檢索結果 - Ellis, Colin

Authors’ Reply to Drs Bourque and Breiner, Re: Cerebrospinal Fluid in Posterior Reversible Encephalopathy Syndrome 由 Ellis, Colin A., Balu, Ramani

獲取全文 獲取全文 獲取全文

Early-onset genetic epilepsies reaching adult clinics 由 Lewis-Smith, David, Ellis, Colin A, Helbig, Ingo, Thomas, Rhys H

獲取全文 獲取全文 獲取全文

The “Maternal Effect” on Epilepsy Risk: Analysis of Familial Epilepsies and Reassessment of Prior Evidence 由 Ellis, Colin A., Berkovic, Samuel F., Epstein, Michael P., Ottman, Ruth

獲取全文 獲取全文 獲取全文

Generalized, Focal, and Combined Epilepsies in Families: New Evidence for Distinct Genetic Factors 由 Ellis, Colin A., Ottman, Ruth, Epstein, Michael P., Berkovic, Samuel F.

獲取全文 獲取全文 獲取全文

Timing Is Everything: Where Status Epilepticus Treatment Fails 由 Hill, Chloe E., Parikh, Alomi O., Ellis, Colin, Myers, Jennifer S., Litt, Brian

獲取全文 獲取全文 獲取全文

Epilepsy risk in offspring of affected parents; a cohort study of the “maternal effect” in epilepsy 由 Dreier, Julie W., Ellis, Colin A., Berkovic, Samuel F., Cotsapas, Chris, Ottman, Ruth, Christensen, Jakob

獲取全文 獲取全文 獲取全文

Unilateral thalamic lesion mimicking genetic generalized epilepsy 由 Kulick-Soper, Catherine V., Stein, Joel M., Chen, Isaac H., Ellis, Colin A., Davis, Kathryn A.

獲取全文 獲取全文 獲取全文

Seizure Detection in Continuous Inpatient EEG: A Comparison of Human vs Automated Review 由 Ganguly, Taneeta Mindy, Ellis, Colin A., Tu, Danni, Shinohara, Russell T., Davis, Kathryn A., Litt, Brian, Pathmanathan, Jay

獲取全文 獲取全文 獲取全文

Epilepsy in Families: Age at onset is a familial trait, independent of syndrome 由 Ellis, Colin A., Churilov, Leonid, Epstein, Michael P., Xie, Sharon X., Bellows, Susannah T., Ottman, Ruth, Berkovic, Samuel F.

獲取全文 獲取全文 獲取全文

Cerebrospinal Fluid in Posterior Reversible Encephalopathy Syndrome: Implications of Elevated Protein and Pleocytosis 由 Ellis, Colin A., McClelland, Andrew C., Mohan, Suyash, Kuo, Emory, Kasner, Scott E., Zhang, Cen, Khankhanian, Pouya, Balu, Ramani

獲取全文 獲取全文 獲取全文

Randomized Controlled Trial of Melatonin for Sleep Disturbance in Dravet Syndrome: The DREAMS Study 由 Myers, Kenneth A., Davey, Margot J., Ching, Michael, Ellis, Colin, Grinton, Bronwyn E., Roten, Annie, Lightfoot, Paul A., Scheffer, Ingrid E.

獲取全文 獲取全文 獲取全文

A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation 由 Ganesan, Shiva, Galer, Peter D., Helbig, Katherine L., McKeown, Sarah E., O’Brien, Margaret, Gonzalez, Alexander K., Felmeister, Alex S., Khankhanian, Pouya, Ellis, Colin A., Helbig, Ingo

獲取全文 獲取全文 獲取全文

Correction: A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation 由 Ganesan, Shiva, Galer, Peter D., Helbig, Katherine L., McKeown, Sarah E., O’Brien, Margaret, Gonzalez, Alexander K., Felmeister, Alex S., Khankhanian, Pouya, Ellis, Colin A., Helbig, Ingo

獲取全文 獲取全文 獲取全文

Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractable 由 Lewis-Smith, David, Galer, Peter D., Balagura, Ganna, Kearney, Hugh, Ganesan, Shiva, Cosico, Mahgenn, O’Brien, Margaret, Vaidiswaran, Priya, Krause, Roland, Ellis, Colin A., Thomas, Rhys H., Robinson, Peter N., Helbig, Ingo

獲取全文 獲取全文 獲取全文

Phenotypic homogeneity in childhood epilepsies evolves in gene-specific patterns across 3251 patient-years of clinical data 由 Lewis-Smith, David, Ganesan, Shiva, Galer, Peter D., Helbig, Katherine L., McKeown, Sarah E., O’Brien, Margaret, Khankhanian, Pouya, Kaufman, Michael C., Gonzalez, Alexander K., Felmeister, Alex S., Krause, Roland, Ellis, Colin A., Helbig, Ingo

獲取全文 獲取全文 獲取全文

Using Generalized Polyspike Train to Predict Drug-Resistant Idiopathic Generalized Epilepsy 由 Conrad, Erin C., Chugh, Nanak, Ganguly, Taneeta M., Gugger, James J., Tizazu, Etsegenet F., Shinohara, Russell T., Raghupathi, Ramya, Becker, Danielle A., Gelfand, Michael A., Omole, Armina T., Decker, Barbara M., Pathmanathan, Jay S., Davis, Kathryn A., Ellis, Colin A.

獲取全文 獲取全文 獲取全文

Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders 由 Crawford, Katherine, Xian, Julie, Helbig, Katherine L., Galer, Peter D., Parthasarathy, Shridhar, Lewis-Smith, David, Kaufman, Michael C., Fitch, Eryn, Ganesan, Shiva, O’Brien, Margaret, Codoni, Veronica, Ellis, Colin A., Conway, Laura J., Taylor, Deanne, Krause, Roland, Helbig, Ingo

獲取全文 獲取全文 獲取全文

Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies 由 Galer, Peter D., Ganesan, Shiva, Lewis-Smith, David, McKeown, Sarah E., Pendziwiat, Manuela, Helbig, Katherine L., Ellis, Colin A., Rademacher, Annika, Smith, Lacey, Poduri, Annapurna, Seiffert, Simone, von Spiczak, Sarah, Muhle, Hiltrud, van Baalen, Andreas, Thomas, Rhys H., Krause, Roland, Weber, Yvonne, Helbig, Ingo

獲取全文 獲取全文 獲取全文

Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery 由 Oliver, Karen L., Ellis, Colin A., Scheffer, Ingrid E., Ganesan, Shiva, Leu, Costin, Sadleir, Lynette G., Heinzen, Erin L., Mefford, Heather C., Bass, Andrew J., Curtis, Sarah W., Harris, Rebekah V., Whiteman, David C., Helbig, Ingo, Ottman, Ruth, Epstein, Michael P., Bahlo, Melanie, Berkovic, Samuel F.

獲取全文 獲取全文 獲取全文

The role of common genetic variation in presumed monogenic epilepsies 由 Campbell, Ciarán, Leu, Costin, Feng, Yen-Chen Anne, Wolking, Stefan, Moreau, Claudia, Ellis, Colin, Ganesan, Shiva, Martins, Helena, Oliver, Karen, Boothman, Isabelle, Benson, Katherine, Molloy, Anne, Brody, Lawrence, Michaud, Jacques L., Hamdan, Fadi F., Minassian, Berge A., Lerche, Holger, Scheffer, Ingrid E., Sisodiya, Sanjay, Girard, Simon, Cosette, Patrick, Delanty, Norman, Lal, Dennis, Cavalleri, Gianpiero L.

獲取全文 獲取全文 獲取全文