Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Etsushi Tsuchida"'
Autor:
Satomi Okano, Ryosuke Tanaka, Akie Okayama, Etsushi Tsuchida, Fumikatsu Nohara, Nao Suzuki, Toshio Okamoto, Ken Nagaya, Satoru Takahashi, Hiroshi Azuma
Publikováno v:
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-3 (2017)
Abstract Background Basal meningoceles are rare congenital defects and often clinically occult until they result in life-threatening complications. Therefore, it is important to know the diagnostic clues to early diagnosis. Case presentation We descr
Externí odkaz:
https://doaj.org/article/a3f63a8779894987898bef5f942693c2
Autor:
Akie Okayama, Ryosuke Tanaka, Ken Nagaya, Toshio Okamoto, Etsushi Tsuchida, Hiroshi Azuma, Satomi Okano, Nao Suzuki, Satoru Takahashi, Fumikatsu Nohara
Publikováno v:
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-3 (2017)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background Basal meningoceles are rare congenital defects and often clinically occult until they result in life-threatening complications. Therefore, it is important to know the diagnostic clues to early diagnosis. Case presentation We describe three
Publikováno v:
Journal of Neuroimaging. 24:603-606
BACKGROUND AND PURPOSE A thrombosed dural sinus malformation (DSM) is a rare condition, the clinical features of which have not yet been completely characterized. Here, we describe the clinical course of a patient with a thrombosed DSM and discuss th
Publikováno v:
Pediatric Pulmonology. 50:173-178
Summary Objective There is little available data on airway humidity during high-frequency ventilation (HFV). The purpose of this study is to evaluate the temperature drop in an endotracheal tube (ETT) during HFV. Methods We examined the airway temper
Autor:
Hiroshi Azuma, Masafumi Koga, Shigeru Suzuki, Noriyasu Niizeki, Akiko Furuya, Toshio Okamoto, Yusuke Tanahashi, Ken Nagaya, Kumihiro Matsuo, Fumikatsu Nohara, Etsushi Tsuchida
Publikováno v:
Pediatric Diabetes. 14:267-272
Background As the presence of fetal hemoglobin (HbF) affects the accuracy of hemoglobin A1c (HbA1c) analysis methods, HbA1c measurement may not be a good indicator for patients with neonatal diabetes mellitus, whereas glycated albumin (GA) may be a g
Autor:
Ken Nagaya, Fumikatsu Nohara, Toshio Okamoto, Gen Nishimura, Akiko Yamashita, Tokitsugi Hayashi, Hiroshi Azuma, Hiroko Asai, Etsushi Tsuchida
Publikováno v:
American journal of medical genetics. Part A. (8):1953-1956
Author
Heterozygous COL2A1 mutations create a group of skeletal dysplasias collectively termed type II collagenopathies. Sporadic cases of type II collagenopathies are almost exclusively caused by de novo mutations. Very few cases with intrafami
Heterozygous COL2A1 mutations create a group of skeletal dysplasias collectively termed type II collagenopathies. Sporadic cases of type II collagenopathies are almost exclusively caused by de novo mutations. Very few cases with intrafami
Autor:
Akiko Furuya, Masafumi Koga, Shigeru Suzuki, Hiroko Asai, Noriyasu Niizeki, Hiroshi Azuma, Yusuke Tanahashi, Yumi Kawata, Etsushi Tsuchida, Kumihiro Matsuo, Fumikatsu Nohara, Ken Nagaya, Hironori Takahashi, Toshio Okamoto
Publikováno v:
Pediatric Diabetes. 14:25-30
Background Glycated albumin (GA) reflects glycemic control in patients with neonatal diabetes mellitus (NDM). However, GA in NDM patients is apparently low in relation to glycemia. Objective To establish the reference intervals for GA in healthy infa
Autor:
Hiroko Asai, Tokitsugi Hayashi, Etsushi Tsuchida, Fumikatsu Nohara, Hiroshi Sakata, Toshio Okamoto, Ken Nagaya, Hiroshi Azuma, Yutaka Terao
Publikováno v:
Pediatrics International. 55:519-521
Since the mid-1980s, there have been increasing reports of severe invasive group A streptococcal (GAS) disease in children and adults. There are few reports, however, of neonatal invasive disease, particularly neonatal pleural empyema caused by GAS.
Autor:
Toshio, Okamoto, Ken, Nagaya, Yumi, Kawata, Hiroko, Asai, Etsushi, Tsuchida, Fumikatsu, Nohara, Kazuki, Okajima, Hiroshi, Azuma
Publikováno v:
Congenital anomalies. 55(3)
Short-rib polydactyly syndrome type III is an autosomal recessive lethal skeletal ciliopathy, which is phenotypically similar to nonlethal asphyxiating thoracic dystrophy. Mutations in DYNC2H1 have been identified in both of these disorders, indicati
Autor:
Satomi Igawa, Etsushi Tsuchida, Masako Minami-Hori, Hajime Iizuka, Masaru Honma, Akemi Ishida-Yamamoto
Publikováno v:
The Journal of Dermatology. 43:103-104