Ohnishi H - Search Results

1

A case of A20 haploinsufficiency complicated by autoimmune hepatitis.

Iwasa T, Miwa T, Unome S, Hanai T, Imai K, Takai K, Miwa Y, Hori T, Ohnishi H, Matsumoto M, Niwa A, Miyazaki T, Shimizu M. Iwasa T, et al. Among authors: ohnishi h. Hepatol Res. 2023 Dec 21. doi: 10.1111/hepr.14003. Online ahead of print. Hepatol Res. 2023. PMID: 38126665

2

Autosomal-dominant chronic mucocutaneous candidiasis with STAT1-mutation can be complicated with chronic active hepatitis and hypothyroidism.

Hori T, Ohnishi H, Teramoto T, Tsubouchi K, Naiki T, Hirose Y, Ohara O, Seishima M, Kaneko H, Fukao T, Kondo N. Hori T, et al. Among authors: ohnishi h. J Clin Immunol. 2012 Dec;32(6):1213-20. doi: 10.1007/s10875-012-9744-6. Epub 2012 Jul 31. J Clin Immunol. 2012. PMID: 22847544

3

Single-nucleotide substitution T to A in the polypyrimidine stretch at the splice acceptor site of intron 9 causes exon 10 skipping in the ACAT1 gene.

Sasai H, Aoyama Y, Otsuka H, Abdelkreem E, Nakama M, Hori T, Ohnishi H, Turner L, Fukao T. Sasai H, et al. Among authors: ohnishi h. Mol Genet Genomic Med. 2017 Feb 8;5(2):177-184. doi: 10.1002/mgg3.275. eCollection 2017 Mar. Mol Genet Genomic Med. 2017. PMID: 28361105 Free PMC article.

4

Prepubertal onset of slipped capital femoral epiphysis associated with hypothyroidism: a case report and literature review.

Kadowaki S, Hori T, Matsumoto H, Kanda K, Ozeki M, Shirakami Y, Kawamoto N, Ohnishi H, Fukao T. Kadowaki S, et al. Among authors: ohnishi h. BMC Endocr Disord. 2017 Sep 18;17(1):59. doi: 10.1186/s12902-017-0210-6. BMC Endocr Disord. 2017. PMID: 28923047 Free PMC article. Review.

5

Haploinsufficiency of A20 causes autoinflammatory and autoimmune disorders.

Kadowaki T, Ohnishi H, Kawamoto N, Hori T, Nishimura K, Kobayashi C, Shigemura T, Ogata S, Inoue Y, Kawai T, Hiejima E, Takagi M, Imai K, Nishikomori R, Ito S, Heike T, Ohara O, Morio T, Fukao T, Kanegane H. Kadowaki T, et al. Among authors: ohnishi h. J Allergy Clin Immunol. 2018 Apr;141(4):1485-1488.e11. doi: 10.1016/j.jaci.2017.10.039. Epub 2017 Dec 11. J Allergy Clin Immunol. 2018. PMID: 29241730 No abstract available.

6

Autosomal dominant Hashimoto's thyroiditis with a mutation in TNFAIP3.

Hori T, Ohnishi H, Kadowaki T, Kawamoto N, Matsumoto H, Ohara O, Fukao T. Hori T, et al. Among authors: ohnishi h. Clin Pediatr Endocrinol. 2019;28(3):91-96. doi: 10.1297/cpe.28.91. Epub 2019 Jul 20. Clin Pediatr Endocrinol. 2019. PMID: 31384100 Free PMC article.

7

Immunophenotyping of A20 haploinsufficiency by multicolor flow cytometry.

Kadowaki T, Ohnishi H, Kawamoto N, Kadowaki S, Hori T, Nishimura K, Kobayashi C, Shigemura T, Ogata S, Inoue Y, Hiejima E, Izawa K, Matsubayashi T, Matsumoto K, Imai K, Nishikomori R, Ito S, Kanegane H, Fukao T. Kadowaki T, et al. Among authors: ohnishi h. Clin Immunol. 2020 Jul;216:108441. doi: 10.1016/j.clim.2020.108441. Epub 2020 Apr 23. Clin Immunol. 2020. PMID: 32335289

8

Neonatal bacteremia caused by emm type 80 group A Streptococcus: A case report.

Shinoda Y, Hori T, Sasai H, Ikebe T, Ohnishi H. Shinoda Y, et al. Among authors: ohnishi h. Pediatr Int. 2020 Nov;62(11):1305-1306. doi: 10.1111/ped.14349. Epub 2020 Nov 3. Pediatr Int. 2020. PMID: 33145863 No abstract available.

9

A20 Haploinsufficiency in East Asia.

Kadowaki T, Kadowaki S, Ohnishi H. Kadowaki T, et al. Among authors: ohnishi h. Front Immunol. 2021 Nov 26;12:780689. doi: 10.3389/fimmu.2021.780689. eCollection 2021. Front Immunol. 2021. PMID: 34899744 Free PMC article. Review.

10

Case Report: Analysis of Preserved Umbilical Cord Clarified X-Linked Anhidrotic Ectodermal Dysplasia With Immunodeficiency in Deceased, Undiagnosed Uncles.

Inaba S, Aizawa Y, Miwa Y, Imai C, Ohnishi H, Kanegane H, Saitoh A. Inaba S, et al. Among authors: ohnishi h. Front Immunol. 2021 Dec 22;12:786164. doi: 10.3389/fimmu.2021.786164. eCollection 2021. Front Immunol. 2021. PMID: 35003103 Free PMC article.

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