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AJNR. American Journal of Neuroradiology
|
July 1, 2026
Comprehensive Structural MRI Phenotyping in <i>Oligophrenin 1-</i>Related Disorder Reveals Characteristic Brain Malformations
Asthik Biswas, Matthew T Whitehead, Parthiv Haldipur, et al.
Neuropediatrics
|
August 27, 2016
Update on Leukodystrophies: A Historical Perspective and Adapted Definition
Sietske H Kevelam, Marjan E Steenweg, Siddharth Srivastava, et al.
American Journal of Medical Genetics. Part A
|
May 16, 2012
Brain abnormalities in patients with Beckwith-Wiedemann syndrome
Kate Gardiner, David Chitayat, Sanaa Choufani, et al.
The Laryngoscope
|
June 28, 2016
Midline posterior glossectomy and lingual tonsillectomy in obese and nonobese children with down syndrome: Biomarkers for success
Evan J Propst, Reshma Amin, Natasha Talwar, et al.
Prenatal Diagnosis
|
December 12, 2018
Fetal myelomeningocele surgery: Only treating the tip of the iceberg
Alyaa AlRefai, James Drake, Abhaya V Kulkarni, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
April 15, 2019
Anticoagulation therapy and the risk of perioperative brain injury in neonates with congenital heart disease
Lara M Leijser, Vann Chau, Mike Seed, et al.
American Journal of Medical Genetics. Part A
|
July 9, 2011
Further expansion of the phenotypic spectrum associated with mutations in ALDH18A1, encoding Δ¹-pyrroline-5-carboxylate synthase (P5CS)
David L Skidmore, David Chitayat, Tim Morgan, et al.
Brain : a Journal of Neurology
|
October 1, 2010
Magnetic resonance imaging pattern recognition in hypomyelinating disorders
Marjan E Steenweg, Adeline Vanderver, Susan Blaser, et al.
Human Molecular Genetics
|
October 11, 2018
Bi-allelic mutations of LONP1 encoding the mitochondrial LonP1 protease cause pyruvate dehydrogenase deficiency and profound neurodegeneration with progressive cerebellar atrophy
Graeme A M Nimmo, Sundararajan Venkatesh, Ashutosh K Pandey, et al.
Early Human Development
|
January 9, 2025
Predictive model of neurodevelopmental outcome in neonatal hypoxic ischemic encephalopathy
Amr I El Shahed, Helen M Branson, Anil Chacko, et al.
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of 18
Search research articles
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Showing results (141-150 of 178) with videos related to
Sort By:
Page
of 18
AJNR. American Journal of Neuroradiology
|
July 1, 2026
Comprehensive Structural MRI Phenotyping in <i>Oligophrenin 1-</i>Related Disorder Reveals Characteristic Brain Malformations
Asthik Biswas, Matthew T Whitehead, Parthiv Haldipur, et al.
Neuropediatrics
|
August 27, 2016
Update on Leukodystrophies: A Historical Perspective and Adapted Definition
Sietske H Kevelam, Marjan E Steenweg, Siddharth Srivastava, et al.
American Journal of Medical Genetics. Part A
|
May 16, 2012
Brain abnormalities in patients with Beckwith-Wiedemann syndrome
Kate Gardiner, David Chitayat, Sanaa Choufani, et al.
The Laryngoscope
|
June 28, 2016
Midline posterior glossectomy and lingual tonsillectomy in obese and nonobese children with down syndrome: Biomarkers for success
Evan J Propst, Reshma Amin, Natasha Talwar, et al.
Prenatal Diagnosis
|
December 12, 2018
Fetal myelomeningocele surgery: Only treating the tip of the iceberg
Alyaa AlRefai, James Drake, Abhaya V Kulkarni, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
April 15, 2019
Anticoagulation therapy and the risk of perioperative brain injury in neonates with congenital heart disease
Lara M Leijser, Vann Chau, Mike Seed, et al.
American Journal of Medical Genetics. Part A
|
July 9, 2011
Further expansion of the phenotypic spectrum associated with mutations in ALDH18A1, encoding Δ¹-pyrroline-5-carboxylate synthase (P5CS)
David L Skidmore, David Chitayat, Tim Morgan, et al.
Brain : a Journal of Neurology
|
October 1, 2010
Magnetic resonance imaging pattern recognition in hypomyelinating disorders
Marjan E Steenweg, Adeline Vanderver, Susan Blaser, et al.
Human Molecular Genetics
|
October 11, 2018
Bi-allelic mutations of LONP1 encoding the mitochondrial LonP1 protease cause pyruvate dehydrogenase deficiency and profound neurodegeneration with progressive cerebellar atrophy
Graeme A M Nimmo, Sundararajan Venkatesh, Ashutosh K Pandey, et al.
Early Human Development
|
January 9, 2025
Predictive model of neurodevelopmental outcome in neonatal hypoxic ischemic encephalopathy
Amr I El Shahed, Helen M Branson, Anil Chacko, et al.
Page
of 18