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Epilepsia|March 24, 2023
The presence and severity of epilepsy coincide with reduced γ-aminobutyrate and cortical excitatory markers in succinic semialdehyde dehydrogenase deficiencyItay Tokatly Latzer, Mariarita Bertoldi, Melissa L DiBacco, et al.Molecular Genetics and Metabolism|February 7, 2025
The neuropsychological profile of SSADH deficiency, a neurotransmitter disorder of GABA metabolismItay Tokatly Latzer, Ellen Hanson, Mariarita Bertoldi, et al.Journal of Clinical Medicine|April 23, 2022
Comparisons of Clinical Features and Outcomes of COVID-19 between Patients with Pediatric Onset Inflammatory Rheumatic Diseases and Healthy ChildrenFatih Haslak, Sevki Erdem Varol, Aybuke Gunalp, et al.The Journal of Experimental Medicine|July 9, 2026
Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosisDiana Olguín Calderón, Laura E Kilpatrick, Clément Conil, et al.Biorxiv : the Preprint Server for Biology|April 3, 2026
Homozygosity for rare or common hypomorphic IL23R variants confers a predisposition to tuberculosis in humansDiana Olguín Calderón, Laura E Kilpatrick, Clément Conil, et al.Frontiers in Pediatrics|May 31, 2021
Epidemiological, Clinical, and Laboratory Features of Children With COVID-19 in TurkeyAdem Karbuz, Gulsen Akkoc, Tugba Bedir Demirdag, et al.European Journal of Pediatrics|July 14, 2026
Clinical characteristics and predictors of severe pertussis in hospitalized children after the COVID-19 period in Türkiye: a multicenter studySevliya Ocal-Demir, Pınar Canizci Erdemli, Esra Cakmak Taskin, et al.Pageof 3