Zobrazeno 1 - 10
of 12
pro vyhledávání: '"AKIRA TSURU"'
Autor:
Tetsuo Matsuzaka, Hiroyuki Moriuchi, Chisato Kawasaki, Atsuko Matsuo, Shigeki Tanaka, Hiroshi Baba, Akira Tsuru
Publikováno v:
Epilepsia. 42:9-12
Purpose: To define the most appropriate time for surgery for medically intractable epilepsies in infants and young children. Methods: First we examined retrospectively the changes in developmental quotients (DQs) during the clinical course and the cl
Autor:
Nakamichi Saitoh, Tomomi Tsujii, Tatsuro Kondoh, Tadashi Matsumoto, Kimiko Tamagawa, Akira Tsuru, Takashi Shimizu, Nagisa Amamoto
Publikováno v:
Journal of Human Genetics. 48:0125-0129
The childhood cerebral form of X-linked adrenoleukodystrophy (X-ALD) is a severe congenital metabolic disease without a definite effective therapy except for hematopoietic stem cell transplantation in the appropriate disease stage. Seven Japanese fam
Autor:
Ayako Hamada, Hiroyuki Moriuchi, Norio Tominaga, Tadashi Matsumoto, Tetsuo Matsuzaka, Tatsuro Kondoh, Akira Tsuru, Tsutomu Kamei
Publikováno v:
Pediatrics International. 44:686-689
Autor:
Shigeki Tanaka, Tetsuo Matsuzaka, Chikako Baba, Yoshio Nakashita, Kunio Tomimasu, Atsuko Matsuo, Hiroyuki Moriuchi, Akira Tsuru
Publikováno v:
Brain and Development. 23:575-579
Recent advances in diagnostic and therapeutic techniques may have changed incidence and etiologies of West syndrome (WS). We performed a retrospective epidemiological study of WS that occurred in 47 children in Nagasaki Prefecture during a recent 10-
Autor:
Yoshiro Tsuji, Tsuneyoshi Baba, Tadamichi Yanagi, Tomoko Sawai, Tetsuya Yokoo, Eiichi Kinoshita, Akira Tsuru, Masaaki Yoshimoto
Publikováno v:
Pediatrics International. 32:146-150
A new system for selective low density lipoprotein apheresis with an automated regenerating column using dextran-sulfate (DS) as ligand was evaluated for six months in a 13-year-old boy homozygous for familial hypercholesterolemia. Two columns each c
Autor:
Yasuharu Ohno, Izumi Muraoka, Hiroyuki Moriuchi, Eiichi Kinoshita, Taichirou Kosaka, Takashi Kanematsu, Akira Tsuru
Publikováno v:
World journal of gastroenterology. 12(16)
We report the remission of primary gastric lymphoma of the mucosa-associated lymphoid tissue (MALT) type in two immunocompromised pediatric patients. Patient 1, a 14-year-old boy in an immunocompromised state of unknown cause, complained of repeated
Autor:
Hiroshi Hayashi, Mariko Oishi, Hiroki Yokoyama, Shin-ichi Araki, Koichi Kawai, Katsuya Yamazaki, Osamu Tomonaga, Shin-ichiro Shirabe, Hiroshi Maegawa, Miyoko Saito, Yoshio Kurihara, Takeshi Osonoi, Daijiro Kabata, Ayumi Shintani, Hiroshi Yamaguchi, Masahiro Iwamoto, Haruhiko Yoshimura, Yasushi Ishigaki, Yoshihiko Takahashi, Hiroshi Takamura, Daigaku Uchida, Atsunori Kashiwagi, Masae Minami, Hiroshi Takeda, Akira Kanamori, Akiko Hosokawa, Azuma Kanatsuka, Noriharu Yagi, Atsushi Hasegawa, Masakazu Kato, Naoki Manda, Kazuhiro Miyazawa, Tetsuya Moriai, Kenichi Tsuchida, Daishiro Yamada, Makoto Nakazono, Fuminobu Okuguchi, Takashi Ajihara, Shigetake Ko, Susumu Nakamura, Akira Tsuruoka, Mitsutoshi Kato, Akio Ueki, Koichi Hirao, Kotaro Iemitsu, Hajime Maeda, Masahiko Takai, Masato Takaki, Hikari Suzuki, Yuki Kono, Sumio Kato, Ituko Miyazawa, Takashi Noto, Koichi Iwasaki, Hiroshi Ninomiya, Kokichi Tanaka, Yoshifumi Yokomizo, Kohei Yamaguchi, Katsushige Abe, Nobuyuki Abe, Nobuki Yano, Michiko Chosa, Takako Arakaki
Publikováno v:
BMJ Open Diabetes Research & Care, Vol 10, Iss 3 (2022)
Externí odkaz:
https://doaj.org/article/3a3b6c618a2146ec95286df435ad7085
Autor:
Hiroyuki Moriuchi, Naohisa Kamimura, Akira Tsuru, Tadashi Matsumoto, Tetsuo Matsuzaka, Tatsuro Kondoh
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 43(2)
Autor:
Tadashi Matsumoto, Tatsuro Kondoh, Yoshihiko Imamura, Tsutomu Kamei, Yukiharu Shimasaki, Akira Tsuru, Hiroyuki Moriuchi, Eiichi Kinoshita
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 42(5)
Publikováno v:
Journal of human genetics. 44(1)
The disease "deafness and onychodystrophy" (DOD) is characterized by congenital hearing impairment and dystrophic or absent nails and teeth. The autosomal dominant form of the disorder has been previously reported only in one family. We describe here