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American Journal of Medical Genetics. Part A
|
September 12, 2012
Overgrowth with increased proliferation of fibroblast and matrix metalloproteinase activity related to reduced TIMP1: a newly recognized syndrome?
Brian Chung, Aleksander Hinek, Sarah Keating, et al.
AJNR. American Journal of Neuroradiology
|
January 21, 2026
Periventricular Nodular Heterotopia, Cerebellar Hypodysgenesis, and Mesial Temporal Malformation detected on Fetal MRI: An Under-Recognized Association
Vivek Pai, Shiri Shinar, Pradeep Krishnan, et al.
Neuroimaging Clinics of North America
|
November 22, 2025
Fetal and Neonatal Brain Tumors: An Imaging Review
Vivek Pai, Neetika Gupta, Elka Miller, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 27, 2015
Exome sequencing identifies complex I NDUFV2 mutations as a novel cause of Leigh syndrome
Jessie M Cameron, Nevena MacKay, Annette Feigenbaum, et al.
Prenatal Diagnosis
|
August 20, 2010
Fetal cardiac tumors: a single-center experience of 40 cases
Yoav Yinon, David Chitayat, Susan Blaser, et al.
International Journal of Pediatric Otorhinolaryngology
|
January 4, 2005
Retropharyngeal and parapharyngeal infections in children: the Toronto experience
Hamid Daya, Stephen Lo, Blake C Papsin, et al.
The Laryngoscope
|
December 6, 2006
Inner ear dysplasia is common in children with Down syndrome (trisomy 21)
Susan Blaser, Evan J Propst, Daniel Martin, et al.
The Laryngoscope
|
December 6, 2006
Temporal bone imaging in GJB2 deafness
Evan J Propst, Susan Blaser, Tracy L Stockley, et al.
Retina (Philadelphia, Pa.)
|
March 25, 2017
RETINAL DETACHMENT AND RETROBULBAR CYSTS IN A LARGE COHORT OF OPTIC NERVE COLOBOMA
Yufeng N Chen, C K Patel, Peter J Kertes, et al.
American Journal of Medical Genetics. Part A
|
November 23, 2011
Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: expanding the spectrum of Timothy syndrome
Jane Gillis, Elena Burashnikov, Charles Antzelevitch, et al.
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of 18
Search research articles
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Showing results (91-100 of 178) with videos related to
Sort By:
Page
of 18
American Journal of Medical Genetics. Part A
|
September 12, 2012
Overgrowth with increased proliferation of fibroblast and matrix metalloproteinase activity related to reduced TIMP1: a newly recognized syndrome?
Brian Chung, Aleksander Hinek, Sarah Keating, et al.
AJNR. American Journal of Neuroradiology
|
January 21, 2026
Periventricular Nodular Heterotopia, Cerebellar Hypodysgenesis, and Mesial Temporal Malformation detected on Fetal MRI: An Under-Recognized Association
Vivek Pai, Shiri Shinar, Pradeep Krishnan, et al.
Neuroimaging Clinics of North America
|
November 22, 2025
Fetal and Neonatal Brain Tumors: An Imaging Review
Vivek Pai, Neetika Gupta, Elka Miller, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 27, 2015
Exome sequencing identifies complex I NDUFV2 mutations as a novel cause of Leigh syndrome
Jessie M Cameron, Nevena MacKay, Annette Feigenbaum, et al.
Prenatal Diagnosis
|
August 20, 2010
Fetal cardiac tumors: a single-center experience of 40 cases
Yoav Yinon, David Chitayat, Susan Blaser, et al.
International Journal of Pediatric Otorhinolaryngology
|
January 4, 2005
Retropharyngeal and parapharyngeal infections in children: the Toronto experience
Hamid Daya, Stephen Lo, Blake C Papsin, et al.
The Laryngoscope
|
December 6, 2006
Inner ear dysplasia is common in children with Down syndrome (trisomy 21)
Susan Blaser, Evan J Propst, Daniel Martin, et al.
The Laryngoscope
|
December 6, 2006
Temporal bone imaging in GJB2 deafness
Evan J Propst, Susan Blaser, Tracy L Stockley, et al.
Retina (Philadelphia, Pa.)
|
March 25, 2017
RETINAL DETACHMENT AND RETROBULBAR CYSTS IN A LARGE COHORT OF OPTIC NERVE COLOBOMA
Yufeng N Chen, C K Patel, Peter J Kertes, et al.
American Journal of Medical Genetics. Part A
|
November 23, 2011
Long QT, syndactyly, joint contractures, stroke and novel CACNA1C mutation: expanding the spectrum of Timothy syndrome
Jane Gillis, Elena Burashnikov, Charles Antzelevitch, et al.
Page
of 18