Alpha 2.0
Login Register
» Authors » Tetsuo Morioka

Tetsuo Morioka

Explore the profile of Tetsuo Morioka including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 38
Citations 361
Followers 0
Related Specialties
Nephrology
Biology
Neurology
Top 10 Co-Authors
Takashi Oite
Jian Yao
Ichiei Narita
Yuko Oyama
Yoichi Iwafuchi
Bing Li
Yutaka Tsubata
Takashi Morita
Noriko Saito
Fumitake Gejyo
Published In
CEN Case Rep
Kidney Int
Nephron Exp Nephrol
Clin Exp Nephrol
Case Rep Nephrol Dial
Affiliations
Soon will be listed here.
Recent Articles
1.
A case of non-lupus full-house nephropathy diagnosed by kidney biopsy but observed IgA nephropathy on second biopsy
Iwafuchi Y, Morioka T, Oyama Y, Narita I
CEN Case Rep . 2024 Feb; 13(5):373-380. PMID: 38421587
We describe a case of full-house nephropathy without any underlying disease, including systemic lupus erythematosus. A 40-year-old woman was referred to our hospital with mild proteinuria and microscopic hematuria. The...
2.
Fatal acute portal vein thrombosis associated with hepatic cysts in a patient with autosomal dominant polycystic kidney disease
Tsuchida Y, Tsubata Y, Nozawa R, Maruyama S, Ikarashi K, Saito N, et al.
CEN Case Rep . 2023 May; 13(1):32-36. PMID: 37162720
Autosomal dominant polycystic kidney disease (ADPKD) often involves polycystic liver disease (PLD). In severe cases, PLD can develop various complications. However, fatal acute portal vein thrombosis (APVT) associated with PLD...
3.
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
CEN Case Rep . 2021 Nov; 11(2):247-253. PMID: 34787826
Various forms of glomerular lesions have been described in primary Sjögren's syndrome (pSjS); however, myeloperoxidase (MPO)-antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis is rarely reported, and the disease onset and clinical course...
4.
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
Case Rep Nephrol . 2021 Nov; 2021:2519918. PMID: 34733563
We report the case of a patient with gene variant, who developed thrombotic microangiopathy on a mixed clinical background. A 79-year-old woman was transferred to Sanjo General Hospital for maintenance...
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
Oyama Y, Iwafuchi Y, Morioka T, Narita I
Case Rep Nephrol Dial . 2020 May; 10(1):42-50. PMID: 32399474
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....
6.
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, et al.
J Neuropathol Exp Neurol . 2018 Dec; 78(2):181-186. PMID: 30561700
Retinal vasculopathy with cerebral leukodystrophy (RVCL) is an autosomal-dominant disorder involving the cerebral, retinal, renal, and other systemic microvessels due to frameshift mutations in the TREX1 gene. Under physiological conditions,...
7.
Severe hypermagnesemia induced by magnesium oxide ingestion: a case series
Yamaguchi H, Shimada H, Yoshita K, Tsubata Y, Ikarashi K, Morioka T, et al.
CEN Case Rep . 2018 Aug; 8(1):31-37. PMID: 30136128
Hypermagnesemia is generally considered an exceptional iatrogenic condition usually caused by magnesium-containing cathartics. In particular, this condition often develops when magnesium-containing cathartics are administered to elderly patients with renal insufficiency...
8.
Atrial Fibrillation Had Less Impact on the Risk of Ischemic Stroke in Non-anticoagulated Patients Undergoing Hemodialysis: Insight from the RAKUEN study
Mitsuma W, Matsubara T, Hatada K, Imai S, Tamura M, Tsubata Y, et al.
Intern Med . 2018 Apr; 57(16):2295-2300. PMID: 29607945
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...
9.
Renal histopathological findings of retinal vasculopathy with cerebral leukodystrophy
Tsubata Y, Morita T, Morioka T, Sasagawa T, Ikarashi K, Saito N, et al.
CEN Case Rep . 2018 Jan; 7(1):83-89. PMID: 29322432
Retinal vasculopathy with cerebral leukodystrophy (RVCL) is a rare autosomal dominant systemic microvascular disease. Neurological disorders and visual disturbance are highlighted as manifestations of RVCL; however, there are few reports...
10.
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, et al.
CEN Case Rep . 2017 Oct; 6(2):210-214. PMID: 29019163
Fabry disease is a rare X-linked lysosomal storage disorder of glycosphingolipid catabolism caused by deficient activity of the lysosomal hydrolase alpha-galactosidase A (ɑ-Gal A). A 20-year-old woman was referred to...