Author Fujiwara, Shintaro| Harada, Ko| Hagiya, Hideharu| Koyama, Toshihiro| Hasegawa, Kosei| Tsukahara, Hirokazu| Otsuka, Fumio|
Keywords childhood obesity epidemiology joinpoint regression analysis paediatrics trend analysis
Note This is the peer reviewed version of the following article: [Fujiwara S, Harada K, Hagiya H, et al. Trends in childhood obesity in Japan: A nationwide observational study from 2012 to 2021. Clinical Obesity. 2023;e12636. doi:10.1111/cob.12636], which has been published in final form at [https://doi.org/10.1111/cob.12636]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.| This fulltext file will be available in Dec. 2024.|
Published Date 2023-12-29
Publication Title Clinical Obesity
Publisher Wiley
Start Page e12636
ISSN 1758-8103
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2023 World Obesity Federation.
File Version author
PubMed ID 38156435
DOI 10.1111/cob.12636
Web of Science KeyUT 001133999100001
Related Url isVersionOf https://doi.org/10.1111/cob.12636
Author Miyahara, Daisuke| Hasegawa, Kosei| Ago, Yuko| Futagawa, Natsuko| Miyahara, Hiroyuki| Higuchi, Yousuke| Yamada, Kazuki| Tetsunaga, Tomonori| Moriwake, Tadashi| Tanaka, Hiroyuki| Tsukahara, Hirokazu|
Keywords bone development dwarfism growth infant radiography
Note This is the peer reviewed version of the following article: [Miyahara, D., Hasegawa, K., Ago, Y., Futagawa, N., Miyahara, H., Higuchi, Y., Yamada, K., Tetsunaga, T., Moriwake, T., Tanaka, H., & Tsukahara, H. (2023). Radiological characteristics of skeletal growth in neonates and infants with achondroplasia. American Journal of Medical Genetics Part A, 1–8. https://doi.org/10.1002/ajmg.a.63525], which has been published in final form at [https://doi.org/10.1002/ajmg.a.63525]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.| This fulltext file will be available in Dec. 2024.|
Published Date 2023-12-29
Publication Title American Journal of Medical Genetics Part A
Publisher Wiley
ISSN 1552-4825
NCID AA11815067
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2023 Wiley Periodicals LLC.
File Version author
PubMed ID 38158382
DOI 10.1002/ajmg.a.63525
Web of Science KeyUT 001133715300001
Related Url isVersionOf https://doi.org/10.1002/ajmg.a.63525
FullText URL fulltext20231110-02.pdf
Author Hasegawa, Kosei| Futagawa, Natsuko| Ago, Yuko| Miyahara, Hiroyuki| Harada, Daisuke| Miyazawa, Mari| Yoshimoto, Junko| Baba, Kenji| Moriwake, Tadashi| Tanaka, Hiroyuki| Tsukahara, Hirokazu|
Keywords infant skeleton spine cartilage growth
Published Date 2023
Publication Title Clinical Pediatric Endocrinology
Volume volume32
Issue issue4
Publisher Japanese Society for Pediatric Endocrinology
Start Page 221
End Page 227
ISSN 0918-5739
NCID AA11006467
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2023 by The Japanese Society for Pediatric Endocrinology
File Version publisher
PubMed ID 37842142
DOI 10.1297/cpe.2023-0035
Web of Science KeyUT 001085272200003
Related Url isVersionOf https://doi.org/10.1297/cpe.2023-0035
Title Alternative Achondroplasia
Author Hasegawa, Kosei| Futagawa, Natsuko| Miyahara, Hiroyuki| Tsukahara, Hirokazu|
Keywords 骨系統疾患 FGFR3 指定難病 成長ホルモン ガイドライン
Publication Title Journal of Okayama Medical Association
Published Date 2022-12-01
Volume volume134
Issue issue3
Start Page 176
End Page 179
ISSN 0030-1558
Related Url isVersionOf https://doi.org/10.4044/joma.134.176
language Japanese
Copyright Holders Copyright (c) 2022 岡山医学会
File Version publisher
DOI 10.4044/joma.134.176
FullText URL fulltext.pdf
Author Miyahara, Hiroyuki| Hasegawa, Kosei| Yashiro, Masato| Ohara, Toshiaki| Fujisawa, Masayoshi| Yoshimura, Teizo| Matsukawa, Akihiro| Tsukahara, Hirokazu|
Published Date 2022-03-21
Publication Title Scientific Reports
Volume volume12
Issue issue1
Publisher Nature Portfolio
Start Page 4819
ISSN 2045-2322
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © The Author(s) 2022
File Version publisher
PubMed ID 35314758
DOI 10.1038/s41598-022-08791-z
Web of Science KeyUT 000771589000002
Related Url isVersionOf https://doi.org/10.1038/s41598-022-08791-z
FullText URL fulltext20210908-1.pdf
Author Hasegawa, Kosei| Tanaka, Hiroyuki| Futagawa, Natsuko| Miyahara, Hiroyuki| Higuchi, Yousuke| Tsukahara, Hirokazu|
Note This is the peer reviewed version of the following article: [Hasegawa, K., Tanaka, H., Futagawa, N., Miyahara, H., Higuchi, Y., & Tsukahara, H. (2021). A novel pathogenic variant p.Asp797Val in IFIH1 in a Japanese boy with overlapping Singleton-Merten syndrome and Aicardi-Goutières syndrome. American Journal of Medical Genetics Part A, 188A: 249– 252. ], which has been published in final form at [https://doi.org/10.1002/ajmg.a.62478]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages there of by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.|
Published Date 2021-8-28
Publication Title American Journal of Medical Genetics Part A
Volume volume188A
Publisher Wiley
Start Page 249
End Page 252
ISSN 1552-4825
NCID AA11815067
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2021 Wiley Periodicals LLC.
File Version author
PubMed ID 34453469
DOI 10.1002/ajmg.a.62478
Web of Science KeyUT 000690679100001
Related Url isVersionOf https://doi.org/10.1002/ajmg.a.62478
FullText URL fulltext.pdf
Author Higuchi, Yousuke| Hasegawa, Kosei| Futagawa, Natsuko| Yamashita, Miho| Tanaka, Hiroyuki| Tsukahara, Hirokazu|
Keywords COL1A1 COL1A2 IFITM5 Osteogenesis imperfecta variant
Note This is an Accepted Manuscript of an article published by Wiley|
Published Date 2021-05-03
Publication Title Molecular Genetics & Genomic Medicine
Publisher Wiley
Start Page e1675
ISSN 2324-9269
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version publisher
PubMed ID 33939306
NAID 120007037392
DOI 10.1002/mgg3.1675
Web of Science KeyUT 000646270800001
Related Url isVersionOf https://doi.org/10.1002/mgg3.1675
FullText URL fulltext.pdf Fig1.tif SupplementaryMaterial1.pdf SupplementaryMaterial2.pdf SupplementaryMaterial3.pdf
Author Akiyama, Tomoyuki| Hyodo, Yuki| Hasegawa, Kosei| Oboshi, Taikan| Imai, Katsumi| Ishihara, Naoko| Dowa, Yuri| Koike, Takayoshi| Yamamoto, Toshiyuki| Shibasaki, Jun| Shimbo, Hiroko| Fukuyama, Tetsuhiro| Takano, Kyoko| Shiraku, Hiroshi| Takeshita, Saoko| Okanishi, Tohru| Baba, Shimpei| Kubota, Masaya| Hamano, Shin-ichiro| Kobayashi, Katsuhiro|
Keywords ALDH7A1 PLPBP PLPHP PROSC Pyridoxal 5′-phosphate homeostasis protein deficiency Pyridoxine-dependent epilepsy
Note © 2020 Elsevier Inc.. This manuscript version is made available under the CC-BY-NC-ND 4.0 License.http://creativecommons.org/licenses/by-nc-nd/4.0/.This is the accepted manuscript version. The formal published version is available at https://doi.org/10.1016/j.pediatrneurol.2020.08.020|
Published Date 2020-12
Publication Title Pediatric Neurology
Volume volume113
Publisher Elsevier
Start Page 33
End Page 41
ISSN 0887-8994
NCID AA10472238
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version author
PubMed ID 32980745
DOI 10.1016/j.pediatrneurol.2020.08.020
Web of Science KeyUT 000591640100007
Related Url isVersionOf https://doi.org/10.1016/j.pediatrneurol.2020.08.020
FullText URL PI_62_5_587_592.pdf PI_62_5_Fig1.tif PI_62_5_Fig2.tif
Author Miyahara, Hiroyuki| Akiyama, Tomoyuki| Hasegawa, Kosei| Akiyama, Mari| Oka, Makio| Kobayashi, Katsuhiro| Tsukahara, Hirokazu|
Keywords adrenocorticotropic hormone therapy calcium crystal renal tubular epithelial cell urinary sediment
Note This is the peer reviewed version of the following article: Miyahara, Hiroyuki et.al. "Laboratory changes during adrenocorticotropic hormone therapy associated with renal calcified lesions" Pediatrics International 62(5) 587-592 (2020), which has been published in final form at https://doi.org/10.1111/ped.14158. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.|
Published Date 2020-01-19
Publication Title Pediatrics International
Volume volume62
Issue issue5
Publisher Wiley
Start Page 587
End Page 592
ISSN 1328-8067
NCID AA11320483
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2020 Japan Pediatric Society
File Version author
PubMed ID 31957090
DOI 10.1111/ped.14158
Web of Science KeyUT 000536494300014
Related Url isVersionOf https://doi.org/10.1111/ped.14158
FullText URL CPE28_4_155.pdf
Author Hasegawa, Kosei| Ihoriya, Hiromi| Futagawa, Natsuko| Higuchi, Yousuke| Tsuchiya, Hiroki| Shibata, Takashi| Hayashi, Yumiko| Kobayashi, Katsuhiro| Tsukahara, Hirokazu|
Keywords developmental delay polyuria polydipsia fever poor weight gain
Note 本文データは学協会の許諾に基づきCiNiiから複製したものである|
Published Date 2019-10-19
Publication Title Clinical Pediatric Endocrinology
Volume volume28
Issue issue4
Publisher Japanese Society for Pediatric Endocrinology
Start Page 155
End Page 158
ISSN 0918-5739
NCID AA11006467
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders The Japanese Society for Pediatric Endocrinology
File Version publisher
PubMed ID 31666769
DOI 10.1297/cpe.28.155
Web of Science KeyUT 000491469300008
Related Url isVersionOf https://doi.org/10.1297/cpe.28.155
JaLCDOI 10.18926/AMO/54805
FullText URL 70_6_435.pdf
Author Yamashita, Miho| Hasegawa, Kosei| Higuchi, Yousuke| Miyai, Takayuki| Okada, Ayumi| Tanaka, Hiroyuki| Tsukahara, Hirokazu|
Abstract The urinary cross-linked N-terminal telopeptide of type I collagen (uNTx) levels in infantile osteogenesis imperfecta (OI) have not been well studied. Here we investigated the levels of uNTx in infants with OI and healthy infants. We collected spot urine samples from 30 infants with OI (male/female, 14/16; Sillence classification, I/II/III/IV: 15/3/6/6; age, 5.2±4.4 months) and 120 healthy infants (male/female, 75/45; age, 5.1±4.1 months) for the measurement of uNTx levels. The uNTx levels of the OI infants were significantly lower than those of the healthy infants (mean±SD, 1,363.7±530.1 vs. 2,622.2±1,202.6 nmol BCE/mmol Cr; p<0.001). The uNTx levels of the infants with type I OI were significantly lower than those of the age-matched healthy infants, although an overlap was observed between the 2 groups. Among the 1-month-old infants, the uNTx levels of the infants with types I, III or IV OI were significantly lower than those of the healthy infants, without overlap (1,622.5±235.8 vs. 3,781.0±1,027.1 nmol BCE/mmol Cr; p<0.001). These results indicate that uNTx levels are significantly lower in infants with OI than in healthy infants, and they suggest that uNTx might be useful as a reference for diagnosing OI.
Keywords bone resorption marker bone turnover bone mass
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2016-12
Volume volume70
Issue issue6
Publisher Okayama University Medical School
Start Page 435
End Page 439
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2016 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 28003667
Author Hasegawa, Kosei|
Published Date 2008-03-25
Publication Title
Content Type Thesis or Dissertation
Author Hasegawa, Kosei|
Published Date 2004-03-25
Publication Title
Content Type Thesis or Dissertation