Search Results - "Shubha, G N"

Duchenne muscular dystrophy: A clinical, histopathological and genetic study at a neurology tertiary care center in southern India by Swaminathan, Bhairavi, Shubha, G. N, Shubha, D, Murthy, A. Ram, Kiran Kumar, H. B, Shylashree, S, Gayathri, N, Jamuna, R, Jain, Sanjeev, Purushottam, Meera, Nalini, A

“…Background : Duchenne muscular dystrophy (DMD) is the most common muscular dystrophy that affects young boys and the dystrophin gene on the X chromosome has…”
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Association of serotonin transporter gene polymorphisms with obsessive-compulsive disorder (OCD) in a south Indian population by Tibrewal, Prashant, Kumar, H B Kiran, Shubha, G N, Subhashree, D, Purushottam, Meera, Thennarasu, K, Reddy, Y C J, Jain, Sanjeev

“…Serotonin transporter polymorphisms, 5-HTTVNTR and 5-HTTLPR, have been found to be associated with obsessive-compulsive disorder (OCD) and particularly with…”
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Paternal inheritance or a de novo mutation in a Duchenne Muscular Dystrophy pedigree from South India by Purushottam, Meera, Ram Murthy, A, Shubha, G.N, Gayathri, N, Nalini, A

“…Abstract A six year old boy presented with classical features of Duchenne Muscular Dystrophy (DMD) and was confirmed by absent dystrophin staining on muscle…”
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Advanced Material for Newer Applications by Shubha, G.N., Tejaswini, M.L., Lakshmi, K.P.

“…Silicon based components are the heart of today’s electronic devices. The improvisation and optimization of devices based on silicon components are reaching…”
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Patemal inheritance or a de novo mutation in a Duchenne Muscular Dystrophy pedigree from South India by PURUSHOTTAM, Meera, RAM MURTHY, A, SHUBHA, G. N, GAYATHRI, N, NALINI, A

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