Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Yoshiyuki Baba"'
Autor:
Akihiro Fujino, Yasushi Fuchimoto, Teizaburo Mori, Motohiro Kano, Yohei Yamada, Michinobu Ohno, Yoshiyuki Baba, Nobutaka Isogawa, Katsuhiro Arai, Takako Yoshioka, Makoto Abe, Nobuo Kanai, Ryo Takagi, Masanori Maeda, Akihiro Umezawa
Publikováno v:
Stem Cell Research & Therapy, Vol 14, Iss 1, Pp 1-9 (2023)
Abstract Background We performed the first autologous oral mucosa-derived epithelial cell sheet transplantation therapy in a patient with refractory postoperative anastomotic stricture in congenital esophageal atresia (CEA) and confirmed its safety.
Externí odkaz:
https://doaj.org/article/71b419a3e31449bf9c0e7eb3f6093eb8
Autor:
Akihiro Fujino, Yasushi Fuchimoto, Yoshiyuki Baba, Nobutaka Isogawa, Takanori Iwata, Katsuhiro Arai, Makoto Abe, Nobuo Kanai, Ryo Takagi, Masanori Maeda, Akihiro Umezawa
Publikováno v:
Stem Cell Research & Therapy, Vol 13, Iss 1, Pp 1-10 (2022)
Abstract Background Congenital esophageal atresia postoperative anastomotic stricture occurs in 30–50% of cases. Patients with severe dysphagia are treated with endoscopic balloon dilatation (EBD) and/or local injection of steroids, but many patien
Externí odkaz:
https://doaj.org/article/3fd7fc5355374d2985a7ceb4eb0b52e9
Publikováno v:
Journal of Craniofacial Surgery. 34:350-355
Costochondral grafting is performed in the reconstruction of severe micrognathia. In this study, we report our experience with graft take, as well as unique findings that have not been focused on in the past literature such as postoperative position
Autor:
Yasushi Fuchimoto, Yoshiyuki Baba, Akihiro Fujino, Makoto Abe, Katsuhiro Arai, Nobuo Kanai, Masanori Maeda, Takanori Iwata, Nobutaka Isogawa, Akihiro Umezawa, Ryo Takagi
Publikováno v:
Stem Cell Research & Therapy, Vol 13, Iss 1, Pp 1-10 (2022)
Stem Cell Research & Therapy
Stem Cell Research & Therapy
Background Congenital esophageal atresia postoperative anastomotic stricture occurs in 30–50% of cases. Patients with severe dysphagia are treated with endoscopic balloon dilatation (EBD) and/or local injection of steroids, but many patients contin
Autor:
Nobutaka Isogawa, Yoshiyuki Baba
Publikováno v:
Pediatric Dental Journal. 31:275-280
The favorable conditions for revascularization of replanted immature primary teeth after avulsion are not well understood. We report a case of replantation of an avulsed immature mandibular primary central incisor in a 7-month-old male infant. The av
Autor:
Akihiro Fujino, Yasushi Fuchimoto, Teizaburo Mori, Motohiro Kano, Yohei Yamada, Michinobu Ohno, Yoshiyuki Baba, Nobutaka Isogawa, Katsuhiro Arai, Takako Yoshioka, Makoto Abe, Nobuo Kanai, Ryo Takagi, Masanori Maeda, Akihiro Umezawa
BackgroundWe performed the first autologous oral mucosa-derived epithelial cell sheet transplantation therapy in a patient with refractory postoperative anastomotic stricture in congenital esophageal atresia (CEA) and confirmed its safety. In this st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f432ebe93feb5ae0e2645eda4948b30
https://doi.org/10.1101/2022.09.04.22279376
https://doi.org/10.1101/2022.09.04.22279376
Publikováno v:
Plastic and Aesthetic Research. 9:51
This case report aimed to present the course of surgically combined comprehensive orthodontic treatment of a male adult with cleft lip and palate, showing a left alveolar cleft, lateral deviation of the major segment of the maxilla, and palatal trans
Autor:
Rina Hikita, Keiji Moriyama, Michiko Tsuji, Tsutomu Matsumoto, Sahori Matsuno, Yoshiyuki Baba
Publikováno v:
Congenital Anomalies. 59:162-168
Williams syndrome (WS) is a rare congenital anomaly that is characterized by distinctive facial features, congenital heart disease, and behavioral characteristics that include mental retardation. However, only a few reports have documented the dentoc
Publikováno v:
Congenital Anomalies. 59:11-17
Turner syndrome is associated with an X chromosome abnormality in women and is characterized by infantilism, congenital webbed neck, and cubitus valgus. The aim of this study was to determine the maxillofacial morphology and oral characteristics of J
Publikováno v:
Pediatric Dental Journal. 27:101-104
Background/Purpose Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disorder characterized by anhidrosis, lack of pain sensation, and mental retardation. Mutations in the NTRK1 gene are responsible for this disord