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Pediatric Radiology
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May 8, 2013
Temporal and occipital lobe features in children with hypochondroplasia/FGFR3 gene mutation
Cristina 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 Disease
Rebecca Barmherzig, Garrett Bullivant, Dawn Cordeiro, et al.
Journal of Neurosurgery. Pediatrics
|
November 28, 2008
Meningioma with dural venous sinus invasion and jugular vein extension
Shobhan Vachhrajani, Andrew Jea, John A Rutka, et al.
Neurology
|
December 29, 2017
<i>COL4A1</i> and fetal vascular origins of schizencephaly
Roha 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 meningomyelocele
H 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 intervention
Tran D Le, Eugene S Liu, Feisal A Adatia, et al.
Journal of Neuropathology and Experimental Neurology
|
December 10, 2024
Mesencephalosynapsis and aqueductal stenosis
Yael Fisher, Patrick Shannon, Orli Greenberg, et al.
Journal of Child Neurology
|
May 7, 2003
Pontocerebellar hypoplasia type 1: new leads for an earlier diagnosis
Michael S Salman, Susan Blaser, J Raymond Buncic, et al.
Prenatal Diagnosis
|
April 8, 2025
Brain Abnormalities in Prenatally Diagnosed Rubinstein-Taybi Syndrome
Laurence 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 clinic
Aaisha Al Balushi, Diana Matviychuk, Rebekah Jobling, et al.
Page
of 18
Search research articles
Search
Showing results (71-80 of 177) with videos related to
Sort By:
Page
of 18
Pediatric Radiology
|
May 8, 2013
Temporal and occipital lobe features in children with hypochondroplasia/FGFR3 gene mutation
Cristina 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 Disease
Rebecca Barmherzig, Garrett Bullivant, Dawn Cordeiro, et al.
Journal of Neurosurgery. Pediatrics
|
November 28, 2008
Meningioma with dural venous sinus invasion and jugular vein extension
Shobhan Vachhrajani, Andrew Jea, John A Rutka, et al.
Neurology
|
December 29, 2017
<i>COL4A1</i> and fetal vascular origins of schizencephaly
Roha 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 meningomyelocele
H 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 intervention
Tran D Le, Eugene S Liu, Feisal A Adatia, et al.
Journal of Neuropathology and Experimental Neurology
|
December 10, 2024
Mesencephalosynapsis and aqueductal stenosis
Yael Fisher, Patrick Shannon, Orli Greenberg, et al.
Journal of Child Neurology
|
May 7, 2003
Pontocerebellar hypoplasia type 1: new leads for an earlier diagnosis
Michael S Salman, Susan Blaser, J Raymond Buncic, et al.
Prenatal Diagnosis
|
April 8, 2025
Brain Abnormalities in Prenatally Diagnosed Rubinstein-Taybi Syndrome
Laurence 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 clinic
Aaisha Al Balushi, Diana Matviychuk, Rebekah Jobling, et al.
Page
of 18