Molecular Genetic Studies in Isolated Growth Hormone Deficiency (IGHD) Meena P. DesaiShilpa M. MithbawkarMadhava Vijaykumar Original Article 23 February 2013 Pages: 623 - 630
Entire DAX1 Gene Deletion in an Indian Boy with Adrenal Hypoplasia Congenita Vaman V. KhadilkarHari R. MangtaniAnuradha V. Khadilkar Original Article 22 December 2012 Pages: 631 - 635
Blood Lead Levels among School Children after Phasing-Out of Leaded Petrol in Delhi, India Veena KalraJitendra Kumar SahuR. M. Pandey Original Article 29 March 2013 Pages: 636 - 640
Consensus on Hypotonia via Delphi Process Pragashnie NaidooRobin W. E. Joubert Original Article 17 May 2013 Pages: 641 - 650
Is Indian Childhood Cirrhosis an Extinct Disease Now?—An Observational Study Susama PatraMukul VijSubash C. Samal Original Article 22 December 2012 Pages: 651 - 654
Effect of Deferasirox Chelation on Liver Iron and Total Body Iron Concentration Javed AhmedNoor AhmadRashid H. Merchant Original Article 29 May 2013 Pages: 655 - 658
Prevalence and Risk Factors for Hepatitis C Virus, Hepatitis B Virus, and Human Immunodeficiency Virus in Transfused Children in Kinshasa M. KatabukaM. E. MafutaJ. R. Gini Original Article 24 November 2012 Pages: 659 - 662
Consensus on Timing of Intervention for Common Congenital Heart Diseases: Part II - Cyanotic Heart Defects P. Syamasundar Rao Special Article 03 May 2013 Pages: 663 - 674
Umbilical Cord Blood Transplant for Malignancies: A Hope or Hype Ankur BahlSameer Bakhshi Special Article 10 May 2013 Pages: 675 - 680
Common Endocrine Problems in Children (Hypothyroidism and Type 1 Diabetes Mellitus) Anju SethAnu Maheshwari General Practitioners' Column 29 June 2013 Pages: 681 - 687
Congenital Central Hypoventilation Syndrome with PHOX2B Gene Mutation: Are We Missing the Diagnosis? Nilay NirupamRajni SharmaVirendra Kumar Clinical Brief 25 July 2012 Pages: 688 - 690
Mutations in the Nebulin Gene in a Child with Nemaline (Rod) Myopathy Seema KapoorAnkur SinghVineeta Vijay Batra Clinical Brief 02 September 2012 Pages: 691 - 693
CLN6 p.I154del Mutation Causing Late Infantile Neuronal Ceroid Lipofuscinosis in a Large Consanguineous Moroccan Family Ahmed BouhoucheWafae RegraguiMohamed Yahyaoui Clinical Brief 22 November 2012 Pages: 694 - 696
Pulmonary Hypertension in an Infant Treated with Ibuprofen Arvind SehgalPrasanna S. N. Kumarshingri Clinical Brief 29 July 2012 Pages: 697 - 699
Isolated Pulmonary Langerhans Cell Histiocytosis Sneha VarkkiMintoo TergestinaSophy Korula Clinical Brief 23 September 2012 Pages: 700 - 703
Detection of Carrier Status and Mutations in Family Members of a Child with Complete Deletion of the DAX1 Gene using Multiplex Ligation-Dependent Probe Amplification Nikhil D. PhadkeKavita A. KhatodAnuradha V. Khadilkar Scientific Letter 29 May 2013 Pages: 704 - 705
Spontaneous Pneumothorax with Symmetrical Digital Gangrene -A Rare Complication of Chickenpox Yashpal SinghTanvir Roshan KhanK. P. Kushwaha Scientific Letter to the Editor 16 November 2012 Pages: 706 - 707
Direct Economic Cost of Acute Asthma in Emergency Department Raheleh DashtiMostafa SedighyMostafa Moin Scientific Letter to the Editor 24 November 2012 Pages: 708 - 709
Tuberculin Skin Test, Chest Radiography and Contact Screening in Young Children Somsri WiwanitkitViroj Wiwanitkit Correspondence 29 September 2012 Pages: 710 - 711
Incomplete Conjoined Twin Shasanka Shekhar PandaRashmi Ranjan Das Picture of the Month 12 April 2013 Pages: 712 - 712
Pediatric Nephrology: Rees L, Brogan PA, Bockenhauer D, Webb NJA (eds) Kanav Anand Book Review 28 June 2013 Pages: 713 - 713
