Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Toru Kawanami"'
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-5 (2017)
Abstract Background Joubert syndrome and related disorders (JSRD) is a clinically and genetically heterogeneous condition with autosomal recessive or X-linked inheritance, which share a distinctive neuroradiological hallmark, the so-called molar toot
Externí odkaz:
https://doaj.org/article/1c77f7e7f084454391ca18e0174d85b8
Autor:
Hidenori Sato, Yoshimi Takahashi, Luna Kimihira, Chifumi Iseki, Hajime Kato, Yuya Suzuki, Ryosuke Igari, Hiroyasu Sato, Shingo Koyama, Shigeki Arawaka, Toru Kawanami, Masakazu Miyajima, Naoyuki Samejima, Shinya Sato, Masahiro Kameda, Shinya Yamada, Daisuke Kita, Mitsunobu Kaijima, Isao Date, Yukihiko Sonoda, Takamasa Kayama, Nobumasa Kuwana, Hajime Arai, Takeo Kato
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0166615 (2016)
Little is known about genetic risk factors for idiopathic normal pressure hydrocephalus (iNPH). We examined whether a copy number loss in intron 2 of the SFMBT1 gene could be a genetic risk for shunt-responsive, definite iNPH. Quantitative and digita
Externí odkaz:
https://doaj.org/article/5d089864b8564de38d512b8d99b28516
Autor:
Katsumi Mizuta, Makoto Kuroda, Masayuki Kurimura, Yoshikazu Yahata, Tsuyoshi Sekizuka, Yoko Aoki, Tatsuya Ikeda, Chieko Abiko, Masahiro Noda, Hirokazu Kimura, Tetsuya Mizutani, Takeo Kato, Toru Kawanami, Tadayuki Ahiko
Publikováno v:
Emerging Infectious Diseases, Vol 18, Iss 11, Pp 1787-1793 (2012)
Human parechovirus has rarely been shown to cause clinical disease in adults. During June–August 2008, a total of 22 adults sought treatment at Yonezawa City Hospital in Yamagata, Japan, for muscle pain and weakness of all limbs; most also had feve
Externí odkaz:
https://doaj.org/article/07e22cb3e02640ef951c22a2be677012
Autor:
Manabu Wada, Shingo Koyama, Takeo Kato, Shinobu Kawakatsu, Masayuki Kurimura, Toru Kawanami, Ryota Kobayashi, Hidenori Sato
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
Scientific Reports
Scientific Reports
Primary familial brain calcification (PFBC) is a rare neuropsychiatric disorder with characteristic symmetrical brain calcifications. Patients with PFBC may have a variety of symptoms, although they also may be clinically asymptomatic. Parkinsonism i
Autor:
Takeo Kato, Manabu Wada, Hiroyasu Sato, Haruko Tanji, Hiroaki Okada, Koichi Wakabayashi, Yoshimi Takahashi, Toru Kawanami, Ryosuke Igari, Yoshitaka Yamaguchi, Shigeki Arawaka, Shingo Koyama
Publikováno v:
Internal Medicine. 55:1911-1916
A 58-year-old woman with a 1-month history of right hand clumsiness and speaking difficulty was admitted to our hospital. A neurological examination revealed sensory aphasia and right hemiparesis. Her laboratory tests showed elevated serum levels of
Autor:
Kentaro Watanabe, Toru Kawanami, Shinji Susa, Kenzo Oba, Manabu Wada, Motoshi Ouchi, Takeo Kato, Tatsuya Suzuki, Wataru Kameda, Toshihide Oizumi, Makoto Ohara
Publikováno v:
Geriatrics & Gerontology International. 15:1023-1030
Aim The present study aimed to evaluate the relationship between the change of carotid intima-media thickness (CIMT) and clinical characteristics in Japanese patients without a history of cardiovascular disease. Methods The study participants were 14
Publikováno v:
Journal of the Neurological Sciences. 339:108-112
Background The epidemiology and pathophysiology of iNPH remain unclear. We aimed to investigate the incidence of iNPH in elderly inhabitants of the community, and to identify how ventriculomegaly develops on brain MRIs and how symptoms develop in iNP
Autor:
Hidenori Sato, Yoshitaka Yamaguchi, Toru Kawanami, Manabu Wada, Shingo Koyama, Yoshimi Takahashi, Hikaru Nagasawa, Takeo Kato
Publikováno v:
American Journal of Hypertension. 27:1257-1267
BACKGROUND Recent epidemiological studies reported a relationship between 24-hour ambulatory blood pressure (ABP) variability and cardiovascular events. However, the impact of ABP variability on small vessel disease (SVD) progression or cognitive dec
Publikováno v:
Internal Medicine. 53:151-154
A 38-year-old woman was suffering from irregular headaches and sleepiness. She had used soap containing Glupearl 19S (hydrolyzed wheat proteins) every day for approximately one year and had experienced an episode of rash eruption on her face seven mo
Publikováno v:
Magnetic Resonance in Medical Sciences. 13:123-126
In 2 cases of Wernicke encephalopathy in which the initial symptom was double vision, the only abnormal finding on magnetic resonance (MR) imaging was abnormal enhancement of the mammillary bodies. The mammillary bodies are the region most vulnerable