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Artificial Intelligence in Medicine|April 26, 2023
Enriching representation learning using 53 million patient notes through human phenotype ontology embeddingMaryam Daniali, Peter D Galer, David Lewis-Smith, et al.
Developmental Medicine and Child Neurology|May 6, 2022
Visits of concern in child neurology telemedicineMarisa Prelack, Sara Fridinger, Alexander K Gonzalez, et al.
Nature Communications|March 12, 2021
Microtubules orchestrate local translation to enable cardiac growthEmily A Scarborough, Keita Uchida, Maria Vogel, et al.
Basic Research in Cardiology|August 25, 2022
Extracellular stiffness induces contractile dysfunction in adult cardiomyocytes via cell-autonomous and microtubule-dependent mechanismsAlexia Vite, Matthew A Caporizzo, Elise A Corbin, et al.
Genome Biology|July 7, 2025
Conserved missense variant pathogenicity and correlated phenotypes across paralogous genesTobias Brünger, Alina Ivaniuk, Eduardo Pérez-Palma, et al.
Annals of Clinical and Translational Neurology|May 23, 2026
White Matter Microstructural Abnormalities in Neonatal Onset Genetic EpilepsyAmanda G Sandoval Karamian, Tianjia Zhu, Hao Huang, et al.
Frontiers in Neurology|April 20, 2023
Investigating the genetic contribution in febrile infection-related epilepsy syndrome and refractory status epilepticusDanielle deCampo, Julie Xian, Alexis Karlin, et al.
Epilepsia|November 11, 2025
Clinical trajectories and medication response in TBC1D24-related epilepsiesEaling Mondragon, Jan H Magielski, Bintou Bane, et al.
Epilepsia|January 28, 2016
Seizures as presenting and prominent symptom in chorea-acanthocytosis with c.2343del VPS13A gene mutationFelix Benninger, Zaid Afawi, Amos D Korczyn, et al.
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