Utilization of Sustainable Resources for Promoting Energy Efficiency in Environment Using Smart Technologies von Vedanarayanan, V., Vibhakar, Chirag, Sujaatha, A., Chavda, Jiten K., Karthik, M., Pramila, P. V., Raghavan, Ishwarya Komalnu

Volltext

Synthesis of Modified Phase-Changing Material with Latent Heat and Thermal Conductivity to Store Solar Energy Using a Carbon Nanotube von Vedanarayanan, V., Srinivasan, J. Dilli, Arulvendhan, K., Kumaran, P. Thirusenthil, Selvakumar, R., Asif, H. S., Siddique, M. H., Chimdi, Jifara

Volltext

Performance Development and Evaluation of Solar Air Collector with Novel Phase Change Material von Vedanarayanan, V., Srinivasan, J. Dilli, Arulvendhan, K., Kumaran, P. Thirusenthil, Selvakumar, R., Maridurai, T., Sudhakar, M., Al Obaid, Sami, Alfarraj, Saleh, Raj, M. M., Raghavan, Ishwarya Komalnu

Volltext

Update on Inclusion Body Myositis von Jabari, Duaa, Vedanarayanan, V. V., Barohn, Richard J., Dimachkie, Mazen M.

Volltext

Design and Analysis of a novel 2D Edge Preservation Adaptive Wavelet Anisotropic Bilateral Filter for Image Restoration of Palm Leaf Manuscripts von T, Jerry Alexander, S, Suresh Kumar, V, Vedanarayanan

Volltext

Experimental Investigation on Mechanical Behaviour of Kevlar and Ramie Fibre Reinforced Epoxy Composites von Vedanarayanan, V., Kumar, B. S. Praveen, Karuna, M. S., Jayanthi, A., Kumar, K. V. Pradeep, Radha, A., Ramkumar, G., Christopher, David

Volltext

Carpal Tunnel Syndrome in Children von Davis, Lamar, MD, Vedanarayanan, V.V., MD, FRCPC

Volltext

Detection and classification of lung cancer using CNN and Google net von Pandian, R., Vedanarayanan, V., Ravi Kumar, D.N.S., Rajakumar, R.

Volltext

Intravenous immunoglobulin in drug and device refractory patients with the symptoms of gastroparesis—an open‐label study von Ashat, M., Lewis, A., Liaquat, H., Stocker, A., McElmurray, L., Vedanarayanan, V., Soota, K., Howell, T., Kedar, A., Obert, J., Abell, T. L.

Volltext

Progressive Muscular Dystrophy in Adults from Mutations in LAMA2 Gene (1520) von Vedanarayanan, V, Sreenivasan, Varun

Volltext

Variable clinical presentation of HMGCR antibody associated necrotizing myopathy (2911) von Sreenivasan, Varun, Vedanarayanan, V

Volltext

CINRG randomized controlled trial of creatine and glutamine in Duchenne muscular dystrophy von Escolar, Diana M., Buyse, Gunnar, Henricson, Erik, Leshner, Robert, Florence, Julaine, Mayhew, Jill, Tesi-Rocha, Carolina, Gorni, Ksenija, Pasquali, Livia, Patel, Kantilal M., McCarter, Robert, Huang, Jennifer, Mayhew, Thomas, Bertorini, Tulio, Carlo, Jose, Connolly, Anne M., Clemens, Paula R., Goemans, Nathalie, Iannaccone, Susan T., Igarashi, Masanori, Nevo, Yoram, Pestronk, Alan, Subramony, S. H., Vedanarayanan, V. V., Wessel, Henry

Volltext

Efficient Classification of Breast Lesion based on Deep Learning Technique von Sen, Bandita, Vedanarayanan, V.

Volltext

Cerebrospinal Fluid Opening Pressure in Children: Experience in a Controlled Setting von Lee, Marcus W., MD, Vedanarayanan, Vettakikoru V., MD

Volltext

Sensory ataxic neuropathy as the presenting feature of a novel mitochondrial disease von FADIC, R, RUSSELL, J. A, VEDANARAYANAN, V. V, LEHAR, M, KUNCL, R. W, JOHNS, D. R

Volltext

Tick paralysis in children: Electrophysiology and possibility of misdiagnosis von VENKATARAMAN VEDANARAYANAN, V, EVANS, Owen B, SUBRAMONY, S. H

Volltext

Confirmation of the severe phenotypic effect of serine at codon 41 of the superoxide dismutase 1 gene von Subramony, S. H., Ashizawa, Tetsuo, Langford, Leigh, Mckenna, Robert, Avvaru, Balu, Siddique, Teepu, Vedanarayanan, V.

Volltext

Novel mutations in collagen VI genes: Expansion of the Bethlem myopathy phenotype von SCACHERI, P. C, GILLANDERS, E. M, SUBRAMONY, S. H, VEDANARAYANAN, V, CROWE, C. A, THAKORE, N, BINGLER, M, HOFFMAN, E. P

Volltext

Ryanodine Receptor RYR1 Gene Mutations in African American Men with Hypertrophied Muscles and Persistently Elevated Serum Creatine Kinase (S05.004) von Vedanarayanan, V., Sinclair, David

Volltext

Sequence variation in GAA repeat expansions may cause differential penotype display in Friedreich's ataxia von McDaniel, D. Olga, Keats, Bronya, Vedanarayanan, V.V., Subramony, S.H.

Volltext