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Daisuke Ariyasu

Observed names: Ariyasu, Daisuke, Daisuke ARIYASU
Observed institutions: Keio University, Kawasaki Municipal Hospital, Tokyo Metropolitan Children's Medical Center, Tokyo Metropolitan Kiyose Children's Hospital, Institute of Resource Development and Analysis, Kumamoto University, Kumamoto University
ORCID: 0000-0002-9261-6050
Observed ORCID: 0000-0002-9261-6050
OpenAlex ID: A5000910034
Endoplasmic Reticulum (ER) Stress and Endocrine Disorders
2017 · Daisuke Ariyasu, Hiderou Yoshida, et al. · International Journal of Molecular Sciences · 104
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High iFGF23 level despite hypophosphatemia is one of the clinical indicators to make diagnosis of XLH
2011 · Junko Miyamoto Igaki, Makoto Yamada, et al. · Endocrine Journal · 29
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Serum FSH level below 10 mIU/mL at twelve years old is an index of spontaneous and cyclical menstruation in Turner syndrome
2010 · Keiko Aso, Shinobu Koto, et al. · Endocrine Journal · 29
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Three Children With Plastic Bronchitis Associated With 2009 H1n1 Influenza Virus Infection
2010 · Chikako Terano, Masaru Miura, et al. · The Pediatric Infectious Disease Journal · 27
Genetic and enzymatic analysis for two Japanese patients with idiopathic infantile arterial calcification
2005 · Chikahiko Numakura, Makoto Yamada, et al. · Journal of Bone and Mineral Metabolism · 26
Gradually increasing ethinyl estradiol for Turner syndrome may produce good final height but not ideal BMD
2016 · Yukihiro Hasegawa, Daisuke Ariyasu, et al. · Endocrine Journal · 21
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Hypophosphatemic rickets developed after treatment with etidronate disodium in a patient with generalized arterial calcification in infancy
2015 · Kentaro Miyai, Daisuke Ariyasu, et al. · Bone Reports · 12
Endoplasmic Reticulum Stress and Apoptosis Contribute to the Pathogenesis of Dominantly Inherited Isolated GH Deficiency Due to GH1 Gene Splice Site Mutations
2013 · Daisuke Ariyasu, Hiderou Yoshida, et al. · Endocrinology · 11
Microduplication of Xq24 and Hartsfield syndrome with holoprosencephaly, ectrodactyly, and clefting
2012 · Toshiki Takenouchi, Hironobu Okuno, et al. · American Journal of Medical Genetics Part A · 10
Patients with Hypophosphatemic Osteomalacia Need Continuous Treatment during Adulthood
2009 · Eri Suzuki, Makoto Yamada, et al. · Clinical Pediatric Endocrinology · 10
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Pregnanetriol in the Range of 1.2-2.1mg/m2/day as an Index of Optimal Control in CYP21A2 Deficiency
2007 · Masako Izawa, Keiko Aso, et al. · Clinical Pediatric Endocrinology · 10
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The Range of 2.2-3.3 mg/gCr of Pregnanetriol in the First Morning Urine Sample as an Index of Optimal Control in CYP21 Deficiency
2008 · Masako Izawa, Keiko Aso, et al. · Clinical Pediatric Endocrinology · 9
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WT1 intron 9 splice acceptor site mutation in a 46,XY male with focal segmental glomerulosclerosis
2006 · Katsuyoshi Kanemoto, Kenji Ishikura, et al. · Pediatric Nephrology · 8
Cryptococcal meningitis in an immunocompetent child
2005 · Masayoshi Shinjoh, Isao Miyairi, et al. · European Journal of Pediatrics · 8
Incidence and Risk Factors for Adrenal Crisis in Pediatric-onset Adrenal Insufficiency: A Prospective Study
2023 · Mayumi Hosokawa, Yosuke Ichihashi, et al. · The Journal of Clinical Endocrinology & Metabolism · 7
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Decreased Activity of the Ghrhr and Gh Promoters Causes Dominantly Inherited GH Deficiency in Humanized GH1 Mouse Models
2019 · Daisuke Ariyasu, Emika Kubo, et al. · Endocrinology · 7
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A case of transient neonatal diabetes due to a novel mutation in ABCC8
2016 · Masaki Takagi, Ryojun Takeda, et al. · Clinical Pediatric Endocrinology · 4
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Current understanding and perspectives on growth and long-acting GH therapy in Japan
2024 · Yukihiro Hasegawa, Kento Ikegawa, et al. · Clinical Pediatric Endocrinology · 2
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A Japanese boy with fructose-1,6-bisphosphatase deficiency who had a novel FBP1 mutation (p.Phe90Val)
2017 · Keiko Nagahara, Daisuke Ariyasu, et al. · Clinical Pediatric Endocrinology · 2
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Early-onset urological disorders due to Wolfram syndrome: A case of neonatal onset
2016 · Mami Fukuma, Daisuke Ariyasu, et al. · Clinical Pediatric Endocrinology · 2
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TmP/GFR is a Useful Marker in Making a Clinical Diagnosis of X-Linked Hypophosphataemic Rickets Caused by the PHEX Gene Mutation
2015 · Ryojun Takeda, K Miyai, et al. · 54th ESPE Meeting (ESPE 2015) · 2
Mice with Heterozygous Deletion of Exon 3 in the Gh Gene Demonstrate Growth Retardation Caused by Reduced Ghrhr mRNA
2025 · Daisuke Ariyasu, Daisuke Higa, et al. · International Journal of Molecular Sciences · 1
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en.2019-00306 Supplemental Table 1
2019 · Ariyasu, Daisuke · Figshare · 1
Phenotypic and Genetic Insights Into CNOT3 ‐Related Intellectual Developmental Disorder of Speech Delay, Autism, and Dysmorphic Faces ( IDDSADF ) From the First Two Japanese Cases
2026 · Daisuke Ariyasu, Rika Kosaki, et al. · American Journal of Medical Genetics Part A
A de novo HK1 Variant in a Boy Fulfilling the Diagnostic Criteria for Tuberous Sclerosis Complex: Expanding the Phenotypic Spectrum of NEDVIBA
2025 · Daisuke Ariyasu, Hiroaki Sato, et al. · American Journal of Medical Genetics Part A
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Works count: 44
Citation count: 342
H-index: 10
I10-index: 11
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