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European Journal of Medicinal Chemistry|March 15, 2011
A new class of β-carboline alkaloid-peptide conjugates with therapeutic efficacy in acute limb ischemia/reperfusion injuryWei Bi, Yue Bi, Ping Xue, et al.
Journal of Inherited Metabolic Disease|January 7, 2010
A new case of GABA transaminase deficiency facilitated by proton MR spectroscopyMegumi Tsuji, Noriko Aida, Takayuki Obata, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|May 14, 2009
Hepatocyte transplantation improves phenotype and extends survival in a murine model of intermediate maple syrup urine diseaseKristen J Skvorak, Harbhajan S Paul, Kenneth Dorko, et al.
Journal of Child Neurology|August 31, 2021
Development of a Quality-of-Life Survey for Patients With Succinic Semialdehyde Dehydrogenase Deficiency, a Rare Disorder of GABA MetabolismMousumi Bose, Jean-Baptiste Roullet, K Michael Gibson, et al.
Molecular Genetics and Metabolism Reports|March 1, 2019
Emotional experience in parents of children with Zellweger spectrum disorders: A qualitative studyMousumi Bose, Meena Mahadevan, Dana R Schules, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 18, 2002
Therapeutic intervention in mice deficient for succinate semialdehyde dehydrogenase (gamma-hydroxybutyric aciduria)Maneesh Gupta, Rachel Greven, Erwin E W Jansen, et al.
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