Search Results - "Dhammi, Navjot"

A case of severe acidosis in a 12-month-old: Succinyl-CoA:3-ketoacid-CoA transferase deficiency with OXCT1 gene mutations by Dhammi, Navjot, Essakow, Jenna, Gallagher, Renata, Gaw, Cynthia

“…Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency is a rare autosomal recessive disorder that results in severe ketoacidosis due to a defect in ketone…”
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A case of severe acidosis in a 12-month-old: Succinyl-CoA:3-ketoacidCoA transferase deficiency with gene mutations by Navjot Dhammi, Jenna Essakow, Renata Gallagher, Cynthia Gaw

“…Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency is a rare autosomal recessive disorder that results in severe ketoacidosis due to a defect in ketone…”
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The PREEMPT study - evaluating smartphone-assisted n-of-1 trials in patients with chronic pain: study protocol for a randomized controlled trial by Barr, Colin, Marois, Maria, Sim, Ida, Schmid, Christopher H, Wilsey, Barth, Ward, Deborah, Duan, Naihua, Hays, Ron D, Selsky, Joshua, Servadio, Joseph, Schwartz, Marc, Dsouza, Clyde, Dhammi, Navjot, Holt, Zachary, Baquero, Victor, MacDonald, Scott, Jerant, Anthony, Sprinkle, Ron, Kravitz, Richard L

“…Chronic pain is prevalent, costly, and clinically vexatious. Clinicians typically use a trial-and-error approach to treatment selection. Repeated crossover…”
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A case of severe acidosis in a 12-month-old: Succinyl-CoA:3-ketoacid-CoA transferase deficiency with OXCT1 gene mutations by Dhammi, Navjot, Essakow, Jenna, Gallagher, Renata, Gaw, Cynthia

Get full text