Showing results (181-190 of 255) with videos related to
Sort By:
Pageof 26
Mitochondrion|March 26, 2013
Multiple Symmetrical Lipomatosis--a mitochondrial disorder of brown fatC Plummer, P J Spring, R Marotta, et al.Human Molecular Genetics|June 1, 1997
An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsyO K Steinlein, A Magnusson, J Stoodt, et al.Neurology|November 9, 2005
Effect of antiepileptic medication on bone mineral measuresS J Petty, L M Paton, T J O'Brien, et al.Lancet (London, England)|October 6, 1998
Epileptology of the first-seizure presentation: a clinical, electroencephalographic, and magnetic resonance imaging study of 300 consecutive patientsM A King, M R Newton, G D Jackson, et al.Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|March 14, 2000
A role for E2F1 in the induction of apoptosis during thymic negative selectionI García, M Murga, A Vicario, et al.Neurology|May 16, 2002
Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1BR H Wallace, I E Scheffer, G Parasivam, et al.Archives of Neurology|July 1, 1993
Life-threatening focal status epilepticus due to occult cortical dysplasiaR Desbiens, S F Berkovic, F Dubeau, et al.Neurology|August 8, 2008
Reduced striatal D1 receptor binding in autosomal dominant nocturnal frontal lobe epilepsyM Fedi, S F Berkovic, I E Scheffer, et al.Epilepsia|July 18, 2002
How mutations in the nAChRs can cause ADNFLE epilepsyD Bertrand, F Picard, S Le Hellard, et al.Annals of Neurology|June 1, 1995
Comparison of ictal SPECT and interictal PET in the presurgical evaluation of temporal lobe epilepsyS S Ho, S F Berkovic, S U Berlangieri, et al.Pageof 26