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Kathryn Moseley, MSRD

TitleAssistant Professor of Clinical Pediatrics
InstitutionUniversity of Southern California
DepartmentPediatrics
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.
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    1. Yano S, Moseley K, Fu X, Azen C. 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; PMCID: PMC4981358.
      View in: PubMed, PubMed Central
    2. Moseley K, Ottina MJ, Azen CG, Yano S. 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
    3. Yano S, Moseley K, Azen C. 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
    4. Camp KM, Parisi MA, Acosta PB, Berry GT, Bilder DA, Blau N, Bodamer OA, Brosco JP, Brown CS, Burlina AB, Burton BK, Chang CS, Coates PM, Cunningham AC, Dobrowolski SF, Ferguson JH, Franklin TD, Frazier DM, Grange DK, Greene CL, Groft SC, Harding CO, Howell RR, Huntington KL, Hyatt-Knorr HD, Jevaji IP, Levy HL, Lichter-Konecki U, Lindegren ML, Lloyd-Puryear MA, Matalon K, MacDonald A, McPheeters ML, Mitchell JJ, Mofidi S, Moseley K, Mueller CM, Mulberg AE, Nerurkar LS, Ogata BN, Pariser AR, Prasad S, Pridjian G, Rasmussen SA, Reddy UM, Rohr FJ, Singh RH, Sirrs SM, Stremer SE, Tagle DA, Thompson SM, Urv TK, Utz JR, van Spronsen F, Vockley J, Waisbren SE, Weglicki LS, White DA, Whitley CB, Wilfond BS, Yannicelli S, Young JM. 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
    5. Singh RH, Rohr F, Frazier D, Cunningham A, Mofidi S, Ogata B, Splett PL, Moseley K, Huntington K, Acosta PB, Vockley J, Van Calcar SC. Recommendations for the nutrition management of phenylalanine hydroxylase deficiency. Genet Med. 2014 Feb; 16(2):121-31. PMID: 24385075; PMCID: PMC3918542.
      View in: PubMed, PubMed Central
    6. Yano S, Moseley K, Wong L, Castelnovi C, Azen C, Pavlova Z. 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
    7. Yano S, Moseley K, Bottiglieri T, Arning E, Azen C. 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
    8. Berry SA, Brown C, Grant M, Greene CL, Jurecki E, Koch J, Moseley K, Suter R, van Calcar SC, Wiles J, Cederbaum S. Newborn screening 50 years later: access issues faced by adults with PKU. Genet Med. 2013 Aug; 15(8):591-9. PMID: 23470838; PMCID: PMC3938172.
      View in: PubMed, PubMed Central
    9. Yano S, Moseley K, Azen C. 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
    10. Moseley K, Freed GL, Goold SD. Which sources of child health advice do parents follow? Clin Pediatr (Phila). 2011 Jan; 50(1):50-6. PMID: 20837618.
      View in: PubMed
    11. Moseley K, Hudson EJ. 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. PMID: 19476193.
      View in: PubMed
    12. Younessi D, Moseley K, Yano S. Creatine metabolism in combined methylmalonic aciduria and homocystinuria disease revisited. Ann Neurol. 2009 Apr; 65(4):481-2; author reply 482-3. PMID: 19399869.
      View in: PubMed
    13. Moseley K, Freed GL, Bullard CM, Goold SD. Measuring African-American parents' cultural mistrust while in a healthcare setting: a pilot study. J Natl Med Assoc. 2007 Jan; 99(1):15-21. PMID: 17304964; PMCID: PMC2569607.
      View in: PubMed, PubMed Central
    14. Kemper AR, Uren RL, Moseley K, Clark SJ. Primary care physicians' attitudes regarding follow-up care for children with positive newborn screening results. Pediatrics. 2006 Nov; 118(5):1836-41. PMID: 17079552.
      View in: PubMed
    15. Moseley K. After Flexner: the challenge. J Natl Med Assoc. 2006 Sep; 98(9):1430-1. PMID: 17019908; PMCID: PMC2569731.
      View in: PubMed, PubMed Central
    16. Koch R, Moseley K, Guttler F. Tetrahydrobiopterin and maternal PKU. Mol Genet Metab. 2005 Dec; 86 Suppl 1:S139-41. PMID: 16338627.
      View in: PubMed
    17. Moseley K, Church A, Hempel B, Yuan H, Goold SD, Freed GL. 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. PMID: 15253324; PMCID: PMC2568418.
      View in: PubMed, PubMed Central
    18. 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. Biopterin responsive phenylalanine hydroxylase deficiency. Genet Med. 2004 Jan-Feb; 6(1):27-32. PMID: 14726806.
      View in: PubMed
    19. Moats RA, Moseley K, Koch R, Nelson M. Brain phenylalanine concentrations in phenylketonuria: research and treatment of adults. Pediatrics. 2003 Dec; 112(6 Pt 2):1575-9. PMID: 14654668.
      View in: PubMed
    20. Ianchulev T, Kolin T, Moseley K, Sadun A. Optic nerve atrophy in propionic acidemia. Ophthalmology. 2003 Sep; 110(9):1850-4. PMID: 13129889.
      View in: PubMed
    21. Koch R, Moseley K, Yano S, Nelson M, Moats RA. Large neutral amino acid therapy and phenylketonuria: a promising approach to treatment. Mol Genet Metab. 2003 Jun; 79(2):110-3. PMID: 12809641.
      View in: PubMed
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