy (DMD) gene

First two cases of adult‐onset type II citrullinemia successfully treated by deceased‐donor liver transplantation in Japan

The Characteristics of Food Intake in Patients with Type II Citrullinemia

Gastro-protective action of lafutidine mediated by capsaicin-sensitive afferent neurons without interaction with TRPV1 and involvement of endogenous prostaglandins

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