Saisho-hattori Takako | 宮城県立こども病院血液腫瘍科

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著作論文

The analysis of the functions of human B and T cells in humanized NOD/shi-scid/γc^ (NOG) mice (hu-HSC NOG mice)
Phylogenetic, ontogenetic, and pathological aspects of the urine-concentrating mechanism
The Nutrient Formula Containing Eicosapentaenoic Acid and Docosahexaenoic Acid Benefits the Fatty Acid Status of Patients Receiving Long-Term Enteral Nutrition
Olfactory Stimulation Using Black Pepper Oil Facilitates Oral Feeding in Pediatric Patients Receiving Long-Term Enteral Nutrition
Fludarabine- and Cyclophosphamide-Based Nonmyelobalative Conditioning Regimen for Transplantation of Chronic Granulomatous Disease : Possible Correlation with Prolonged Pure Red Cell Aplasia
A novel JAK3 mutation in a Japanese patient with severe combined immunodeficiency
Novel mutations in five Japanese patients with 3-methylcrotonyl-CoA carboxylase deficiency
Refractory chronic immune thrombocytopenic purpura in a child with acute lymphoblastic leukemia
Neonatal-Onset Brainstem Reticular Reflex Myoclonus Following a Prenatal Brain Insult : Generalized Myoclonic Jerk and a Brainstem Lesion
Characterization of a Novel Nonsense Mutation in the Interleukin-7 Receptor α Gene in a Korean Patient with Severe Combined Immunodeficiency
The Absolute Number of Peripheral Blood CD34+ Cells Predicts a Timing for Apheresis and Progenitor Cell Yield in Patients with Hematologic Malignancies and Solid Tumors
Evaluation of Hematological Reconstitution Potential of Autologous Peripheral Blood Progenitor Cells Cryopreserved by a Simple Controlled-Rate Freezing Method
Abdominal Migraine Associated with Ecchymosis of the Legs and Buttocks : Does the Symptom Imply an Unknown Mechanism of Migraine?
The Cerebrospinal Fluid Level of 5-Methylterahydrofolate in a Japanese Boy with Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum
Molecular analysis of a presymptomatic case of carnitine palmitoyl transferase I (CPT I) deficiency detected by tandem mass spectrometry newborn screening in Japan
Mutation and haplotype analyses of the MUT gene in Japanese patients with methylmalonic acidemia
Quality assessment of umbilical cord blood units at the time of transplantation
Vincristine-resistant Kasabach-Merritt phenomenon successfully treated with low-dose radiotherapy
A genome-wide association study identifies RNF213 as the first Moyamoya disease gene
Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies

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