Showing results (191-200 of 661) with videos related to

Sort By:
Pageof 67
American Journal of Medical Genetics. Part A|May 21, 2013
Deletions of 16p11.2 and 19p13.2 in a family with intellectual disability and generalized epilepsyAlexander G Bassuk, Eileen Geraghty, Shu Wu, et al.
Epilepsia|March 28, 2007
SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrumEric Herlenius, Sarah E Heron, Bronwyn E Grinton, et al.
Archives of Neurology|May 10, 2006
Distinguishing sleep disorders from seizures: diagnosing bumps in the nightChristopher Paul Derry, Margot Davey, Murray Johns, et al.
Epilepsia|February 28, 2006
Thalamic atrophy in childhood absence epilepsyChow Huat Patrick Chan, Regula S Briellmann, Gaby S Pell, et al.
Epilepsy & Behavior : E&B|March 2, 2010
Neuropsychological function in patients with a single gene mutation associated with autosomal dominant nocturnal frontal lobe epilepsyAmanda G Wood, Michael M Saling, Marco Fedi, et al.
European Journal of Human Genetics : EJHG|August 9, 2022
Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencingHaloom Rafehi, Cherie Green, Kiymet Bozaoglu, et al.
Developmental Medicine and Child Neurology|February 23, 2026
Developmental stuttering with common and complex phenotypesSarah E Horton, Daisy A Shepherd, Stephanie Siemers, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 14, 2020
Levetiracetam efficacy in PCDH19 Girls Clustering EpilepsyLynette G Sadleir, Kristy L Kolc, Chontelle King, et al.
Epilepsia|May 29, 2020
A proposed guideline for vagus nerve stimulator handling in palliative care and after deathGhadd Alhajaj, Jeffrey Atkinson, Mark R Keezer, et al.
Biochemical and Biophysical Research Communications|October 19, 2007
Osteoblast-like cells and fluid flow: cytoskeleton-dependent shear sensitivityKenneth A Myers, Jerome B Rattner, Nigel G Shrive, et al.
Pageof 67