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Showing results (41-50 of 46) with videos related to

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Acta Anaesthesiologica Scandinavica|January 21, 2012
Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndromeA V Vanlander, P G Jorens, J Smet, et al.
Neurology|September 30, 2010
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutationsL Deprez, S Weckhuysen, P Holmgren, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 19, 2009
Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>CB Dermaut, S Seneca, L Dom, et al.
Nature Communications|November 21, 2019
Author Correction: A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutationS J Tavernier, V Athanasopoulos, P Verloo, et al.
Nature Communications|October 23, 2019
A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutationS J Tavernier, V Athanasopoulos, P Verloo, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathiesLorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
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Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Acta Anaesthesiologica Scandinavica|January 21, 2012
Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndromeA V Vanlander, P G Jorens, J Smet, et al.
Neurology|September 30, 2010
Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutationsL Deprez, S Weckhuysen, P Holmgren, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 19, 2009
Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>CB Dermaut, S Seneca, L Dom, et al.
Nature Communications|November 21, 2019
Author Correction: A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutationS J Tavernier, V Athanasopoulos, P Verloo, et al.
Nature Communications|October 23, 2019
A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutationS J Tavernier, V Athanasopoulos, P Verloo, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathiesLorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
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