Výsledky vyhledávání - "Tomoko Hatata"

Akademický článek

Safety, efficacy and pharmacokinetics of palivizumab in off-label neonates, infants, and young children at risk for serious respiratory syncytial virus infection: a multicenter phase II clinical trialResearch in context

Autor: Masaaki Mori, Kanako Yoshizaki, Shinichi Watabe, Mika Ishige, Akinari Hinoki, Takuya Kondo, Tomoaki Taguchi, Hisaya Hasegawa, Tomoko Hatata, Naoyuki Tanuma, Kosuke Kirino, Akihiro Hirakawa, Takuya Naruto, Minoru Imai, Ryuji Koike, Kenichiro Hosoi, Satoshi Kusuda

Publikováno v: The Lancet Regional Health. Western Pacific, Vol 39, Iss , Pp 100847- (2023)

Summary: Background: Pediatric patients with certain rare diseases are at increased risk of severe respiratory syncytial virus (RSV) infection. However, the prophylactic use of anti-RSV antibody (palivizumab) in these patients is not indicated at pre

Externí odkaz: https://doaj.org/article/faeb27805df24a098986fb0ed51c5afa

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A strategy to prevent tracheo-innominate artery fistula in the course of laryngotracheal separation: 9-year experience in a children's hospital

Autor: Katsumi Yoshizawa, Tomoko Hatata, Shigeru Takamizawa, Junya Ishii, Toru Shimizu

Publikováno v: Journal of pediatric surgery. 57(2)

Aim of the Study : Laryngotracheal separation (LTS) is known to be the definitive solution for intractable aspiration pneumonia in neurologically impaired children. Postoperatively, a tracheostomy cannula is usually required. However, there are fatal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00cd366802173a022a69e1793b0aa4e3
https://pubmed.ncbi.nlm.nih.gov/34844740

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Preoperative sonographic evaluation of the defect size and the diaphragm rim in congenital diaphragmatic hernia - preliminary experience

Autor: Tomoko Furukawa, Shigeru Takamizawa, Yoshiaki Kondo, Kengo Hattori, Yuichiro Miyake, Tomoko Hatata, Katsumi Yoshizawa

Publikováno v: Pediatric radiology. 48(11)

Sonographic assessment before congenital diaphragmatic hernia repair has rarely been studied. To evaluate the accuracy of preoperative ultrasound in measuring the defect size and in anticipating the presence of a rim and thereby to determine ultrasou

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfd497d8bf9a3c31ef4ee67191747a04
https://pubmed.ncbi.nlm.nih.gov/29978294

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Safety and efficacy of noncardiac surgical procedures in the management of patients with trisomy 13: A single institution-based detailed clinical observation

Autor: Tomoki Kosho, Takehiko Hiroma, Masahiko Noguchi, Soichi Shibuya, Kenya Fujita, Kazuki Yoshizawa, Tomoko Hatata, Katsumi Yoshizawa, Shigeru Takamizawa, Tomohiko Nakamura, Eriko Nishi, Jun Ohata, Yuichiro Miyake

Publikováno v: American journal of medical genetics. Part A. 176(5)

Intensive treatment including surgery for patients with trisomy 13 (T13) remains controversial. This study aimed to evaluate the safety and efficacy of noncardiac surgical intervention for T13 patients. Medical records of patients with karyotypically

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::612b2de877c11133e5ef52a9f694e588
https://pubmed.ncbi.nlm.nih.gov/29681109

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Surgical intervention for esophageal atresia in patients with trisomy 18

Autor: Seiji Mizuno, Kenji Iio, Eriko Nishi, Tomoki Kosho, Yasumasa Yamada, Katsumi Yoshizawa, Yoshimitsu Fukushima, Takehiko Hiroma, Hiroshi Kawame, Tomoko Hatata, Shigeru Takamizawa, Tomohiko Nakamura

Publikováno v: American Journal of Medical Genetics Part A. 164:324-330

Trisomy 18 is a common chromosomal aberration syndrome involving growth impairment, various malformations, poor prognosis, and severe developmental delay in survivors. Although esophageal atresia (EA) with tracheoesophageal fistula (TEF) is a potenti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0da9385221d7918f2927fc6458765d3
https://doi.org/10.1002/ajmg.a.36294

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Use of transabdominal (external) ultrasound during balloon dilatation to diagnose tracheobronchial remnant in congenital esophageal stenosis

Autor: Tomoko Furukawa, Kengo Hattori, Katsumi Yoshizawa, Shigeru Takamizawa, Yoshiaki Kondo, Tomoko Hatata, Yuichiro Miyake

Publikováno v: World Journal of Pediatric Surgery. 1:e000006

Preoperativedifferential diagnosis between tracheobronchial remnant (TBR) and other typesof congenital esophageal stenosis (CES) is challenging, even when usingendoscopic ultrasonography (EUS). This report is the first to demonstrate theuse of transa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bd7cf8297f6479ebf1a66502893a3641
https://doi.org/10.1136/wjps-2018-000006

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Long-term Outcome of Children With Biliary Atresia Who Were Not Transplanted After the Kasai Operation: >20-year Experience at a Children's Hospital

Autor: Tomoko Hatata, Kyoko Mochizuki, Masato Shinkai, Hiroshi Take, Hironori Kudo, Youkatsu Ohhama, Norihiko Kitagawa

Publikováno v: Journal of Pediatric Gastroenterology & Nutrition. 48:443-450

Sequential strategies combining the Kasai operation as a first-line treatment and liver transplantation as a second-line option, if necessary, have been accepted for patients with biliary atresia (BA). To understand the role of the Kasai operation in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c08ab5ea74e166176161bba7d908ec1
https://doi.org/10.1097/mpg.0b013e318189f2d5

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Extraosseous Ewing sarcoma in the mesentery: the first report of cases in children

Autor: Yoshifumi Ogiso, Kazutoshi Komori, Soichi Shibuya, Kazuki Yoshizawa, Tomoko Hatata, Katsumi Yoshizawa, Shigeru Takamizawa

Publikováno v: Pediatric surgery international. 31(10)

Extraosseous ewing sarcoma (EES) is a rare soft-tissue tumor usually found in the extremities or paraspinal region. We describe the case of a 4-year-old boy with a large cystic mass in the mesentery diagnosed as mesenteric lymphangioma preoperatively

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3efb7d9a475e7ea035ebf86bbcb323bf
https://pubmed.ncbi.nlm.nih.gov/26280743

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Discordant clinical phenotype in monozygotic twins with Alagille syndrome: Possible influence of non-genetic factors

Autor: Eriko Nishi, Michiko Arakawa, Nancy B. Spinner, Daisuke Hayashi, Tomohiko Nakamura, Alexandra M. Falsey, Takehiko Hiroma, Kosuke Izumi, Eiko Hidaka, Yoshifumi Ogiso, Noriko Kubota, Christopher M. Grochowski, Tomoko Hatata

Publikováno v: American journal of medical genetics. Part A. (2)

Alagille syndrome is a multisystem developmental disorder characterized by bile duct paucity, congenital heart disease, vertebral anomalies, posterior embryotoxon, and characteristic facial features. Alagille syndrome is typically the result of germl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72a4c9d130cd681a444bcc764d4cdbe8
https://pubmed.ncbi.nlm.nih.gov/26463753

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