1. Utility of serum lysosomal enzyme assay in the detection of cerebral sphingolipidoses in patients with progressive neurologic dysfunction

   • Rita Christopher
   • K. Taranath Shetty

   Lysosomal Disorders Pages: 102 - 107

2. Lipid metabolism in tumour bearing mice treated withAeromonas L-asparaginase

   • P. J. Benny
   • G. Muraleedhara Kurup
   • K. Sreejith

   Cancer Pages: 108 - 113

3. Polymorphonuclear leukocytic sialic acid and sialidase activity in obesity

   • Raj K. Das
   • M. G. Muddeshwar

   Obesity Pages: 114 - 118

4. Biochemical changes during exchange transfusion in hyperbilirubinemia in term newborn babies

   • Amit Jain
   • D. Puri
   • M. M. A. Faridi

   Hyperbilirubinemia Pages: 119 - 124

5. Vitamin E status in protein energy malnutrition

   • Pankaj Abrol
   • Neeraj Sharma
   • Harbans Lal

   Nutrition Pages: 125 - 127

6. Urinary iodine levels in three ecological zones of Bangladesh

   • Salamatullah Quazi
   • M. Mohiduzzaman
   • Harun K. M. Yusuf

   Nutrition Pages: 128 - 133

7. Preparation of lyophilised lipid rich quality control serum by isolating lipids using large scale chromatography technology

   • Sumant S. Karnik
   • Saroj P. Taskar

   Quality Control Pages: 134 - 138

8. Method evaluation of an enzymatic method for serum creatinine

   • K. S. S. Saibaba
   • P. V. L. N. Srinivasa Rao
   • M. Vijaya Bhaskar

   Quality Control Pages: 139 - 141

9. Detection of non-deletional type of hereditary persistence of fetal hemoglobin (HPFH) condition associated with 619 bp β^°-thalassemia deletion

   • Syed Mazher Husain
   • M. P. J. S. Anandaraj

   Quality Control Pages: 142 - 145

10. Hereditary methaemoglobinaemia due to Cytochrome b-5 reductase deficiency—A case report

    • U. K. Saha
    • I. Chakraborty
    • A. K. Chakrabarti

    Quality Control Pages: 146 - 147