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Nina S Ma

TitleAssociate Professor
InstitutionUniversity of Colorado Denver - Anschutz Medical Campus
DepartmentSOM-PEDS
Phone720/777-0780

    Collapse Biography 
    Collapse awards and honors
    2019Ed and Jeannette Kerr Family Endowed Chair in Endocrinology, Children's Hospital Colorado

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Warner LA, Sewell RL, Ma NS. Vitamin D Update in the Pediatric Population. Adv Pediatr. 2021 Aug; 68:171-194. PMID: 34243851.
      View in: PubMed
    2. Eswarakumar AS, Ma NS, Ward LM, Backeljauw P, Wasserman H, Weber DR, DiMeglio LA, Imel EA, Gagne J, Cody D, Zimakas P, Topor LS, Agrawal S, Calabria A, Tebben P, Faircloth RS, Gordon R, Casey L, Carpenter TO. Long-Term Follow-up of Hypophosphatemic Bone Disease Associated With Elemental Formula Use: Sustained Correction of Bone Disease After Formula Change or Phosphate Supplementation. Clin Pediatr (Phila). 2020 10; 59(12):1080-1085. PMID: 32666808.
      View in: PubMed
    3. Cree-Green M, Carreau AM, Davis SM, Frohnert BI, Kaar JL, Ma NS, Nokoff NJ, Reusch JEB, Simon SL, Nadeau KJ. Peer mentoring for professional and personal growth in academic medicine. J Investig Med. 2020 08; 68(6):1128-1134. PMID: 32641352.
      View in: PubMed
    4. Whyte MP, Ma NS, Mumm S, Gottesman GS, McAlister WH, Nenninger AR, Bijanki VN, Ericson KL, Magnusson P. Persistent idiopathic hyperphosphatasemia from bone alkaline phosphatase in a healthy boy. Bone. 2020 09; 138:115459. PMID: 32474245.
      View in: PubMed
    5. Stefater MA, Wolfsdorf JI, Ma NS, Majzoub JA. Glycogen storage disease presenting as Cushing syndrome. JIMD Rep. 2019 May; 47(1):17-22. PMID: 31240162.
      View in: PubMed
    6. Martinez EE, Quinn N, Arouchon K, Anzaldi R, Tarrant S, Ma NS, Griffin J, Darras BT, Graham RJ, Mehta NM. Comprehensive nutritional and metabolic assessment in patients with spinal muscular atrophy: Opportunity for an individualized approach. Neuromuscul Disord. 2018 06; 28(6):512-519. PMID: 29699728.
      View in: PubMed
    7. Zarate YA, Steinraths M, Matthews A, Smith WE, Sun A, Wilson LC, Brain C, Allgove J, Jacobs B, Fish JL, Powell CM, Wasserman WW, van Karnebeek CD, Wakeling EL, Ma NS. Bone health and SATB2-associated syndrome. Clin Genet. 2018 03; 93(3):588-594. PMID: 28787087.
      View in: PubMed
    8. Zenlea IS, Melvin P, Huh SY, Mehta N, Reidy SJ, Rhodes ET, Ma NS. Risk Factors for Fractures in Children Hospitalized in Intensive and Intermediate Care Units. Hosp Pediatr. 2017 Jul; 7(7):395-402. PMID: 28588070.
      View in: PubMed
    9. Gonzalez Ballesteros LF, Ma NS, Gordon RJ, Ward L, Backeljauw P, Wasserman H, Weber DR, DiMeglio LA, Gagne J, Stein R, Cody D, Simmons K, Zimakas P, Topor LS, Agrawal S, Calabria A, Tebben P, Faircloth R, Imel EA, Casey L, Carpenter TO. Unexpected widespread hypophosphatemia and bone disease associated with elemental formula use in infants and children. Bone. 2017 04; 97:287-292. PMID: 28167344.
      View in: PubMed
    10. Zalewski A, Ma NS, Legeza B, Renthal N, Fl├╝ck CE, Pandey AV. Vitamin D-Dependent Rickets Type 1 Caused by Mutations in CYP27B1 Affecting Protein Interactions With Adrenodoxin. J Clin Endocrinol Metab. 2016 09; 101(9):3409-18. PMID: 27399352.
      View in: PubMed
    11. Ma NS, Thompson C, Weston S. Brief Report: Scurvy as a Manifestation of Food Selectivity in Children with Autism. J Autism Dev Disord. 2016 Apr; 46(4):1464-70. PMID: 26590972.
      View in: PubMed
    12. Ma NS, Gordon CM. The truth about vitamin D and adolescent skeletal health. Adolesc Med State Art Rev. 2012 Dec; 23(3):457-70. PMID: 23437682.
      View in: PubMed
    13. Fink C, Vedin AM, Garcia-Filion P, Ma NS, Geffner ME, Borchert M. Newborn thyroid-stimulating hormone in children with optic nerve hypoplasia: associations with hypothyroidism and vision. J AAPOS. 2012 Oct; 16(5):418-23. PMID: 23084376.
      View in: PubMed
    14. Ma NS, Gordon CM. Pediatric osteoporosis: where are we now? J Pediatr. 2012 Dec; 161(6):983-90. PMID: 22974578.
      View in: PubMed
    15. Venkatramani R, Ma NS, Pitukcheewanont P, Malogolowkin MH, Mascarenhas L. Gorham's disease and diffuse lymphangiomatosis in children and adolescents. Pediatr Blood Cancer. 2011 Apr; 56(4):667-70. PMID: 21298758.
      View in: PubMed
    16. Ma NS, Fink C, Geffner ME, Borchert M. Evolving central hypothyroidism in children with optic nerve hypoplasia. J Pediatr Endocrinol Metab. 2010 Jan-Feb; 23(1-2):53-8. PMID: 20432806.
      View in: PubMed
    17. Franklin SL, Austin J, Reh CS, Ma NS, Kim M. 2009 Annual Meeting of the Endocrine Society Washington DC, United States (June 10-13, 2009)--selected highlights. Pediatr Endocrinol Rev. 2009 Dec; 7(2):50-8. PMID: 20183933.
      View in: PubMed
    18. Ma NS, Shah AJ, Geffner ME, Kapoor N. Igf-I stimulates in vivo thymopoiesis after stem cell transplantation in a child with Omenn syndrome. J Clin Immunol. 2010 Jan; 30(1):114-20. PMID: 19777327.
      View in: PubMed
    19. Ma NS, Malloy PJ, Pitukcheewanont P, Dreimane D, Geffner ME, Feldman D. Hereditary vitamin D resistant rickets: identification of a novel splice site mutation in the vitamin D receptor gene and successful treatment with oral calcium therapy. Bone. 2009 Oct; 45(4):743-6. PMID: 19523546.
      View in: PubMed
    20. Ma NS, Geffner ME. Gynecomastia in prepubertal and pubertal men. Curr Opin Pediatr. 2008 Aug; 20(4):465-70. PMID: 18622206.
      View in: PubMed
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