1,728 results on '"Kato, Motohiro"'
Search Results
252. Long-term survivor of relapsed stage IV malignant rhabdoid tumor of the kidney
253. Prophylactic Administration of Prothrombin Complex Concentrates for Congenital Prothrombin Deficiency With a Novel Frameshift Mutation, Prothrombin Saitama
254. Which concentration of the inhibitor should be used to predict in vivo drug interactions from in vitro data?
255. Genetic features of precursor B‐cell phenotype Burkitt leukemia with IGH‐MYC rearrangement.
256. Extrapolation of In Vitro Metabolic and P-Glycoprotein-Mediated Transport Data to In Vivo by Modeling and Simulations
257. Effects of stimulus orientation on spatial frequency function of the visual evoked potential
258. An international retrospective study for tolerability of 6-mercaptopurine on NUDT15 bi-allelic variants in children with acute lymphoblastic leukemia
259. Fatal Epstein‐Barr virus‐associated hemophagocytic lymphohistiocytosis with virus‐infected T cells after pediatric multivisceral transplantation: A proof‐of‐concept case report
260. ATRT-11. PREVALENCE OF GERMLINE VARIANTS IN SMARCB1 INCLUDING SOMATIC MOSAICISM IN AT/RT AND OTHER RHABDOID TUMORS
261. HGG-49. A PEDIATRIC THALAMIC HIGH-GRADE GLIOMA WITH H3F3A K27M AND BRAF V600E DOUBLE MUTATIONS
262. ETMR-11. A CASE OF PRIMARY DIFFUSE LEPTOMENINGEAL PRIMITIVE NEUROECTODERMAL TUMOR
263. Current Status of Aggressive End-of-Life Care in Children with Hematologic Malignancy: A Population Based Study
264. Hematopoietic stem cell transplantation in children and adolescents with nonremission acute lymphoblastic leukemia
265. Mass decrease in contaminants by photocatalytic decomposition of TiO2 in vacuum
266. Unrelated cord blood transplantation with myeloablative conditioning for pediatric acute lymphoblastic leukemia in remission: prognostic factors
267. Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7
268. Clinical utility of target capture‐based panel sequencing in hematological malignancies: A multicenter feasibility study
269. A case of pure erythroid leukemia with MYB–GATA1 fusion that developed tumor lysis syndrome with dexamethasone
270. Successful Treatment With ATRA and Arsenic Trioxide for a Child With Down Syndrome and Acute Promyelocytic Leukemia
271. Nationwide study of pediatric B‐cell precursor acute lymphoblastic leukemia with chromosome 8q24/ MYC rearrangement in Japan
272. High prevalence of SMARCB1 constitutional abnormalities including mosaicism in malignant rhabdoid tumors
273. In vitro–in vivo extrapolation of metabolic clearance using human liver microsomes: factors showing variability and their normalization
274. Comparison of child and family reports of health-related quality of life in pediatric acute lymphoblastic leukemia patients after induction therapy
275. Age-Related Trend in Tacrolimus Clearance Among Children Undergoing Stem Cell Transplantation
276. Myelodysplastic syndrome in a patient with Barth syndrome (3‐methylglutaconic aciduria type II).
277. Prediction of Human Blood-to-Plasma Drug Concentration Ratio
278. Voriconazole–micafungin combination therapy for acute lymphoblastic leukemia
279. IgD myeloma indicated by plasma cells in the peripheral blood and massive pleural effusion
280. Mechanism of the upregulation of erythropoietin-induced uptake clearance by the spleen
281. Chromosomal abnormalities and novel disease-related regions in progression from Barrettʼs esophagus to esophageal adenocarcinoma
282. Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms
283. Frequent inactivation of A20 in B-cell lymphomas
284. The Quantitative Prediction of In Vivo Enzyme-Induction Caused by Drug Exposure from In Vitro Information on Human Hepatocytes
285. Effect of buformin and metformin on formation of advanced glycation end products by methylglyoxal
286. Genomic analysis of two rare cases of pediatric Ph‐positive T‐ALL.
287. Differentiating between multiple system atrophy and Parkinson’s disease by positron emission tomography with18F-dopa and18F-FDG
288. Characterization of adenocarcinoma of the lung in a familial adenomatous polyposis patient
289. Estimation of Serum Protein Binding of Compounds Metabolized in Serum Using Matrix Inhibition
290. Whole-genome profiling of chromosomal aberrations in hepatoblastoma using high-density single-nucleotide polymorphism genotyping microarrays
291. New Method for the Simultaneous Estimation of Intrinsic Hepatic Clearance and Protein Binding by Matrix Inhibition
292. High-resolution copy number analysis of hepatoblastoma using ultrahigh-density SNP-genotyping microarrays: O-084
293. Existence of two nonlinear elimination mechanisms for hepatocyte growth factor in rats
294. Pediatric acute lymphoblastic leukemia
295. Nationwide study of pediatric B-cell precursor acute lymphoblastic leukemia with chromosome 8q24/MYC rearrangement in Japan
296. Semi-Active Vibration Isolation System for Launch Vehicles
297. Aggressive Transformation of Juvenile Myelomonocytic Leukemia Associated with Duplication of Oncogenic KRAS due to Acquired Uniparental Disomy
298. Mucopolysaccharidosis II with neonatal respiratory distress syndrome and bronchopulmonary dysplasia.
299. Genomic analysis of Kabuki syndrome with multiple abnormalities in infancy.
300. Transplantation using targeted busulfan for Diamond–Blackfan anemia.
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