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Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance. [electronic resource] by
- Crompton, Douglas E
- Scheffer, Ingrid E
- Taylor, Isabella
- Cook, Mark J
- McKelvie, Penelope A
- Vears, Danya F
- Lawrence, Kate M
- McMahon, Jacinta M
- Grinton, Bronwyn E
- McIntosh, Anne M
- Berkovic, Samuel F
Producer: 20101130
In:
Brain : a journal of neurology vol. 133
Availability: No items available.
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10.
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PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures. [electronic resource] by
- Scheffer, Ingrid E
- Grinton, Bronwyn E
- Heron, Sarah E
- Kivity, Sara
- Afawi, Zaid
- Iona, Xenia
- Goldberg-Stern, Hadassa
- Kinali, Maria
- Andrews, Ian
- Guerrini, Renzo
- Marini, Carla
- Sadleir, Lynette G
- Berkovic, Samuel F
- Dibbens, Leanne M
Producer: 20130118
In:
Neurology vol. 79
Availability: No items available.
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11.
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A variant of KCC2 from patients with febrile seizures impairs neuronal Cl- extrusion and dendritic spine formation. [electronic resource] by
- Puskarjov, Martin
- Seja, Patricia
- Heron, Sarah E
- Williams, Tristiana C
- Ahmad, Faraz
- Iona, Xenia
- Oliver, Karen L
- Grinton, Bronwyn E
- Vutskits, Laszlo
- Scheffer, Ingrid E
- Petrou, Steven
- Blaesse, Peter
- Dibbens, Leanne M
- Berkovic, Samuel F
- Kaila, Kai
Producer: 20150114
In:
EMBO reports vol. 15
Availability: No items available.
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12.
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Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy. [electronic resource] by
- Berkovic, Samuel F
- Heron, Sarah E
- Giordano, Lucio
- Marini, Carla
- Guerrini, Renzo
- Kaplan, Robert E
- Gambardella, Antonio
- Steinlein, Ortrud K
- Grinton, Bronwyn E
- Dean, Joanne T
- Bordo, Laura
- Hodgson, Bree L
- Yamamoto, Toshiyuki
- Mulley, John C
- Zara, Federico
- Scheffer, Ingrid E
Producer: 20040507
In:
Annals of neurology vol. 55
Availability: No items available.
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13.
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Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations. [electronic resource] by
- Scheffer, Ingrid E
- Harkin, Louise A
- Grinton, Bronwyn E
- Dibbens, Leanne M
- Turner, Samantha J
- Zielinski, Marta A
- Xu, Ruwei
- Jackson, Graeme
- Adams, Judith
- Connellan, Mary
- Petrou, Steven
- Wellard, R Mark
- Briellmann, Regula S
- Wallace, Robyn H
- Mulley, John C
- Berkovic, Samuel F
Producer: 20070201
In:
Brain : a journal of neurology vol. 130
Availability: No items available.
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14.
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Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families. [electronic resource] by
- Marini, Carla
- Scheffer, Ingrid E
- Crossland, Kathryn M
- Grinton, Bronwyn E
- Phillips, Fiona L
- McMahon, Jacinta M
- Turner, Samantha J
- Dean, Joanne T
- Kivity, Sara
- Mazarib, Aziz
- Neufeld, Miriam Y
- Korczyn, Amos D
- Harkin, Louise A
- Dibbens, Leanne M
- Wallace, Robyn H
- Mulley, John C
- Berkovic, Samuel F
Producer: 20040528
In:
Epilepsia vol. 45
Availability: No items available.
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15.
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Genetic epilepsy with febrile seizures plus: Refining the spectrum. [electronic resource] by
- Zhang, Yue-Hua
- Burgess, Rosemary
- Malone, Jodie P
- Glubb, Georgie C
- Helbig, Katherine L
- Vadlamudi, Lata
- Kivity, Sara
- Afawi, Zaid
- Bleasel, Andrew
- Grattan-Smith, Padraic
- Grinton, Bronwyn E
- Bellows, Susannah T
- Vears, Danya F
- Damiano, John A
- Goldberg-Stern, Hadassa
- Korczyn, Amos D
- Dibbens, Leanne M
- Ruzzo, Elizabeth K
- Hildebrand, Michael S
- Berkovic, Samuel F
- Scheffer, Ingrid E
Producer: 20171004
In:
Neurology vol. 89
Availability: No items available.
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16.
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Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome. [electronic resource] by
- Grinton, Bronwyn E
- Heron, Sarah E
- Pelekanos, James T
- Zuberi, Sameer M
- Kivity, Sara
- Afawi, Zaid
- Williams, Tristiana C
- Casalaz, Dan M
- Yendle, Simone
- Linder, Ilan
- Lev, Dorit
- Lerman-Sagie, Tally
- Malone, Stephen
- Bassan, Haim
- Goldberg-Stern, Hadassa
- Stanley, Thorsten
- Hayman, Michael
- Calvert, Sophie
- Korczyn, Amos D
- Shevell, Michael
- Scheffer, Ingrid E
- Mulley, John C
- Berkovic, Samuel F
Producer: 20150916
In:
Epilepsia vol. 56
Availability: No items available.
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17.
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Epidemiology and etiology of infantile developmental and epileptic encephalopathies in Tasmania. [electronic resource] by
- Ware, Tyson L
- Huskins, Shannon R
- Grinton, Bronwyn E
- Liu, Yu-Chi
- Bennett, Mark F
- Harvey, Michael
- McMahon, Jacinta
- Andreopoulos-Malikotsinas, Danae
- Bahlo, Melanie
- Howell, Katherine B
- Hildebrand, Michael S
- Damiano, John A
- Rosenfeld, Alexander
- Mackay, Mark T
- Mandelstam, Simone
- Leventer, Richard J
- Harvey, A Simon
- Freeman, Jeremy L
- Scheffer, Ingrid E
- Jones, Dean L
- Berkovic, Samuel F
Publication details: Epilepsia open Sep 2019
In:
Epilepsia open vol. 4
Availability: No items available.
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18.
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PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome. [electronic resource] by
- Heron, Sarah E
- Grinton, Bronwyn E
- Kivity, Sara
- Afawi, Zaid
- Zuberi, Sameer M
- Hughes, James N
- Pridmore, Clair
- Hodgson, Bree L
- Iona, Xenia
- Sadleir, Lynette G
- Pelekanos, James
- Herlenius, Eric
- Goldberg-Stern, Hadassa
- Bassan, Haim
- Haan, Eric
- Korczyn, Amos D
- Gardner, Alison E
- Corbett, Mark A
- Gécz, Jozef
- Thomas, Paul Q
- Mulley, John C
- Berkovic, Samuel F
- Scheffer, Ingrid E
- Dibbens, Leanne M
Producer: 20120312
In:
American journal of human genetics vol. 90
Availability: No items available.
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