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Kathryn Moseley, MSRD

Title(s)Assistant Professor of Clinical Pediatrics
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. Priest N, Slopen N, Woolford S, Philip JT, Singer D, Kauffman AD, Moseley K, Davis M, Ransome Y, Williams D. Stereotyping across intersections of race and age: Racial stereotyping among White adults working with children. PLoS One. 2018; 13(9):e0201696. PMID: 30208023.
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    2. 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. Can untreated PKU patients escape from intellectual disability? A systematic review. Orphanet J Rare Dis. 2018 08 29; 13(1):149. PMID: 30157945.
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    3. 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.
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    4. Singh RH, Cunningham AC, Mofidi S, Douglas TD, Frazier DM, Hook DG, Jeffers L, McCune H, Moseley KD, Ogata B, Pendyal S, Skrabal J, Splett PL, Stembridge A, Wessel A, Rohr F. 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.
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    5. Moseley KD, 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.
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    6. 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.
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    7. 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 KD, 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.
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    8. 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.
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    9. 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.
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    10. 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.
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    11. 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.
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    12. 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.
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    13. Yano S, Baskin B, Bagheri A, Watanabe Y, Moseley K, Nishimura A, Matsumoto N, Ray PN. 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. PMID: 20950395.
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    14. Moseley KL, Freed GL, Goold SD. Which sources of child health advice do parents follow? Clin Pediatr (Phila). 2011 Jan; 50(1):50-6. PMID: 20837618.
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    15. Castelnovi C, Moseley K, Yano S. 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. PMID: 20807522.
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    16. Edwards RL, Moseley K, Watanabe Y, Wong LJ, Ottina J, Yano S. 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. PMID: 19562505.
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    17. Moseley KL, 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.
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    18. 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.
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    19. Yano S, Moseley K, Pavlova Z. 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. PMID: 19308670.
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    20. Moseley KL, 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.
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    21. Kemper AR, Uren RL, Moseley KL, 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.
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    22. Moseley KL. After Flexner: the challenge. J Natl Med Assoc. 2006 Sep; 98(9):1430-1. PMID: 17019908.
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    23. Koch R, Moseley K, Guttler F. Tetrahydrobiopterin and maternal PKU. Mol Genet Metab. 2005 Dec; 86 Suppl 1:S139-41. PMID: 16338627.
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    24. Moseley KL, 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.
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    25. 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.
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    26. 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. The Resource Mothers Study of Maternal Phenylketonuria: preliminary findings. J Inherit Metab Dis. 2004; 27(2):145-55. PMID: 15159645.
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    27. Moats RA, Moseley KD, 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.
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    28. Ianchulev T, Kolin T, Moseley K, Sadun A. Optic nerve atrophy in propionic acidemia. Ophthalmology. 2003 Sep; 110(9):1850-4. PMID: 13129889.
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    29. Koch R, Moseley KD, 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.
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    30. Koch R, Moseley KD, Moats R, Yano S, Matalon R, Guttler F. Danger of high-protein dietary supplements to persons with hyperphenylalaninaemia. J Inherit Metab Dis. 2003; 26(4):339-42. PMID: 12971421.
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    31. Yano S, Li L, Le TP, Moseley K, Guedalia A, Lee J, Gonzalez I, Boles RG. 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. PMID: 14518828.
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    32. Moseley K, Koch R, Moser AB. 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. PMID: 11999981.
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    33. Moats RA, Koch R, Moseley K, Guldberg P, Guttler F, Boles RG, Nelson MD. Brain phenylalanine concentration in the management of adults with phenylketonuria. J Inherit Metab Dis. 2000 Feb; 23(1):7-14. PMID: 10682303.
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    34. Koch R, Moseley K, Ning J, Romstad A, Guldberg P, Guttler F. Long-term beneficial effects of the phenylalanine-restricted diet in late-diagnosed individuals with phenylketonuria. Mol Genet Metab. 1999 Jun; 67(2):148-55. PMID: 10356314.
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