Publications by authors named "Curtis R Coughlin"

42Publications

Development and application of an ethical framework for pediatric metabolic and bariatric surgery evaluation.

Surg Obes Relat Dis 2021 Feb 16;17(2):425-433. Epub 2020 Sep 16.

Department of Pediatrics, Section of Nutrition, University of Colorado School of Medicine, Children's Hospital Colorado, Aurora, Colorado.

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February 2021

Abnormal expression of GABA receptor subunits and hypomotility upon loss of in zebrafish.

Biol Open 2020 04 13;9(4). Epub 2020 Apr 13.

Department of Biological Sciences, Border Biomedical Research Center, University of Texas El Paso, El Paso, TX 79968, USA

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April 2020

Pyridoxine-dependent epilepsy is more than just epilepsy.

Dev Med Child Neurol 2020 03 25;62(3):268. Epub 2019 Nov 25.

Section of Clinical Genetics and Metabolism, Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

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March 2020

Genetic Testing: Consent and Result Disclosure for Primary Care Providers.

Med Clin North Am 2019 Nov 20;103(6):967-976. Epub 2019 Aug 20.

Department of Pediatrics, Section of Genetics, University of Colorado Anschutz Medical Campus, East 17th Avenue, Aurora, CO 80045, USA.

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November 2019

Brain imaging in classic nonketotic hyperglycinemia: Quantitative analysis and relation to phenotype.

J Inherit Metab Dis 2019 05 20;42(3):438-450. Epub 2019 Mar 20.

Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado, Aurora, Colorado.

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May 2019

Identification of a novel biomarker for pyridoxine-dependent epilepsy: Implications for newborn screening.

J Inherit Metab Dis 2019 05 11;42(3):565-574. Epub 2019 Mar 11.

Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, Colorado.

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May 2019

Comment on Late-Onset Nonketotic Hyperglycinemia With a Heterozygous Novel Point Mutation of the GLDC Gene.

Pediatr Neurol 2018 02 28;79:e1. Epub 2017 Sep 28.

Department of Pediatrics, Section of Clinical Genetics and Metabolism, University of Colorado School of Medicine, Aurora, CO 80045, USA.. Electronic address:

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February 2018

Lethal neonatal hyperammonemia in severe ornithine transcarbamylase (OTC) deficiency compounded by large hepatic portosystemic shunt.

J Inherit Metab Dis 2017 01 10;40(1):159-160. Epub 2016 Nov 10.

Division of Clinical Genetics and Metabolism, Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO, USA.

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January 2017