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Ayako Chida

Showing results (21-30 of 37) with videos related to

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European Journal of Pediatrics|August 21, 2021
Risk factors for hospitalisation due to respiratory syncytial virus infection in children receiving prophylactic palivizumabAyako Chida-Nagai, Hiroki Sato, Itsumi Sato, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 6, 2013
Soluble ST2 and N-terminal pro-brain natriuretic peptide combination. Useful biomarker for predicting outcome of childhoodpulmonary arterial hypertensionAyako Chida, Hiroki Sato, Masaki Shintani, et al.
Heart and Vessels|April 15, 2020
Pulmonary vasodilators can lead to various complications in pulmonary "arterial" hypertension associated with congenital heart diseaseAyako Chida-Nagai, Koichi Sagawa, Takao Tsujioka, et al.
Plos One|February 1, 2019
Role of BRCA1-associated protein (BRAP) variant in childhood pulmonary arterial hypertensionAyako Chida-Nagai, Masaki Shintani, Hiroki Sato, et al.
Molecular Genetics & Genomic Medicine|May 15, 2023
A case of infantile Barth syndrome with severe heart failure: Importance of splicing variants in the TAZ geneAtsuhito Takeda, Masahiro Ueki, Jiro Abe, et al.
International Journal of Stroke : Official Journal of the International Stroke Society|April 25, 2026
Biallelic loss-of-function variants in <i>PTGIS</i> cause recurrent cervical internal carotid artery vasospasmHiroyuki Akagawa, Hideaki Onda, Yosuke Moteki, et al.
Molecular Genetics & Genomic Medicine|June 18, 2014
Mutations of NOTCH3 in childhood pulmonary arterial hypertensionAyako Chida, Masaki Shintani, Yoshihisa Matsushita, et al.
Clinical Genetics|January 15, 2024
Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasiaShuhei Morita, Shunsuke Nomura, Kenko Azuma, et al.
American Journal of Medical Genetics. Part A|August 9, 2023
A Noonan-like pediatric patient with a de novo CBL pathogenic variant and an RNF213 polymorphism p.R4810K presenting with cardiopulmonary arrest due to left main coronary artery ostial atresiaAyako Chida-Nagai, Hidefumi Tonoki, Naomasa Makita, et al.
Scientific Reports|October 4, 2024
Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndromeAkikazu Nakamura, Shunsuke Nomura, Shoko Hara, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
European Journal of Pediatrics|August 21, 2021
Risk factors for hospitalisation due to respiratory syncytial virus infection in children receiving prophylactic palivizumabAyako Chida-Nagai, Hiroki Sato, Itsumi Sato, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 6, 2013
Soluble ST2 and N-terminal pro-brain natriuretic peptide combination. Useful biomarker for predicting outcome of childhoodpulmonary arterial hypertensionAyako Chida, Hiroki Sato, Masaki Shintani, et al.
Heart and Vessels|April 15, 2020
Pulmonary vasodilators can lead to various complications in pulmonary "arterial" hypertension associated with congenital heart diseaseAyako Chida-Nagai, Koichi Sagawa, Takao Tsujioka, et al.
Plos One|February 1, 2019
Role of BRCA1-associated protein (BRAP) variant in childhood pulmonary arterial hypertensionAyako Chida-Nagai, Masaki Shintani, Hiroki Sato, et al.
Molecular Genetics & Genomic Medicine|May 15, 2023
A case of infantile Barth syndrome with severe heart failure: Importance of splicing variants in the TAZ geneAtsuhito Takeda, Masahiro Ueki, Jiro Abe, et al.
International Journal of Stroke : Official Journal of the International Stroke Society|April 25, 2026
Biallelic loss-of-function variants in <i>PTGIS</i> cause recurrent cervical internal carotid artery vasospasmHiroyuki Akagawa, Hideaki Onda, Yosuke Moteki, et al.
Molecular Genetics & Genomic Medicine|June 18, 2014
Mutations of NOTCH3 in childhood pulmonary arterial hypertensionAyako Chida, Masaki Shintani, Yoshihisa Matsushita, et al.
Clinical Genetics|January 15, 2024
Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasiaShuhei Morita, Shunsuke Nomura, Kenko Azuma, et al.
American Journal of Medical Genetics. Part A|August 9, 2023
A Noonan-like pediatric patient with a de novo CBL pathogenic variant and an RNF213 polymorphism p.R4810K presenting with cardiopulmonary arrest due to left main coronary artery ostial atresiaAyako Chida-Nagai, Hidefumi Tonoki, Naomasa Makita, et al.
Scientific Reports|October 4, 2024
Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndromeAkikazu Nakamura, Shunsuke Nomura, Shoko Hara, et al.
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