Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Kouichi Nakau"'
Autor:
Keita Ito, Hideharu Oka, Yuki Shibagaki, Yuki Sasaki, Rina Imanishi, Sorachi Shimada, Yuki Akiho, Kazunori Fukao, Sadahiro Nakagawa, Kunihiro Iwata, Kouichi Nakau, Satoru Takahashi
Publikováno v:
The Egyptian Heart Journal, Vol 76, Iss 1, Pp 1-6 (2024)
Abstract Background Four-dimensional flow magnetic resonance imaging (MRI) enables blood flow visualization. The absence of left atrial vortex flow (LAVF) has been implicated in the development of thrombus formation and arrhythmias. However, the clin
Externí odkaz:
https://doaj.org/article/98d511fa699e4bbeb526178b22ef04ab
Autor:
Rina Imanishi, Kouichi Nakau, Sorachi Shimada, Hideharu Oka, Ryo Takeguchi, Ryosuke Tanaka, Tatsutoshi Sugiyama, Mitsumaro Nii, Toshio Okamoto, Ken Nagaya, Yoshio Makita, Kumiko Yanagi, Tadashi Kaname, Satoru Takahashi
Publikováno v:
Human Genome Variation, Vol 10, Iss 1, Pp 1-3 (2023)
Abstract Pathogenic variants of HECW2 have been reported in cases of neurodevelopmental disorder with hypotonia, seizures, and absent language (NDHSAL; OMIM #617268). A novel HECW2 variant (NM_001348768.2:c.4343 T > C,p.Leu1448Ser) was identified in
Externí odkaz:
https://doaj.org/article/759a403f14234af1881497e323c091ca
Autor:
Hideharu Oka, MD, PhD, Kouichi Nakau, MD, Rina Imanishi, MD, Takuo Furukawa, MD, PhD, Yasuko Tanabe, MD, PhD, Keiichi Hirono, MD, PhD, Yukiko Hata, PhD, Naoki Nishida, MD, PhD, Hiroshi Azuma, MD, PhD
Publikováno v:
CJC Open, Vol 3, Iss 9, Pp 1195-1198 (2021)
Hypertrophic cardiomyopathy (HCM) is the primary cause of sudden cardiac death in children and adolescents. Patients with HCM frequently have ventricular tachycardia and ventricular fibrillation, although complete atrioventricular block (CAVB) is ver
Externí odkaz:
https://doaj.org/article/72062631d0c34150b02caf6ab4790a5e
Autor:
Tomoaki Sasaki, MD, PhD, Miki Ogata, MD, Aya Kajihama, MD, Kouichi Nakau, MD, Atsutaka Okizaki, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 16, Iss 3, Pp 656-660 (2021)
Mucopolysaccharidosis type 2 is a congenital lysosomal disease characterized by iduronate-2-sulfatase deficiency, which leads to excessive accumulation of glycosaminoglycans in tissue. Dysostosis, which primarily involves decreased bone mineralizatio
Externí odkaz:
https://doaj.org/article/e87b21e82e2b4ef3aa060a06e2b0694e
Publikováno v:
Case Reports in Cardiology, Vol 2018 (2018)
Asplenia syndrome is frequently complicated by a total anomalous pulmonary venous connection. Pulmonary venous obstruction, following total anomalous pulmonary venous connection surgery, is one of the risk factors for morbidity and mortality. In some
Externí odkaz:
https://doaj.org/article/946edcb4353c4eca83ccbb924258dfd3
Autor:
Jingshan Gao, Takeru Makiyama, Yuta Yamamoto, Takuya Kobayashi, Hisaaki Aoki, Thomas L. Maurissen, Yimin Wuriyanghai, Asami Kashiwa, Tomohiko Imamura, Takanori Aizawa, Hai Huang, Hirohiko Kohjitani, Misato Nishikawa, Kazuhisa Chonabayashi, Megumi Fukuyama, Hiromi Manabe, Kouichi Nakau, Tsutomu Wada, Koichi Kato, Futoshi Toyoda, Yoshinori Yoshida, Naomasa Makita, Knut Woltjen, Seiko Ohno, Nagomi Kurebayashi, Takashi Murayama, Takashi Sakurai, Minoru Horie, Takeshi Kimura
Publikováno v:
Circulation: Arrhythmia and Electrophysiology. 16
Background: CaM (calmodulin) is a ubiquitously expressed, multifunctional Ca 2+ sensor protein that regulates numerous proteins. Recently, CaM missense variants have been identified in patients with malignant inherited arrhythmias, such as long QT sy
Autor:
Naoki Nishida, Hiroshi Azuma, Hideharu Oka, Takuo Furukawa, Yukiko Hata, Yasuko Tanabe, Rina Imanishi, Kouichi Nakau, Keiichi Hirono
Publikováno v:
CJC Open, Vol 3, Iss 9, Pp 1195-1198 (2021)
CJC Open
CJC Open
Hypertrophic cardiomyopathy (HCM) is the primary cause of sudden cardiac death in children and adolescents. Patients with HCM frequently have ventricular tachycardia and ventricular fibrillation, although complete atrioventricular block (CAVB) is ver
Autor:
Kouichi Nakau, Rina Imanishi, Sadahiro Nakagawa, Hideharu Oka, Hiroshi Azuma, Yuki Kobayashi, Kunihiro Iwata
Publikováno v:
Cardiology in the Young. 32:925-929
Background:T1 mapping is a recently developed imaging analysis method that allows quantitative assessment of myocardial T1 values obtained using MRI. In children, MRI is performed under free-breathing. Thus, it is important to know the changes in T1
Autor:
Hideharu Oka, Kouichi Nakau, Sadahiro Nakagawa, Rina Imanishi, Sorachi Shimada, Yuki Mikami, Kazunori Fukao, Kunihiro Iwata, Satoru Takahashi
Publikováno v:
Cardiology in the young.
Background: Assessing the hepatic status of children with CHD is very important in the post-operative period. This study aimed to assess the usefulness of paediatric liver T1/T2 values and to evaluate the impact of respiration on liver T1/T2 values.
Publikováno v:
Korean Circulation Journal
BACKGROUND AND OBJECTIVES There are few reports on renal dysfunction in the remote period after biventricular repair, and biomarkers for early detection of renal dysfunction are not well understood. We examined whether early fluctuation of biomarkers