スポンサーリンク
Department of Pediatrics, Kyoto prefectural University of Medicine | 論文
- A Case of Budd-Chiari Syudrome Successfully Treated by Transcatheter Recanalixation of the Right Hepatic Vein and Transjugular Intrahepatic Portosystemic Shunt
- Identification of a novel fusion gene in a pre-B acute lymphoblastic leukemia with t(1 ; 19)(q23 ; p13)
- Hemophagocytic lymphohistiocytosis during maintenance treatment of precursor B-cell acute lymphoblastic leukemia
- A Novel Perforin Gene Mutation in a Japanese Family with Hemophagocytic Lymphohistiocytosis
- Multi-color FISH : Application to the Simultaneous Detection of Chromosome Aberrations in Neuro-epithelial Tumor Cell Lines
- Infected urachal cyst ruptured during medical palliation
- Tissue culture sture study on neuronal migration in the rat cerebral cortex; effects of low dose radiation
- Response to Imatinib Mesylate in a Patient with Idiopathic Hypereosinophilic Syndrome Associated with Cyclic Eosinophil Oscillations
- Hb Bristol-Alesha Presenting Thalassemia-Type Hyperunstable Hemoglobinopathy
- Hemophagocytic Syndrome Associated with Severe Adenoviral Pneumonia : Usefulness of Real-Time Polymerase Chain Reaction for Diagnosis
- Hemophagocytosis by leukemic blasts in a case a of acute megakaryoblastic leukemia with t(16 ; 21) (p11 ; q22)
- Hypercalcemia in children presenting with acute lymphoblastic leukemia
- A review of 331 rhabdomyosarcoma cases in patients treated between 1991 and 2002 in Japan
- Low Frequency of KIT Gene Mutation in Pediatric Acute Myeloid Leukemia with inv(16)(p13q22) : A Study of the Japanese Childhood AML Cooperative Study Group
- Measurement of carnitine precursors, ε-trimethyllysine and γ-butyrobetaine in human serum by tandem mass spectrometry
- Effect of sports activity on carnitine metabolism Measurement of free carnitine, γ-butyrobetaine and acylcarnitines by tandem mass spectrometry
- A Case of XYY Syndrome with Short Stature
- Subcellular and Subnuclear Distributions of Estrogen Receptor α in Living Cells Using Green Fluorescent Protein and Immunohistochemistry
- A Case of Chronic Infantile Neurological Cutaneous Articular (CINCA) Syndrome with Marked Growth Disturbance
- A Case of Severe Hypoglycemia during Infancy Turned out to be Turner Syndrome with Ringed X