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Annals of Neurology|October 22, 2005
Status epilepticus in mice deficient for succinate semialdehyde dehydrogenase: GABAA receptor-mediated mechanismsYing Wu, Andrea Buzzi, Marina Frantseva, et al.
Molecular Genetics and Metabolism|September 5, 2002
Structure of human succinic semialdehyde dehydrogenase gene: identification of promoter region and alternatively processed isoformsPaola Blasi, Pietro Pilo Boyl, Mario Ledda, et al.
Biophysical Journal|February 1, 2023
Allosteric modulation of α1β3γ2 GABA<sub>A</sub> receptors by farnesol through the neurosteroid sitesJeevan B Gc, Christopher T Szlenk, Ayobami Diyaolu, et al.
Biological Psychiatry|September 27, 2003
Significant behavioral disturbances in succinic semialdehyde dehydrogenase (SSADH) deficiency (gamma-hydroxybutyric aciduria)K Michael Gibson, Maneesh Gupta, Phillip L Pearl, et al.
Journal of Inherited Metabolic Disease|February 21, 2018
Succinic semialdehyde dehydrogenase deficiency, a disorder of GABA metabolism: an update on pharmacological and enzyme-replacement therapeutic strategiesKara R Vogel, Garrett R Ainslie, Dana C Walters, et al.
Neurology|February 14, 2014
Taurine trial in succinic semialdehyde dehydrogenase deficiency and elevated CNS GABAPhillip L Pearl, John Schreiber, William H Theodore, et al.
Pediatrics|February 4, 2003
Mevalonate kinase deficiency: enlarging the clinical and biochemical spectrumViola Prietsch, Ertan Mayatepek, Hermann Krastel, et al.
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