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Cureus
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July 18, 2022
A Comparison of Pathogenic Eukaryotic Elongation Factor 2 (EEF2) Variants in Spinocerebellar Ataxia 26 Versus De Novo Mutations
Hongfei Zhao, Nikolas Mata-Machado
Frontiers in Child and Adolescent Psychiatry
|
March 23, 2026
Gabapentin may promote language development in a pediatric patient with autism spectrum disorder: a case report
Tobias Kremsmayer, Robert Blakey, Hugo Hidrogo, et al.
Current Neurology and Neuroscience Reports
|
January 14, 2016
Neurocutaneous Disorders for the Practicing Neurologist: a Focused Review
Anna Carolina Paiva Costa T Figueiredo, Nikolas Mata-Machado, Matthew McCoyd, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences
|
July 10, 2012
A multidisciplinary approach to the treatment of anti-NMDA-receptor antibody encephalitis: a case and review of the literature
Andrea Mann, Nikolas Mata Machado, Ni Liu, et al.
Human Genome Variation
|
December 10, 2020
A novel TSC1 variant associated with tuberous sclerosis and sacrococcygeal teratoma
Saba Ahmad, Luis Manon, Gifty Bhat, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Cureus
|
July 18, 2022
A Comparison of Pathogenic Eukaryotic Elongation Factor 2 (EEF2) Variants in Spinocerebellar Ataxia 26 Versus De Novo Mutations
Hongfei Zhao, Nikolas Mata-Machado
Frontiers in Child and Adolescent Psychiatry
|
March 23, 2026
Gabapentin may promote language development in a pediatric patient with autism spectrum disorder: a case report
Tobias Kremsmayer, Robert Blakey, Hugo Hidrogo, et al.
Current Neurology and Neuroscience Reports
|
January 14, 2016
Neurocutaneous Disorders for the Practicing Neurologist: a Focused Review
Anna Carolina Paiva Costa T Figueiredo, Nikolas Mata-Machado, Matthew McCoyd, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences
|
July 10, 2012
A multidisciplinary approach to the treatment of anti-NMDA-receptor antibody encephalitis: a case and review of the literature
Andrea Mann, Nikolas Mata Machado, Ni Liu, et al.
Human Genome Variation
|
December 10, 2020
A novel TSC1 variant associated with tuberous sclerosis and sacrococcygeal teratoma
Saba Ahmad, Luis Manon, Gifty Bhat, et al.
Page
of 1