Incidence and clinical risk factors of Bednar's aphthae in Japanese newborns
Narukama, Risako, Takahashi, Keigo, Arimitsu, Takeshi, Hara‐Isono, Kaori, Shimizu, Hajime, Ikeda, Kazushige
Published in Pediatrics international (01.01.2023)
Published in Pediatrics international (01.01.2023)
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A patient with Silver-Russell syndrome with multilocus imprinting disturbance, and Schimke immuno-osseous dysplasia unmasked by uniparental isodisomy of chromosome 2
Hara-Isono, Kaori, Matsubara, Keiko, Hamada, Riku, Shimada, Shun, Yamaguchi, Tomomi, Wakui, Keiko, Miyazaki, Osamu, Muroya, Koji, Kurosawa, Kenji, Fukami, Maki, Ogata, Tsutomu, Kosho, Tomoki, Kagami, Masayo
Published in Journal of human genetics (01.11.2021)
Published in Journal of human genetics (01.11.2021)
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Journal Article
Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum
Fuke, Tomoko, Nakamura, Akie, Inoue, Takanobu, Kawashima, Sayaka, Hara, Kaori Isono, Matsubara, Keiko, Sano, Shinichiro, Yamazawa, Kazuki, Fukami, Maki, Ogata, Tsutomu, Kagami, Masayo
Published in The journal of clinical endocrinology and metabolism (08.03.2021)
Published in The journal of clinical endocrinology and metabolism (08.03.2021)
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Journal Article
The cut-off values of vitamin D deficiency in early infancy
Ikeda, Kazushige, Hara-Isono, Kaori, Takahashi, Keigo, Arimitsu, Takeshi, Sato, Yasunori
Published in Pediatrics and neonatology (01.07.2022)
Published in Pediatrics and neonatology (01.07.2022)
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Journal Article
Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system
Fuke, Tomoko, Nakamura, Akie, Inoue, Takanobu, Kawashima, Sayaka, Hara-Isono, Kaori, Matsubara, Keiko, Sano, Shinichiro, Yamazawa, Kazuki, Fukami, Maki, Ogata, Tsutomu, Kagami, Masayo
Published in Journal of human genetics (01.10.2022)
Published in Journal of human genetics (01.10.2022)
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Journal Article
Assisted reproductive technology represents a possible risk factor for development of epimutation-mediated imprinting disorders for mothers aged ≥ 30 years
Hara-Isono, Kaori, Matsubara, Keiko, Mikami, Masashi, Arima, Takahiro, Ogata, Tsutomu, Fukami, Maki, Kagami, Masayo
Published in Clinical epigenetics (22.07.2020)
Published in Clinical epigenetics (22.07.2020)
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Journal Article
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, Kaori, Matsubara, Keiko, Nakamura, Akie, Sano, Shinichiro, Inoue, Takanobu, Kawashima, Sayaka, Fuke, Tomoko, Yamazawa, Kazuki, Fukami, Maki, Ogata, Tsutomu, Kagami, Masayo
Published in Clinical epigenetics (06.05.2023)
Published in Clinical epigenetics (06.05.2023)
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Journal Article
Comprehensive orthodontic treatment for Silver–Russell syndrome patient with large overjet and overbite
Murata, Yuka, Kurosaka, Hiroshi, Hirose, Takumi, Fujiwara, Makoto, Miyoshi, Yoko, Kagami, Masayo, Hara-Isono, Kaori, Ozono, Keiichi, Yamashiro, Takashi
Published in Clinical and investigative orthodontics (Online) (03.07.2022)
Published in Clinical and investigative orthodontics (Online) (03.07.2022)
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Journal Article
Genome-wide methylation analysis in Silver-Russell syndrome, Temple syndrome, and Prader-Willi syndrome
Hara-Isono, Kaori, Matsubara, Keiko, Fuke, Tomoko, Yamazawa, Kazuki, Satou, Kazuhito, Murakami, Nobuyuki, Saitoh, Shinji, Nakabayashi, Kazuhiko, Hata, Kenichiro, Ogata, Tsutomu, Fukami, Maki, Kagami, Masayo
Published in Clinical epigenetics (22.10.2020)
Published in Clinical epigenetics (22.10.2020)
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Journal Article
CDKN1C hyperexpression in two patients with severe growth failure and microdeletions affecting the paternally inherited KCNQ1OT1:TSS-DMR
Hara-Isono, Kaori, Yamazawa, Kazuki, Tanaka, Satsuki, Nishi, Eriko, Fukami, Maki, Kagami, Masayo
Published in Journal of medical genetics (01.12.2022)
Published in Journal of medical genetics (01.12.2022)
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Journal Article
Pathogenic copy number and sequence variants in children born SGA with short stature without imprinting disorders
Hara-Isono, Kaori, Nakamura, Akie, Fuke, Tomoko, Inoue, Takanobu, Kawashima, Sayaka, Matsubara, Keiko, Sano, Shinichiro, Yamazawa, Kazuki, Fukami, Maki, Ogata, Tsutomu, Kagami, Masayo
Published in The journal of clinical endocrinology and metabolism (01.08.2022)
Published in The journal of clinical endocrinology and metabolism (01.08.2022)
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Journal Article
A boy with overgrowth caused by multi-locus imprinting disturbance including hypomethylation of MEST:alt-TSS-DMR
Narusawa, Hiromune, Sasaki, Sunao, Hara-Isono, Kaori, Matsubara, Keiko, Fukami, Maki, Nagasaki, Keisuke, Kagami, Masayo
Published in European journal of medical genetics (01.06.2022)
Published in European journal of medical genetics (01.06.2022)
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Journal Article
Discordant responses of bone formation and absorption markers in Japanese infants with vitamin D deficiency: a comprehensive matched case-control study
Takahashi, Keigo, Ikeda, Kazushige, Hara-Isono, Kaori, Nitta, Akihisa, Nagano, Nobuhiko, Arimitsu, Takeshi
Published in JBMR plus (01.05.2024)
Published in JBMR plus (01.05.2024)
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Journal Article
ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbance
Kagami, Masayo, Hara-Isono, Kaori, Matsubara, Keiko, Nakabayashi, Kazuhiko, Narumi, Satoshi, Fukami, Maki, Ohkubo, Yumiko, Saitsu, Hirotomo, Takada, Shuji, Ogata, Tsutomu
Published in Clinical epigenetics (26.05.2021)
Published in Clinical epigenetics (26.05.2021)
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