Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Takeshi Futatani"'
Autor:
Yu Saito, Kenta Matsumura, Misao Kageyama, Yuichi Kato, Eiji Ohta, Kiyoaki Sumi, Takeshi Futatani, Taketoshi Yoshida
Publikováno v:
BMC Research Notes, Vol 13, Iss 1, Pp 1-6 (2020)
Abstract Objective Patients with congenital myotonic dystrophy (CDM) tend to be born preterm. Although the CDM severity generally depends on the CTG repeat length, prematurity may also affect the prognosis in patients with CDM. Given that preterm bir
Externí odkaz:
https://doaj.org/article/fb50f0d5804c4050ae0b61e4f4a520d2
Autor:
Asghar Aghamohammadi, Nima Parvaneh, Hirokazu Kanegana, Mostafa Moin, Ali Akbar Amirzargar, Abolhassan Farhoudi, Zahra Pourpak, Masoud Movahedi, Mohammad Gharagozlou, Nima Rezaei, Takeshi Futatani, Toshio Miyawaki "
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 3, Iss 4 (2004)
X-linked agammaglobulinemia (XLA) is an immunodeficiency caused by mutations in the Bruton tyrosine kinase (Btk) gene. In order to identify the mutations in Btk gene in Iranian patients with antibody deficiency, 13 male patients with an XLA phenotype
Externí odkaz:
https://doaj.org/article/1c24d940a39a41c2823c27834c469816
Autor:
Shuhei Fujita, Takeshi Futatani, Eriko Kabata, Keigo Nishida, Akira Murata, Kazuyuki Ueno, Noboru Igarashi, Kiyoshi Hatasaki
Publikováno v:
J Cardiol Cases
A 9-year-old boy, diagnosed with double outlet right ventricle after birth, suffered sinus node dysfunction and non-sustained junctional tachycardia after an extracardiac total cavopulmonary connection (TCPC). Spontaneous atrial tachycardia appeared
Autor:
Takeshi Futatani, Ayako Shimao, Shihomi Ina, Hiroyuki Higashiyama, Kiyoshi Hatasaki, Masami Makimoto, Taketoshi Yoshida, Hiroaki Imamura, Jiro Ogawa, Kazuhiro Watanabe, Michio Konishi
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 64(1)
Severe neonatal hypoglycemia may cause irreversible neurological sequelae. Although blood glucose (BG) screening in term neonates without risk factors for hypoglycemia (non-risk neonates) is not recommended in the current guidelines, severe hypoglyce
Autor:
Hiroyuki Higashiyama, Yoshiteru Ohsone, Rieko Takatani, Takeshi Futatani, Rika Kosaki, Masayo Kagami
Publikováno v:
European Journal of Medical Genetics. 65:104580
Kagami-Ogata syndrome (KOS) is an imprinting disorder characterized by polyhydramnios, bell-shaped thorax with coat-hanger appearance (curved ribs), respiratory distress, abdominal wall defects, and distinct facial features, together with intellectua
Autor:
Takeshi Futatani, Noboru Igarashi, Kiyoshi Hatasaki, Ayako Shimao, Shuhei Fujita, Hiroyuki Higashiyama, Shihomi Ina
Publikováno v:
Pediatrics International. 61:471-474
Background Blood sodium and ketone are parameters of dehydration and fasting, respectively. Little is known, however, about the postnatal changes in these parameters in healthy, term, exclusively breast-fed neonates. Methods Capillary blood sodium,
Autor:
Takeshi Futatani, Yoshiki Nagata, Ryo Nakagawa, Hitoshi Irabu, Noboru Igarashi, Shuhei Fujita, Keigo Nishida, Kiyoshi Hatasaki, Minoru Horie, Kazuo Usuda, Seiko Ohno
Publikováno v:
Pediatrics International. 60:998-1001
Background In pediatric patients, syncope commonly occurs as vasovagal syncope, or in epilepsy or orthostatic dysregulation. Cardiogenic syncope is rare but it is lethal, and needs to be promptly diagnosed and treated. Methods and results We describe
Autor:
Rika Usuda, Toshinari Takamura, Kosuke R. Shima, Takeshi Futatani, Hiroshi Akahori, Tohru Yorifuji, Shuichi Kaneko
Publikováno v:
Endocrine Journal. 65:1055-1059
Gain-of-function ATP-binding cassette subfamily C member 8 (ABCC8) mutations are known to cause neonatal diabetes mellitus and maturity-onset diabetes in the young. However, the intrafamilial heterogeneous nature of diabetes caused by the ABCC8 mutat
Publikováno v:
Pediatrics International. 61:1048-1050
Autor:
Kentaro Tamura, Taketoshi Yoshida, Takeshi Futatani, Satomi Inomata, Shigeru Saito, Yosuke Ono
Publikováno v:
Pediatrics & Neonatology. 60:339-341