Evidence for a shared genetic susceptibility to migraine and epilepsy von Winawer, Melodie R., Connors, Robert

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SLC35A2 somatic variants in drug resistant epilepsy: FCD and MOGHE von Elziny, Soad, Crino, Peter B., Winawer, Melodie

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Association of depression and COVID-induced PTSD with cognitive symptoms after COVID-19 illness von Liyanage-Don, Nadia A., Winawer, Melodie R., Hamberger, Marla J., Agarwal, Sachin, Trainor, Alison R., Quispe, Kristal A., Kronish, Ian M.

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Issues related to symptomatic and disease‐modifying treatments affecting cognitive and neuropsychiatric comorbidities of epilepsy von Brooks‐Kayal, Amy R., Bath, Kevin G., Berg, Anne T., Galanopoulou, Aristea S., Holmes, Gregory L., Jensen, Frances E., Kanner, Andres M., O'Brien, Terence J., Whittemore, Vicky H., Winawer, Melodie R., Patel, Manisha, Scharfman, Helen E.

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Familial aggregation of focal seizure semiology in the Epilepsy Phenome/Genome Project von Tobochnik, Steven, Fahlstrom, Robyn, Shain, Catherine, Winawer, Melodie R

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Reproductive decision‐making in families containing multiple individuals with epilepsy von Nakamura, Jacquelyn, Sorge, Shawn T., Winawer, Melodie R., Phelan, Jo C., Chung, Wendy K., Ottman, Ruth

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Increased seizure severity and seizure‐related death in mice lacking HCN1 channels von Santoro, Bina, Lee, Janet Y., Englot, Dario J., Gildersleeve, Sandra, Piskorowski, Rebecca A., Siegelbaum, Steven A., Winawer, Melodie R., Blumenfeld, Hal

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Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy von Winawer, Melodie R., Griffin, Nicole G., Samanamud, Jorge, Baugh, Evan H., Rathakrishnan, Dinesh, Ramalingam, Senthilmurugan, Zagzag, David, Schevon, Catherine A., Dugan, Patricia, Hegde, Manu, Sheth, Sameer A., McKhann, Guy M., Doyle, Werner K., Grant, Gerald A., Porter, Brenda E., Mikati, Mohamad A., Muh, Carrie R., Malone, Colin D., Bergin, Ann Marie R., Peters, Jurriaan M., McBrian, Danielle K., Pack, Alison M., Akman, Cigdem I., LaCoursiere, Christopher M., Keever, Katherine M., Madsen, Joseph R., Yang, Edward, Lidov, Hart G. W., Shain, Catherine, Allen, Andrew S., Canoll, Peter D., Crino, Peter B., Poduri, Annapurna H., Heinzen, Erin L.

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Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene von Barba, Carmen, Blumcke, Ingmar, Winawer, Melodie R., Hartlieb, Till, Kang, Hoon-Chul, Grisotto, Laura, Chipaux, Mathilde, Bien, Christian G., Heřmanovská, Barbora, Porter, Brenda E., Lidov, Hart G.W., Cetica, Valentina, Woermann, Friedrich G., Lopez-Rivera, Javier A., Canoll, Peter D., Mader, Irina, D'Incerti, Ludovico, Baldassari, Sara, Yang, Edward, Gaballa, Ahmed, Vogel, Hannes, Straka, Barbora, Macconi, Letizia, Polster, Tilman, Grant, Gerald A., Krsková, Lenka, Shin, Hui Jin, Ko, Ara, Crino, Peter B., Krsek, Pavel, Lee, Jeong Ho, Lal, Dennis, Baulac, Stéphanie, Poduri, Annapurna, Guerrini, Renzo

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Familial aggregation of status epilepticus in generalized and focal epilepsies von Weisenberg, Judith L.Z., Fitzgerald, Robert T., Constantino, John N., Winawer, Melodie R., Thio, Liu Lin

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Genetic causal attribution of epilepsy and its implications for felt stigma von Sabatello, Maya, Phelan, Jo C., Hesdorffer, Dale C., Shostak, Sara, Goldsmith, Jeff, Sorge, Shawn T., Winawer, Melodie R., Chung, Wendy K., Ottman, Ruth

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Genetic effects on sleep/wake variation of seizures von Winawer, Melodie R., Shih, Jerry, Beck, Erin S., Hunter, Jessica E., Epstein, Michael P.

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Genetic attribution and perceived impact of epilepsy in multiplex epilepsy families von Garofalo, Diana C., Sorge, Shawn T., Hesdorffer, Dale C., Winawer, Melodie R., Phelan, Jo C., Chung, Wendy K., Ottman, Ruth

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Glyoxalase 1 and its substrate methylglyoxal are novel regulators of seizure susceptibility von Distler, Margaret G., Gorfinkle, Naomi, Papale, Ligia A., Wuenschell, Gerald E., Termini, John, Escayg, Andrew, Winawer, Melodie R., Palmer, Abraham A.

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Depression and genetic causal attribution of epilepsy in multiplex epilepsy families von Sorge, Shawn T., Hesdorffer, Dale C., Phelan, Jo C., Winawer, Melodie R., Shostak, Sara, Goldsmith, Jeff, Chung, Wendy K., Ottman, Ruth

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Recruitment for genetic studies of epilepsy von Misiewicz, Sylwia, Winawer, Melodie R

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Migraine, epilepsy, and psychiatric comorbidity: partners in crime von Winawer, Melodie R, Hesdorffer, Dale C

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Genetic testing preferences in families containing multiple individuals with epilepsy von Okeke, Janice O., Tangel, Virginia E., Sorge, Shawn T., Hesdorffer, Dale C., Winawer, Melodie R., Goldsmith, Jeff, Phelan, Jo C., Chung, Wendy K., Shostak, Sara, Ottman, Ruth

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Parents’ interest in genetic testing of their offspring in multiplex epilepsy families von Caminiti, Courtney B., Hesdorffer, Dale C., Shostak, Sara, Goldsmith, Jeff, Sorge, Shawn T., Winawer, Melodie R., Phelan, Jo C., Chung, Wendy K., Ottman, Ruth

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Mapping a mouse limbic seizure susceptibility locus on chromosome 10 von Winawer, Melodie R., Gildersleeve, Sandra S., Phillips, Austin G., Rabinowitz, Daniel, Palmer, Abraham A.

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