Keck School Faculty

Kathryn Moseley, MSRD
Kathryn Moseley, MSRD
Assistant Professor of Clinical Pediatrics
GLB 1-G24 1801 Marengo Street Off Campus Los Angeles
Kathryn Moseley is an Assistant Professor of Pediatrics at the University of Southern California, LAC+USC Medical Center in Los Angeles, California. She is a genetic metabolic dietitian and has participated in many research projects in the area of PKU. She did her undergraduate work at California State University Long Beach, Ca and received her Masters in Human Nutrition from the University of New Haven. She is currently on the Medical Advisory Board for the National PKU Alliance and the Dietitian's Advisory Board for BioMarin. She is the Public Policy Chair for the American Dietetic Association's Pediatric Nutrition Practice Group and is the President of the California Coalition for PKU nd Allied Disorders. She has had the great honor of working with and being mentored by Dr. Richard Koch, who is a pioneer in the area of PKU. She also has an adult daughter with PKU.

Stereotyping across intersections of race and age: Racial stereotyping among White adults working with children PLoS One. 2018; 13(9):e0201696. . View in PubMed

Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach Mol Genet Metab. 2016 06; 118(2):72-83. . View in PubMed

Evaluation of Tetrahydrobiopterin Therapy with Large Neutral Amino Acid Supplementation in Phenylketonuria: Effects on Potential Peripheral Biomarkers, Melatonin and Dopamine, for Brain Monoamine Neurotransmitters PLoS One. 2016; 11(8):e0160892. . View in PubMed

Pilot study to evaluate the effects of tetrahydrobiopterin on adult individuals with phenylketonuria with measurable maladaptive behaviors CNS Spectr. 2015 Apr; 20(2):157-63. . View in PubMed

Melatonin and dopamine as biomarkers to optimize treatment in phenylketonuria: effects of tryptophan and tyrosine supplementationJ Pediatr. 2014 Jul; 165(1):184-189. e1. . View in PubMed

Phenylketonuria Scientific Review Conference: state of the science and future research needs Mol Genet Metab. 2014 Jun; 112(2):87-122. . View in PubMed

Glycosaminoglycan metabolism defects and atherosclerosis: frequent association of endothelial dysfunction in patients with Mucopolysaccharidosis J Inherit Metab Dis. 2014 Mar; 37(2):255-61. . View in PubMed

Recommendations for the nutrition management of phenylalanine hydroxylase deficiency Genet Med. 2014 Feb; 16(2):121-31. . View in PubMed

Maternal Phenylketonuria International Collaborative Study revisited: evaluation of maternal nutritional risk factors besides phenylalanine for fetal congenital heart defects J Inherit Metab Dis. 2014 Jan; 37(1):39-42. . View in PubMed

Newborn screening 50 years later: access issues faced by adults with PKU Genet Med. 2013 Aug; 15(8):591-9. . View in PubMed

Large neutral amino acid supplementation increases melatonin synthesis in phenylketonuria: a new biomarker J Pediatr. 2013 May; 162(5):999-1003. . View in PubMed

Which sources of child health advice do parents follow? Clin Pediatr (Phila). 2011 Jan; 50(1):50-6.. View in PubMed

Steroid inhaler adherence, flu vaccine receipt, and race: associations with the quality of the parent-physician relationship for asthmatic children J Natl Med Assoc. 2009 May; 101(5):407-13. . View in PubMed

Creatine metabolism in combined methylmalonic aciduria and homocystinuria disease revisited Ann Neurol. 2009 Apr; 65(4):481-2; author reply 482-3. . View in PubMed

Measuring African-American parents' cultural mistrust while in a healthcare setting: a pilot study J Natl Med Assoc. 2007 Jan; 99(1):15-21. . View in PubMed

Primary care physicians' attitudes regarding follow-up care for children with positive newborn screening results Pediatrics. 2006 Nov; 118(5):1836-41. . View in PubMed

After Flexner: the challenge J Natl Med Assoc. 2006 Sep; 98(9):1430-1. . View in PubMed

Tetrahydrobiopterin and maternal PKU Mol Genet Metab. 2005 Dec; 86 Suppl 1:S139-41. . View in PubMed

End-of-life choices for African-American and white infants in a neonatal intensive-care unit: a pilot study J Natl Med Assoc. 2004 Jul; 96(7):933-7. . View in PubMed

Biopterin responsive phenylalanine hydroxylase deficiency Genet Med. 2004 Jan-Feb; 6(1):27-32. . View in PubMed

Brain phenylalanine concentrations in phenylketonuria: research and treatment of adults Pediatrics. 2003 Dec; 112(6 Pt 2):1575-9. . View in PubMed

Optic nerve atrophy in propionic acidemia Ophthalmology. 2003 Sep; 110(9):1850-4. . View in PubMed

Large neutral amino acid therapy and phenylketonuria: a promising approach to treatment Mol Genet Metab. 2003 Jun; 79(2):110-3. . View in PubMed

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