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	1.	An 8-year-old girl with a history of stiff and painful joints. [electronic resource] by Raiman, Julian D'Aco, Kristin Producer: 20150512 In: Pediatric annals vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Clinical neurogenetics: neurologic presentations of metabolic disorders. [electronic resource] by Kwon, Jennifer M D'Aco, Kristin E Producer: 20140618 In: Neurologic clinics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutation in the mitochondrial tRNA(Val) causes mitochondrial encephalopathy, lactic acidosis and stroke-like episodes. [electronic resource] by Glatz, Catherine D'Aco, Kristin Smith, Sabrina Sondheimer, Neal Producer: 20110922 In: Mitochondrion vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	What is in the can? The dilemma with dietary supplements. [electronic resource] by D'Aco, Kristin Mooney, Robert Cusmano-Ozog, Kristina Hofherr, Sean Lichter-Konecki, Uta Producer: 20150716 In: Molecular genetics and metabolism vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Severe 5,10-methylenetetrahydrofolate reductase deficiency and two MTHFR variants in an adolescent with progressive myoclonic epilepsy. [electronic resource] by D'Aco, Kristin E Bearden, David Watkins, David Hyland, Keith Rosenblatt, David S Ficicioglu, Can Producer: 20151021 In: Pediatric neurology vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Mitochondrial tRNA(Phe) mutation as a cause of end-stage renal disease in childhood. [electronic resource] by D'Aco, Kristin E Manno, Megan Clarke, Colleen Ganesh, Jaya Meyers, Kevin E C Sondheimer, Neal Producer: 20130726 In: Pediatric nephrology (Berlin, Germany) vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Compound heterozygosity with a novel S222N GALT mutation leads to atypical galactosemia with loss of GALT activity in erythrocytes but little evidence of clinical disease. [electronic resource] by Cocanougher, Benjamin Aypar, Umut McDonald, Amber Hasadsri, Linda Bennett, Michael J Edward Highsmith, W D'Aco, Kristin Publication details: Molecular genetics and metabolism reports Mar 2015 In: Molecular genetics and metabolism reports vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Diagnosis and treatment trends in mucopolysaccharidosis I: findings from the MPS I Registry. [electronic resource] by D'Aco, Kristin Underhill, Lisa Rangachari, Lakshmi Arn, Pamela Cox, Gerald F Giugliani, Roberto Okuyama, Torayuki Wijburg, Frits Kaplan, Paige Producer: 20121017 In: European journal of pediatrics vol. 171 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome. [electronic resource] by DeSanto, Cori D'Aco, Kristin Araujo, Gabriel C Shannon, Nora Vernon, Hilary Rahrig, April Monaghan, Kristin G Niu, Zhiyv Vitazka, Patrik Dodd, Jonathan Tang, Sha Manwaring, Linda Martir-Negron, Arelis Schnur, Rhonda E Juusola, Jane Schroeder, Audrey Pan, Vivian Helbig, Katherine L Friedman, Bethany Shinawi, Marwan Producer: 20160801 In: Journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)