Výsledky vyhledávání - "Kunitaka Joh"

Ventricular mechanics in the bidirectional glenn procedure and total cavopulmonary connection

Autor: Akira Sese, Yoshihisa Tanoue, Kunitaka Joh, Yutaka Imoto

Publikováno v: The Annals of Thoracic Surgery. 76:562-566

Background The time course of ventricular efficiency in Fontan candidates who underwent both the bidirectional Glenn procedure (BDG) and total cavopulmonary connection (TCPC) were analyzed in this study. We previously reported that volume-load reduct

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2535f1cc8fd6526db697bdd4110d5e44
https://doi.org/10.1016/s0003-4975(03)00467-3

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Bidirectional Glenn Procedure Improves the Mechanical Efficiency of a Total Cavopulmonary Connection in High-Risk Fontan Candidates

Autor: Yoshihisa Tanoue, Kunitaka Joh, Akira Sese, Takayuki Hijii, Yasutaka Ueno

Publikováno v: Circulation. 103:2176-2180

Background —A total cavopulmonary connection (TCPC) is a widely performed surgical procedure for Fontan candidates. High-risk candidates who have undergone the bidirectional Glenn procedure (BDG) before TCPC have shown good results. The exact mecha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::255fb97b17b5e58768ac031c228727e2
https://doi.org/10.1161/01.cir.103.17.2176

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Molecular cytogenetic diagnosis of Williams syndrome

Autor: Atsuyoshi Takao, Shin-ichiro Imamura, Kazuo Momma, Misa Kimura, Hamao Hirota, Kunitaka Joh-o, Masahiko Ando, Rumiko Matsuoka

Publikováno v: American Journal of Medical Genetics. 64:473-477

Williams syndrome (WS) is characterized by distinct facial changes, growth deficiency, mental retardation, and congenital heart defect (particularly supravalvular aortic stenosis), associated at times with infantile hypercalcemia. Molecular genetic s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f5c30113430d0b7e17163083bd7cf99
https://doi.org/10.1002/(sici)1096-8628(19960823)64:3<473::aid-ajmg5>3.0.co

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Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2

Autor: Misa Kimura, Kunitaka Joh-o, Chisato Kondo, Shin-ichiro Imamura, Atsuyoshi Takao, Makoto Nishibatake, Rumiko Matsuoka, Kazuo Momma, Masahiko Ando, Kazuo Ikeda

Publikováno v: American Journal of Medical Genetics. 53:285-289

The so-called "conotruncal anomaly face syndrome" (CTAFS) is characterized by a peculiar facial appearance associated with congenital heart disease (CHD), especially cardiac outflow tract defects such as tetralogy of Fallot (TOF), double outlet right

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09c06ce653324e5d5cdd0674122666e2
https://doi.org/10.1002/ajmg.1320530314

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Survey of pediatric ward hospitalization due to respiratory syncytial virus infection after the introduction of palivizumab to high-risk infants in Japan

Autor: Satoshi, Kusuda, Naoto, Takahashi, Takami, Saitoh, Masaru, Terai, Hisashi, Kaneda, Yuichi, Kato, Atsushi, Ohashi, Shinichi, Watabe, Kunitaka, Joh-o, Katsuki, Hirai

Publikováno v: Pediatrics international : official journal of the Japan Pediatric Society. 53(3)

Respiratory syncytial virus (RSV) infection is a major cause of hospitalization during the winter among infants and young children. In 2002 palivizumab was introduced to high-risk infants for RSV hospitalization in Japan. It is important to character

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3ac50b53e3fffbac699478677dbebd56
https://pubmed.ncbi.nlm.nih.gov/20854284

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Redirection of the hepatic venous flow for the treatment of pulmonary arteriovenous malformations after Fontan operation

Autor: Yutaka Imoto, Akira Sese, Kunitaka Joh

Publikováno v: Pediatric cardiology. 27(4)

A 45-month-old boy who had complex cardiac anomalies with interrupted inferior vena cava and polysplenia underwent extracardiac Fontan operation. He redeveloped deep cyanosis postoperatively. Cardiac catheterization showed a preferential flow of the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d31abe5d92b1582647b0a90ed546d68
https://pubmed.ncbi.nlm.nih.gov/16830083

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Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein Ib-beta

Autor: Taichi Kato, Kunitaka Joh-o, Misa Kimura, Kazuki Kosaka, Masahiko Ando, Atsuyoshi Takao, Osamu Yamada, Akira Ohtake, Rumiko Matsuoka, Kazumasa Iwai, Kenji Kuroe, Shin-ichiro Imamura, Kazuo Momma

Publikováno v: Genetics in medicine : official journal of the American College of Medical Genetics. 5(2)

Purpose: To elucidate whether thrombocytopenia in 22q11.2 deletion syndrome patients is associated with the hemizygosity of glycoprotein Ib-β and to clarify the correlation of phenotype and genotype of this gene in 22q11.2 deletion syndrome patients

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::076cb7b92cf1230c0088482a43cc9930
https://pubmed.ncbi.nlm.nih.gov/12644781

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Serum hepatocyte growth factor combined with vascular endothelial growth factor as a predictive indicator for the occurrence of coronary artery lesions in Kawasaki disease

Autor: Tetsuji Yuge, Toshiro Hara, Kouichi Kusuhara, Takuro Ohno, Kunitaka Joh-o, Hidehiko Kariyazono, Hisaji Igarashi, Naoko Kinugawa

Publikováno v: European journal of pediatrics. 161(2)

We investigated the possible use of serum hepatocyte growth factor (HGF) and vascular endothelial growth factor (VEGF) levels as a predictive indicator for the occurrence of coronary artery lesions (CAL) in Kawasaki disease (KD). Serum HGF and VEGF l

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13187d348144c7dbc5be5fed689f0c79
https://pubmed.ncbi.nlm.nih.gov/11954744

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Surgical management of aortopulmonary window

Autor: Akira Sese, Yasutaka Ueno, Yoshihisa Tanoue, Kunitaka Joh

Publikováno v: The Japanese journal of thoracic and cardiovascular surgery : official publication of the Japanese Association for Thoracic Surgery = Nihon Kyobu Geka Gakkai zasshi. 48(9)

Objective: Aortopulmonary window is a rare congenital malformation involving a window-like communication between the ascending aorta and the pulmonary artery. Here, we present our experience regarding the surgical repair of an aortopulmonary window,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a614500c086a4e4d56939b07f9b9497
https://pubmed.ncbi.nlm.nih.gov/11030126

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