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Pediatric Radiology
|
February 12, 2025
Overview of neuroimaging in primary mitochondrial disorders
Sedat Giray Kandemirli, Khalid Al-Dasuqi, Bulent Aslan, et al.
Pediatric Radiology
|
January 5, 2023
Magnetic resonance imaging protocols in pediatric stroke
Susan T Sotardi, Cesar Augusto P F Alves, Suraj D Serai, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
October 31, 2019
Brain abnormalities in myelomeningocele patients
Bárbara Albuquerque Morais, Davi Jorge Fontoura Solla, Vitor Nagai Yamaki, et al.
Neuroradiology
|
April 22, 2022
Spinal involvement in pediatric familial cavernous malformation syndrome
Ana Filipa Geraldo, Aysha Luis, Cesar Augusto P F Alves, et al.
Neuroradiology
|
October 5, 2022
Natural history of familial cerebral cavernous malformation syndrome in children: a multicenter cohort study
Ana Filipa Geraldo, Cesar Augusto P F Alves, Aysha Luis, et al.
AJNR. American Journal of Neuroradiology
|
September 29, 2025
Neuroimaging Findings in Carbonic Anhydrase VA Deficiency: A Case Series Highlighting Diagnostic and Prognostic Patterns in a Potentially Reversible Mitochondrial Dysfunction
Diego Cardoso Fragoso, Eiman Al-Ajmi, Agustin M Cardenas, et al.
Molecular Genetics and Metabolism Reports
|
November 24, 2022
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature
Jessica R C Priestley, Lisa M Pace, Kuntal Sen, et al.
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Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Pediatric Radiology
|
February 12, 2025
Overview of neuroimaging in primary mitochondrial disorders
Sedat Giray Kandemirli, Khalid Al-Dasuqi, Bulent Aslan, et al.
Pediatric Radiology
|
January 5, 2023
Magnetic resonance imaging protocols in pediatric stroke
Susan T Sotardi, Cesar Augusto P F Alves, Suraj D Serai, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
October 31, 2019
Brain abnormalities in myelomeningocele patients
Bárbara Albuquerque Morais, Davi Jorge Fontoura Solla, Vitor Nagai Yamaki, et al.
Neuroradiology
|
April 22, 2022
Spinal involvement in pediatric familial cavernous malformation syndrome
Ana Filipa Geraldo, Aysha Luis, Cesar Augusto P F Alves, et al.
Neuroradiology
|
October 5, 2022
Natural history of familial cerebral cavernous malformation syndrome in children: a multicenter cohort study
Ana Filipa Geraldo, Cesar Augusto P F Alves, Aysha Luis, et al.
AJNR. American Journal of Neuroradiology
|
September 29, 2025
Neuroimaging Findings in Carbonic Anhydrase VA Deficiency: A Case Series Highlighting Diagnostic and Prognostic Patterns in a Potentially Reversible Mitochondrial Dysfunction
Diego Cardoso Fragoso, Eiman Al-Ajmi, Agustin M Cardenas, et al.
Molecular Genetics and Metabolism Reports
|
November 24, 2022
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature
Jessica R C Priestley, Lisa M Pace, Kuntal Sen, et al.
Page
of 1