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Susan Blaser

Showing results (71-80 of 177) with videos related to

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Pediatric Radiology|May 8, 2013
Temporal and occipital lobe features in children with hypochondroplasia/FGFR3 gene mutationCristina M Philpott, Elysa Widjaja, Charles Raybaud, et al.
Pediatric Neurology|July 1, 2017
A New Patient With Intermediate Severe Salla Disease With Hypomyelination: A Literature Review for Salla DiseaseRebecca Barmherzig, Garrett Bullivant, Dawn Cordeiro, et al.
Journal of Neurosurgery. Pediatrics|November 28, 2008
Meningioma with dural venous sinus invasion and jugular vein extensionShobhan Vachhrajani, Andrew Jea, John A Rutka, et al.
Neurology|December 29, 2017
<i>COL4A1</i> and fetal vascular origins of schizencephalyRoha Khalid, Pradeep Krishnan, Kathleen Andres, et al.
Journal of the International Neuropsychological Society : JINS|September 4, 2008
Auditory interhemispheric transfer in relation to patterns of partial agenesis and hypoplasia of the corpus callosum in spina bifida meningomyeloceleH Julia Hannay, Amy Walker, Maureen Dennis, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 14, 2014
The effect of adding orbital computed tomography findings to the Chandler criteria for classifying pediatric orbital cellulitis in predicting which patients will require surgical interventionTran D Le, Eugene S Liu, Feisal A Adatia, et al.
Journal of Neuropathology and Experimental Neurology|December 10, 2024
Mesencephalosynapsis and aqueductal stenosisYael Fisher, Patrick Shannon, Orli Greenberg, et al.
Journal of Child Neurology|May 7, 2003
Pontocerebellar hypoplasia type 1: new leads for an earlier diagnosisMichael S Salman, Susan Blaser, J Raymond Buncic, et al.
Prenatal Diagnosis|April 8, 2025
Brain Abnormalities in Prenatally Diagnosed Rubinstein-Taybi SyndromeLaurence S Carmant, Elka Miller, Susan Blaser, et al.
JIMD Reports|February 20, 2020
Phenotypes and genotypes of mitochondrial aminoacyl-tRNA synthetase deficiencies from a single neurometabolic clinicAaisha Al Balushi, Diana Matviychuk, Rebekah Jobling, et al.
Pageof 18

Showing results (71-80 of 177) with videos related to

Sort By:
Pageof 18
Pediatric Radiology|May 8, 2013
Temporal and occipital lobe features in children with hypochondroplasia/FGFR3 gene mutationCristina M Philpott, Elysa Widjaja, Charles Raybaud, et al.
Pediatric Neurology|July 1, 2017
A New Patient With Intermediate Severe Salla Disease With Hypomyelination: A Literature Review for Salla DiseaseRebecca Barmherzig, Garrett Bullivant, Dawn Cordeiro, et al.
Journal of Neurosurgery. Pediatrics|November 28, 2008
Meningioma with dural venous sinus invasion and jugular vein extensionShobhan Vachhrajani, Andrew Jea, John A Rutka, et al.
Neurology|December 29, 2017
<i>COL4A1</i> and fetal vascular origins of schizencephalyRoha Khalid, Pradeep Krishnan, Kathleen Andres, et al.
Journal of the International Neuropsychological Society : JINS|September 4, 2008
Auditory interhemispheric transfer in relation to patterns of partial agenesis and hypoplasia of the corpus callosum in spina bifida meningomyeloceleH Julia Hannay, Amy Walker, Maureen Dennis, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 14, 2014
The effect of adding orbital computed tomography findings to the Chandler criteria for classifying pediatric orbital cellulitis in predicting which patients will require surgical interventionTran D Le, Eugene S Liu, Feisal A Adatia, et al.
Journal of Neuropathology and Experimental Neurology|December 10, 2024
Mesencephalosynapsis and aqueductal stenosisYael Fisher, Patrick Shannon, Orli Greenberg, et al.
Journal of Child Neurology|May 7, 2003
Pontocerebellar hypoplasia type 1: new leads for an earlier diagnosisMichael S Salman, Susan Blaser, J Raymond Buncic, et al.
Prenatal Diagnosis|April 8, 2025
Brain Abnormalities in Prenatally Diagnosed Rubinstein-Taybi SyndromeLaurence S Carmant, Elka Miller, Susan Blaser, et al.
JIMD Reports|February 20, 2020
Phenotypes and genotypes of mitochondrial aminoacyl-tRNA synthetase deficiencies from a single neurometabolic clinicAaisha Al Balushi, Diana Matviychuk, Rebekah Jobling, et al.
Pageof 18