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Your search keyword '"Jackson, Graeme"' showing total 24 results
Start Over Author "Jackson, Graeme" Journal neurology (ovid)
24 results on '"Jackson, Graeme"'

5. Multicenter Validation of a Deep Learning Detection Algorithm for Focal Cortical Dysplasia

Author

Gill, Ravnoor Singh, Lee, Hyo-Min, Caldairou, Benoit, Hong, Seok-Jun, Barba, Carmen, Deleo, Francesco, D'Incerti, Ludovico, Mendes Coelho, Vanessa Cristina, Lenge, Matteo, Semmelroch, Mira, Schrader, Dewi Victoria, Bartolomei, Fabrice, Guye, Maxime, Schulze-Bonhage, Andreas, Urbach, Horst, Cho, Kyoo Ho, Cendes, Fernando, Guerrini, Renzo, Jackson, Graeme, Hogan, R. Edward, Bernasconi, Neda, and Bernasconi, Andrea

Published
2021
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6. One-Stage, Limited-Resection Epilepsy Surgery for Bottom-of-Sulcus Dysplasia

Author

Macdonald-Laurs, Emma, Maixner, Wirginia J., Bailey, Catherine A., Barton, Sarah M., Mandelstam, Simone A., Yuan-Mou Yang, Joseph, Warren, Aaron E.L., Kean, Michael J., Francis, Peter, MacGregor, Duncan, D'Arcy, Colleen, Wrennall, Jacquie A., Davidson, Andrew, Pope, Kate, Leventer, Richard J., Freeman, Jeremy L., Wray, Alison, Jackson, Graeme D., and Harvey, A. Simon

Published
2021
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9. Multiplex families with epilepsy

Author

Afawi, Zaid, Oliver, Karen L., Kivity, Sara, Mazarib, Aziz, Blatt, Ilan, Neufeld, Miriam Y., Helbig, Katherine L., Goldberg-Stern, Hadassa, Misk, Adel J., Straussberg, Rachel, Walid, Simri, Mahajnah, Muhammad, Lerman-Sagie, Tally, Ben-Zeev, Bruria, Kahana, Esther, Masalha, Rafik, Kramer, Uri, Ekstein, Dana, Shorer, Zamir, Wallace, Robyn H., Mangelsdorf, Marie, MacPherson, James N., Carvill, Gemma L., Mefford, Heather C., Jackson, Graeme D., Scheffer, Ingrid E., Bahlo, Melanie, Gecz, Jozef, Heron, Sarah E., Corbett, Mark, Mulley, John C., Dibbens, Leanne M., Korczyn, Amos D., and Berkovic, Samuel F.

Published
2016
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10. The surgically remediable syndrome of epilepsy associated with bottom-of-sulcus dysplasia

Author

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., and Jackson, Graeme D.

Abstract

To determine clinical and EEG features that might help identify patients with epilepsy harboring small, intrinsically epileptogenic, surgically treatable, bottom-of-sulcus dysplasias (BOSDs).

Published
2015
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12. Abnormal neurovascular coupling during status epilepticus migrainosus in Sturge-Weber syndrome

Author

Sethi, Moksh, Kowalczyk, Magdalena A., Dalic, Linda J., Archer, John S., and Jackson, Graeme D.

Abstract

Sturge-Weber syndrome is a rare, sporadic, neurocutaneous disorder classically characterized by a facial nevus in the trigeminal distribution (port wine stain), leptomeningeal angiomatosis, and glaucoma, although intracranial changes can be present without cutaneous involvement.1Seizures occur in up to 75% of individuals, are often associated with headache, and stroke-like episodes causing prolonged neurologic deficits are also described.1,2

Published
2017
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13. Networks underlying paroxysmal fast activity and slow spike and wave in Lennox-Gastaut syndrome

Author

Pillay, Neelan, Archer, John S., Badawy, Radwa A.B., Flanagan, Danny F., Berkovic, Samuel F., and Jackson, Graeme

Abstract

To use EEG-fMRI to determine which structures are critically involved in the generation of paroxysmal fast activity (PFA) and slow spike and wave (SSW) (1.5–2.5 Hz), the characteristic interictal discharges of Lennox-Gastaut syndrome (LGS).

Published
2013
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14. Etiology of hippocampal sclerosis

Author

Tsai, Meng-Han, Pardoe, Heath R., Perchyonok, Yuliya, Fitt, Gregory J., Scheffer, Ingrid E., Jackson, Graeme D., and Berkovic, Samuel F.

Abstract

We sought evidence of a hereditary component for hippocampal sclerosis (HS) by determining whether close relatives of probands with temporal lobe epilepsy (TLE) with HS also had asymptomatic HS or subtle variation in hippocampal morphology.

Published
2013
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17. Cortical/subcortical BOLD changes associated with epileptic discharges

Author

Federico, Paolo, Archer, John S., Abbott, David F., and Jackson, Graeme D.

Abstract

Malformations of cortical development have characteristic interictal discharges, yet the mechanisms of generation of these discharges are not known in humans. Interictal discharges in malformations of cortical development were studied with EEG-fMRI.

Published
2005
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18. Hippocampal pathology in refractory temporal lobe epilepsy

Author

Briellmann, Regula S., Kalnins, Renate M., Berkovic, Samuel F., and Jackson, Graeme D.

Abstract

The MR and pathologic features of hippocampal sclerosis (HS) are well described and include volume decrease and T2-weighted signal increase for MRI, and neuron cell loss and gliosis for pathology. ObjectiveTo confirm the established correlation between hippocampal volumes and neuron cell counts, and to study the still controversial association between signal change and gliosis.

Published
2002

21. Hippocampal sclerosis studied in identical twins

Author

Jackson, Graeme D., McIntosh, Anne M., Briellmann, Regula S., and Berkovic, Samuel F.

Abstract

To test both the genetic and acquired hypotheses for the etiology of hippocampal sclerosis (HS) by studying with optimized and quantitative MRI three monozygous (MZ) twin pairs in which the index twin had temporal lobe epilepsy and HS.

Published
1998

22. Hippocampal sclerosis following brief generalized seizures in adulthood

Author

Briellmann, Regula S., Newton, Mark R., Wellard, R. Mark, and Jackson, Graeme D.

Abstract

This report describes a patient who had a first generalized tonic clonic seizure (GTCS) at the age of 18 years. The initial MRI scan was normal on visual and quantitative examination. After a further six GTCS, a second MRI scan showed reduced hippocampal volume and increased hippocampal T2 signal, which was confirmed in a third scan. Therefore, hippocampal sclerosis may be acquired in adulthood after brief GTCS.

Published
2001

23. Author response: Mechanisms of memory impairment in epilepsy depend on age at disease onset

Author

Rayner, Genevieve, Jackson, Graeme D., and Wilson, Sarah J.

Abstract

We thank Dr. Heilman for the comment on our article, which showed that antecedents of autobiographic memory impairments common to patients with focal epilepsy differ as a function of age at seizure onset.1Impairments in those with childhood-onset epilepsy were predicted by young age at onset, frequent seizures, and reduced working memory, whereas in adult-onset epilepsy, depression was the major factor.1

Published
2017
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