|1.||Blümcke, Ingmar: 3 articles (08/2004 - 01/2002)|
|2.||Wiestler, Otmar D: 3 articles (08/2004 - 01/2002)|
|3.||Schramm, Johannes: 3 articles (08/2004 - 01/2002)|
|4.||Becker, Albert J: 2 articles (08/2004 - 07/2002)|
|5.||Elger, Christian E: 2 articles (08/2004 - 07/2002)|
|6.||Lahl, Rainer: 2 articles (08/2004 - 07/2002)|
|7.||Scheffler, Björn: 2 articles (07/2002 - 01/2002)|
|8.||Urbach, Horst: 2 articles (07/2002 - 01/2002)|
|9.||Sarnat, Harvey B: 1 article (05/2015)|
|10.||Philippart, Michel: 1 article (05/2015)|
05/24/2005 - "Adult-onset epilepsy in focal cortical dysplasia of Taylor type."
01/01/2002 - "Focal cortical dysplasia of Taylor's balloon-cell type (FCD-BC) are a frequent cause of pharmacoresistant epilepsy in young patients. "
05/24/2005 - "Focal cortical dysplasia of Taylor type (FCDT) usually presents with seizures at an early age, whereas adult onset of epilepsy is uncommon. "
01/11/2005 - "Children with cortical dysplasia of Taylor type have in common a very-early-onset, severe epilepsy with neurologic co-morbidity. "
|2.||Tuberous Sclerosis (Bourneville's Disease)
07/01/2002 - "Focal cortical dysplasia of Taylor's balloon cell type: mutational analysis of the TSC1 gene indicates a pathogenic relationship to tuberous sclerosis."
01/01/2008 - "Expression of tuberin and hamartin in tuberous sclerosis complex-associated and sporadic cortical dysplasia of Taylor's balloon cell type."
|4.||Malformations of Cortical Development
05/01/2015 - "Malformations that arise at different times can share a common pathogenesis with variations on the extent: timing of mitotic cycles in mosaic somatic mutations may distinguish hemimegalencephaly from focal cortical dysplasia type 2. Timing should always be considered in interpreting cerebral dysgeneses in both imaging and neuropathological diagnoses."
|5.||Chromosomal Instability (Chromosome Stability)
|2.||tuberous sclerosis complex 1 protein (hamartin)
|3.||tuberous sclerosis complex 2 protein (tuberin)