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Trends in Neurosciences|August 17, 2001
LIS1: from cortical malformation to essential protein of cellular dynamicsR J Leventer, C Cardoso, D H Ledbetter, et al.Human Genetics|August 1, 1988
Familial pericentric and paracentric inversions of chromosome 1D D Johnson, W B Dobyns, H Gordon, et al.American Journal of Human Genetics|January 1, 1992
Microdeletions of chromosome 17p13 as a cause of isolated lissencephalyS A Ledbetter, A Kuwano, W B Dobyns, et al.Neurology|August 15, 2001
LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQR J Leventer, C Cardoso, D H Ledbetter, et al.Journal of Medical Genetics|May 10, 2005
Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotypeU Moog, M C Jones, L M Bird, et al.Journal of Child Neurology|August 2, 2000
Diffuse polymicrogyria associated with congenital hydrocephalus, craniosynostosis, severe mental retardation, and minor facial and genital anomaliesL Pavone, R Rizzo, P Pavone, et al.Brain Research|May 9, 1983
Participation of cortical recurrent inhibition in the genesis of spike and wave discharges in feline generalized penicillin epilepsyG Kostopoulos, M Avoli, P GloorHippocampus|January 1, 1997
In vitro electrophysiology of rat subicular bursting neuronsD Mattia, H Kawasaki, M AvoliNeuroscience|October 26, 2013
Neurosteroids modulate epileptiform activity and associated high-frequency oscillations in the piriform cortexR Herrington, M Lévesque, M AvoliNeuroradiology|October 1, 1996
Congenital pontocerebellar atrophy in three patients: clinical, radiologic and etiologic considerationsN Zelnik, W B Dobyns, S L Forem, et al.Pageof 64