Masato Nishioka
Overview
Explore the profile of Masato Nishioka including associated specialties, affiliations and a list of published articles.
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Articles
23
Citations
141
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0
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Recent Articles
1.
Inamura N, Taniguchi H, Yoshida S, Nishioka M, Ishihara K
Sci Rep
. 2024 Jan;
14(1):1089.
PMID: 38212465
Ultra-endurance events have gained global participation, whereas the critical factors of competition results remain to be well elucidated. This study used a nutritional approach to evaluate the association of competition...
2.
Hatano M, Udagawa T, Kanamori T, Sutani A, Mori T, Sohara E, et al.
Hum Genome Var
. 2022 Nov;
9(1):42.
PMID: 36450716
Familial renal glucosuria (FRG) is characterized by persistent glucosuria despite normal blood glucose levels in the absence of overt tubular dysfunction. SGLT2 is a sodium-glucose cotransporter expressed in the proximal...
3.
Hatano M, Shimizu M, Miyaoka F, Kanai H, Nishioka M
Pediatr Int
. 2022 Mar;
64(1):e15013.
PMID: 35278252
No abstract available.
4.
Kurokami T, Takasawa R, Takeda S, Kurobe M, Takasawa K, Nishioka M, et al.
Turk J Pediatr
. 2019 Mar;
60(4):429-432.
PMID: 30859769
Kurokami T, Takasawa R, Takeda S, Kurobe M, Takasawa K, Nishioka M, Shimohira M. Venous thromboembolism in two adolescents with Down syndrome. Turk J Pediatr 2018; 60: 429-432. Although venous...
5.
Shimbo A, Takasawa K, Nishioka M, Morio T, Shimohira M
Pediatr Int
. 2018 Jun;
60(5):491-492.
PMID: 29878630
No abstract available.
6.
Shimoyama T, Matsuda N, Kurobe M, Hayakawa T, Nishioka M, Shimohira M, et al.
Paediatr Int Child Health
. 2018 Apr;
39(3):219-223.
PMID: 29621936
About 50-75% of patients with Henoch-Schönlein purpura (HSP) develop gastro-intestinal symptoms with surgical complications such as intussusception occurring in 0.7-13.6%. In 10-40% of patients, however, gastro-intestinal manifestations may precede the...
7.
Satoh K, Wakejima Y, Gau M, Kiguchi T, Matsuda N, Takasawa R, et al.
Int J Rheum Dis
. 2017 Nov;
21(3):746-754.
PMID: 29105337
Aim: To examine clinical characteristics of Kawasaki disease (KD) in infants younger than 3 months of age and to develop a method for detecting KD in febrile infants. Method: In...
8.
Kobayashi A, Takasawa R, Takasawa K, Nishioka M, Kaneko M, Ono H, et al.
Allergol Int
. 2016 Nov;
66(3):479-481.
PMID: 27843080
No abstract available.
9.
Murakoshi M, Takasawa K, Nishioka M, Asakawa M, Kashimada K, Yoshimoto T, et al.
Am J Med Genet A
. 2016 Oct;
173(2):495-500.
PMID: 27774766
1p36 deletion syndrome is the most common terminal deletion syndrome, and the genomic regions that contribute to specific 1p36 deletion syndrome-related phenotypes were recently identified. Deletions in the 1p36 region...
10.
Takasawa K, Takeda S, Nishioka M, Sakuma H, Morio T, Shimohira M
Pediatr Infect Dis J
. 2016 Jan;
35(2):227-8.
PMID: 26756268
No abstract available.