Nancy Leslie

Nancy Leslie

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Nancy Leslie

Nancy Leslie

Publications by authors named "Nancy Leslie"

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Acquired ornithine transcarbamylase deficiency in pediatric and adolescent patients with fibrolamellar hepatocellular carcinoma.

Pediatr Blood Cancer 2018 12 9;65(12):e27392. Epub 2018 Aug 9.

Division of Pediatric Oncology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

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http://dx.doi.org/10.1002/pbc.27392DOI Listing
December 2018

Bilateral cataracts in a 6-yr-old with new onset diabetes: a novel presentation of a known INS gene mutation.

Pediatr Diabetes 2016 11 4;17(7):535-539. Epub 2015 Nov 4.

Division of Endocrinology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

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http://dx.doi.org/10.1111/pedi.12335DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854816PMC
November 2016

Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules.

Hum Pathol 2016 Mar 28;49:27-32. Epub 2015 Oct 28.

Divisions of Human Genetics, Gastroenterology, and Pathology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229. Electronic address:

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http://dx.doi.org/10.1016/j.humpath.2015.09.039DOI Listing
March 2016

Prolonged QTc interval in association with medium-chain acyl-coenzyme A dehydrogenase deficiency.

Pediatrics 2014 Jun 5;133(6):e1781-6. Epub 2014 May 5.

Perinatal Institute, Division of Neonatology;Department of Pediatrics; and

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http://dx.doi.org/10.1542/peds.2013-1105DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4035587PMC
June 2014

Recurrent pancreatitis in ornithine transcarbamylase deficiency.

Mol Genet Metab 2012 Aug 15;106(4):482-4. Epub 2012 Jun 15.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, USA.

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http://dx.doi.org/10.1016/j.ymgme.2012.06.005DOI Listing
August 2012

Malonyl coenzyme A decarboxylase deficiency: early dietary restriction and time course of cardiomyopathy.

Pediatrics 2012 Aug 9;130(2):e456-60. Epub 2012 Jul 9.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, 3333 Burnet Ave, MLC 4006, Cincinnati, OH 45229, USA.

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http://dx.doi.org/10.1542/peds.2011-2927DOI Listing
August 2012

Cardiac disease in methylmalonic acidemia.

J Pediatr 2011 Nov 23;159(5):862-4. Epub 2011 Jul 23.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA.

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http://dx.doi.org/10.1016/j.jpeds.2011.06.005DOI Listing
November 2011

The effects of gestational age and birth weight on false-positive newborn-screening rates.

Pediatrics 2010 Nov 25;126(5):910-6. Epub 2010 Oct 25.

Cincinnati Children's Hospital Medical Center, Division of Neonatology, University of Cincinnati College of Medicine, 3333 Burnet Ave, Cincinnati, OH 45229-3039, USA.

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http://pediatrics.aappublications.org/cgi/doi/10.1542/peds.2
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http://dx.doi.org/10.1542/peds.2010-0943DOI Listing
November 2010

C-Reactive protein, a valuable predictive marker in chronic kidney disease.

Saudi J Kidney Dis Transpl 2009 Sep;20(5):811-5

Department of Internal Medicine, Sri Ramachandra Medical College and Research Institute, Porur, Chennai, Tamil Nadu, India.

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September 2009

A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24-2q31.

Mov Disord 2009 Feb;24(3):364-70

Division of Neurology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati School of Medicine, Cincinnati, Ohio 45229-3039, USA.

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http://dx.doi.org/10.1002/mds.22363DOI Listing
February 2009

Review of the use of idursulfase in the treatment of mucopolysaccharidosis II.

Biologics 2008 Jun;2(2):311-20

The Division of Human Genetics, Cincinnati Children's Hospital Medical Center, and the Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2721351PMC
June 2008

Prolactin signaling through the short form of its receptor represses forkhead transcription factor FOXO3 and its target gene galt causing a severe ovarian defect.

Mol Endocrinol 2008 Feb 1;22(2):513-22. Epub 2007 Nov 1.

Department of Physiology and Biophysics, College of Medicine, University of Illinois at Chicago, 835 South Wolcott, M/C 901, Chicago, IL 60612, USA.

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http://dx.doi.org/10.1210/me.2007-0399DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2234584PMC
February 2008

Enzyme reconstitution/replacement therapy for lysosomal storage diseases.

Curr Opin Pediatr 2007 Dec;19(6):628-35

Division of Human Genetics, Cincinnati Children's Hospital Medical Center and the Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio 45229-3039, USA.

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http://pdfs.journals.lww.com/co-pediatrics/2007/12000/Enzyme
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http://dx.doi.org/10.1097/MOP.0b013e3282f161f2DOI Listing
December 2007

Correlation of anemia, secondary hyperparathyroidism with left ventricular hypertrophy in Chronic Kidney Disease patients.

J Assoc Physicians India 2006 Sep;54:699-703

Department of Medicine, Madras Medical Mission, Chennai.

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September 2006

An updated review of the long-term neurological effects of galactosemia.

Pediatr Neurol 2005 Sep;33(3):153-61

University of Cincinnati School of Medicine, Cincinnati, Ohio, USA.

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http://dx.doi.org/10.1016/j.pediatrneurol.2005.02.015DOI Listing
September 2005

UDP-galactose pyrophosphorylase in mice with galactose-1-phosphate uridyltransferase deficiency.

Mol Genet Metab 2005 May 23;85(1):21-7. Epub 2005 Feb 23.

Division of Human Genetics, Cincinnati Children's Hospital Research Foundation, Cincinnati, OH 45229, USA.

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http://dx.doi.org/10.1016/j.ymgme.2005.01.004DOI Listing
May 2005

Undetectable maternal serum uE3 and postnatal abnormal sterol and steroid metabolism in Antley-Bixler syndrome.

Am J Med Genet A 2004 Aug;129A(1):1-7

Cincinnati Children's Hospital Medical Center, Division of Human Genetics, Cincinnati, Ohio 45229, USA.

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http://dx.doi.org/10.1002/ajmg.a.30170DOI Listing
August 2004

Galactitol and galactonate accumulation in heart and skeletal muscle of mice with deficiency of galactose-1-phosphate uridyltransferase.

Mol Genet Metab 2004 Feb;81(2):105-11

Metabolic Research Laboratory, The Children's Hospital of Philadelphia, and the Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.

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February 2004

Insights into the pathogenesis of galactosemia.

Authors:
Nancy D Leslie

Annu Rev Nutr 2003 9;23:59-80. Epub 2003 Apr 9.

Division of Human Genetics, Cincinnati Children's Hospital Research Foundation, 3333 Burnet Avenue, Cincinnati, Ohio 45229, USA.

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http://dx.doi.org/10.1146/annurev.nutr.23.011702.073135DOI Listing
November 2003