A Timely Review of the Genetics of Epileptic Encephalopathies

Por Freeman, Jeremy L.
Publicado no Pediatr Neurol Briefs (2015)

Prognostic Factors in Patients with Multiple Recurrences of Well-Differentiated Thyroid Carcinoma

Por Holler, Theresa, Theriault, Jenna, Payne, Richard J., Clark, Jonathan, Eski, Spiro, Freeman, Jeremy L.
Publicado em 2009

EpCAM nuclear localization identifies aggressive Thyroid Cancer and is a marker for poor prognosis

Por MacMillan Christina, Lim Terence, Cao Jun, Ralhan Ranju, Freeman Jeremy L, Walfish Paul G
Publicado em 2010-06-01

EpCAM nuclear localization identifies aggressive Thyroid Cancer and is a marker for poor prognosis

Por Ralhan, Ranju, Cao, Jun, Lim, Terence, MacMillan, Christina, Freeman, Jeremy L, Walfish, Paul G
Publicado em 2010

An Ep-ICD Based Index Is a Marker of Aggressiveness and Poor Prognosis in Thyroid Carcinoma

Por He, Helen C.-H., Kashat, Lawrence, Kak, Ipshita, Kunavisarut, Tada, Gundelach, Raefe, Kim, Dae, So, Anthony K.-C., MacMillan, Christina, Freeman, Jeremy L., Ralhan, Ranju, Walfish, Paul G.
Publicado em 2012

Nuclear and Cytoplasmic Accumulation of Ep-ICD Is Frequently Detected in Human Epithelial Cancers

Por Ralhan, Ranju, He, Helen C.-H., So, Anthony K.-C., Tripathi, Satyendra C., Kumar, Manish, Hasan, Md. Raghibul, Kaur, Jatinder, Kashat, Lawrence, MacMillan, Christina, Chauhan, Shyam Singh, Freeman, Jeremy L., Walfish, Paul G.
Publicado em 2010

SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures

Por Howell, Katherine B., McMahon, Jacinta M., Carvill, Gemma L., Tambunan, Dimira, Mackay, Mark T., Rodriguez-Casero, Victoria, Webster, Richard, Clark, Damian, Freeman, Jeremy L., Calvert, Sophie, Olson, Heather E., Mandelstam, Simone, Poduri, Annapurna, Mefford, Heather C., Harvey, A. Simon, Scheffer, Ingrid E.
Publicado no Neurology (2015)

Survival from Differentiated Thyroid Cancer: What Has Age Got to Do with It?

Por Ganly, Ian, Nixon, Iain J., Wang, Laura Y., Palmer, Frank L., Migliacci, Jocelyn C., Aniss, Ahmad, Sywak, Mark, Eskander, Antoine E., Freeman, Jeremy L., Campbell, Michael J., Shen, Wen T., Vaisman, Fernanda, Momesso, Denise, Corbo, Rossana, Vaisman, Mario, Shaha, Ashok, Tuttle, R. Michael, Shah, Jatin P., Patel, Snehal G.
Publicado no Thyroid (2015)

Rare copy number variants are an important cause of epileptic encephalopathies

Por Mefford, Heather C., Yendle, Simone C., Hsu, Cynthia, Cook, Joseph, Geraghty, Eileen, McMahon, Jacinta M., Eeg-Olofsson, Orvar, Sadleir, Lynette G., Gill, Deepak, Ben-Zeev, Bruria, Lerman-Sagie, Tally, Mackay, Mark, Freeman, Jeremy L., Andermann, Eva, Pelakanos, James, Andrews, Ian, Wallace, Geoffrey, Eichler, Evan E., Berkovic, Samuel F., Scheffer, Ingrid E.
Publicado em 2011

Mutations of the Sonic Hedgehog Pathway Underlie Hypothalamic Hamartoma with Gelastic Epilepsy

Por Hildebrand, Michael S., Griffin, Nicole G., Damiano, John A., Cops, Elisa J., Burgess, Rosemary, Ozturk, Ezgi, Jones, Nigel C., Leventer, Richard J., Freeman, Jeremy L., Harvey, A. Simon, Sadleir, Lynette G., Scheffer, Ingrid E., Major, Heather, Darbro, Benjamin W., Allen, Andrew S., Goldstein, David B., Kerrigan, John F., Berkovic, Samuel F., Heinzen, Erin L.
Publicado no Am J Hum Genet (2016)

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1

Por Carvill, Gemma L., Heavin, Sinéad B., Yendle, Simone C., McMahon, Jacinta M., O’Roak, Brian J., Cook, Joseph, Khan, Adiba, Dorschner, Michael O, Weaver, Molly, Calvert, Sophie, Malone, Stephen, Wallace, Geoffrey, Stanley, Thorsten, Bye, Ann M. E., Bleasel, Andrew, Howell, Katherine B., Kivity, Sara, Mackay, Mark T., Rodriguez-Casero, Victoria, Webster, Richard, Korczyn, Amos, Afawi, Zaid, Zelnick, Nathanel, Lerman-Sagie, Tally, Lev, Dorit, Møller, Rikke S., Gill, Deepak, Andrade, Danielle M., Freeman, Jeremy L., Sadleir, Lynette G., Shendure, Jay, Berkovic, Samuel F., Scheffer, Ingrid E., Mefford, Heather C.
Publicado em 2013