Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Shin-ichiro Miyagawa"'
Autor:
Kazuoki Kubota, Takakuni Tanizawa, Hiroaki Inomata, Shun Soneda, Chuken Miyagi, Mari Murashita, Naoko Sato, Shin-ichiro Miyagawa, Takahiro Mochizuki, Masakuni Tokuda, Eiichi Kinoshita, Sachiko Kitanaka, Hiroki Nozue, Katsura Ishizu, Osamu Nose, Susumu Konda, Kentaro Kishi, Atsuko Ogasawara, Masahiro Noda, Toshiaki Tanaka, Yukiko Nakano, Kumiko Araki
Publikováno v:
Hormone Research in Paediatrics. 94:211-218
Background: About twice as many boys as girls undergo growth hormone (GH) therapy in GH deficiency (GHD). However, this sex difference may not correctly reflect a real incidence. Objectives: We analyzed the evidence of a selection bias whereby more b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39c707c7d598d76f745446e1adcf07d1
https://doi.org/10.1159/000518995
https://doi.org/10.1159/000518995
Autor:
Kazuhiko Jinno, Kazuhiro Nakamura, Akari Utsunomiya, Takashi Sato, Masao Kobayashi, Shin-ichiro Miyagawa, Mizuka Miki, Yoshiyuki Kobayashi, Satoshi Okada, Yoko Mizoguchi, Keiichi Hara
Publikováno v:
Pediatrics International. 55:e96-e99
A 2-year-old boy presented with a 21-hydroxylase deficiency, associated with advanced-stage neuroblastoma primarily occurring in the left adrenal gland. He required intensive chemotherapy with polypharmacy, followed by cord blood stem cell transplant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dffe7c5f1ba67b16255128c19614a110
https://doi.org/10.1111/ped.12093
https://doi.org/10.1111/ped.12093
Autor:
Hiroyuki Nunoi, Ayumi Awaya, Tomoyuki Mizukami, Asako Hiraoka, Masao Kobayashi, Shin-ichiro Miyagawa, Fumio Hidaka, Rie Onodera, Mizuka Miki, Atsushi Ono, Emi Kurita
Publikováno v:
Pediatrics International. 51:838-841
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eee298a469050ca636565f9d4bc36bb
https://doi.org/10.1111/j.1442-200x.2009.02931.x
https://doi.org/10.1111/j.1442-200x.2009.02931.x
Autor:
Seiji Mizuno, Kentaro Matsuoka, Tatsuro Kondoh, Masayo Kagami, Tsutomu Ogata, Yukihiro Hasegawa, Reiko Horikawa, Kazuki Yamazawa, Shin-ichiro Miyagawa, Tomonobu Hasegawa, Kazumichi Onigata, Toshio Yamazaki, Toshiro Nagai, Katsuhiro Maeyama, Yoko Miyoshi
Publikováno v:
Journal of Molecular Medicine. 86:1171-1181
Silver-Russell syndrome (SRS) is characterized by growth failure and dysmorphic features and is frequently caused by hypomethylation (epimutation) of the H19-DMR. Although molecular and clinical studies have extensively been performed for SRS patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b10e452d1bf062f9d6106fd5bfdab1f5
https://doi.org/10.1007/s00109-008-0377-4
https://doi.org/10.1007/s00109-008-0377-4
Autor:
Shin-ichiro Miyagawa, Teruyuki Kajiume, Satoshi Okada, Yoko Mizoguchi, Yoshikazu Nishi, Masao Kobayashi
Publikováno v:
Hormone Research in Paediatrics. 67:257-262
Aims: Metyrapone causes a decrease in the serum cortisol level without affecting ACTH production in ectopic tumors. We report a case who presented with Cushing’s syndrome due to an ectopic ACTH-producing thymic carcinoid. In the present case, it wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e98b4182f932d381ab505ef08a33f23
https://doi.org/10.1159/000098548
https://doi.org/10.1159/000098548
Autor:
Shin-Ichiro Nishimura, Kazuhiro Nakamura, Masao Kobayashi, Koji Arihiro, Shin-ichiro Miyagawa, Yoko Mizoguchi
Publikováno v:
International Journal of Hematology. 81:330-334
Primary adrenal lymphoma is uncommon, and the majority cases of this disorder are found in elderly individuals. We describe a 17-year-old boy with persistent fever, hemophagocytic lymphohistiocytosis, and a bilateral tumor of the adrenal glands. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd4a63687389608972e469dca6e571e5
https://doi.org/10.1532/ijh97.04143
https://doi.org/10.1532/ijh97.04143
Autor:
Yoshihiro Komada, Kazuhiro Nakamura, Masao Kobayashi, Hidemi Toyoda, Takashi Sato, Shin-ichiro Miyagawa, Osamu Katoh, Seiji Kojima, Hiroshi Kawaguchi, Kazuhiro Ueda, Nakao Konishi
Publikováno v:
Blood. 96:4366-4369
To define the basis for faulty granulopoiesis in patients with severe congenital neutropenia (SCN), the expression of granulocyte colony-stimulating factor receptor (G-CSFR) in primitive myeloid progenitor cells and their responsiveness to hematopoie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0f1e92ac674ae8dfe4c183fa982b2b6
https://doi.org/10.1182/blood.v96.13.4366.h8004366_4366_4369
https://doi.org/10.1182/blood.v96.13.4366.h8004366_4366_4369
Publikováno v:
British Journal of Haematology. 109:555-562
The effects of insulin and insulin-like growth factor I (IGF-I) on the proliferation of erythroid progenitor cells in bone marrow were studied in serum-deprived culture. Primitive human bone marrow cells were purified by cell sorting on the basis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f8b3adb8a7ea311c3d907903ea96a39
https://doi.org/10.1046/j.1365-2141.2000.02047.x
https://doi.org/10.1046/j.1365-2141.2000.02047.x
Autor:
Michiko Hayashidani, Shin-ichiro Miyagawa, Akari Nakamura-Utsunomiya, Rie Fukuhara, Keiichi Ozono, Yusei Nakata, Kanako Tachikawa, Kanae Takeda, Keiichi Hara, Masao Kobayashi, Toshimi Michigami, Satoshi Okada
Publikováno v:
Clinical Pediatric Endocrinology
Hypophosphatasia is a rare inherited disorder caused by deficient tissue-nonspecific alkaline phosphatase activity. It is classified into 6 subtypes, and the perinatal lethal form of hypophosphatasia is the most severe. Patients with this form suffer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ab6b73950c067e72fcb3a3ce9ce0638
https://pubmed.ncbi.nlm.nih.gov/23926372
https://pubmed.ncbi.nlm.nih.gov/23926372
Autor:
Takashi Sato, Kazuhiro Nakamura, Masao Kobayashi, Shin-Ichiro Nishimura, Teruyuki Kajiume, Hussam Mahmood Salih, Yoshiyuki Kobayashi, Shin-ichiro Miyagawa
Publikováno v:
Journal of pediatric hematology/oncology. 29(3)
Perforin deficiency characterized by markedly reduced cytotoxic T and natural killer cell activities is one type of familial hemophagocytic lymphohistiocytosis (FHL). FHL is a fatal inherited disease, and treatment with stem cell transplantation has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d9a9dc666312f260fa625e6613ed98c
https://pubmed.ncbi.nlm.nih.gov/17356398
https://pubmed.ncbi.nlm.nih.gov/17356398