Autosomal Dominant Inheritance of Centrotemporal Sharp Waves in Rolandic Epilepsy Families

Por Bali, Bhavna, Kull, Lewis L., Strug, Lisa J., Clarke, Tara, Murphy, Peregrine L., Akman, Cigdem I., Greenberg, David A., Pal, Deb K.
Publicado em 2007

A microRNA‐328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy

Por Panjwani, Naim, Wilson, Michael D., Addis, Laura, Crosbie, Jennifer, Wirrell, Elaine, Auvin, Stéphane, Caraballo, Roberto H., Kinali, Maria, McCormick, David, Oren, Caroline, Taylor, Jacqueline, Trounce, John, Clarke, Tara, Akman, Cigdem I., Kugler, Steven L., Mandelbaum, David E., McGoldrick, Patricia, Wolf, Steven M., Arnold, Paul, Schachar, Russell, Pal, Deb K., Strug, Lisa J.
Publicado no Ann Clin Transl Neurol (2016)

Risk factors for reading disability in rolandic epilepsy families

Por Vega, Yaiza Hernández, Smith, Anna, Cockerill, Hannah, Tang, Shan, Agirre-Arrizubieta, Zaloa, Goyal, Sushma, Pina, Marisa, Akman, Cigdem I, Jolleff, Nicola, McGinnity, Colm, Gomez, Kumudini, Gupta, Rajesh, Hughes, Elaine, Jackman, John, McCormick, David, Oren, Caroline, Scott, David, Taylor, Jacqueline, Trounce, John, Clarke, Tara, Kugler, Steven, Mandelbaum, David E, McGoldrick, Patricia, Wolf, Steven, Strug, Lisa J, Pal, Deb K
Publicado no Epilepsy Behav (2015)

Recurrent Distal 7q11.23 Deletion Including HIP1 and YWHAG Identified in Patients with Intellectual Disabilities, Epilepsy, and Neurobehavioral Problems

Por Ramocki, Melissa B., Bartnik, Magdalena, Szafranski, Przemyslaw, Kołodziejska, Katarzyna E., Xia, Zhilian, Bravo, Jaclyn, Miller, G. Steve, Rodriguez, Diana L., Williams, Charles A., Bader, Patricia I., Szczepanik, Elżbieta, Mazurczak, Tomasz, Antczak-Marach, Dorota, Coldwell, James G., Akman, Cigdem I., McAlmon, Karen, Cohen, Melinda P., McGrath, James, Roeder, Elizabeth, Mueller, Jennifer, Kang, Sung-Hae L., Bacino, Carlos A., Patel, Ankita, Bocian, Ewa, Shaw, Chad A., Cheung, Sau Wai, Mazurczak, Tadeusz, Stankiewicz, Paweł
Publicado em 2010