Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Yutaka Awaya"'
Autor:
Yutaka Awaya, Risa Uno, Masaru Nishida, Toshisaburou Nagai, Tetsuzo Tagawa, Hidenori Imaishi, Hiroshi Arai, Takuya Tanabe, Junko Tanaka, Kihei Maekawa
Publikováno v:
Pediatrics International. 53:626-629
Background: Primary care physicians in Japan are often unwilling to vaccinate children with neurological disorders. The aim of the present study was to determine the state of vaccination in children who are severely handicapped and/or have convulsive
Autor:
Fumiyuki Araki, Shiro Amano, Mieko Yanagisawa, Norihiko Honda, Kyoko Ono, Shima Fukuoka, Tatsuya Mimura, Yutaka Awaya, Makoto Araie, Makiko Ochiai, Tomohiko Usui, Satoru Yamagami, Reiko Arita
Publikováno v:
Current Eye Research. 33:940-945
To observe the morphology of the corneal cells and corneal nerve fibers in patients with type IV or V hereditary sensory and autonomic neuropathy (HSAN) by in vivo confocal microscopy and elucidate the mechanism leading to the loss of corneal sensati
Publikováno v:
Brain and Development. 24:231-238
This study investigated the clinical and EEG characteristics of initial status epilepticus (SE) during infancy in patients with mesial temporal lobe epilepsy (MTLE). The subjects were six patients who had been brought to our emergency clinic and trea
Autor:
Toshiya Tomioka, Hiroshi Sekiyama, Yutaka Awaya, Shigehito Sawamura, Kazuo Hanaoka, Kenji Nihei
Publikováno v:
Anesthesia & Analgesia. 94:271-274
We investigated the anesthetic management of patients with congenital insensitivity to pain and anhidrosis (CIPA) in Japan. CIPA is a rare inherited disease characterized by a lack of pain sensation and thermoregulation. Although lacking pain sensati
Publikováno v:
Brain and Development. 23:736-748
Severe myoclonic epilepsy in infants (SME) is one of the most malignant epileptic syndromes recognized in the latest classification of epileptic syndromes. The clinical details and electroencephalographic (EEG) characteristics have been elucidated by
Autor:
Tatsuya Takahashi, Tetsuo Sakai, Hideki Nagatomo, Izumi Kawachi, Masatoyo Nishizawa, Osamu Onodera, Kiyoshi Iwabuchi, Yoshiki Sekijima, Kayoko Saito, Hajime Tanaka, Yoshihisa Takiyama, Tatsuhiko Yuasa, Sumio Sugano, Yutaka Awaya, Shuichi Igarashi, Tadashi Hiroi, Shoji Tsuji, Ryoko Koike, Hidetoshi Date, Kazutoshi Uekawa, Nobuyoshi Fukuhara
Publikováno v:
Nature Genetics. 29:184-188
Friedreich ataxia (FRDA), the most common autosomal recessive neurodegenerative disease among Europeans and people of European descent, is characterized by an early onset (usually before the age of 25), progressive ataxia, sensory loss, absence of te
Autor:
Makiko Osawa, Kayoko Saito, Yutaka Awaya, Teruyuki Tanaka, Hiroyuki Shimizu, Nobutaka Arai, Kyoko Mukahira, Ichiro Suzuki, Masaya Oda, Hirokazu Oguni
Publikováno v:
Epilepsia. 41:21-25
Summary: Recent progress in surgical intervention for medically refractory epilepsy has helped to shed light on more complex epileptogenic problems in children and infants. Surgical treatment increasingly is being used in pediatric patients, but the
Autor:
Ichiro Matsuda, Sek Mardy, Yasuhiro Indo, Yutaka Awaya, Fumio Endo, Kenji Nihei, Yuichi Miura
Publikováno v:
Human Genetics. 106:116-124
The human TRKA gene encodes a high-affinity tyrosine kinase receptor for nerve growth factor. Congenital insensitivity to pain with anhidrosis (CIPA) is an autosomal recessive genetic disorder reported from various countries and characterized by anhi
Autor:
Ichiro Suzuki, Yutaka Awaya, Kayoko Saito, Makiko Osawa, Nobutaka Arai, Hiroyuki Shimizu, Hirokazu Oguni, Teruyuki Tanaka, Masaya Oda, Kyoko Mukahira
Publikováno v:
Brain and Development. 20:154-164
We studied the clinical details of 14 children with intractable epilepsies, all of whom underwent epilepsy surgery before age 18 years. All 14 suffered catastrophic seizures, which were resistant to the full range of available medical treatments. The
Autor:
Yasuhiro Indo, Mohammad Azharul Karim, Hidefumi Tonoki, Yumi Hayashida, Tomoyasu Kawano, Ichiro Matsuda, Hiroshi Mitsubuchi, Motoko Tsuruta, Yutaka Awaya, Kohji Ohta
Publikováno v:
Nature Genetics. 13(4):485-488
Congenital insensitivity to pain with anhidrosis (CIPA; MIM 256800) is an autosomal-recessive disorder characterized by recurrent episodes of unexplained fever, anhidrosis (absence of sweating) and absence of reaction to noxious stimuli, self-mutilat