Morioka T - Search Results

1

Renal histopathological findings of retinal vasculopathy with cerebral leukodystrophy.

Tsubata Y, Morita T, Morioka T, Sasagawa T, Ikarashi K, Saito N, Shimada H, Miyazaki S, Sakai S, Tanaka H, Saito R, Toyoshima Y, Nozaki H, Narita I. Tsubata Y, et al. Among authors: morioka t. CEN Case Rep. 2018 May;7(1):83-89. doi: 10.1007/s13730-017-0300-3. Epub 2018 Jan 10. CEN Case Rep. 2018. PMID: 29322432 Free PMC article.

2

Severe hypermagnesemia induced by magnesium oxide ingestion: a case series.

Yamaguchi H, Shimada H, Yoshita K, Tsubata Y, Ikarashi K, Morioka T, Saito N, Sakai S, Narita I. Yamaguchi H, et al. Among authors: morioka t. CEN Case Rep. 2019 Feb;8(1):31-37. doi: 10.1007/s13730-018-0359-5. Epub 2018 Aug 22. CEN Case Rep. 2019. PMID: 30136128 Free PMC article.

3

Retinal Vasculopathy With Cerebral Leukodystrophy: Clinicopathologic Features of an Autopsied Patient With a Heterozygous TREX 1 Mutation.

Saito R, Nozaki H, Kato T, Toyoshima Y, Tanaka H, Tsubata Y, Morioka T, Horikawa Y, Oyanagi K, Morita T, Onodera O, Kakita A. Saito R, et al. Among authors: morioka t. J Neuropathol Exp Neurol. 2019 Feb 1;78(2):181-186. doi: 10.1093/jnen/nly115. J Neuropathol Exp Neurol. 2019. PMID: 30561700

4

Nephrotic Syndrome without Hematuria due to Infection-Related Glomerulonephritis Mimicking Minimal-Change Disease in a Child.

Iwafuchi Y, Morioka T, Morita T, Watanabe K, Oyama Y, Narita I. Iwafuchi Y, et al. Among authors: morioka t. Case Rep Nephrol Dial. 2016 Jan 15;6(1):14-20. doi: 10.1159/000443727. eCollection 2016 Jan-Apr. Case Rep Nephrol Dial. 2016. PMID: 26889476 Free PMC article.

5

Diverse Renal Phenotypes Observed in a Single Family with a Genetic Mutation in Paired Box Protein 2.

Iwafuchi Y, Morioka T, Morita T, Yanagihara T, Oyama Y, Morisada N, Iijima K, Narita I. Iwafuchi Y, et al. Among authors: morioka t. Case Rep Nephrol Dial. 2016 Apr 14;6(1):61-9. doi: 10.1159/000445679. eCollection 2016 Jan-Apr. Case Rep Nephrol Dial. 2016. PMID: 27226968 Free PMC article.

6

Enzyme replacement therapy in a patient of heterozygous Fabry disease: clinical and pathological evaluations by repeat kidney biopsy and a successful pregnancy.

Iwafuchi Y, Maruyama H, Morioka T, Noda S, Nagata H, Oyama Y, Narita I. Iwafuchi Y, et al. Among authors: morioka t. CEN Case Rep. 2017 Nov;6(2):210-214. doi: 10.1007/s13730-017-0277-y. Epub 2017 Oct 10. CEN Case Rep. 2017. PMID: 29019163 Free PMC article.

7

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.

Oyama Y, Iwafuchi Y, Morioka T, Narita I. Oyama Y, et al. Among authors: morioka t. Case Rep Nephrol Dial. 2020 Apr 22;10(1):42-50. doi: 10.1159/000507426. eCollection 2020 Jan-Apr. Case Rep Nephrol Dial. 2020. PMID: 32399474 Free PMC article.

8

A case of smoldering antineutrophil cytoplasmic antibody-associated vasculitis development during the course of primary Sjögren's syndrome.

Iwafuchi Y, Morioka T, Oyama Y, Narita I. Iwafuchi Y, et al. Among authors: morioka t. CEN Case Rep. 2022 May;11(2):247-253. doi: 10.1007/s13730-021-00663-1. Epub 2021 Nov 17. CEN Case Rep. 2022. PMID: 34787826 Free PMC article.

9

A Case of Transforming Growth Factor-β-Induced Gene-Related Oculorenal Syndrome: Granular Corneal Dystrophy Type II with a Unique Nephropathy.

Iwafuchi Y, Morioka T, Oyama Y, Nozu K, Iijima K, Narita I. Iwafuchi Y, et al. Among authors: morioka t. Case Rep Nephrol Dial. 2016 Sep 13;6(3):106-113. doi: 10.1159/000449129. eCollection 2016 Sep-Dec. Case Rep Nephrol Dial. 2016. PMID: 27781206 Free PMC article.

10

Complement Factor H Gene Variant in a Patient with Thrombotic Microangiopathy on a Mixed Clinical Background.

Iwafuchi Y, Morioka T, Oyama Y, Goto S, Narita I. Iwafuchi Y, et al. Among authors: morioka t. Case Rep Nephrol. 2021 Oct 25;2021:2519918. doi: 10.1155/2021/2519918. eCollection 2021. Case Rep Nephrol. 2021. PMID: 34733563 Free PMC article.

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