Early Progenitor Cell Marker Expression Distinguishes Type II From Type I Focal Cortical Dysplasias
- Author
- ORLOVA, Ksenia A1 ; TSAI, Victoria1 ; BAYBIS, Marianna1 ; HEUER, Gregory G2 ; SISODIYA, Sanjay3 ; THOM, Maria3 ; STRAUSS, Kevin4 ; ARONICA, Eleonora5 6 ; STORM, Phillip B7 ; CRINO, Peter B1
[1] PENN Epilepsy Center and Department of Neurology, University of Pennsylvania Medical Center, Philadelphia, Pennsylvania, United States
[2] Department of Neurosurgery, University of Pennsylvania Medical Center, Philadelphia, Pennsylvania, United States
[3] Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, London, United Kingdom
[4] The Clinic for Special Children, Lancaster, Pennsylvania, United States
[5] Department of (Neuro)Pathology, Academic Medical Center, University of Amsterdam, Netherlands
[6] Stichting Epilepsie Instellingen Nederland, Heemstede, Netherlands
[7] Department of Neurosurgery, Children Hospital of Philadelphia, Philadelphia, Pennsylvania, United States - Source
Journal of neuropathology and experimental neurology. 2010, Vol 69, Num 8, pp 850-863, 14 p ; ref : 39 ref
- Publisher
- Lippincott Williams & Wilkins, Hagerstown, MD
- Publication country
- United States
- Document type
- Article
- Language
- English
- Author keyword
- Cortical dysplasia Epilepsy STRADα Tuberous sclerosis complex mTOR
- Keyword (fr)
- Dysplasie Epilepsie Pathologie du système nerveux Phacomatose de Bourneville Précoce Maladie héréditaire Pathologie de l'encéphale Pathologie du système nerveux central Tumeur
- Keyword (en)
- Dysplasia Epilepsy Nervous system diseases Bourneville syndrome Early Genetic disease Cerebral disorder Central nervous system disease Tumor
- Keyword (es)
- Displasia Epilepsia Sistema nervioso patología Facomatosis Bourneville Precoz Enfermedad hereditaria Encéfalo patología Sistema nervosio central patología Tumor
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D03 Carbohydrates (enzymatic deficiencies). Glycogenosis
- Discipline
- Metabolic diseases Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 23087776
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1097/NEN.0b013e3181eac1f5 
https://dx.doi.org/10.1097/NEN.0b013e3181eac1f5
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