Nina S Ma
Title | Associate Professor |
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Institution | University of Colorado Denver - Anschutz Medical Campus |
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Department | SOM-PEDS |
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Biography 2019 | Ed and Jeannette Kerr Family Endowed Chair in Endocrinology, Children's Hospital Colorado |
Overview Nutritional and genetic forms of rickets (such as hypophosphatemic rickets); hypoparathyroidism; disorders of vitamin D metabolism (such as 1-alpha-hydroxylase deficiency [CYP27B1], vitamin D resistance [VDR]); rare bone diseases (such as multicentric carpotarsal osteolysis or MCTO [MAFB]).
Bibliographic
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Humphrey MB, Russell L, Danila MI, Fink HA, Guyatt G, Cannon M, Caplan L, Gore S, Grossman J, Hansen KE, Lane NE, Ma NS, Magrey M, McAlindon T, Robinson AB, Saha S, Womack C, Abdulhadi B, Charles JF, Cheah JTL, Chou S, Goyal I, Haseltine K, Jackson L, Mirza R, Moledina I, Punni E, Rinden T, Turgunbaev M, Wysham K, Turner AS, Uhl S. 2022 American College of Rheumatology Guideline for the Prevention and Treatment of Glucocorticoid-Induced Osteoporosis. Arthritis Care Res (Hoboken). 2023 12; 75(12):2405-2419. PMID: 37884467.
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Humphrey MB, Russell L, Danila MI, Fink HA, Guyatt G, Cannon M, Caplan L, Gore S, Grossman J, Hansen KE, Lane NE, Ma NS, Magrey M, McAlindon T, Robinson AB, Saha S, Womack C, Abdulhadi B, Charles JF, Cheah JTL, Chou S, Goyal I, Haseltine K, Jackson L, Mirza R, Moledina I, Punni E, Rinden T, Turgunbaev M, Wysham K, Turner AS, Uhl S. 2022 American College of Rheumatology Guideline for the Prevention and Treatment of Glucocorticoid-Induced Osteoporosis. Arthritis Rheumatol. 2023 12; 75(12):2088-2102. PMID: 37845798.
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Savarirayan R, Hoernschemeyer DG, Ljungberg M, Zarate YA, Bacino CA, Bober MB, Legare JM, H?gler W, Quattrin T, Abuzzahab MJ, Hofman PL, White KK, Ma NS, Schnabel D, Sousa SB, Mao M, Smith A, Chakraborty M, Giwa A, Winding B, Volck B, Shu AD, McDonnell C. Once-weekly TransCon CNP (navepegritide) in children with achondroplasia (ACcomplisH): a phase 2, multicentre, randomised, double-blind, placebo-controlled, dose-escalation trial. EClinicalMedicine. 2023 Nov; 65:102258. PMID: 37823031.
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Trinkino B, Ma NS. Treatment of a young child with multicentric carpotarsal osteolysis exhibiting joint inflammation and dysfunctional bone formation. Bone Rep. 2023 Dec; 19:101701. PMID: 37576926.
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Ma NS, Mumm S, Takahashi S, Levine MA. Multicentric Carpotarsal Osteolysis: a Contemporary Perspective on the Unique Skeletal Phenotype. Curr Osteoporos Rep. 2023 02; 21(1):85-94. PMID: 36477366.
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Cohen LL, Berry JG, Ma NS, Cook DL, Hedequist DJ, Karlin LI, Emans JB, Hresko MT, Snyder BD, Glotzbecker MP. Spinal Fusion in Pediatric Patients With Low Bone Density: Defining the Value of DXA. J Pediatr Orthop. 2022 Aug 01; 42(7):e713-e719. PMID: 35605209.
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Warner LA, Sewell RL, Ma NS. Vitamin D Update in the Pediatric Population. Adv Pediatr. 2021 08; 68:171-194. PMID: 34243851.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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Ma NS, Gordon CM. Pediatric osteoporosis: where are we now? J Pediatr. 2012 Dec; 161(6):983-90. PMID: 22974578.
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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.
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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.
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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.
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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.
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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.
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Ma NS, Geffner ME. Gynecomastia in prepubertal and pubertal men. Curr Opin Pediatr. 2008 Aug; 20(4):465-70. PMID: 18622206.
This graph shows the total number of publications by year, by first, middle/unknown, or last author.
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Year | Publications |
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2008 | 1 | 2009 | 3 | 2010 | 2 | 2012 | 3 | 2016 | 2 | 2017 | 3 | 2018 | 1 | 2019 | 1 | 2020 | 3 | 2021 | 1 | 2022 | 2 | 2023 | 4 |
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