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Ingrid E Scheffer

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Credit Name
Ingrid E Scheffer
Full Name
Scheffer, Ingrid E
 
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Publications

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Subject:  Electroencephalography
Subject:  Pedigree

Results 1-11 of 11 (Search time: 0.007 seconds).

Publication YearTitleAuthor(s)
17-Jun-2013Etiology of hippocampal sclerosis: evidence for a predisposing familial morphologic anomaly.Tsai, Meng-Han; Pardoe, Heath R; Perchyonok, Yuliya ; Fitt, Gregory J ; Scheffer, Ingrid E ; Jackson, Graeme D ; Berkovic, Samuel F 
216-Apr-2013Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26.Klein, Karl Martin; Bromhead, Catherine J; Smith, Katherine R; O'Callaghan, Christopher J ; Corcoran, Susan J; Heron, Sarah E; Iona, Xenia; Hodgson, Bree L; McMahon, Jacinta M; Lawrence, Kate M; Scheffer, Ingrid E ; Dibbens, Leanne M; Bahlo, Melanie; Berkovic, Samuel F 
310-Jul-2012Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrum.Klein, Karl Martin; O'Brien, Terence J; Praveen, Kavita; Heron, Sarah E; Mulley, John C; Foote, Simon; Berkovic, Samuel F ; Scheffer, Ingrid E 
45-Jan-2012Clinical genetic studies in benign childhood epilepsy with centrotemporal spikes.Vears, Danya F; Tsai, Meng-Han; Sadleir, Lynette G; Grinton, Bronwyn E; Lillywhite, Leasha M; Carney, Patrick W ; Harvey, A Simon; Berkovic, Samuel F ; Scheffer, Ingrid E 
59-Jul-2008Benign occipital epilepsies of childhood: clinical features and genetics.Taylor, Isabella; Berkovic, Samuel F ; Kivity, Sara; Scheffer, Ingrid E 
629-Jan-2008Epilepsy and mental retardation limited to females: an under-recognized disorder.Scheffer, Ingrid E ; Turner, Samantha J; Dibbens, Leanne M; Bayly, Marta A; Friend, Kathryn; Hodgson, Bree; Burrows, Linda; Shaw, Marie; Wei, Chen; Ullmann, Reinhard; Ropers, Hans-Hilger; Szepetowski, Pierre; Haan, Eric; Mazarib, Aziz; Afawi, Zaid; Neufeld, Miriam Y; Andrews, P Ian; Wallace, Geoffrey; Kivity, Sara; Lev, Dorit; Lerman-Sagie, Tally; Derry, Christopher P; Korczyn, Amos D; Gecz, Jozef; Mulley, John C; Berkovic, Samuel F 
71-Jan-2003Childhood absence epilepsy and febrile seizures: a family with a GABA(A) receptor mutation.Marini, Carla; Harkin, Louise A; Wallace, Robyn H; Mulley, John C; Scheffer, Ingrid E ; Berkovic, Samuel F 
82000Autosomal dominant rolandic epilepsy with speech dyspraxia.Scheffer, Ingrid E 
91-Jan-1999Generalized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndrome.Singh, R; Scheffer, Ingrid E ; Crossland, K; Berkovic, Samuel F 
101-Dec-1998Familial partial epilepsy with variable foci: a new partial epilepsy syndrome with suggestion of linkage to chromosome 2.Scheffer, Ingrid E ; Phillips, H A; O'Brien, C E; Saling, Michael M ; Wrennall, J A; Wallace, Robyn H; Mulley, John C; Berkovic, Samuel F 
111-Oct-1995Autosomal dominant rolandic epilepsy and speech dyspraxia: a new syndrome with anticipation.Scheffer, Ingrid E ; Jones, L; Pozzebon, M; Howell, R A; Saling, Michael M ; Berkovic, Samuel F