Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hiromi Tsuneta"'
Autor:
Yasuo Takekoshi, Yukio Sakiyama, Tadashi Ariga, Hiromi Tsuneta, Yutaka Takahashi, Tohru Watanabe, Toshiaki Ishii, Shuzo Matsumoto
Publikováno v:
Pediatrics International. 28:226-231
15-year-old boy with Wiskott-aldrich syndrome (WAS) associated with nephrotic syndrome was reported. Histological findings on a renal biopsy specimen by light, fluorescence and electron mictroscopies disclosed pathologic changes typical of mambranous
Publikováno v:
Pediatrics International. 26:51-55
Ataxia telangiectasia is agenetically determined immunodeficiency with predisposition to malignancy. Herein we report a case of ataxia telangiectasis in a child who had showed high antibody titers to viral capsid antigen (VCA), presence of antibodies
Autor:
Yukio Sakiyama, Akemi Wakisaka, T. Okuyama, Shuzo Matsumoto, Kaname Togashi, Yoshinori Wagatsuma, Hiromi Tsuneta, Yuko Nakai, Miki Aizawa
Publikováno v:
Pediatrics International. 25:356-360
Autor:
Akemi Wakisaka, Toyoko Kano, Kaname Togashi, Junko Moriuchi, Yuko Nakai, Yoshinori Wagatsuma, Yukio Sakiyama, Hiromi Tsuneta, Miki Aizawa, Shuzo Matsumoto
Publikováno v:
Human Immunology. 4:265-270
Twenty-three unrelated Japanese patients with asthma who showed a high total serum IgE level, a strong skin test response to Dermatophagoides farinae, and a high score on a radioallergosorbent test (RAST) using Dermatophagoides farinae were typed for
Autor:
Norio Niikawa, Hiromichi Kojima, Hiroyoshi Itoh, Toshio Lmai, Shuzo Matsumoto, Yutaka Takahashi, Masahiko Okada, Kazue Sasaki, Hiromi Tsuneta, Yukio Sakiyama
Publikováno v:
Pediatrics International. 23:268-268
Autor:
Hiromi Tsuneta, Tohru Watanabe, Shuzo Matsumoto, B. Nagai, R. Mitsuyama, O. Okada, Shinichiro Arashima
Publikováno v:
Pediatrics International. 23:222-222
Publikováno v:
Archives of Pediatrics & Adolescent Medicine. 131:522
• The case presented here may be the first identified report of Down syndrome with 21 trisomy in one child of triplets. One triplet died at 1 month of age; his facial appearance was not typical of Down syndrome. Detailed testing of blood groups sug
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