Shinya Iwasawa

Scopus著者プロファイル

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年別の研究成果

Pureに変更を加えた場合、すぐここに表示されます。

フィンガープリント

Shinya Iwasawaが活動している研究トピックを掘り下げます。このトピックラベルは、この研究者の研究成果に基づきます。これらがまとまってユニークなフィンガープリントを構成します。

1 類似のプロファイル

8 Article
1 Comment/debate

Male infant with Noonan syndrome with RAF-1 gene mutation who survived hypertrophic cardiomyopathy-induced fatal heart failure and uncontrollable arrhythmias
Hagino, M., Ota, C., Onoki, T. & Iwasawa, S., 2022 9月 28, In: BMJ case reports. 15, 9, e250342.
研究成果: Article › 査読

Open Access
Two Distinct Cases of Adult-onset Kawasaki Disease
Onoki, T., Metoki, T., Iwasawa, S., Kawano, K., Kimura, M., Kure, S. & Ota, C., 2022, In: Internal Medicine. 61, 23, p. 3525-3529 5 p.
研究成果: Article › 査読

Open Access
A sublethal ATP11A mutation associated with neurological deterioration causes aberrant phosphatidylcholine flipping in plasma membranes
Segawa, K., Kikuchi, A., Noji, T., Sugiura, Y., Hiraga, K., Suzuki, C., Haginoya, K., Kobayashi, Y., Matsunaga, M., Ochiai, Y., Yamada, K., Nishimura, T., Iwasawa, S., Shoji, W., Sugihara, F., Nishino, K., Kosako, H., Ikawa, M., Uchiyama, Y., Suematsu, M., & 3 othersIshikita, H., Kure, S. & Nagata, S., 2021 9月 15, In: Journal of Clinical Investigation. 131, 18, e148005.
研究成果: Article › 査読

Open Access
10 被引用数 (Scopus)
Bilateral lung transplantation in a 9-year-old girl with bronchopulmonary dysplasia with pulmonary hypertension
Ota, C., Saito, R., Tominaga, J., Iwasawa, S., Hirama, T., Matsuda, Y., Ono, K., Onoki, T., Kimura, M., Kawabata, Y. & Okada, Y., 2021 10月, In: Pediatric Pulmonology. 56, 10, p. 3417-3421 5 p.
研究成果: Article › 査読
Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia (Genetics in Medicine, (2019), 21, 6, (1286-1294), 10.1038/s41436-018-0340-x)
Wada, Y., Kikuchi, A., Arai-Ichinoi, N., Sakamoto, O., Takezawa, Y., Iwasawa, S., Niihori, T., Nyuzuki, H., Nakajima, Y., Ogawa, E., Ishige, M., Hirai, H., Sasai, H., Fujiki, R., Shirota, M., Funayama, R., Yamamoto, M., Ito, T., Ohara, O., Nakayama, K., & 4 othersAoki, Y., Koshiba, S., Fukao, T. & Kure, S., 2020 7月 1, In: Genetics in Medicine. 22, 7, p. 1281 1 p.
研究成果: Comment/debate › 査読

Open Access

岩澤伸哉

フィンガープリント

ネットワーク

詳細を開く

Male infant with Noonan syndrome with RAF-1 gene mutation who survived hypertrophic cardiomyopathy-induced fatal heart failure and uncontrollable arrhythmias

Two Distinct Cases of Adult-onset Kawasaki Disease

A sublethal ATP11A mutation associated with neurological deterioration causes aberrant phosphatidylcholine flipping in plasma membranes

Bilateral lung transplantation in a 9-year-old girl with bronchopulmonary dysplasia with pulmonary hypertension

Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia (Genetics in Medicine, (2019), 21, 6, (1286-1294), 10.1038/s41436-018-0340-x)

岩澤 伸哉

フィンガープリント

ネットワーク

研究成果

Male infant with Noonan syndrome with RAF-1 gene mutation who survived hypertrophic cardiomyopathy-induced fatal heart failure and uncontrollable arrhythmias

Two Distinct Cases of Adult-onset Kawasaki Disease

A sublethal ATP11A mutation associated with neurological deterioration causes aberrant phosphatidylcholine flipping in plasma membranes

Bilateral lung transplantation in a 9-year-old girl with bronchopulmonary dysplasia with pulmonary hypertension

Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia (Genetics in Medicine, (2019), 21, 6, (1286-1294), 10.1038/s41436-018-0340-x)

岩澤伸哉