Browsing by Author "Lalwani, S G"
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Item Chinese paralytic syndrome.(1996-04-01) Lalwani, S G; Karande, S C; Menon, J; Chaudhuri, A; Nadkarni, U B; Jain, M KItem Defrosting a refrigerator used to store vaccine.(1999-04-16) Lalwani, S GItem Mucolipidoses--II: A report of three cases.(1995-09-01) Lalwani, S G; Kher, A; Shridhar, N; Bharucha, B A; Naik, G GMucolipidoses II is a rare lysosomal storage disorder with autosomal recessive inheritance. There cases with typical clinical features in early infancy like coarse facial features, severe psychomotor retardation and joint contractures are being reported. All the cases had no mucopolysacchariduria. These cases had normal values of lysosomal enzymes in leucocytes but markedly increased values in serum thus confirming mucolipidoses II. Despite the fact that there is no specific treatment, genetic counselling and prenatal diagnosis is indicated.Item Systemic lupus erythematosus with aortoarteritis.(1996-03-01) Menon, J; Karande, S C; Khambekar, K P; Lalwani, S G; Nadkarni, U B; Jain, M KItem Ultrasonographic evaluation of hepatic steatosis in malnutrition.(1998-07-27) Lalwani, S G; Karande, S; Khemani, R; Jain, M K