Publications by authors named "Kathryn C Chatfield"

17Publications

Alteration of cardiolipin biosynthesis and remodeling in single right ventricle congenital heart disease.

Am J Physiol Heart Circ Physiol 2020 04 14;318(4):H787-H800. Epub 2020 Feb 14.

Division of Cardiology, Department of Pediatrics, University of Colorado School of Medicine, Children's Hospital Colorado, Aurora, Colorado.

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http://dx.doi.org/10.1152/ajpheart.00494.2019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7191493PMC
April 2020

Cardiac transplantation in children with Noonan syndrome.

Pediatr Transplant 2019 09 1;23(6):e13535. Epub 2019 Jul 1.

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

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http://dx.doi.org/10.1111/petr.13535DOI Listing
September 2019

Costello syndrome: Clinical phenotype, genotype, and management guidelines.

Am J Med Genet A 2019 09 20;179(9):1725-1744. Epub 2019 Jun 20.

Division of Genomic Medicine, Department of Pediatrics, University of California Davis, Sacramento, California.

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http://dx.doi.org/10.1002/ajmg.a.61270DOI Listing
September 2019

Elamipretide Improves Mitochondrial Function in the Failing Human Heart.

JACC Basic Transl Sci 2019 Apr 29;4(2):147-157. Epub 2019 Apr 29.

Department of Medicine/Division of Cardiology, University of Colorado School of Medicine, Aurora, Colorado.

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http://dx.doi.org/10.1016/j.jacbts.2018.12.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488757PMC
April 2019

In-utero idiopathic ductal constriction: a prenatal manifestation of Alagille and Williams syndrome arteriopathy.

J Perinatol 2018 11 10;38(11):1453-1456. Epub 2018 Sep 10.

Section of Cardiology, Department of Pediatrics, Children's Hospital Colorado, The University of Colorado School of Medicine, Aurora, CO, USA.

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http://dx.doi.org/10.1038/s41372-018-0221-9DOI Listing
November 2018

Discovery of a potentially deleterious variant in TMEM87B in a patient with a hemizygous 2q13 microdeletion suggests a recessive condition characterized by congenital heart disease and restrictive cardiomyopathy.

Cold Spring Harb Mol Case Stud 2016 May;2(3):a000844

Department of Pediatrics, Section of Genetics, University of Colorado School of Medicine, Aurora, Colorado 80045, USA;; Colorado Intellectual and Developmental Disabilities Research Center (IDDRC), University of Colorado School of Medicine, Aurora, Colorado 80045, USA.

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http://dx.doi.org/10.1101/mcs.a000844DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853521PMC
May 2016

Genome-wide expression analysis in fibroblast cell lines from probands with Pallister Killian syndrome.

PLoS One 2014 16;9(10):e108853. Epub 2014 Oct 16.

The Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America; The Perelman School of Medicine at The University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0108853PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199614PMC
June 2015

Dysregulation of cardiolipin biosynthesis in pediatric heart failure.

J Mol Cell Cardiol 2014 Sep 14;74:251-9. Epub 2014 Jun 14.

Department of Medicine/Division of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA; Department of Integrative Physiology, University of Colorado, Boulder, CO, USA; Division of Cardiology, Denver Health Medical Center, Denver, CO, USA.

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http://dx.doi.org/10.1016/j.yjmcc.2014.06.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4114989PMC
September 2014

Congenital heart disease in Cornelia de Lange syndrome: phenotype and genotype analysis.

Am J Med Genet A 2012 Oct 10;158A(10):2499-505. Epub 2012 Sep 10.

Department of Pediatrics, Section of Pediatric Cardiology, The Children's Hospital of Colorado, Denver, USA.

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http://dx.doi.org/10.1002/ajmg.a.35582DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551981PMC
October 2012