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Extracellular Vesicle Therapeutics in Regenerative Medicine

Cell Biology and Translational Medicine, Volume 11, 2021-01, Vol.1312, p.131-138

2021

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Rapidly progressive glomerulonephritis caused by tegafur/gimeracil/oteracil resulted in diabetes nephropathy, in a patient with minor risk of diabetes nephropathy: a case report

CEN case reports, 2020-11, Vol.9 (4), p.347-353

2020

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How to resolve confusion in the clinical setting for the diagnosis of heterozygous COL4A3 or COL4A4 gene variants? Discussion and suggestions from nephrologists

Clinical and experimental nephrology, 2020-08, Vol.24 (8), p.651-656

2020

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Isolation and Characterization of Extracellular Vesicles from Keratinocyte Cultures

Methods in molecular biology (Clifton, N.J.), 2020, Vol.2109, p.35

2020

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Rat Mesenchymal Stromal Cell Sheets Suppress Renal Fibrosis via Microvascular Protection

Stem cells translational medicine, 2019-12, Vol.8 (12), p.1330-1341

2019

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Exosomes derived from clinical-grade oral mucosal epithelial cell sheets promote wound healing

Journal of extracellular vesicles, 2019-12, Vol.8 (1), p.1565264-n/a

2019

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Incidence and risk factors of new-onset hypertrophic pachymeningitis in patients with anti-neutrophil antibody-associated vasculitis: using logistic regression and classification tree analysis

Clinical rheumatology, 2019-04, Vol.38 (4), p.1039-1046

2019

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Acute Kidney Injury by Renal Hemosiderosis Secondary to Primary Cold Agglutinin Disease Associated with an Excessive Alcohol Intake

Internal Medicine, 2018/11/15, Vol.57(22), pp.3261-3265

2018

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Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically

Nephrology (Carlton, Vic.), 2018-10, Vol.23 (10), p.940-947

2018

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Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome

Journal of the American Society of Nephrology, 2018-08, Vol.29 (8), p.2244-2254

2018

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Primary Central Nervous System Post-transplant Lymphoproliferative Disorder Diagnosed by Peripheral Facial Nerve Palsy

Internal Medicine, 2018/07/01, Vol.57(13), pp.1899-1903

2018

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Risk factors of ceftriaxone-associated biliary pseudolithiasis in adults: influence of renal dysfunction

Clinical and experimental nephrology, 2018-06, Vol.22 (3), p.613-619

2018

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A clinical staging score to measure the severity of dialysis-related amyloidosis

Clinical and experimental nephrology, 2017-04, Vol.21 (2), p.300-306

2017

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Multicentric Castleman’s disease associated with IgA vasculitis (Henoch-Schönlein purpura) responding well to tocilizumab: a case report

Clinical rheumatology, 2017-03, Vol.36 (3), p.729-733

2017

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Acquired hemophilia A that developed during the induction of hemodialysis: the use of double-filtration plasmapheresis

Clinical nephrology, 2017-03, Vol.87 (2017) (3), p.147

2017

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Intracystic magnetic resonance imaging in patients with autosomal dominant polycystic kidney disease: features of severe cyst infection in a case-control study

BMC nephrology, 2016-11, Vol.17 (1), p.170-170, Article 170

2016

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Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome

Clinical journal of the American Society of Nephrology, 2016-08, Vol.11 (8), p.1441-1449

2016

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Suitability of Patients with Autosomal Dominant Polycystic Kidney Disease for Renal Transcatheter Arterial Embolization

Journal of the American Society of Nephrology, 2016-07, Vol.27 (7), p.2177-2187

2016

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Clinicopathological Analysis of Allogeneic Hematopoietic Stem Cell Transplantation-related Membranous Glomerulonephritis

Human pathology, 2016-04, Vol.50, p.187-194

2016

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Ursodeoxycholic Acid for Treatment of Enlarged Polycystic Liver

Therapeutic apheresis and dialysis, 2016-02, Vol.20 (1), p.73-78

2016

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Effect of Proteinuria and Glomerular Filtration Rate on Renal Outcome in Patients with Biopsy-Proven Benign Nephrosclerosis

PloS one, 2016-01, Vol.11 (1), p.e0147690-e0147690

2016

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Bone Histology of Two Cases with Osteomalacia Related to Low-dose Adefovir

Internal Medicine, 2016/10/15, Vol.55(20), pp.3013-3019

2016

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AA-negative and Kappa-positive Amyloidosis in a Patient with Rheumatoid Arthritis

Internal Medicine, 2016/09/01, Vol.55(17), pp.2491-2495

2016

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Recurrent Cholangitis in a Patient with Autosomal Dominant Polycystic Kidney Disease (ADPKD) and Caroli's Disease

Internal Medicine, 2016/10/15, Vol.55(20), pp.3009-3012

2016

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A Case of Chronic Microscopic Hematuria

Nihon Naika Gakkai Zasshi, 2015/10/10, Vol.104(10), pp.2237-2240

2015

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Extracellular Vesicle Therapeutics in Regenerative Medicine

Rapidly progressive glomerulonephritis caused by tegafur/gimeracil/oteracil resulted in diabetes nephropathy, in a patient with minor risk of diabetes nephropathy: a case report

How to resolve confusion in the clinical setting for the diagnosis of heterozygous COL4A3 or COL4A4 gene variants? Discussion and suggestions from nephrologists

Isolation and Characterization of Extracellular Vesicles from Keratinocyte Cultures

Rat Mesenchymal Stromal Cell Sheets Suppress Renal Fibrosis via Microvascular Protection

Exosomes derived from clinical-grade oral mucosal epithelial cell sheets promote wound healing

Incidence and risk factors of new-onset hypertrophic pachymeningitis in patients with anti-neutrophil antibody-associated vasculitis: using logistic regression and classification tree analysis

Acute Kidney Injury by Renal Hemosiderosis Secondary to Primary Cold Agglutinin Disease Associated with an Excessive Alcohol Intake

Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically

Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome

Primary Central Nervous System Post-transplant Lymphoproliferative Disorder Diagnosed by Peripheral Facial Nerve Palsy

Risk factors of ceftriaxone-associated biliary pseudolithiasis in adults: influence of renal dysfunction

A clinical staging score to measure the severity of dialysis-related amyloidosis

Multicentric Castleman’s disease associated with IgA vasculitis (Henoch-Schönlein purpura) responding well to tocilizumab: a case report

Acquired hemophilia A that developed during the induction of hemodialysis: the use of double-filtration plasmapheresis

Intracystic magnetic resonance imaging in patients with autosomal dominant polycystic kidney disease: features of severe cyst infection in a case-control study

Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome

Suitability of Patients with Autosomal Dominant Polycystic Kidney Disease for Renal Transcatheter Arterial Embolization

Clinicopathological Analysis of Allogeneic Hematopoietic Stem Cell Transplantation-related Membranous Glomerulonephritis

Ursodeoxycholic Acid for Treatment of Enlarged Polycystic Liver

Effect of Proteinuria and Glomerular Filtration Rate on Renal Outcome in Patients with Biopsy-Proven Benign Nephrosclerosis

Bone Histology of Two Cases with Osteomalacia Related to Low-dose Adefovir

AA-negative and Kappa-positive Amyloidosis in a Patient with Rheumatoid Arthritis

Recurrent Cholangitis in a Patient with Autosomal Dominant Polycystic Kidney Disease (ADPKD) and Caroli's Disease

A Case of Chronic Microscopic Hematuria

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