Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tetsuro Nagashima"'
Autor:
Kuniko Takanashi, Yashuto Suzuki, Ayumu Noro, MInako Sugiyama, Masanori Nakanishi, Tetsuro Nagashima, Akie Nakamura, Ishizu Katsura, Toshihiro Tajima
Publikováno v:
Pediatric Reports, Vol 3, Iss 3, Pp e20-e20 (2011)
The clinical phenotype of congenital pituitary hormone deficiency is variable and can be associated with a number of structural abnormalities of the central nervous system. We report three Japanese patients with congenital pituitary hormone deficienc
Externí odkaz:
https://doaj.org/article/ed31a85d542d4c498b700ef64c394abd
Autor:
Daisuke Takahashi, Masanori Nakanishi, Katsura Ishizu, Kanako Kubota, Akie Nakamura, Yasuto Suzuki, Hiroyuki Kobayashi, Tetsuro Nagashima, Toshihiro Tajima
Publikováno v:
jpem. 26:949-953
We report an 18-year-old Japanese male with a lack of secondary sex characterization and growth failure caused by a rare association between Rathke’s cyst and hypophysitis. He was referred to us because of delayed secondary sex characterization. En
Autor:
Kenji Kishimoto, Daisuke Suzuki, Masanori Nakanishi, Ryoji Kobayashi, Kazue Yasuda, Hirozumi Sano, Kunihiko Kobayashi, Tetsuro Nagashima
Publikováno v:
International Journal of Hematology. 97:782-785
Langerhans cell histiocytosis (LCH) is sometimes resistant to conventional chemotherapies, and treatment with 2-chlorodeoxyadenosine (2-CdA) is gaining importance as a salvage treatment for refractory or recurrent LCH. Secondary malignancies such as
Autor:
Tomihiro Imai, Yuki Ueda, Kazuyori Yagyu, Tomoshiro Itoh, Tetsuro Nagashima, Yumi Takahashi, Shinji Saitoh, Masakatsu Motomura, Masanori Nakanishi, Minako Sugiyama, Hideaki Shiraishi, Yukayo Ukeba-Terashita
Publikováno v:
Brain and Development. 34:784-786
Anti-muscle-specific tyrosine kinase antibody (MuSK-Ab) is the second most frequent autoantibody identified in adult patients with myasthenia gravis (MG). Adult patients with MuSK-Ab demonstrate characteristic clinical features but very little inform
Autor:
Tetsuro Nagashima, Koji Okuhara, Yuichi Ishikawa, Toshihiro Tajima, Jun Nakae, Kouhei Satoh, Kenji Fujieda
Publikováno v:
Journal of Human Genetics. 46:426-430
Pseudohypoparathyroidism Ia (PHP-Ia), is an inherited disease with clinical hypoparathyroidism caused by parathyroid hormone resistance (PTH), and shows the phenotype of Albright hereditary osteodystrophy (AHO), including short stature, obesity, roun
Autor:
Masafumi Yamada, Tetsuro Nagashima, Kazue Yasuda, Hirozumi Sano, Daisuke Suzuki, Masanori Nakanishi, Ryoji Kobayashi, Kunihiko Kobayashi
Publikováno v:
International journal of hematology. 96(2)
A male infant exhibited thrombocytopenia at birth, and later developed leukocytosis, monocytosis, and bloody stool. The bone marrow was hypercellular with dysplasia. Spontaneous granulocyte/macrophage-colony formation and hypersensitivity to granuloc
Autor:
Yasutsugu Koga, Masahiko Mizumoto, Kenji Fujieda, Yasuo Tahara, Yoshinori Matsumoto, Masahiro Hagisawa, Seiichiro Fujimoto, Tsukasa Hattori, Tetsuro Nagashima
Publikováno v:
Pediatrics International. 36:71-74
We evaluated the validity of the Ballard scoring system for assessing gestational age in Japanese low birthweight infants. Infants included in this study were 116 neonates who were admitted to seven hospitals in Hokkaido. Gestational ages of all infa
Autor:
Tetsuro Nagashima, Akie Nakamura, Minako Sugiyama, Yashuto Suzuki, Toshihiro Tajima, Ishizu Katsura, Ayumu Noro, Kuniko Takanashi, Masanori Nakanishi
Publikováno v:
Pediatric Reports
Volume 3
Issue 3
Pediatric Reports, Vol 3, Iss 3, Pp e20-e20 (2011)
Volume 3
Issue 3
Pediatric Reports, Vol 3, Iss 3, Pp e20-e20 (2011)
The clinical phenotype of congenital pituitary hormone deficiency is variable and can be associated with a number of structural abnormalities of the central nervous system. We report three Japanese patients with congenital pituitary hormone deficienc
Autor:
Masahiro Hagisawa, Masahiko Mizumoto, Takeshi Kida, Takeo Nakajima, Seiichiro Fujimoto, Yasutugu Koga, Satoshi Hattori, Yoshinori Matsumoto, Shunichi Sageshima, Satoru Makinoda, Nobuhiro Takahashi, Kenji Fujieda, Yasuo Tahara, Yutaka Takahashi, Tetsuro Nagashima, Seido Iwata
Publikováno v:
Clinical Pediatric Endocrinology. 3:148-149
Publikováno v:
Brain and Development. 7:611-614
Sixty patients (age-range one month to 14 years) with other types of epilepsy than infantile spasms were treated with clonazepam. Disappearance of seizures and normalization of abnormal EEG with disappearance of seizures were recognized in 77% and 50