Search Results - "Imafuku, Aya"
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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
Published in Clinical and experimental nephrology (01-08-2020)“…Both thin basement membrane nephropathy (TBMN) and autosomal dominant Alport syndrome (ADAS) are types of hereditary nephritis resulting from heterozygous…”
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Rat Mesenchymal Stromal Cell Sheets Suppress Renal Fibrosis via Microvascular Protection
Published in Stem cells translational medicine (01-12-2019)“…Renal fibrosis is one of the largest global health care problems, and microvascular (MV) injury is important in the development of progressive fibrosis…”
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Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome
Published in Journal of the American Society of Nephrology (01-08-2018)“…X-linked Alport syndrome (XLAS) is a progressive hereditary nephropathy caused by mutations in the gene. Genotype-phenotype correlation in male XLAS is…”
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Denosumab for Low Bone Mass in Hemodialysis Patients: A Noncontrolled Trial
Published in American journal of kidney diseases (01-07-2015)Get full text
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Exosomes derived from clinical-grade oral mucosal epithelial cell sheets promote wound healing
Published in Journal of extracellular vesicles (01-01-2019)“…The oral mucosa exhibits unique regenerative properties, sometimes referred to as foetal-like wound healing. Researchers from our institute have used sheets of…”
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Primary Central Nervous System Post-transplant Lymphoproliferative Disorder Diagnosed by Peripheral Facial Nerve Palsy
Published in Internal Medicine (01-07-2018)“…Although primary central nervous system post-transplant lymphoproliferative disorder (PCNS-PTLD) causes various symptoms depending on the tumor region, there…”
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Risk factors of ceftriaxone-associated biliary pseudolithiasis in adults: influence of renal dysfunction
Published in Clinical and experimental nephrology (01-06-2018)“…Background Ceftriaxone (CTRX) is a known cause of biliary pseudolithiasis (BPL) mainly in children. Biliary elimination of CTRX increases in patients with…”
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Clinicopathological Analysis of Allogeneic Hematopoietic Stem Cell Transplantation-related Membranous Glomerulonephritis
Published in Human pathology (01-04-2016)“…Summary Allogeneic hematopoietic stem cell transplantation (HSCT)-related membranous glomerulonephritis (MGN) is poorly understood. A total of 830 patients who…”
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Acute Kidney Injury by Renal Hemosiderosis Secondary to Primary Cold Agglutinin Disease Associated with an Excessive Alcohol Intake
Published in Internal Medicine (15-11-2018)“…Renal hemosiderosis occurs in the context of severe intravascular hemolysis, with the most common cause being paroxysmal nocturnal hematuria. Patients with…”
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A pathological scoring system to predict renal outcome in diabetic nephropathy
Published in American journal of nephrology (01-01-2015)“…With the association between diabetic nephropathy (DN) and renal outcome being increasingly clear, we aimed at creating a new DN pathological scoring system…”
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Effect of Proteinuria and Glomerular Filtration Rate on Renal Outcome in Patients with Biopsy-Proven Benign Nephrosclerosis
Published in PloS one (25-01-2016)“…Reduced estimated glomerular filtration rate (eGFR) and proteinuria are risk factors for end-stage renal disease (ESRD), of which benign nephrosclerosis is a…”
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A clinical staging score to measure the severity of dialysis-related amyloidosis
Published in Clinical and experimental nephrology (01-04-2017)“…Background The ongoing effort to prevent dialysis-related amyloidosis (DRA) has been hampered by lack of any way to measure DRA’s severity. Yet, such…”
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Recurrent Cholangitis in a Patient with Autosomal Dominant Polycystic Kidney Disease (ADPKD) and Caroli's Disease
Published in Internal Medicine (01-01-2016)“…We herein present a rare case of an autosomal dominant polycystic kidney disease (ADPKD) patient with Caroli's disease, a congenital embryonic biliary tree…”
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Ursodeoxycholic Acid for Treatment of Enlarged Polycystic Liver
Published in Therapeutic apheresis and dialysis (01-02-2016)“…Patients with autosomal dominant polycystic kidney disease and polycystic liver disease (PLD) often have elevated serum levels of alkaline phosphatase (ALP)…”
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Bone Histology of Two Cases with Osteomalacia Related to Low-dose Adefovir
Published in Internal Medicine (01-01-2016)“…We performed a bone histomorphometric analysis in two patients demonstrating Fanconi syndrome with hypophosphatemia, adefovir-related bone disease and chronic…”
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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
Published in CEN case reports (01-11-2020)“…A 79-year-old Japanese male with a history of type 2 diabetes mellitus (T2DM) for 16 years was admitted to evaluate possible renal disease. The T2DM was well…”
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AA-negative and Kappa-positive Amyloidosis in a Patient with Rheumatoid Arthritis
Published in Internal Medicine (01-01-2016)“…A 57-year-old Japanese woman with a 5-year history of rheumatoid arthritis (RA) was admitted to our hospital for an evaluation of nephrotic range proteinuria…”
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IgG4-related Disease: A Mass Lesion in the Intrarenal Sinus near the Renal Pelvis
Published in Internal Medicine (01-01-2015)“…A 52-year-old Japanese woman was admitted to our hospital with the renal pelvic mass lesion detected on a health screening examination. The surgical specimen…”
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Malignant Nephrosclerosis in a Patient with Familial Mediterranean Fever
Published in Internal Medicine (01-01-2015)“…A 37-year-old man was admitted to our hospital for an evaluation of renal dysfunction and hypertension. The C-reactive protein level was 6.0 mg/dL, and the…”
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Peritoneal Dialysis is Limited by Kidney and Liver Volume in Autosomal Dominant Polycystic Kidney Disease
Published in Therapeutic apheresis and dialysis (01-06-2015)“…We evaluated the influence of kidney volume (KV) and liver volume (LV) on continuation of peritoneal dialysis (PD) in patients with autosomal dominant…”
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