All Stories

  1. Pulmonary Arteriovenous Malformation Causing Systemic Hypoxemia in Early Infancy
  2. Sensorineural hearing loss in Kawasaki disease
  3. Electrocardiogram before starting stimulant medications: to order or not?
  4. PRKAG2 mutation: An easily missed cardiac specific non-lysosomal glycogenosis
  5. Plasmodium vivaxmalaria complicated by splenic infarct
  6. Role of Calcium Deficiency in Development of Nutritional Rickets in Indian Children: A Case Control Study
  7. Hemothorax and Hematocele: Unusual Presentations of Vitamin K Deficiency Bleeding Disorder
  8. Hypothyroidism in Children Beyond 5 y of Age: Delayed Diagnosis of Congenital Hypothyroidism
  9. Outcome of HIV Exposed Infants: Experience of a Regional Pediatric Center for HIV in North India
  10. Metachronous Occurrence of Multifocal Phaeochromocytoma
  11. The Renal Cysts and Diabetes (RCAD) Syndrome in a Child with Deletion of the Hepatocyte Nuclear Factor-1β Gene
  12. Congenital Langerhans cell histiocytosis with skin and lung involvement: Spontaneous regression
  13. Persistent jaundice in an infant with homozygous beta thalassemia due to co‐inherited Crigler–Najjar syndrome
  14. Rosai-Dorfman Disease