Nina Ma

Title(s)Affiliate
SchoolViterbi School of Engineering, Bme
Address1042 Downey Way
University Park Campus
Los Angeles CA 90089
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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. Multicentric Carpotarsal Osteolysis: a Contemporary Perspective on the Unique Skeletal Phenotype. Curr Osteoporos Rep. 2023 02; 21(1):85-94. Ma NS, Mumm S, Takahashi S, Levine MA. PMID: 36477366; PMCID: PMC10393442.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    2. Persistent idiopathic hyperphosphatasemia from bone alkaline phosphatase in a healthy boy. Bone. 2020 09; 138:115459. Whyte MP, Ma NS, Mumm S, Gottesman GS, McAlister WH, Nenninger AR, Bijanki VN, Ericson KL, Magnusson P. PMID: 32474245.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    3. Glycogen storage disease presenting as Cushing syndrome. JIMD Rep. 2019 May; 47(1):17-22. Stefater MA, Wolfsdorf JI, Ma NS, Majzoub JA. PMID: 31240162; PMCID: PMC6498823.
      View in: PubMed   Mentions: 3  
    4. Unexpected widespread hypophosphatemia and bone disease associated with elemental formula use in infants and children. Bone. 2017 04; 97:287-292. 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. PMID: 28167344; PMCID: PMC5884631.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    5. 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. Zalewski A, Ma NS, Legeza B, Renthal N, Flück CE, Pandey AV. PMID: 27399352.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    6. Brief Report: Scurvy as a Manifestation of Food Selectivity in Children with Autism. J Autism Dev Disord. 2016 Apr; 46(4):1464-70. Ma NS, Thompson C, Weston S. PMID: 26590972.
      View in: PubMed   Mentions: 42     Fields:    Translation:Humans
    7. The truth about vitamin D and adolescent skeletal health. Adolesc Med State Art Rev. 2012 Dec; 23(3):457-70. Ma NS, Gordon CM. PMID: 23437682.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    8. Newborn thyroid-stimulating hormone in children with optic nerve hypoplasia: associations with hypothyroidism and vision. J AAPOS. 2012 Oct; 16(5):418-23. Fink C, Vedin AM, Garcia-Filion P, Ma NS, Geffner ME, Borchert M. PMID: 23084376; PMCID: PMC3481172.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansPHPublic Health
    9. Pediatric osteoporosis: where are we now? J Pediatr. 2012 Dec; 161(6):983-90. Ma NS, Gordon CM. PMID: 22974578.
      View in: PubMed   Mentions: 33     Fields:    Translation:Humans
    10. Gorham's disease and diffuse lymphangiomatosis in children and adolescents. Pediatr Blood Cancer. 2011 Apr; 56(4):667-70. Venkatramani R, Ma NS, Pitukcheewanont P, Malogolowkin MH, Mascarenhas L. PMID: 21298758.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    11. Evolving central hypothyroidism in children with optic nerve hypoplasia. J Pediatr Endocrinol Metab. 2010 Jan-Feb; 23(1-2):53-8. Ma NS, Fink C, Geffner ME, Borchert M. PMID: 20432806.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    12. 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. Franklin SL, Austin J, Reh CS, Ma NS, Kim M. PMID: 20183933.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    13. 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. Ma NS, Shah AJ, Geffner ME, Kapoor N. PMID: 19777327.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCellsPHPublic Health
    14. 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. Ma NS, Malloy PJ, Pitukcheewanont P, Dreimane D, Geffner ME, Feldman D. PMID: 19523546; PMCID: PMC2782671.
      View in: PubMed   Mentions: 14     Fields:    
    15. Gynecomastia in prepubertal and pubertal men. Curr Opin Pediatr. 2008 Aug; 20(4):465-70. Ma NS, Geffner ME. PMID: 18622206.
      View in: PubMed   Mentions: 27  Translation:Humans
    16. 2007 Annual Meeting of the Endocrine Society Toronto, Canada (June 2-5, 2007): selected pediatric highlights. Pediatr Endocrinol Rev. 2008 Mar; 5(3):796-803. Numbenjapon N, Nawaporn N, Rapaport R, Monzavi R, Pitukcheewanont P, Ma N. PMID: 18368002.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
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