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51. Memory B cells predict outcome in primary podocytopathies of adults.

55. Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part three

56. Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part two

57. A Novel CEBPE Variant Causes Severe Infections and Profound Neutropenia

58. Granulomatous inflammation and hypogammaglobulinemia: Clinical conundrum of familial hemophagocytic lymphohistiocytosis type 5

59. Biomarkers for Kawasaki Disease: Clinical Utility and the Challenges Ahead

67. Uncommon histopathological features of cytomegalovirus encephalitis and measles inclusion body encephalitis on autopsy in two patients with primary immunodeficiency

68. Juvenile dermatomyositis associated with autoantibodies to small ubiquitin-like modifier activating enzyme: a report of 4 cases from North India and a review of literature

69. Challenges in the diagnosis of periodic fever, aphthous stomatitis, pharyngitis, and adenitis syndrome in developing countries—A decade of experience from North India

71. Blau syndrome: Lessons learned in a tertiary care centre at Chandigarh, North India

74. Clinical profile, long-term follow-up and outcome of juvenile systemic scleroderma: 25 years of clinical experience from North-West India

78. Emerging pediatric visceral leishmaniasis in Kashmir valley: A report of three cases

80. Correspondence

84. Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity

86. Features of Hemophagocytic Lymphohistiocytosis in Infants With Severe Combined Immunodeficiency: Our Experience From Chandigarh, North India

87. Coronary arterial abnormalities detected in children over 10 years following initial Kawasaki disease using cardiac computed tomography

90. Deficiency of Human Adenosine Deaminase Type 2 – A Diagnostic Conundrum for the Hematologist

91. Distal coronary artery abnormalities in Kawasaki disease: experience on CT coronary angiography in 176 children

93. Kawasaki disease in siblings in close temporal proximity to each other—what are the implications?

98. Phenomic Analysis of Chronic Granulomatous Disease Reveals More Severe Integumentary Infections in X-Linked Compared With Autosomal Recessive Chronic Granulomatous Disease

100. Distal coronary artery abnormalities in Kawasaki disease: experience on CT coronary angiography in 176 children.

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