Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Shigeo Yamaki"'
Publikováno v:
Pulmonary Medicine, Vol 2015 (2015)
A few reports have provided histopathological insight into pulmonary hypertension developing after antitumor chemotherapy. In general, plexogenic pulmonary arteriopathy is a commonly observed finding in patients with severe pulmonary hypertension. We
Externí odkaz:
https://doaj.org/article/f28cb31f19e249ae8bf204fd8b2fb602
Autor:
Hideyuki Hawaka, Mitsunobu Sugino, Risa Morita, Masahiro Tahara, Shigeo Yamaki, Kotarou Urayama, Naoki Masaki, Kazuya Sanada
Publikováno v:
American Journal of Medical Genetics Part A. 185:1059-1066
The aim of this study was to evaluate the features of pulmonary histopathological changes in cases of trisomy 18 complicated with congenital heart disease and pulmonary arterial hypertension. Twenty-eight patients with trisomy 18 underwent open lung
Autor:
Masahiro Tahara, Kazuya Sanada, Risa Morita, Hideyuki Hawaka, Kotarou Urayama, Mitsunobu Sugino, Naoki Masaki, Shigeo Yamaki
Publikováno v:
American Journal of Medical Genetics. Part A; Apr2021, Vol. 185 Issue 4, p1059-1066, 8p
Autor:
Takanari Fujii, Kazuto Fujimoto, Hiroaki Kise, Yoshitaka Watanabe, Takeshi Yamazaki, Hideshi Tomita, Shigeru Uemura, Kozue Kobayashi, Kazuo Itabashi, Satoshi Hibino, Junya Iwasaki, Takashi Soga, Shigeo Yamaki, Shunsuke Sakurai, Takeshi Shimizu
Publikováno v:
Journal of Cardiology Cases. 9(1):3-7
Primary pulmonary vein stenosis (PVS) is rare within the pediatric population and its pathophysiology remains unclear, especially as to how the histopathology relates to its refractoriness to treatment. We report the case of a 4-month-old girl with p
Publikováno v:
American Journal of Medical Genetics Part A. 164:319-323
Congestive heart failure is a major cause of early death in patients with trisomy 13 or 18 and congenital heart disease (CHD). Pulmonary artery banding for these patients early in life is preferred to protect the lungs from high pulmonary flow rates
Autor:
Shigeo Yamaki
Publikováno v:
General Thoracic and Cardiovascular Surgery
Purpose Diagnosis from lung biopsy or autopsy was performed in 445 patients with congenital (385) or acquired (60) heart disease from all over Japan. The purpose of this study is the presentation of these prospective data collections. Methods Of the
Publikováno v:
Pulmonary Medicine
Pulmonary Medicine, Vol 2015 (2015)
Pulmonary Medicine, Vol 2015 (2015)
A few reports have provided histopathological insight into pulmonary hypertension developing after antitumor chemotherapy. In general, plexogenic pulmonary arteriopathy is a commonly observed finding in patients with severe pulmonary hypertension. We
Autor:
Katsuhide Maeda, Arata Murakami, Toshihide Asou, Shinichi Takamoto, Shigeo Yamaki, Hideaki Kado
Publikováno v:
The Annals of Thoracic Surgery. 78:1371-1381
Background The various types of cavopulmonary connection are occasionally unsuccessful even when the indications have been strictly fulfilled based on preoperative hemodynamic studies. We performed a detailed study of lung specimens from 60 patients
Autor:
Munetaka Kumate, Koichi Tabayashi, Susumu Yonesaka, Shigeo Yamaki, Katsuhide Maeda, Masato Endo
Publikováno v:
Chest. 126:1042-1047
Objective: Surgical indication was determined by lung biopsy in 91 patients with secundum atrial septal defect (ASD) and severe pulmonary hypertension > 70 mm Hg of pulmonary arterial peak pressure and/or pulmonary vascular resistance of > 8 U/m 2 .
Publikováno v:
The Japanese Journal of Thoracic and Cardiovascular Surgery. 52:213-216
The hemodynamic determination of operability in atrial septal defect (ASD) with severe pulmonary hypertension is problematic. Therefore, we perform an open lung biopsy prior to the corrective surgery in cases with pulmonary vascular resistance greate