Saul A Mullen

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Credit Name
Saul A Mullen
Full Name
Mullen, Saul A
 
 
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Publications

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Subject:  Humans

Results 1-11 of 11 (Search time: 0.008 seconds).

Publication YearTitleAuthor(s)
122-Sep-2014Lamotrigine can be beneficial in patients with Dravet syndrome.Dalic, Linda; Mullen, Saul A ; Roulet Perez, Eliane; Scheffer, Ingrid E 
231-Jan-2014Glucose metabolism transporters and epilepsy: only GLUT1 has an established role.Hildebrand, Michael S ; Damiano, John Anthony; Mullen, Saul A ; Bellows, Susannah T; Oliver, Karen L; Dahl, Hans-Henrik M; Scheffer, Ingrid E ; Berkovic, Samuel F 
310-Jan-2014Does variation in NIPA2 contribute to genetic generalized epilepsy?Hildebrand, Michael S ; Damiano, John Anthony; Mullen, Saul A ; Bellows, Susannah T; Scheffer, Ingrid E ; Berkovic, Samuel F 
425-Sep-2013Copy number variants are frequent in genetic generalized epilepsy with intellectual disability.Mullen, Saul A ; Carvill, Gemma L; Bellows, Susannah; Bayly, Marta A; Trucks, Holger; Lal, Dennis; Sander, Thoman; Berkovic, Samuel F ; Dibbens, Leanne M; Scheffer, Ingrid E ; Mefford, Heather C
58-Jan-2013Epilepsy in 2012: Advances in epilepsy shed light on key questions.Scheffer, Ingrid E ; Mullen, Saul A 
61-Nov-2012Glucose transporter 1 deficiency in the idiopathic generalized epilepsies.Arsov, Todor; Mullen, Saul A ; Rogers, Sue; Phillips, A Marie; Lawrence, Kate M; Damiano, John Anthony; Goldberg-Stern, Hadassa; Afawi, Zaid; Kivity, Sara; Trager, Chantal; Petrou, Steven; Berkovic, Samuel F ; Scheffer, Ingrid E 
725-Oct-2012Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency.Arsov, Todor; Mullen, Saul A ; Damiano, John Anthony; Lawrence, Kate M; Huh, Linda L; Nolan, Melinda; Young, Helen ; Thouin, Anaïs; Dahl, Hans-Henrik M; Berkovic, Samuel F ; Crompton, Douglas E; Sadleir, Lynette G; Scheffer, Ingrid E 
85-May-2011Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6.Arsov, Todor; Smith, Katherine R; Damiano, John Anthony; Franceschetti, Silvana; Canafoglia, Laura; Bromhead, Catherine J; Andermann, Eva; Vears, Danya F; Cossette, Patrick; Rajagopalan, Sulekha; McDougall, Alan; Sofia, Vito; Farrell, Michael; Aguglia, Umberto; Zini, Andrea; Meletti, Stefano; Morbin, Michela; Mullen, Saul A ; Andermann, Frederick; Mole, Sara E; Bahlo, Melanie; Berkovic, Samuel F 
923-Jun-2010Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency.Mullen, Saul A ; Suls, A; De Jonghe, Peter; Berkovic, Samuel F ; Scheffer, Ingrid E 
1010-Feb-2009A neurologist's guide to genome-wide association studies.Mullen, Saul A ; Crompton, Douglas E; Carney, Patrick W ; Helbig, Ingo; Berkovic, Samuel F 
111-Jan-2009Translational research in epilepsy genetics: sodium channels in man to interneuronopathy in mouse.Mullen, Saul A ; Scheffer, Ingrid E