ゴーシェ病での骨リモデリングと造血における特定のサイトカインの役割
スポンサーリンク
概要
- 論文の詳細を見る
- 2007-12-01
著者
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芳野 信
Department Of Pediatrics And Child Health Kurume University School Of Medicine
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HARADA Masaru
Second Department of Medicine, Kurume University School of Medicine
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Fujii Chieko
Department Of Medicine Tokyo Women's Medical University Medical Center East
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Fujii Chieko
Department Of Pediatrics And Child Health Kurume University School Of Medicine
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HARADA Eimei
Department of Pediatrics and Child Health, Kurume University School of Medicine
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NUMATA Sanae
Department of Pediatrics and Child Health, Kurume University School of Medicine
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WATANABE Yoriko
Department of Pediatrics and Child Health, Kurume University School of Medicine
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TOKUNAGA YASUYUKI
Department of Pediatrics and Child Health, Kurume University School of Medicine
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HARADA EIMIEI
Department of Pediatrics and Child Health, Kurume University School of Medicine
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TAJIMA ASAKO
Department of Pediatrics, Tokyo Jikei University School of Medicine
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IDA HIROYUKI
Department of Pediatrics, Tokyo Jikei University School of Medicine
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Harada Eimei
久留米大学 医学部小児科学
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Harada Eimei
Department Of Pediatrics And Child Health Kurume University School Of Medicine
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Numata Sanae
Department Of Pediatrics And Child Health Kurume University School Of Medicine
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Numata Sanae
久留米大学 医学部小児科学
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Tajima Asako
Department Of Pediatrics Jikei University School Of Medicine
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Tajima Asako
Department Of Pediatrics Tokyo Jikei University School Of Medicine
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Ida Hiroyuki
Department Of Pediatrics Tokyo Jikei University School Of Medicine
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Harada Masaru
Second Department Of Internal Medicine Kurume University School Of Medicine
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Tokunaga Yasuyuki
Department Of Pediatrics And Child Health Kurume University School Of Medicine
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Tokunaga Yasuyuki
Department Of Neonatology Osaka Medical Center For Maternal And Child Health
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Fujii Chieko
Department Of Environmental Ecosystem Graduate School Of Medicine University Of Tsukuba
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Ida Hiroyuki
Department Of Materials Science And Engineering Kyoto University
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Watanabe Yoriko
Department Of Biology Graduate School Of Science Tohoku University
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Ida Hiroyuki
Department of Bioengineering, Graduate School of Engineering, Osaka City University
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- ゴーシェ病での骨リモデリングと造血における特定のサイトカインの役割
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- Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency
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- Antiphospholipid syndrome modifies the clinical features of systemic lupus erythematosus
- OE-148 Exercise Tolerability of Japanese Heart Transplant Patients(Transplantation/LVAD (M) OE25,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- PE-275 Ultrasonic Tissue Characterization With Integrated Backscatter As A Non-Invasive Marker To Assess The Effectiveness Of Beta-Blocker Therapy In Japanese Patient(Cardiomyopathy, Clinical 2 (M) : PE47)(Poster Session (English))
- PE-268 Change in Quality of Life from before to after Heart Transplantation in Japanese Patients(Transplantation 1 (M) : PE46)(Poster Session (English))
- P1-26 Effect of artificial gravity with exercise training during bed rest on cardiorespiratory response to exercise(The Proceedings of the 12th Annual Meetings of Japan Society of Exercise and Sports Physiology)
- P1-9 Effect of artificial gravity with exercise training during 20-d bed rest on skeletal muscle mass and function in humans(The Proceedings of the 12th Annual Meetings of Japan Society of Exercise and Sports Physiology)
- Case-control study of perinatal factors and hepatoblastoma in children with an extremely low birthweight
- Dextromethorphan for neuropathic pain with Churg-Strauss syndrome
- Polyarteritis nodosa with mesenteric aneurysms demonstrated by angiography : report of a case and successful treatment of the patient with prednisolone and cyclophosphamide
- PHYSICAL MAP OF A YAC CONTIG CONTAINING THE REGION OF THE HUMAN GENE (HYRC) COMPLEMENTING HYPER-RADIOSENSITIVITY OF THE SCID MOUSE MUTATION
- Functional liver imaging with asialoglycoprotein receptors and serum hyaluronate in a patient with amyloidosis
- Successful Intrauterine Therapy for Fetal Goitrous Hypothyroidism during Late Gestation
- Enzyme Therapy in Gaucher Disease Type 2 : An Autopsy Case
- Programming of Cell Death during Xylogenesis
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- Wilson disease
- Adult-type metachromatic leukodystrophy with a compound heterozygote mutation showing character change and dementia
- A Case with Acute Quadriplegic Myopathy Following Intensive Care for Idiopathic Interstitial Pneumonia
- 胎児性ゴーシェ病 (fetal Gaucher disease) の一剖検例
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- Wilson Disease and Hepatocellular Carcinoma
- Identification of Glass and Ceramics by X-ray Fluorescence Analysis with a Pyroelectric X-ray Generator
- Clinical and genetic studies of five fatal cases of Japanese Gaucher disease type 1
- A long-term survival case of arginase deficiency with severe multicystic white matter and compound mutations
- Effectiveness and safety of non-intravenous high-dose phenobarbital therapy for intractable epilepsy during childhood
- Development and validation of an HPLC-based screening method to acquire polyhydroxyalkanoate synthase mutants with altered substrate specificity(ENZYMOLOGY, PROTEIN ENGINEERING, AND ENZYME TECHNOLOGY)
- Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies
- Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations
- A familial case of LEOPARD syndrome associated with a high-functioning autism spectrum disorder
- Shield Optimization Study for Choke Coil of Tandem Mirror Fusion Reactor "GAMMA R"
- Biosynthesis of poly(3-hydroxybutyrate-co-3-hydroxy-4-methylvalerate) by recombinant Escherichia coli expressing leucine metabolism-related enzymes derived from Clostridium difficile(GENETICS, MOLECULAR BIOLOGY, AND GENE ENGINEERING)