756 results on '"Ariga, Tadashi"'
Search Results
52. Barth syndrome diagnosed in the subclinical stage of heart failure based on the presence of lipid storage myopathy and isolated noncompaction of the ventricular myocardium
53. The first confirmed case with C3 deficiency caused by compound heterozygous mutations in the C3 gene; a new aspect of pathogenesis for C3 deficiency
54. Comparison of the clinical effectiveness of zanamivir and laninamivir octanoate for children with influenza A(H3N2) and B in the 2011–2012 season
55. Selective expansion of donor-derived regulatory T cells after allogeneic bone marrow transplantation in a patient with IPEX syndrome
56. A possible turning point in the hematopoietic stem cell gene therapy for primary immunodeficiency diseases? Lentiviral vectors could take the place of retroviral vectors
57. Constitutive ER stress and Wolfram syndrome
58. A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM)
59. Rapid progression to pulmonary arterial hypertension crisis associated with mixed connective tissue disease in an 11-year-old girl
60. Successful bone marrow transplantation with reduced intensity conditioning in a patient with delayed-onset adenosine deaminase deficiency
61. Eponym: Barth syndrome
62. Methylation of the RASSF1A promoter is predictive of poor outcome among patients with Wilms tumor
63. Piperacillin/tazobactam versus cefozopran for the empirical treatment of pediatric cancer patients with febrile neutropenia
64. Outcome of unrelated umbilical cord blood transplantation in 88 patients with primary immunodeficiency in Japan
65. Detection of KI polyomavirus and WU polyomavirus DNA by real-time polymerase chain reaction in nasopharyngeal swabs and in normal lung and lung adenocarcinoma tissues
66. ADA-SCID with ‘WAZA-ARI’ mutations that synergistically abolished ADA protein stability
67. Anti-Melanoma Differentiation-Associated Gene 5 Antibody is a Diagnostic and Predictive Marker for Interstitial Lung Diseases Associated with Juvenile Dermatomyositis
68. Novel compound heterozygous mutations in the C3 gene: hereditary C3 deficiency
69. Investigation on Strength and Microstructural Evolution of Porous Cu/Cu Brazed Joints Using Cu-Ni-Sn-P Filler
70. Coexistence of acute poststreptococcal glomerulonephritis and acute rheumatic fever in a Japanese girl with primary Sjögren’s syndrome
71. Stem Cell Gene Therapy for ADA-Deficiency without Myelopreparative Conditioning
72. Brazing of porous copper foam/copper with amorphous Cu-9.7Sn-5.7Ni-7.0P (wt%) filler metal: interfacial microstructure and diffusion behavior
73. Mesangial C4d deposition at diagnosis in childhood immunoglobulin A nephropathy
74. Identification of Severe Combined Immunodeficiency by T-Cell Receptor Excision Circles Quantification Using Neonatal Guthrie Cards
75. De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family
76. Frequency of malformed infants in a tertiary center over a period of ten years in Hokkaido, Japan
77. Possible application of flow cytometry for evaluation of the structure and functional status of WASP in peripheral blood mononuclear cells
78. Development of Graves' disease during drug-free remission of juvenile dermatomyositis.
79. Detection of a novel silent deletion, a missense mutation and a nonsense mutation in TCOF1
80. A Girl With Down Syndrome and Partial Trisomy for 21pter-q22.13: A Clue to Narrow the Down Syndrome Critical Region
81. Stem cell transplantation in primary immunodeficiency disease patients
82. Induction of NKG2D ligands on human dendritic cells by TLR ligand stimulation and RNA virus infection
83. Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome
84. Epstein–Barr virus-associated B-cell lymphoma in a patient with DNA ligase IV (LIG4) syndrome
85. Congenital arhinia: Molecular-genetic analysis of five patients
86. Human Tyrosine Kinase 2 Deficiency Reveals Its Requisite Roles in Multiple Cytokine Signals Involved in Innate and Acquired Immunity
87. Outcome in patients with Wiskott–Aldrich syndrome following stem cell transplantation: an analysis of 57 patients in Japan
88. Successful treatment of congenital pulmonary alveolar proteinosis with intravenous immunoglobulin G administration
89. A Case of C3 Deficiency With a Novel Homozygous Two-Base Deletion in the C3 Gene
90. Dissolution of solid copper cylinder in molten tin-lead alloys under dynamic conditions
91. The role of common gamma chain in human monocytes in vivo; evaluation from the studies of X-linked severe combined immunodeficiency (X-SCID) carriers and X-SCID patients who underwent cord blood stem cell transplantation
92. Quantification of κ-deleting recombination excision circles in Guthrie cards for the identification of early B-cell maturation defects
93. Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX)
94. Prenatal diagnosis of the Wiskott–Aldrich syndrome by PCR-based methods
95. Genetic studies of three Japanese patients with p22-phox-deficient chronic granulomatous disease: detection of a possible common mutant CYBA allele in Japan and a genotype-phenotype correlation in these patients
96. Detection of lymphocytes and granulocytes expressing the mutant WASP message in carriers of Wiskott-Aldrich syndrome
97. Sustainable activity of engineering education and research of association for advanced education in Asia
98. Open-cell copper foam joining: joint strength and interfacial behaviour
99. Su1917 – Clinical and Endoscopic Features of Xiap Deficiency Mimicking Refractory Crohn’s Disease in Pediatric Patients
100. MP07-04 DETECTING DIFFERENCES WITH MAGNETOENCEPHALOGRAPHY (MEG)-URODYNAMICS STUDY OF SOMATOSENSORY PROCESSING NORMAL DESIRE TO VOID AND MAXIMUM DESIRE TO VOID SENSATION
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