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2008 Journal Article Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosisBerkovic, Samuel F., Dibbens, Leanne M., Oshlack, Alicia, Silver, Jeremy D., Katerelos, Marina, Vears, Danya F., Lüllmann-Rauch, Renate, Blanz, Judith, Zhang, Ke Wei, Stankovich, Jim, Kalnins, Renate M., Dowling, John P., Andermann, Eva, Andermann, Frederick, Faldini, Enrico, D'Hooge, Rudi, Vadlamudi, Lata, Macdonell, Richard A., Hodgson, Bree L., Bayly, Marta A., Savige, Judy, Mulley, John C., Smyth, Gordon K., Power, David A., Saftig, Paul and Bahlo, Melanie (2008). Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis. The American Journal of Human Genetics, 82 (3), 673-684. doi: 10.1016/j.ajhg.2007.12.019 |
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2007 Journal Article Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell linesMcRae, A. F., Matigian, N. A., Vadlamudi, L., Mulley, J. C., Mowry, B., Martin, N. G., Berkovic, S. F., Hayward, N. K. and Visscher, P. M. (2007). Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines. Human Molecular Genetics, 16 (4), 364-373. doi: 10.1093/hmg/ddl456 |
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2006 Journal Article Severe myoclonic epilepsy of infancy (Dravet syndrome): Recognition and diagnosis in adultsJansen, F. E., Sadleir, L. G., Harkin, L. A., Vadlamudi, L., McMahon, J. M., Mulley, J. C., Scheffer, I. E. and Berkovic, S. F. (2006). Severe myoclonic epilepsy of infancy (Dravet syndrome): Recognition and diagnosis in adults. Neurology, 67 (12), 2224-2226. doi: 10.1212/01.wnl.0000249312.73155.7d |
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2006 Journal Article Action myoclonus–renal failure syndrome: A cause for worsening tremor in young adultsVadlamudi, L., Vears, D. F., Hughes, A., Pedagogos, E. and Berkovic, S. F. (2006). Action myoclonus–renal failure syndrome: A cause for worsening tremor in young adults. Neurology, 67 (7), 1310-1311. doi: 10.1212/01.wnl.0000238424.23177.5e |
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2006 Journal Article Analyzing the etiology of benign rolandic epilepsy: A multicenter twin collaborationVadlamudi, Lata, Kjeldsen, Marianne J., Corey, Linda A., Solaas, Marit H., Friis, Mogen L., Pellock, John M., Nakken, Karl O., Milne, Roger L., Sceffer, Ingrid E., Harvey, A. Simon, Hopper, John L. and Berkovic, Samuel F. (2006). Analyzing the etiology of benign rolandic epilepsy: A multicenter twin collaboration. Epilepsia, 47 (3), 550-555. doi: 10.1111/j.1528-1167.2006.00466.x |
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2006 Journal Article Volumetric analysis of a specific language region – the planum temporaleVadlamudi, L., Hatton, R., Byth, K., Harasty, J., Vogrin, S., Cook, M. J. and Bleasel, A. F. (2006). Volumetric analysis of a specific language region – the planum temporale. Journal of Clinical Neuroscience, 13 (2), 206-213. doi: 10.1016/j.jocn.2005.03.026 |
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2005 Journal Article Reply: Genetic influence on rolandic epilepsyVadlamudi, Lata, Harvey, A. Simon, Hopper, John L., Scheffer, Ingrid E. and Berkovic, Samuel F. (2005). Reply: Genetic influence on rolandic epilepsy. Annals of Neurology, 57 (3), 465-465. doi: 10.1002/ana.20398 |
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2004 Journal Article Factors underlying scalp‐EEG interictal epileptiform discharges in intractable frontal lobe epilepsyVadlamudi, Lata, So, Elson L., Worrell, Gregory A., Mosewich, Russell K., Cascino, Gregory D., Meyer, Fredic B. and Lesnick, Timothy G. (2004). Factors underlying scalp‐EEG interictal epileptiform discharges in intractable frontal lobe epilepsy. Epileptic Disorders, 6 (2), 89-95. |
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2004 Journal Article Epilepsy in twins: Insights from unique historical data of William LennoxVadlamudi, L., Andermann, E., Lombroso, C. T. and et al. (2004). Epilepsy in twins: Insights from unique historical data of William Lennox. Neurology, 62 (7), 1127-1133. doi: 10.1212/01.WNL.0000118201.89498.48 |
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2004 Journal Article Is benign Rolandic epilepsy genetically determined?Vadlamudi, Lata, Harvey, Simon A., Connellan, Mary M., Milne, Roger L., Hopper, J. L., Scheffer, I. E. and Berkovic, S. F. (2004). Is benign Rolandic epilepsy genetically determined?. Annals of Neurology, 56 (1), 129-132. doi: 10.1002/ana.20153 |
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2003 Journal Article Electroencephalographic findings in Kufs diseaseVadlamudi, L., Westmoreland, B. F., Klass, D. W. and Parisi, J. E. (2003). Electroencephalographic findings in Kufs disease. Clinical Neurophysiology, 114 (9), 1738-1743. doi: 10.1016/S1388-2457(03)00111-1 |
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2003 Journal Article Genetics of temporal lobe epilepsyVadlamudi, L., Scheffer, I. E. and Berkovic, S. F. (2003). Genetics of temporal lobe epilepsy. Journal of Neurology, Neurosurgery and Psychiatry, 74 (10), 1359-1361. doi: 10.1136/jnnp.74.10.1359 |
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2002 Journal Article Multifocal myoclonus due to verapamil overdoseVadlamudi, Lata and Wijdicks, Eelco F.M. (2002). Multifocal myoclonus due to verapamil overdose. Neurology, 58 (6), 984-985. doi: 10.1212/WNL.58.6.984 |
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2000 Journal Article Rasmussen's syndrome in a 54 year old female: more support for an adult variantVadlamudi, L., Galton, C. J., Jeavons, S. J., Tannenberg, A. E. G. and Boyle, R. S. (2000). Rasmussen's syndrome in a 54 year old female: more support for an adult variant. Journal of Clinical Neuroscience, 7 (2), 154-156. doi: 10.1054/jocn.1999.0173 |
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2000 Journal Article Cerebral arterial gas embolism by helium: An unusual case successfully treated with hyperbaric oxygen and lidocaineMitchell, S. J., Benson, M., Vadlamudi, L. and Miller, P. (2000). Cerebral arterial gas embolism by helium: An unusual case successfully treated with hyperbaric oxygen and lidocaine. Annals of Emergency Medicine, 35 (3), 300-303. doi: 10.1016/S0196-0644(00)70086-2 |
