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Department Of Pediatrics Nagoya City University Medical School | 論文
- Cardiac Vagal Activation by Adrenocorticotropic Hormone Treatment in Infants with West Syndrome
- Periventricular Leukomalacia with Late-Onset Circulatory Dysfunction of Premature Infants : Correlation with Severity of Magnetic Resonance Imaging Findings and Neurological Outcomes
- Molecular genetic studies on hereditary orotic aciduria : 1 Purification of human orotidine 5'-monophosphate decarboxylase and cloning of its cDNA
- ピリミジン・サルベージ経路に関する研究(II) : 先天性オロット酸尿症の EB-virus transformed リンパ球におけるフルオロウラシルの代謝
- Basic Fibroblast Growth Factor as a Candidate Tumor Marker for Renal Cell Carcinoma
- Muscarinic Receptor Subtypes Mediating Positive and Negative Inotropy in the Developing Chick Ventricle
- Risk of Recurrence of Fetal Chromosomal Aberrations : Analysis of Trisomy 21, Trisomy 18, Trisomy 13, and 45, X in 1,076 Japanese Mothers
- Age-specific incidences of chromosome abnormalities at the second trimester amniocentesis for Japanese mothers aged 35 and older : collaborative study of 5484 cases
- 46, XY, t (3;20) (q13. 3; p12. 2 )の核型を認めたAlagille症候群
- 母児感染例でのC型肝炎ウイルスエンベロープ領域の塩基配列の検討
- Regulatory Elements Directing Gut Expression of the GATA6 Gene during Mouse Early Development
- Lysosome and Lysosome-related Organelles Responsible for Specialized Functions in Higher Organisms, with Special Emphasis on Vacuolar-type proton ATPase
- Association of Mouse Sorting Nexin 1 with Early Endosomes
- Upstream Regions Directing Heart-Specific Expression of the GATA6 Gene During Mouse Early Development
- Analysis of 55 Transplantations from Unrelated Volunteer Donors Facilitated by Tokai Marrow Donor Bank
- Quality of Life in Adult Patients after Bone Marrow Transplantation
- ピリミジン系抗HIV剤の副作用予防のための研究 : 第1報 AZT、AZTglucuronide の定量分析法
- ピリミジン系抗HIV剤の副作用予防のための研究 : 第2報 AZT、AZTglucuronide の定量分析法を用いたグルクロン酸抱合能の評価
- STUDY ON ABNORMAL COPPER METABOLISM IN MENKES' KINKY HAIR DISEASE AND WILSON'S DISEASE
- Acylcarnitine Profiles during Carnitine Loading and Fasting Tests in a Japanese Patient with Medium-Chain Acyl-CoA Dehydrogenase Deficiency