Zobrazeno 1 - 10 of 72 pro vyhledávání: '"Tetsuo Morioka"'
1
Akademický článek
Acute Kidney Injury Associated with Minimal Change Nephrotic Syndrome in an Elderly Patient Successfully Treated with both Fluid Management and Specific Therapy Based on Kidney Biopsy Findings
Autor: Yuko Oyama, Yoichi Iwafuchi, Tetsuo Morioka, Ichiei Narita
Publikováno v: Case Reports in Nephrology and Dialysis, Vol 10, Iss 1, Pp 42-50 (2020)
Oliguric acute kidney injury (AKI) with minimal change nephrotic syndrome (MCNS) has long been recognized. Several mechanisms such as hypovolemia due to hypoalbuminemia and the nephrosarca hypothesis have been proposed. However, the precise mechanism
Externí odkaz: https://doaj.org/article/7f6260829d774609b65d915a4690f29e
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2
Akademický článek
Complement Factor H Gene Variant in a Patient with Thrombotic Microangiopathy on a Mixed Clinical Background
Autor: Yoichi Iwafuchi, Tetsuo Morioka, Yuko Oyama, Shin Goto, Ichiei Narita
Publikováno v: Case Reports in Nephrology, Vol 2021 (2021)
We report the case of a patient with complement factor H gene variant, who developed thrombotic microangiopathy on a mixed clinical background. A 79-year-old woman was transferred to Sanjo General Hospital for maintenance hemodialysis. She suffered f
Externí odkaz: https://doaj.org/article/b80004b958a34d0d873da1dbdade9073
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5
Acute Kidney Injury Associated with Minimal Change Nephrotic Syndrome in an Elderly Patient Successfully Treated with both Fluid Management and Specific Therapy Based on Kidney Biopsy Findings
Autor: Tetsuo Morioka, Ichiei Narita, Yoichi Iwafuchi, Yuko Oyama
Publikováno v: Case Reports in Nephrology and Dialysis, Vol 10, Iss 1, Pp 42-50 (2020)
Case Reports in Nephrology and Dialysis
Oliguric acute kidney injury (AKI) with minimal change nephrotic syndrome (MCNS) has long been recognized. Several mechanisms such as hypovolemia due to hypoalbuminemia and the nephrosarca hypothesis have been proposed. However, the precise mechanism
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ddd500c6906ceaac2b7394dd7a25e77
https://doi.org/10.1159/000507426
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6
A case of smoldering antineutrophil cytoplasmic antibody-associated vasculitis development during the course of primary Sjögren's syndrome
Autor: Yoichi Iwafuchi, Tetsuo Morioka, Ichiei Narita, Yuko Oyama
Publikováno v: CEN Case Rep
Various forms of glomerular lesions have been described in primary Sjogren's syndrome (pSjS); however, myeloperoxidase (MPO)-antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis is rarely reported, and the disease onset and clinical cours
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7d71955fb0530f9a4f5d63d1836f778
https://pubmed.ncbi.nlm.nih.gov/34787826
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7
Complement Factor H Gene Variant in a Patient with Thrombotic Microangiopathy on a Mixed Clinical Background
Autor: Tetsuo Morioka, Shin Goto, Yoichi Iwafuchi, Ichiei Narita, Yuko Oyama
Publikováno v: Case Reports in Nephrology, Vol 2021 (2021)
Case Reports in Nephrology
We report the case of a patient with complement factor H gene variant, who developed thrombotic microangiopathy on a mixed clinical background. A 79-year-old woman was transferred to Sanjo General Hospital for maintenance hemodialysis. She suffered f
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c34e07a8da51ebb47df82b92d298d872
https://doaj.org/article/b80004b958a34d0d873da1dbdade9073
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8
Atrial Fibrillation Had Less Impact on the Risk of Ischemic Stroke in Non-anticoagulated Patients Undergoing Hemodialysis: Insight from the RAKUEN study
Autor: Katsuharu Hatada, Taku Matsubara, Tetsuo Morioka, Yutaka Tsubata, Hisaki Shimada, Wataru Mitsuma, Noriko Saito, Kozo Ikarashi, Makoto Tamura, Shigeru Miyazaki, Shunsuke Imai
Publikováno v: Internal Medicine. 57:2295-2300
Objective The progress of non-anticoagulated patients with atrial fibrillation (AF) undergoing hemodialysis has not been determined. Using data from the RAKUEN (Registry of Atrial fibrillation in chronic Kidney disease Under hEmodialysis from Niigata
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8732a2c41d4d2c4640a6a583beba028
https://doi.org/10.2169/internalmedicine.0021-17
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9
A Case of Transforming Growth Factor-β-Induced Gene-Related Oculorenal Syndrome: Granular Corneal Dystrophy Type II with a Unique Nephropathy
Autor: Ichiei Narita, Tetsuo Morioka, Yuko Oyama, Yoichi Iwafuchi, Kazumoto Iijima, Kandai Nozu
Publikováno v: Case Reports in Nephrology and Dialysis
Many types of inherited renal diseases have ocular features that occasionally support a diagnosis. The following study describes an unusual example of a 40-year-old woman with granular corneal dystrophy type II complicated by renal involvement. These
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28d3ec209105c3147f1f05fdaa8de335
http://europepmc.org/articles/PMC5073658
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10
Diverse Renal Phenotypes Observed in a Single Family with a Genetic Mutation in Paired Box Protein 2
Autor: Toshio Yanagihara, Yuko Oyama, Naoya Morisada, Ichiei Narita, Kazumoto Iijima, Yoichi Iwafuchi, Tetsuo Morioka, Takashi Morita
Publikováno v: Case Reports in Nephrology and Dialysis
A common renal phenotype of paired box protein 2 (PAX2) mutations is renal coloboma syndrome. We report a single family with diverse renal phenotypes associated with PAX2 mutation. The proband presented steroid-resistant focal segmental glomeruloscle
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43addb819fdc6a7f672a153871ee1f0e
https://doi.org/10.1159/000445679
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