Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tomoyo Noro"'
Autor:
Kazuie Iinuma, Tomoyo Noro, A.S. Knisely, Yusaku Tazawa, Kohachiro Sugiyama, Daiki Abukawa, Michiko Nakagawa
Publikováno v:
Pediatric and Developmental Pathology. 4:304-309
A 12-year-old Japanese boy had chronic elevation and fluctuation of serum transaminase levels since infancy, with no signs or symptoms of liver failure. Usual infections or metabolic disorders were eliminated from consideration. No coagulopathy or ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1ffa7b6038364b9ce382cc14864815c
https://doi.org/10.1007/s100240010174
https://doi.org/10.1007/s100240010174
Autor:
Masue Imaizumi, Masayuki Yamamoto, Hoshiro Suzuki, Naruyoshi Suwabe, Miyako Yoshinari, Ryo Ichinohasama, Yoshitsugu Koizumi, Yan Cui, Tomoyo Noro, Atsushi Sato, Kazuie Iinuma, Toshiaki Saito
Publikováno v:
Leukemia Research. 19:811-815
Phenotypic characteristics of blasts were studied in a Down's infant with transient abnormal myelopoiesis (TAM). Two major subpopulations were identified: (1) CD33+CD42b+ cells with platelet peroxidase activity, the commitment of which to megakaryocy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d717a35d4bebec05328a17a1a1af42a
https://doi.org/10.1016/0145-2126(95)00065-8
https://doi.org/10.1016/0145-2126(95)00065-8
Autor:
Hoshiro Suzuki, Yoshitsugu Koizumi, Toshiaki Saito, Tomoyo Noro, Yasuhiko Obara, Takako Saisho, Hiroshi Nakai, Yan Cui, Tadao Funato, Masue Imaizumi, Atsushi Sato, Kazuie Iinuma, Miyako Yoshinari
Publikováno v:
British Journal of Haematology. 96:614-616
We report a 13-year-old girl with Down's syndrome (DS) having a mosaic karyotype of 46,XX/46,XX, -21,+i(21q), who developed acute myelogenous leukaemia (AML) (FAB M1). The t(8;21) translocation generating a AML1/MTG8 chimaeric gene of her blasts was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c10ce15c8b33e7879a3b92fd66543db
https://doi.org/10.1046/j.1365-2141.1997.d01-2078.x
https://doi.org/10.1046/j.1365-2141.1997.d01-2078.x
Publikováno v:
Journal of inherited metabolic disease. 17(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fac70e81106c3148216ee22b884b4f77
https://pubmed.ncbi.nlm.nih.gov/7837771
https://pubmed.ncbi.nlm.nih.gov/7837771
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 12(1)
Findings in a 1-month-old male infant with Wolman's disease, a rare autosomal defect characterized by intractable diarrhea and severe malabsorption, are described. Investigations in this case focused on the digestive and absorptive functions of the j
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acc006ae5b624746ab33cbd9c3509b3f
https://pubmed.ncbi.nlm.nih.gov/2061782
https://pubmed.ncbi.nlm.nih.gov/2061782
Publikováno v:
Journal of inherited metabolic disease. 12
Recent clinical and biochemical studies have revealed the existence of a ‘peroxisomal disorder’ originating in dysfunction of peroxisomes. In spite of intensive studies, the primary lesion of Zellweger syndrome is obscure (Aikawa et al., 1987). J
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4536644e71e0ad45afb5c5e90bc17537
https://pubmed.ncbi.nlm.nih.gov/2512445
https://pubmed.ncbi.nlm.nih.gov/2512445