Faculty

Back to Index
Kathryn Moseley, MSRD
Assistant Professor of Clinical Pediatrics
Pediatrics
GLB 1-G24 1801 Marengo Street Off Campus Los Angeles
+1 323 226 3819

Overview

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.

Publications

Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach. Mol Genet Metab. 2016 Jun; 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 supplementation. J 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

Who counsels parents of newborns who are carriers of sickle cell anemia or cystic fibrosis? J Genet Couns. Who counsels parents of newborns who are carriers of sickle cell anemia or cystic fibrosis? J Genet Couns. 2013 Apr; 22(2):218-25. View in: PubMed

Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations. Clin Genet. 2011 Nov; 80(5):466-71. View in: PubMed

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

Maternal isovaleric acidemia: observation of distinctive changes in plasma amino acids and carnitine profiles during pregnancy. Clin Chim Acta. 2010 Dec 14; 411(23-24):2101-3. View in: PubMed

Postmortem studies on a patient with mucopolysaccharidosis type I: histopathological findings after one year of enzyme replacement therapy. J Inherit Metab Dis. 2009 Dec; 32 Suppl 1:S53-7. View in: PubMed

Long-term neurodevelopmental effects of early detection and treatment in a 6-year-old patient with argininaemia diagnosed by newborn screening. J Inherit Metab Dis. 2009 Dec; 32 Suppl 1:S197-200. 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

The Resource Mothers Study of Maternal Phenylketonuria: preliminary findings. J Inherit Metab Dis. 2004; 27(2):145-55. 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

Danger of high-protein dietary supplements to persons with hyperphenylalaninaemia. J Inherit Metab Dis. 2003; 26(4):339-42. View in: PubMed

Infantile mitochondrial DNA depletion syndrome associated with methylmalonic aciduria and 3-methylcrotonyl-CoA and propionyl-CoA carboxylase deficiencies in two unrelated patients: a new phenotype of mtDNA depletion syndrome. J Inherit Metab Dis. 2003; 26(5):481-8. View in: PubMed

Lipid status and long-chain polyunsaturated fatty acid concentrations in adults and adolescents with phenylketonuria on phenylalanine-restricted diet. J Inherit Metab Dis. 2002 Feb; 25(1):56-64. View in: PubMed

Brain phenylalanine concentration in the management of adults with phenylketonuria. J Inherit Metab Dis. 2000 Feb; 23(1):7-14. View in: PubMed

Long-term beneficial effects of the phenylalanine-restricted diet in late-diagnosed individuals with phenylketonuria. Mol Genet Metab. 1999 Jun; 67(2):148-55. View in: PubMed

Powered bySC CTSI