2,247 results on '"Sugiura K"'
Search Results
52. Ripple-pattern lichen amyloidosis in a case of ichthyosis vulgaris with a novel FLG mutation
53. A case of epidermolytic ichthyosis showing a very mild phenotype due to a novel tail extension mutation in KRT10
54. Structural design optimization of wind turbine tower for developing countries
55. Extracting bridge frequencies from dynamic responses of two passing vehicles
56. Short Report: Quantitative Assessment of the Risk of Rabies Entering Japan through the Importation of Dogs and Cats from the USA
57. Cutaneous ischemia‐reperfusion injury is exacerbated by IL‐36 receptor antagonist deficiency
58. Changes of fetal oxygen saturation (SpO2) during labor and maternal oxygen administration effect on fetal SpO2
59. Lipodystrophia centrifugalis abdominalis infantilis accompanied by idiopathic encephalopathy
60. Noteworthy clinical findings of harlequin ichthyosis: digital autoamputation caused by cutaneous constriction bands in a case with novel ABCA12 mutations
61. Anti-transcription intermediary factor 1-γ antibody-positive clinically amyopathic dermatomyositis complicated by interstitial lung disease and breast cancer
62. Serum thymus and activation-regulated chemokine (TARC/CCL17) levels reflect the disease activity in a patient with bullous pemphigoid
63. Effect of plasma heat source characteristics on nitrogen absorption in gas tungsten arc weld metal
64. Successful treatment with infliximab of sibling cases with generalized pustular psoriasis caused by deficiency of interleukin-36 receptor antagonist
65. Fatigue Life Estimation of Existing Bridge Using 3-D FEM and Live Load Simulation
66. Damage assessment of a railway bridge based on vibration monitoring
67. Topical minoxidil improves congenital hypotrichosis caused by LIPH mutations
68. Dowling–Degos disease with mutations in POFUT1 is clinicopathologically distinct from reticulate acropigmentation of Kitamura
69. Disappearance of circulating autoantibodies to RNA polymerase III in a patient with systemic sclerosis successfully treated with corticosteroid and methotrexate
70. The novel GJB3 mutation p.Thr202Asn in the M4 transmembrane domain underlies erythrokeratodermia variabilis
71. PTH-354 The association between metabolic parameters in FDG-PET/CT and pathological findings of colorectal cancer
72. PTH-289 The poor overall survival of right-sided colon cancer compared with left-sided colon cancers: a systematic review and meta-analysis
73. Pustular psoriasis-like lesions associated with hereditary lactate dehydrogenase M subunit deficiency without interleukin-36 receptor antagonist mutation: long-term follow-up of two cases
74. Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait
75. Proposal for an optimum water management method using two-pole simultaneous measurement
76. Canine oocyte maturation in culture: Significance of estrogen and EGF receptor gene expression in cumulus cells
77. Generalized pustular psoriasis caused by deficiency of interleukin-36 receptor antagonist successfully treated with granulocyte and monocyte adsorption apheresis
78. Intermediate valence behavior of Yb2Ni12P7 studied by using 31P NMR
79. Highly prevalent SERPINB7 founder mutation causes pseudodominant inheritance pattern in Nagashima-type palmoplantar keratosis
80. Changes in modal parameters of a steel truss bridge due to artificial damage
81. Structural damage diagnosis of steel truss bridges by outlier detection
82. Percutaneous Radiofrequency Lung Ablation Combined with Transbronchial Saline Injection: An Experimental Study in Swine
83. Reticulate acropigmentation of Kitamura and Dowling-Degos Disease are genetically independent disorders distinct from each other; further confirmation: CS67
84. A case of Björnstad syndrome caused by novel compound heterozygous mutations in the BCS1L gene
85. Independent Control of Low-Energy Resonant States and Polaron States by the Zn-Doping and the Structural Transition in La2−x Sr x CuO4 and La2−x Ba x CuO4 (x=0.11)
86. Creation of a Tumor-Mimic Model Using a Muscle Paste for Radiofrequency Ablation of the Lung
87. Cellular prion protein prevents brain damage after encephalomyocarditis virus infection in mice
88. The novel CTSC homozygous nonsense mutation p.Lys106X in a patient with Papillon–Lefèvre syndrome with all permanent teeth remaining at over 40 years of age
89. Electron detachment of super-excited porphyrin anions in an electrostatic ion storage ring
90. Schottky barrier MOSFETs with epitaxial ferromagnetic MnAs/Si(0 0 1) source and drain: Post-growth annealing and transport characteristics
91. On-line pseudo-dynamic network testing on base-isolated bridges using Internet and wireless Internet
92. Prognostic impact of atrial fibrillation in patients with hypertrophic cardiomyopathy in a community-based Japanese cohort: results from Kochi RYOMA study
93. Structural diagnosis of bridges using traffic-induced vibration measurements
94. Mode shape estimation of a bridge using the responses of passing vehicles
95. Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
96. Vector HTS-SQUID system for ULF magnetic field monitoring
97. Prevention of accelerated presbycusis by bone marrow transplantation in senescence-accelerated mice
98. Simultaneous monitoring of the coupled vibration between a bridge and moving trains
99. Cutaneous ischemia‐reperfusion injury is exacerbated by IL‐36 receptor antagonist deficiency.
100. Field-induced SDW phase and superconductivity of (DMET) 2CuCl 2
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