Hara-Isono K - Search Results

1

Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance.

Urakawa T, Soejima H, Yamoto K, Hara-Isono K, Nakamura A, Kawashima S, Narusawa H, Kosaki R, Nishimura Y, Yamazawa K, Hattori T, Muramatsu Y, Inoue T, Matsubara K, Fukami M, Saitoh S, Ogata T, Kagami M. Urakawa T, et al. Among authors: hara isono k. Clin Epigenetics. 2024 Oct 5;16(1):138. doi: 10.1186/s13148-024-01744-5. Clin Epigenetics. 2024. PMID: 39369220 Free PMC article.

2

Discordant responses of bone formation and absorption markers in Japanese infants with vitamin D deficiency: a comprehensive matched case-control study.

Takahashi K, Ikeda K, Hara-Isono K, Nitta A, Nagano N, Arimitsu T. Takahashi K, et al. Among authors: hara isono k. JBMR Plus. 2024 Mar 18;8(5):ziae033. doi: 10.1093/jbmrpl/ziae033. eCollection 2024 May. JBMR Plus. 2024. PMID: 38623484 Free PMC article.

3

Incidence and clinical risk factors of Bednar's aphthae in Japanese newborns.

Narukama R, Takahashi K, Arimitsu T, Hara-Isono K, Shimizu H, Ikeda K. Narukama R, et al. Among authors: hara isono k. Pediatr Int. 2023 Jan-Dec;65(1):e15631. doi: 10.1111/ped.15631. Pediatr Int. 2023. PMID: 37804067

4

Risk assessment of assisted reproductive technology and parental age at childbirth for the development of uniparental disomy-mediated imprinting disorders caused by aneuploid gametes.

Hara-Isono K, Matsubara K, Nakamura A, Sano S, Inoue T, Kawashima S, Fuke T, Yamazawa K, Fukami M, Ogata T, Kagami M. Hara-Isono K, et al. Clin Epigenetics. 2023 May 6;15(1):78. doi: 10.1186/s13148-023-01494-w. Clin Epigenetics. 2023. PMID: 37147716 Free PMC article.

5

Seasonal variation in vitamin D status of Japanese infants starts to emerge at 2 months of age: a retrospective cohort study.

Takahashi K, Arimitsu T, Hara-Isono K, Ikeda K. Takahashi K, et al. Among authors: hara isono k. Br J Nutr. 2023 Jun 14;129(11):1908-1915. doi: 10.1017/S0007114522002744. Epub 2022 Aug 26. Br J Nutr. 2023. PMID: 36017869

6

CDKN1C hyperexpression in two patients with severe growth failure and microdeletions affecting the paternally inherited KCNQ1OT1:TSS-DMR.

Hara-Isono K, Yamazawa K, Tanaka S, Nishi E, Fukami M, Kagami M. Hara-Isono K, et al. J Med Genet. 2022 Dec;59(12):1241-1246. doi: 10.1136/jmg-2022-108700. Epub 2022 Jul 29. J Med Genet. 2022. PMID: 35906012

7

Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system.

Fuke T, Nakamura A, Inoue T, Kawashima S, Hara-Isono K, Matsubara K, Sano S, Yamazawa K, Fukami M, Ogata T, Kagami M. Fuke T, et al. Among authors: hara isono k. J Hum Genet. 2022 Oct;67(10):607-611. doi: 10.1038/s10038-022-01048-7. Epub 2022 May 24. J Hum Genet. 2022. PMID: 35606504

8

Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting Disorders.

Hara-Isono K, Nakamura A, Fuke T, Inoue T, Kawashima S, Matsubara K, Sano S, Yamazawa K, Fukami M, Ogata T, Kagami M. Hara-Isono K, et al. J Clin Endocrinol Metab. 2022 Jul 14;107(8):e3121-e3133. doi: 10.1210/clinem/dgac319. J Clin Endocrinol Metab. 2022. PMID: 35583390

9

A boy with overgrowth caused by multi-locus imprinting disturbance including hypomethylation of MEST:alt-TSS-DMR.

Narusawa H, Sasaki S, Hara-Isono K, Matsubara K, Fukami M, Nagasaki K, Kagami M. Narusawa H, et al. Among authors: hara isono k. Eur J Med Genet. 2022 Jun;65(6):104502. doi: 10.1016/j.ejmg.2022.104502. Epub 2022 Apr 13. Eur J Med Genet. 2022. PMID: 35427809

10

The cut-off values of vitamin D deficiency in early infancy.

Ikeda K, Hara-Isono K, Takahashi K, Arimitsu T, Sato Y. Ikeda K, et al. Among authors: hara isono k. Pediatr Neonatol. 2022 Jul;63(4):361-367. doi: 10.1016/j.pedneo.2021.12.012. Epub 2022 Mar 22. Pediatr Neonatol. 2022. PMID: 35410821 Free article.

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