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Clinical, pathological and genetic data were recorded in an electronic separate, anonymous, password-protected database.
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The epilepsy history was reviewed in each case and the epilepsy syndrome (based on seizure semiology, electroencephalographic, neuroimaging and in some, genetic data) was recorded (Commission on Classification and Terminology of the International League Against Epilepsy, 1989; Engel, 2006).
For the analyses of genetic diversity and differentiation, genotype data were recorded according to the molecular weight (bp) of SSR alleles, either as homozygous genotypes (120/120, 140/140, 150/150).
Demographic data were recorded.
Methods: all relevant data were recorded prospectively.
Clinical and operative data were recorded.
Data were recorded using training diaries.
Height and weight data were recorded simultaneously.
PbrO2 data were recorded retrospectively.
The data were recorded from 6 subjects.
Data were recorded on a standardized questionnaire.
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