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4. Contributors

5. The Spine

10. Radiology

11. In Reply

14. Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32

16. Mapping the progression of progranulin-associated frontotemporal lobar degeneration

17. Parietal Lobe Deficits in Frontotemporal Lobar Degeneration Caused by a Mutation in the Progranulin Gene

19. Reply of the Authors

21. Role of SOX2 Mutations in Human Hippocampal Malformations and Epilepsy

33. Polymicrogyria and absence of pineal gland due to PAX6 mutation

40. Autopsy-Confirmed Familial Early-Onset Alzheimer Disease Caused by the L153V Presenilin 1 Mutation

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