Anterior Temporal Changes on MR Images of Children with Hippocampal Sclerosis: An Effect of Seizures on the Immature Brain?

od Mitchell, L. Anne, Harvey, A. Simon, Coleman, Lee T., Mandelstam, Simone A., Jackson, Graeme D.
Izdano u AJNR Am J Neuroradiol (2003)

Quantitative assessment of corpus callosum morphology in periventricular nodular heterotopia

od Pardoe, Heath R., Mandelstam, Simone A., Hiess, Rebecca Kucharsky, Kuzniecky, Ruben I., Jackson, Graeme D.
Izdano u Epilepsy Res (2014)

GRIN2A: An aptly named gene for speech dysfunction

od Turner, Samantha J., Mayes, Angela K., Verhoeven, Andrea, Mandelstam, Simone A., Morgan, Angela T., Scheffer, Ingrid E.
Izdano u Neurology (2015)

CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures

od Thomas, Rhys H., Zhang, Lin Mei, Carvill, Gemma L., Archer, John S., Heavin, Sinéad B., Mandelstam, Simone A., Craiu, Dana, Berkovic, Samuel F., Gill, Deepak S., Mefford, Heather C., Scheffer, Ingrid E.
Izdano u Neurology (2015)

The surgically remediable syndrome of epilepsy associated with bottom-of-sulcus dysplasia

od Harvey, A. Simon, Mandelstam, Simone A., Maixner, Wirginia J., Leventer, Richard J., Semmelroch, Mira, MacGregor, Duncan, Kalnins, Renate M., Perchyonok, Yuliya, Fitt, Gregory J., Barton, Sarah, Kean, Michael J., Fabinyi, Gavin C.A., Jackson, Graeme D.
Izdano u Neurology (2015)

Second‐hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIA

od Lee, Wei Shern, Stephenson, Sarah E. M., Howell, Katherine B., Pope, Kate, Gillies, Greta, Wray, Alison, Maixner, Wirginia, Mandelstam, Simone A., Berkovic, Samuel F., Scheffer, Ingrid E., MacGregor, Duncan, Harvey, Anthony Simon, Lockhart, Paul J., Leventer, Richard J.
Izdano u Ann Clin Transl Neurol (2019)

Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5

od Scerri, Thomas, Riseley, Jessica R, Gillies, Greta, Pope, Kate, Burgess, Rosemary, Mandelstam, Simone A, Dibbens, Leanne, Chow, Chung W, Maixner, Wirginia, Harvey, Anthony Simon, Jackson, Graeme D, Amor, David J, Delatycki, Martin B, Crino, Peter B, Berkovic, Samuel F, Scheffer, Ingrid E, Bahlo, Melanie, Lockhart, Paul J, Leventer, Richard J
Izdano u Ann Clin Transl Neurol (2015)

Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

od Marsh, Ashley P L, Heron, Delphine, Edwards, Timothy J, Quartier, Angélique, Galea, Charles, Nava, Caroline, Rastetter, Agnès, Moutard, Marie-Laure, Anderson, Vicki, Bitoun, Pierre, Bunt, Jens, Faudet, Anne, Garel, Catherine, Gillies, Greta, Gobius, Ilan, Guegan, Justine, Heide, Solveig, Keren, Boris, Lesne, Fabien, Lukic, Vesna, Mandelstam, Simone A, McGillivray, George, McIlroy, Alissandra, Méneret, Aurélie, Mignot, Cyril, Morcom, Laura R, Odent, Sylvie, Paolino, Annalisa, Pope, Kate, Riant, Florence, Robinson, Gail A, Spencer-Smith, Megan, Srour, Myriam, Stephenson, Sarah E M, Tankard, Rick, Trouillard, Oriane, Welniarz, Quentin, Wood, Amanda, Brice, Alexis, Rouleau, Guy, Attié-Bitach, Tania, Delatycki, Martin B, Mandel, Jean-Louis, Amor, David J, Roze, Emmanuel, Piton, Amélie, Bahlo, Melanie, de Villemeur, Thierry Billette, Sherr, Elliott H, Leventer, Richard J, Richards, Linda J, Lockhart, Paul J, Depienne, Christel
Izdano u Nat Genet (2017)