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Annals of Hematology|April 1, 1994
Polymyositis associated with chronic myelogenous leukemiaL C Pagliaro, P ManciasPharmacotherapy|July 1, 1995
Amoxapine overdose in a young man: a transient mitochondrial abnormality?P Mancias, L Kramer, I J ButlerEpilepsia|October 17, 1998
Does short-term antiepileptic drug treatment in children result in cognitive or behavioral changes?J Williams, S Bates, M L Griebel, et al.Nature Genetics|April 16, 1998
Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathiesL E Warner, P Mancias, I J Butler, et al.Clinical Pediatrics|May 1, 1996
Behavioral descriptors that differentiate between seizure and nonseizure events in a pediatric populationJ Williams, M Grant, M Jackson, et al.AJNR. American Journal of Neuroradiology|July 11, 1992
CT and ultrasound imaging of retropharyngeal abscesses in childrenC M Glasier, J E Stark, R F Jacobs, et al.Genomics|May 18, 1999
Human bHLH transcription factor gene myogenin (MYOG): genomic sequence and negative mutation analysis in patients with severe congenital myopathiesB S Tseng, S T Cavin, E P Hoffman, et al.Annals of Neurology|November 1, 1996
Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathyE Pegoraro, P Mancias, S H Swerdlow, et al.Journal of Child Neurology|May 3, 2001
Brain plasticity for sensory and linguistic functions: a functional imaging study using magnetoencephalography with children and young adultsA C Papanicolaou, P G Simos, J I Breier, et al.Brain : a Journal of Neurology|February 5, 2003
Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth diseaseA Jordanova, P De Jonghe, C F Boerkoel, et al.Pageof 2