Kathryn Moseley, MSRD

Title(s)Assistant Professor of Clinical Pediatrics
AddressGLB 1-G24 1801 Marengo Street
Off Campus
Los Angeles CA 90033
Phone+1 323 226 3819
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    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.

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Stereotyping across intersections of race and age: Racial stereotyping among White adults working with children. PLoS One. 2018; 13(9):e0201696. Priest N, Slopen N, Woolford S, Philip JT, Singer D, Kauffman AD, Moseley K, Davis M, Ransome Y, Williams D. PMID: 30208023.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    2. Can untreated PKU patients escape from intellectual disability? A systematic review. Orphanet J Rare Dis. 2018 08 29; 13(1):149. van Vliet D, van Wegberg AMJ, Ahring K, Bik-Multanowski M, Blau N, Bulut FD, Casas K, Didycz B, Djordjevic M, Federico A, Feillet F, Gizewska M, Gramer G, Hertecant JL, Hollak CEM, Jørgensen JV, Karall D, Landau Y, Leuzzi V, Mathisen P, Moseley K, Mungan NÖ, Nardecchia F, Õunap K, Powell KK, Ramachandran R, Rutsch F, Setoodeh A, Stojiljkovic M, Trefz FK, Usurelu N, Wilson C, van Karnebeek CD, Hanley WB, van Spronsen FJ. PMID: 30157945.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    3. 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. PMID: 27513937.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    4. Updated, web-based nutrition management guideline for PKU: An evidence and consensus based approach. Mol Genet Metab. 2016 06; 118(2):72-83. PMID: 27211276.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    5. 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. PMID: 25323746.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    6. 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. PMID: 24857519.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    7. Phenylketonuria Scientific Review Conference: state of the science and future research needs. Mol Genet Metab. 2014 Jun; 112(2):87-122. PMID: 24667081.
      View in: PubMed   Mentions: 54     Fields:    Translation:Humans
    8. Recommendations for the nutrition management of phenylalanine hydroxylase deficiency. Genet Med. 2014 Feb; 16(2):121-31. PMID: 24385075.
      View in: PubMed   Mentions: 46     Fields:    Translation:Humans
    9. Glycosaminoglycan metabolism defects and atherosclerosis: frequent association of endothelial dysfunction in patients with Mucopolysaccharidosis. J Inherit Metab Dis. 2014 Mar; 37(2):255-61. PMID: 23893050.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    10. 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. PMID: 23784316.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    11. Newborn screening 50 years later: access issues faced by adults with PKU. Genet Med. 2013 Aug; 15(8):591-9. PMID: 23470838.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansPHPublic Health
    12. Large neutral amino acid supplementation increases melatonin synthesis in phenylketonuria: a new biomarker. J Pediatr. 2013 May; 162(5):999-1003. PMID: 23164313.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    13. 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. Yano S, Baskin B, Bagheri A, Watanabe Y, Moseley K, Nishimura A, Matsumoto N, Ray PN. PMID: 20950395.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    14. Which sources of child health advice do parents follow? Clin Pediatr (Phila). 2011 Jan; 50(1):50-6. Moseley KL, Freed GL, Goold SD. PMID: 20837618.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    15. 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. Castelnovi C, Moseley K, Yano S. PMID: 20807522.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    16. 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. Edwards RL, Moseley K, Watanabe Y, Wong LJ, Ottina J, Yano S. PMID: 19562505.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansPHPublic Health
    17. 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. Moseley KL, Hudson EJ. PMID: 19476193.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    18. Creatine metabolism in combined methylmalonic aciduria and homocystinuria disease revisited. Ann Neurol. 2009 Apr; 65(4):481-2; author reply 482-3. Younessi D, Moseley K, Yano S. PMID: 19399869.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    19. 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. Yano S, Moseley K, Pavlova Z. PMID: 19308670.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    20. Measuring African-American parents' cultural mistrust while in a healthcare setting: a pilot study. J Natl Med Assoc. 2007 Jan; 99(1):15-21. Moseley KL, Freed GL, Bullard CM, Goold SD. PMID: 17304964.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    21. Primary care physicians' attitudes regarding follow-up care for children with positive newborn screening results. Pediatrics. 2006 Nov; 118(5):1836-41. Kemper AR, Uren RL, Moseley KL, Clark SJ. PMID: 17079552.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansPHPublic Health
    22. After Flexner: the challenge. J Natl Med Assoc. 2006 Sep; 98(9):1430-1. Moseley KL. PMID: 17019908.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    23. Tetrahydrobiopterin and maternal PKU. Mol Genet Metab. 2005 Dec; 86 Suppl 1:S139-41. Koch R, Moseley K, Guttler F. PMID: 16338627.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansPHPublic Health
    24. 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. Moseley KL, Church A, Hempel B, Yuan H, Goold SD, Freed GL. PMID: 15253324.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    25. Biopterin responsive phenylalanine hydroxylase deficiency. Genet Med. 2004 Jan-Feb; 6(1):27-32. Matalon R, Koch R, Michals-Matalon K, Moseley K, Surendran S, Tyring S, Erlandsen H, Gamez A, Stevens RC, Romstad A, Møller LB, Guttler F. PMID: 14726806.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCTClinical Trials
    26. The Resource Mothers Study of Maternal Phenylketonuria: preliminary findings. J Inherit Metab Dis. 2004; 27(2):145-55. Rohr F, Munier A, Sullivan D, Bailey I, Gennaccaro M, Levy H, Brereton H, Gleason S, Goss B, Lesperance E, Moseley K, Singh R, Tonyes L, Vespa H, Waisbren S. PMID: 15159645.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCTClinical Trials
    27. Brain phenylalanine concentrations in phenylketonuria: research and treatment of adults. Pediatrics. 2003 Dec; 112(6 Pt 2):1575-9. Moats RA, Moseley KD, Koch R, Nelson M. PMID: 14654668.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCTClinical Trials
    28. Optic nerve atrophy in propionic acidemia. Ophthalmology. 2003 Sep; 110(9):1850-4. Ianchulev T, Kolin T, Moseley K, Sadun A. PMID: 13129889.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    29. Large neutral amino acid therapy and phenylketonuria: a promising approach to treatment. Mol Genet Metab. 2003 Jun; 79(2):110-3. Koch R, Moseley KD, Yano S, Nelson M, Moats RA. PMID: 12809641.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCTClinical Trials
    30. 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. Yano S, Li L, Le TP, Moseley K, Guedalia A, Lee J, Gonzalez I, Boles RG. PMID: 14518828.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    31. Danger of high-protein dietary supplements to persons with hyperphenylalaninaemia. J Inherit Metab Dis. 2003; 26(4):339-42. Koch R, Moseley KD, Moats R, Yano S, Matalon R, Guttler F. PMID: 12971421.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    32. 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. Moseley K, Koch R, Moser AB. PMID: 11999981.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    33. Brain phenylalanine concentration in the management of adults with phenylketonuria. J Inherit Metab Dis. 2000 Feb; 23(1):7-14. Moats RA, Koch R, Moseley K, Guldberg P, Guttler F, Boles RG, Nelson MD. PMID: 10682303.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    34. Long-term beneficial effects of the phenylalanine-restricted diet in late-diagnosed individuals with phenylketonuria. Mol Genet Metab. 1999 Jun; 67(2):148-55. Koch R, Moseley K, Ning J, Romstad A, Guldberg P, Guttler F. PMID: 10356314.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
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