Oka A - Search Results

1

Rituximab-induced serum sickness in a 6-year-old boy with steroid-dependent nephrotic syndrome.

Nakamura M, Kanda S, Yoshioka Y, Takahashi C, Owada K, Kajiho Y, Harita Y, Oka A. Nakamura M, et al. Among authors: oka a. CEN Case Rep. 2020 May;9(2):173-176. doi: 10.1007/s13730-020-00449-x. Epub 2020 Jan 22. CEN Case Rep. 2020. PMID: 31970629 Free PMC article.

2

Altered expression of Crb2 in podocytes expands a variation of CRB2 mutations in steroid-resistant nephrotic syndrome.

Udagawa T, Jo T, Yanagihara T, Shimizu A, Mitsui J, Tsuji S, Morishita S, Onai R, Miura K, Kanda S, Kajiho Y, Tsurumi H, Oka A, Hattori M, Harita Y. Udagawa T, et al. Among authors: oka a. Pediatr Nephrol. 2017 May;32(5):801-809. doi: 10.1007/s00467-016-3549-4. Epub 2016 Dec 10. Pediatr Nephrol. 2017. PMID: 27942854

3

Mild Chest Pain After Gymnastic Backflip in a 14-Year-Old Boy.

Hayakawa I, Harita Y, Oka A. Hayakawa I, et al. Among authors: oka a. Glob Pediatr Health. 2017 Dec 6;4:2333794X17745766. doi: 10.1177/2333794X17745766. eCollection 2017. Glob Pediatr Health. 2017. PMID: 29238739 Free PMC article. No abstract available.

4

Amnionless-mediated glycosylation is crucial for cell surface targeting of cubilin in renal and intestinal cells.

Udagawa T, Harita Y, Miura K, Mitsui J, Ode KL, Morishita S, Urae S, Kanda S, Kajiho Y, Tsurumi H, Ueda HR, Tsuji S, Saito A, Oka A. Udagawa T, et al. Among authors: oka a. Sci Rep. 2018 Feb 5;8(1):2351. doi: 10.1038/s41598-018-20731-4. Sci Rep. 2018. PMID: 29402915 Free PMC article.

5

An infant with X-linked anhidrotic ectodermal dysplasia with immunodeficiency presenting with Pneumocystis pneumonia: A case report.

Toyohara M, Kajiho Y, Toyofuku E, Takahashi C, Owada K, Kanda S, Harita Y, Ohnishi H, Wada T, Imai K, Kanegane H, Morio T, Oka A. Toyohara M, et al. Among authors: oka a. Clin Case Rep. 2021 Nov 16;9(11):e05093. doi: 10.1002/ccr3.5093. eCollection 2021 Nov. Clin Case Rep. 2021. PMID: 34815879 Free PMC article.

6

Incomplete cryptic splicing by an intronic mutation of OCRL in patients with partial phenotypes of Lowe syndrome.

Nakano E, Yoshida A, Miyama Y, Yabuuchi T, Kajiho Y, Kanda S, Miura K, Oka A, Harita Y. Nakano E, et al. Among authors: oka a. J Hum Genet. 2020 Oct;65(10):831-839. doi: 10.1038/s10038-020-0773-3. Epub 2020 May 19. J Hum Genet. 2020. PMID: 32427950

7

A cellular model of albumin endocytosis uncovers a link between membrane and nuclear proteins.

Urae S, Harita Y, Udagawa T, Ode KL, Nagahama M, Kajiho Y, Kanda S, Saito A, Ueda HR, Nangaku M, Oka A. Urae S, et al. Among authors: oka a. J Cell Sci. 2020 Jul 6;133(13):jcs242859. doi: 10.1242/jcs.242859. J Cell Sci. 2020. PMID: 32482797

8

Systemic lupus erythematosus presenting with mixed-type fulminant autoimmune hemolytic anemia.

Hirano Y, Itonaga T, Yasudo H, Isojima T, Miura K, Harita Y, Sekiguchi M, Kato M, Takita J, Oka A. Hirano Y, et al. Among authors: oka a. Pediatr Int. 2016 Jun;58(6):527-530. doi: 10.1111/ped.12849. Epub 2016 Feb 19. Pediatr Int. 2016. PMID: 26892457

9

Deletion in the Cobalamin Synthetase W Domain-Containing Protein 1 Gene Is associated with Congenital Anomalies of the Kidney and Urinary Tract.

Kanda S, Ohmuraya M, Akagawa H, Horita S, Yoshida Y, Kaneko N, Sugawara N, Ishizuka K, Miura K, Harita Y, Yamamoto T, Oka A, Araki K, Furukawa T, Hattori M. Kanda S, et al. Among authors: oka a. J Am Soc Nephrol. 2020 Jan;31(1):139-147. doi: 10.1681/ASN.2019040398. Epub 2019 Dec 20. J Am Soc Nephrol. 2020. PMID: 31862704 Free PMC article.

10

Relationship between post-IVIG IgG levels and clinical outcomes in Kawasaki disease patients: new insight into the mechanism of action of IVIG.

Goto R, Inuzuka R, Shindo T, Namai Y, Oda Y, Harita Y, Oka A. Goto R, et al. Among authors: oka a. Clin Rheumatol. 2020 Dec;39(12):3747-3755. doi: 10.1007/s10067-020-05153-w. Epub 2020 May 27. Clin Rheumatol. 2020. PMID: 32458247

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