Glucose transporter 1 deficiency in the idiopathic generalized epilepsies von Arsov, Todor, Mullen, Saul A., Rogers, Sue, Phillips, A. Marie, Lawrence, Kate M., Damiano, John A., Goldberg-Stern, Hadassa, Afawi, Zaid, Kivity, Sara, Trager, Chantal, Petrou, Steven, Berkovic, Samuel F., Scheffer, Ingrid E.

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The hyperpolarization‐activated cyclic nucleotide‐gated 4 channel as a potential anti‐seizure drug target von Kharouf, Qays, Phillips, A. Marie, Bleakley, Lauren E., Morrisroe, Emma, Oyrer, Julia, Jia, Linghan, Ludwig, Andreas, Jin, Liang, Nicolazzo, Joseph A., Cerbai, Elisabetta, Romanelli, M. Novella, Petrou, Steven, Reid, Christopher A.

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Using a Multiplex Nucleic Acid in situ Hybridization Technique to Determine HCN4 mRNA Expression in the Adult Rodent Brain von Oyrer, Julia, Bleakley, Lauren E., Richards, Kay L., Maljevic, Snezana, Phillips, A. Marie, Petrou, Steven, Nowell, Cameron J., Reid, Christopher A.

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Sodium channel β1 subunit localizes to axon initial segments of excitatory and inhibitory neurons and shows regional heterogeneity in mouse brain von Wimmer, Verena C., Harty, Rosemary C., Richards, Kay L., Phillips, A. Marie, Miyazaki, Haruko, Nukina, Nobuyuki, Petrou, Steven

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Spike-and-wave discharge mediated reduction in hippocampal HCN1 channel function associates with learning deficits in a genetic mouse model of epilepsy von Phillips, A. Marie, Kim, Taehwan, Vargas, Ernesto, Petrou, Steven, Reid, Christopher A

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Impaired Color Recognition in HCN1 Epilepsy: A Single Case Report von Mckenzie, Chaseley E, Ho, Chen-Jui, Forster, Ian C, Soh, Ming S, Phillips, A Marie, Chang, Ying-Chao, Scheffer, Ingrid E, Reid, Christopher A, Tsai, Meng-Han

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Loss of synaptic Zn2+ transporter function increases risk of febrile seizures von Hildebrand, Michael S., Phillips, A. Marie, Mullen, Saul A., Adlard, Paul A., Hardies, Katia, Damiano, John A., Wimmer, Verena, Bellows, Susannah T., McMahon, Jacinta M., Burgess, Rosemary, Hendrickx, Rik, Weckhuysen, Sarah, Suls, Arvid, De Jonghe, Peter, Scheffer, Ingrid E., Petrou, Steven, Berkovic, Samuel F., Reid, Christopher A.

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Gabapentin Modulates HCN4 Channel Voltage-Dependence von Tae, Han-Shen, Smith, Kelly M, Phillips, A Marie, Boyle, Kieran A, Li, Melody, Forster, Ian C, Hatch, Robert J, Richardson, Robert, Hughes, David I, Graham, Brett A, Petrou, Steven, Reid, Christopher A

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Loss‐of‐function variants in Kv11.1 cardiac channels as a biomarker for SUDEP von Soh, Ming S., Bagnall, Richard D., Bennett, Mark F., Bleakley, Lauren E., Mohamed Syazwan, Erlina S., Phillips, A. Marie, Chiam, Mathew D. F., McKenzie, Chaseley E., Hildebrand, Michael, Crompton, Douglas, Bahlo, Melanie, Semsarian, Christopher, Scheffer, Ingrid E., Berkovic, Samuel F., Reid, Christopher A.

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Development of a rapid functional assay that predicts GLUT1 disease severity von Zaman, Sasha M, Mullen, Saul A, Petrovski, Slavé, Maljevic, Snezana, Gazina, Elena V, Phillips, A Marie, Jones, Gabriel Davis, Hildebrand, Michael S, Damiano, John, Auvin, Stéphane, Lerche, Holger, Weber, Yvonne G, Berkovic, Samuel F, Scheffer, Ingrid E, Reid, Christopher A, Petrou, Steven

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Stoned von Phillips, A. Marie, Ramaswami, Mani, Kelly, Leonard E.

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The Potential Antidepressant Compound Org 34167 Modulates HCN Channels Via a Novel Mode of Action von McKenzie, Chaseley E, Hung, Andrew, Phillips, A Marie, Soh, Ming S, Reid, Christopher A, Forster, Ian C

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Multiple molecular mechanisms for a single GABAA mutation in epilepsy von REID, Christopher A, KIM, Taehwan, PHILLIPS, A. Marie, LOW, Jun, BERKOVIC, Samuel F, LUSCHER, Bernhard, PETROU, Steven

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HCN channelopathies: pathophysiology in genetic epilepsy and therapeutic implications von Reid, Christopher A, Phillips, A Marie, Petrou, Steven

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Gain‐of‐function HCN2 variants in genetic epilepsy von Li, Melody, Maljevic, Snezana, Phillips, A. Marie, Petrovski, Slave, Hildebrand, Michael S., Burgess, Rosemary, Mount, Therese, Zara, Federico, Striano, Pasquale, Schubert, Julian, Thiele, Holger, Nürnberg, Peter, Wong, Michael, Weisenberg, Judith L., Thio, Liu Lin, Lerche, Holger, Scheffer, Ingrid E., Berkovic, Samuel F., Petrou, Steven, Reid, Christopher A.

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Molecular and genetic characterization of the interactions between the Drosophila stoned-B protein and DAP-160 (intersectin) von Kelly, Leonard E, Phillips, A Marie

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Effective Translation of the Second Cistron in Two Drosophila Dicistronic Transcripts Is Determined by the Absence of In-frame AUG Codons in the First Cistron von Wall, Adam A., Phillips, A. Marie, Kelly, Leonard E.

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Cation leak: a common functional defect causing HCN1 developmental and epileptic encephalopathy von McKenzie, Chaseley E, Forster, Ian C, Soh, Ming S, Phillips, A Marie, Bleakley, Lauren E, Russ-Hall, Sophie J, Myers, Kenneth A, Scheffer, Ingrid E, Reid, Christopher A

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Functional variants in HCN4 and CACNA1H may contribute to genetic generalized epilepsy von Becker, Felicitas, Reid, Christopher A, Hallmann, Kerstin, Tae, Han-Shen, Phillips, A Marie, Teodorescu, Georgeta, Weber, Yvonne G, Kleefuss-Lie, Ailing, Elger, Christian, Perez-Reyes, Edward, Petrou, Steven, Kunz, Wolfram S, Lerche, Holger, Maljevic, Snezana

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Loss-of-function variants in K v 11.1 cardiac channels as a biomarker for SUDEP von Soh, Ming S, Bagnall, Richard D, Bennett, Mark F, Bleakley, Lauren E, Mohamed Syazwan, Erlina S, Phillips, A Marie, Chiam, Mathew D F, McKenzie, Chaseley E, Hildebrand, Michael, Crompton, Douglas, Bahlo, Melanie, Semsarian, Christopher, Scheffer, Ingrid E, Berkovic, Samuel F, Reid, Christopher A

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