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Reem A Alkhater

Showing results (1-10 of 6) with videos related to

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Annals of Clinical and Translational Neurology|November 24, 2020
SUCLA2 Arg407Trp mutation can cause a nonprogressive movement disorder - deafness syndromeReem A Alkhater, Saija Ahonen, Berge A Minassian
The New England Journal of Medicine|February 1, 2013
Brain dopamine-serotonin vesicular transport disease and its treatmentJennifer J Rilstone, Reem A Alkhater, Berge A Minassian
Annals of Clinical and Translational Neurology|December 20, 2018
<i>PI4K2A</i> deficiency in an intellectual disability, epilepsy, myoclonus, akathisia syndromeReem A Alkhater, Stephen W Scherer, Berge A Minassian, et al.
Annals of Clinical and Translational Neurology|February 23, 2024
Parkinsonism-dystonia-2: Case-series study from Saudi ArabiaMohammed A Almuqbil, Sadia Tabassum, Osama Y Muthaffar, et al.
Annals of Clinical and Translational Neurology|April 26, 2019
Dominant <i>LMAN2L</i> mutation causes intellectual disability with remitting epilepsyReem A Alkhater, Peixiang Wang, Alessandra Ruggieri, et al.
Nature Communications|November 24, 2020
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial diseasePhilipp Gut, Sanna Matilainen, Jesse G Meyer, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Annals of Clinical and Translational Neurology|November 24, 2020
SUCLA2 Arg407Trp mutation can cause a nonprogressive movement disorder - deafness syndromeReem A Alkhater, Saija Ahonen, Berge A Minassian
The New England Journal of Medicine|February 1, 2013
Brain dopamine-serotonin vesicular transport disease and its treatmentJennifer J Rilstone, Reem A Alkhater, Berge A Minassian
Annals of Clinical and Translational Neurology|December 20, 2018
<i>PI4K2A</i> deficiency in an intellectual disability, epilepsy, myoclonus, akathisia syndromeReem A Alkhater, Stephen W Scherer, Berge A Minassian, et al.
Annals of Clinical and Translational Neurology|February 23, 2024
Parkinsonism-dystonia-2: Case-series study from Saudi ArabiaMohammed A Almuqbil, Sadia Tabassum, Osama Y Muthaffar, et al.
Annals of Clinical and Translational Neurology|April 26, 2019
Dominant <i>LMAN2L</i> mutation causes intellectual disability with remitting epilepsyReem A Alkhater, Peixiang Wang, Alessandra Ruggieri, et al.
Nature Communications|November 24, 2020
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial diseasePhilipp Gut, Sanna Matilainen, Jesse G Meyer, et al.
Pageof 1