Poster and Platform Presentations — Alica M. Goldman, M.D., Ph.D.

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    American Clinical Neurophysiology Society (ACNS)
    Virtual 2021 Annual Meeting (Feb. 10-14, 2021)
    • Karimov A, Gavvala J, Goldman A, Haneef Z, Maheshwari A, Sheth S, et al. The utility of additional depth or subdural electrodes following stereotactic EEG evaluation. Presented at the American Clinical Neurophysiology Society (ACNS), Virtual 2021 Annual Meeting (Feb. 10-14, 2021).  
    American Epilepsy Society (AES)
    72nd Annual Meeting in New Orleans, La. (Nov. 30 - Dec. 4, 2018)
    • Houck KM, Haneef Z, Nayak A, Gavvala J, Quach MM, Van Ness PC, et al. Functional involvement of periventricular nodular heterotopia. Abstract No 2.066, 2018, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    American Epilepsy Society (AES)
    71st Annual Meeting in Washington, DC (Dec. 1-5, 2017)
    • Mueller SG, Nei M, Bateman L, Knowlton R, Laxer K, Friedman D, et al. Evidence for brainstem network disruption in focal epilepsy and sudden unexplained death in epilepsy: A first validation study. Abstract No 3.205, 2017, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    American Neurological Association (ANA)
    142nd Annual Meeting in San Diego, Calif. (Oct. 15-17, 2017)
    • Marafie D, Rosenfeld J, Van Ness P, Zohrevand P, Haneef Z, Chen D, et al. Clinical utility of genetic testing in adults with epilepsy: 4-year experience of the Baylor Genetic Epilepsy Clinic. Ann Neurol. 2017;80 suppl 2:S6. 
    American Epilepsy Society (AES)
    70th Annual Meeting in Houston, Texas (Dec. 2-6, 2016)
    • Bateman L, Nei M, Goldman A, Mueller S. Center for SUDEP Research: Brainstem atrophy in SUDEP. Abstract No 3.199, 2016, American Epilepsy Society Annual Meeting, www.aesnet.org.  [View poster]
    • Marafie D, Rosenfeld J, Van Ness P, Zohrevand P, Haneef Z, Chen D, et al. Clinical utility of genetic testing in adults with epilepsy: Pilot experience of the Baylor genetic epilepsy clinic. Abstract No 1.337, 2016, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    American Neurological Association (ANA)
    141st Annual Meeting in Baltimore, Md. (Oct. 16-18, 2016)
    • Marafie D, Schultz R, Glaze D, Suter B, Goldman A. Prevalence and character of severe epileptic encephalopathy in patients affected by MECP2 duplication syndrome. Ann Neurol. 2016;80 suppl 20:S65-6. 
    American Academy of Neurology (AAN)
    68th Annual Meeting in Vancouver, BC, Canada (April 15-21, 2016)
    • Marafie D, Schultz R, Glaze D, Goldman A, Suter B. Severe epileptic encephalopathy is a frequent neurological comorbidity of children affected by the MECP2 duplication syndrome. Neurology. 2016;86(Meeting Abstracts 1):S52.005. [Oral Presentation] 
    American Epilepsy Society (AES)
    69th Annual Meeting in Philadelphia, Penn. (Dec. 4-8, 2015)
    • Marafie D, Suter B, Pacheco VH, Glaze D, Drabek J, Goldman A. MECP2 duplication is associated with severe epileptic encephalopathy in the presence of permissive genetic background. Abstract No 1.301, 2015, American Epilepsy Society Annual Meeting, www.aesnet.org.  [View poster]
    American Epilepsy Society (AES)
    68th Annual Meeting in Seattle, Wash. (Dec. 5-9, 2014)
    • Zohrevand P, Diaz M, Amador A, Goldman A. Treatment resistance correlates with ECG abnormalities in a pilot clinical surveillance of epilepsy patients. Abstract No 2.222, 2014, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    American Academy of Neurology (AAN)
    66th Annual Meeting in Philadelphia, Penn. (April 26 - May 3, 2014)
    • Karas L, Goldsmith C, Ruppelt SC, Goldman A. Epidemiological pilot analysis of epilepsy patients in a community clinic aims to inform effective care. Neurology. 2014;82(Meeting Abstracts 1):P5.046.  [View poster]
    American Epilepsy Society (AES)
    67th Annual Meeting in Washington, DC (Dec. 6-10, 2013)
    • King-Stephens D, Mirro E, Weber P, Laxer K, Van Ness P, Salanova V, et al. Lateralization of temporal lobe epilepsy with long-term ambulatory intracranial monitoring using the RNS system: Experience in 82 patients. Abstract No A.02, 2013, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    • Klassen TL, Tomson T, Sveinsson O, von Dobeln U, Drabek J, Noebels J, et al. STOP SUDEP Program: Application of visual automated fluorescence electrophoresis in the qualitative profiling of archived SUDEP samples. Abstract No 1.053, 2013, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    American Neurological Association (ANA)
    138th Annual Meeting in New Orleans, La. (Oct. 13-15, 2013)
    • Goldman A. Sudden unexplained death in epilepsy: Can genomics help? Presented at the American Neurological Association (ANA), 138th Annual Meeting in New Orleans, La. (Oct. 13-15, 2013). [Plenary Talk] 
    American Epilepsy Society (AES)
    66th Annual Meeting in San Diego, Calif. (Nov. 30 - Dec. 4, 2012)
    • Goldman AM. SUDEP Tissue Donation Program (STOP): Collaborative network in support of SUDEP registry, tissue repository and human translational research. Abstract No 1.030, 2012, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    • Goldman AM, Klassen TL, von Rueden EL, Drabek JM, Noebels JL. Universal DNA extraction protocol for the utilization of alternative tissue sources in downstream epilepsy genetic analysis. Abstract No 1.059, 2012, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    • Goldman AM, Richerson G, Parent JM, Bateman L, Nordli DR, Noebels JL. SUDEP research consortium: A new collaborative network to discover predictive genes, mechanisms and biomarkers of SUDEP. Epilepsy Curr. 2013;13 Suppl 1:326. [Investigators' Workshop] 
    • Klassen TL, Chen TT, Reed JG, Kole MJ, Goldman AM, Marini C, et al. Myotonia in brain: 'Skeletal' chloride channel ClC-1 linked to idiopathic generalized epilepsy with focal myotonia. Abstract No 3.312, 2012, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    • Klassen TL, Goldman A, Davis C, Chen T, Gibbs R, Noebels J. Channotyping epilepsy: Profiling personal variation in ion channel genes. Abstract No 1.090, 2012, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    American Epilepsy Society (AES)
    64th Annual Meeting in San Antonio, Texas (Dec. 3-7, 2010)
    • Goldman A, Klassen T, Gu W, Zhang F, Bomben V, Chen T, et al. High resolution copy number variation of ion channel genes in epilepsy. Abstract No 2.001, 2010, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    American Epilepsy Society (AES)
    63rd Annual Meeting in Boston, Mass. (Dec. 4-8, 2009)
    • Goldman A, Glasscock E, Yoo J, Chen T, Klassen T, Noebels J. Long QT mouse model links the dual phenotype of cardiac arrhythmias and epilepsy with sudden unexplained death in epilepsy. Abstract No 3.109, 2009, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    28th International Epilepsy Congress (IEC)
    Budapest, Hungary (June 29 - July 2, 2009)
    • Goldman A, Glasscock E, Yoo J, Chen T, Klassen T, Noebels J. Human KvLQT1 mutations in mice link the dual phenotype of cardiac arrhythmias and epilepsy with sudden unexplained death in epilepsy. Epilepsia. 2009;50(Suppl 10):7-8. 
    American Epilepsy Society (AES)
    62nd Annual Meeting in Seattle, Wash. (Dec. 5-9, 2008)
    • Dulay MF, Levin HS, York MK, Mizrahi EM, Goldsmith IL, Goldman A, et al. Predictors of individual visual memory decline after right anterior temporal lobe resection. Abstract No 1.303, 2008, American Epilepsy Society Annual Meeting, www.aesnet.org.  [View poster]
    American Epilepsy Society (AES)
    61st Annual Meeting in Philadelphia, Penn. (Nov. 30 - Dec. 4, 2007)
    • Dulay MF, Levin HS, Mizrahi EM, York MK, Li X, Goldsmith IL, et al. Growth curve analysis of changes in spatial and verbal learning characteristics after anterior temporal lobectomy. Abstract No 2.265, 2007, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    • Goldman AM, McGuire AL, Hilsenbeck SG, Noebels JL. Genomic research in the era of identifiable genetic information. Abstract No 3.343, 2007, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    American Epilepsy Society (AES)
    60th Annual Meeting in San Diego, Calif. (Dec. 1-5, 2006)
    • Goldman AM, Burgess DL, Gibbs RA, Chapman KE, Wilfong AA, Hrachovy RA, et al. The prevalence of inter-ictal cardiac arrhythmias and LQT gene variants in patients with idiopathic epilepsy. Abstract No 4.223, 2006, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    American Epilepsy Society (AES)
    57th Annual Meeting in Boston, Mass. (Dec. 5-10, 2003)
    • Goldman AM, Burgess DL, Armstrong DD, Mori M, Noebels JL. Regional and developmental localization of ion-channel genes coexpressed in heart and brain. Abstract No 1.193, 2003, American Epilepsy Society Annual Meeting, www.aesnet.org. 
    25th International Epilepsy Congress (IEC)
    Lisbon, Portugal (Oct. 12-16, 2003)
    • Goldman AM, Burgess DL, Armstrong DD, Mori M, Noebels JL. Expression pattern of candidate epilepsy ion channel genes in mouse and human brains. Epilepsia. 2003;44(Suppl 8):170. 
    American Epilepsy Society (AES)
    55th Annual Meeting in Philadelphia, Penn. (Nov. 30 - Dec. 5, 2001)
    • Goldman AM, Wheless JW, Venkataraman V, Kim HL, Papanicolaou AC. Magnetoencephalography mislocalizes interictal epileptogenic activity in mesial temporal epilepsy. Abstract No B.02, 2001, American Epilepsy Society Annual Meeting, www.aesnet.org.