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10. Severe Phenotype With RECQL4 Syndrome: A Report of Two Cases.

11. Activation of bystander CD8+ T cells in a pediatric patient with acute hepatitis E.

12. Maternal BMI and allergy in children until 3 years of age (JECS)

16. Detailed analysis of Japanese patients with adenosine deaminase 2 deficiency reveals characteristic elevation of type II interferon signature and STAT1 hyperactivation

17. Successful Repair and Management of Severe Scalp Avulsion Incurred during Birth in an Extremely Low Birth Weight Infant.

19. A Case of Anorexia Nervosa with Focal Cortical Dysplasia

28. Possible correlation between serum interleukin-8 levels and the activity of myositis in anti-NXP2 antibody-positive dermatomyositis

29. Identification of a novel splice‐site WWOX variant with paternal uniparental isodisomy in a patient with infantile epileptic encephalopathy.

31. Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol-3-OH kinase δ syndrome type 1

32. Non‐conditioned cord blood transplantation for infection control in athymic CHARGE syndrome

37. The CXCL10-CXCR3 axis plays an important role in Kawasaki Disease

40. Alanine-scanning mutagenesis of human signal transducer and activator of transcription 1 to estimate loss- or gain-of-function variants

42. The CXCL10-CXCR3 axis plays an important role in Kawasaki disease.

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