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Neuroimaging Clinics of North America|May 30, 2006
3.0 T versus 1.5 T pediatric brain imagingRobert A Zimmerman, Larissa T Bilaniuk, Avrum N Pollock, et al.The Journal of Bone and Joint Surgery. American Volume|March 3, 2007
Occipitalization of the atlas in children. Morphologic classification, associations, and clinical relevancePurushottam A Gholve, Harish S Hosalkar, Eric T Ricchetti, et al.Pediatric Radiology|December 17, 2009
Hereditary hemorrhagic telangiectasia and juvenile polyposis: an overlap of syndromesErica D Poletto, Angela M Trinh, Terry L Levin, et al.Pediatrics|July 1, 2009
Estimation of optimal CPR chest compression depth in children by using computer tomographyMatthew S Braga, Troy E Dominguez, Avrum N Pollock, et al.Brain Pathology (Zurich, Switzerland)|July 22, 2014
Chromosome band 7q34 deletions resulting in KIAA1549-BRAF and FAM131B-BRAF fusions in pediatric low-grade GliomasJacquelyn J Roth, Mariarita Santi, Avrum N Pollock, et al.The Journal of Pediatrics|June 26, 2007
Headache in children with sickle cell disease: prevalence and associated factorsAlison E Niebanck, Avrum N Pollock, Kim Smith-Whitley, et al.British Journal of Haematology|June 9, 2009
Silent infarcts in young children with sickle cell diseaseJanet L Kwiatkowski, Robert A Zimmerman, Avrum N Pollock, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|November 13, 2013
Retinal hemorrhage and brain injury patterns on diffusion-weighted magnetic resonance imaging in children with head traumaGil Binenbaum, Cindy W Christian, Rebecca N Ichord, et al.Journal of Neuro-Oncology|December 12, 2007
The role of [18F]-fluorodeoxyglucose positron emission tomography in predicting plexiform neurofibroma progressionMichael J Fisher, Sandip Basu, Eva Dombi, et al.Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|December 26, 2006
Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type 2 mutationsSuzanne K Jadico, David A Young, Alexandra Huebner, et al.Pageof 2