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Anna-kaisa Niemi

TitleAssistant Clinical Professor
InstitutionUniversity of California San Diego
DepartmentPediatrics
Address9500 Gilman Drive #0984
La Jolla CA 92093
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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. McClafferty H, Vohra S, Bailey M, Brown M, Esparham A, Gerstbacher D, Golianu B, Niemi A, Sibinga E, Weydert J, Yeh AM. Pediatric Integrative Medicine. Pediatrics. 2017 Sep; 140(3). PMID: 28847978.
      View in: PubMed
    2. Niemi A. Review of Randomized Controlled Trials of Massage in Preterm Infants. Children (Basel). 2017 Apr 03; 4(4). PMID: 28368368.
      View in: PubMed
    3. Gomez-Ospina N, Scott AI, Oh GJ, Potter D, Goel VV, Destino L, Baugh N, Enns GM, Niemi A, Cowan TM. Expanding the phenotype of hawkinsinuria: new insights from response to N-acetyl-L-cysteine. J Inherit Metab Dis. 2016 11; 39(6):821-829. PMID: 27488560.
      View in: PubMed
    4. Splinter K, Niemi A, Cox R, Platt J, Shah M, Enns GM, Kasahara M, Bernstein JA. Impaired Health-Related Quality of Life in Children and Families Affected by Methylmalonic Acidemia. J Genet Couns. 2016 Oct; 25(5):936-44. PMID: 26667650.
      View in: PubMed
    5. Niemi A, Enns GM. Reply: To PMID 25771389. J Pediatr. 2015 Nov; 167(5):1173-4. PMID: 26362093.
      View in: PubMed
    6. Niemi A, Kim IK, Krueger CE, Cowan TM, Baugh N, Farrell R, Bonham CA, Concepcion W, Esquivel CO, Enns GM. Treatment of methylmalonic acidemia by liver or combined liver-kidney transplantation. J Pediatr. 2015 Jun; 166(6):1455-61.e1. PMID: 25771389.
      View in: PubMed
    7. Myers A, Bernstein JA, Brennan ML, Curry C, Esplin ED, Fisher J, Homeyer M, Manning MA, Muller EA, Niemi A, Seaver LH, Hintz SR, Hudgins L. Perinatal features of the RASopathies: Noonan syndrome, cardiofaciocutaneous syndrome and Costello syndrome. Am J Med Genet A. 2014 Nov; 164A(11):2814-21. PMID: 25250515.
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    8. Enns GM, Moore T, Le A, Atkuri K, Shah MK, Cusmano-Ozog K, Niemi A, Cowan TM. Degree of glutathione deficiency and redox imbalance depend on subtype of mitochondrial disease and clinical status. PLoS One. 2014; 9(6):e100001. PMID: 24941115; PMCID: PMC4062483.
    9. Wilnai Y, Enns GM, Niemi A, Higgins J, Vogel H. Abnormal hepatocellular mitochondria in methylmalonic acidemia. Ultrastruct Pathol. 2014 Oct; 38(5):309-14. PMID: 24933007.
      View in: PubMed
    10. Niemi A, Brown C, Moore T, Enns GM, Cowan TM. Evidence of redox imbalance in a patient with succinic semialdehyde dehydrogenase deficiency. Mol Genet Metab Rep. 2014; 1:129-132. PMID: 27896081.
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    11. Moore T, Le A, Niemi A, Kwan T, Cusmano-Ozog K, Enns GM, Cowan TM. A new LC-MS/MS method for the clinical determination of reduced and oxidized glutathione from whole blood. J Chromatogr B Analyt Technol Biomed Life Sci. 2013 Jun 15; 929:51-5. PMID: 23660247.
      View in: PubMed
    12. Kim IK, Niemi A, Krueger C, Bonham CA, Concepcion W, Cowan TM, Enns GM, Esquivel CO. Liver transplantation for urea cycle disorders in pediatric patients: a single-center experience. Pediatr Transplant. 2013 Mar; 17(2):158-67. PMID: 23347504.
      View in: PubMed
    13. Niemi A, Kwan A, Hudgins L, Cherry AM, Manning MA. Report of two patients and further characterization of interstitial 9p13 deletion--a rare but recurrent microdeletion syndrome? Am J Med Genet A. 2012 Sep; 158A(9):2328-35. PMID: 22887577.
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    14. Zadeh N, Bernstein JA, Niemi A, Dugan S, Kwan A, Liang D, Hyland JC, Hoyme HE, Hudgins L, Manning MA. Ectopia lentis as the presenting and primary feature in Marfan syndrome. Am J Med Genet A. 2011 Nov; 155A(11):2661-8. PMID: 21932315.
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    15. Niemi A, Northrup H, Hudgins L, Bernstein JA. Horseshoe kidney and a rare TSC2 variant in two unrelated individuals with tuberous sclerosis complex. Am J Med Genet A. 2011 Oct; 155A(10):2534-7. PMID: 21910228.
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    16. Atkuri KR, Herzenberg LA, Niemi A, Cowan T, Herzenberg LA. Importance of culturing primary lymphocytes at physiological oxygen levels. Proc Natl Acad Sci U S A. 2007 Mar 13; 104(11):4547-52. PMID: 17360561; PMCID: PMC1838638.
    17. Niemi A, Majamaa K. Mitochondrial DNA and ACTN3 genotypes in Finnish elite endurance and sprint athletes. Eur J Hum Genet. 2005 Aug; 13(8):965-9. PMID: 15886711.
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    18. Niemi A, Moilanen JS, Tanaka M, Hervonen A, Hurme M, Lehtimäki T, Arai Y, Hirose N, Majamaa K. A combination of three common inherited mitochondrial DNA polymorphisms promotes longevity in Finnish and Japanese subjects. Eur J Hum Genet. 2005 Feb; 13(2):166-70. PMID: 15483642.
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    19. Niemi A, Hervonen A, Hurme M, Karhunen PJ, Jylhä M, Majamaa K. Mitochondrial DNA polymorphisms associated with longevity in a Finnish population. Hum Genet. 2003 Jan; 112(1):29-33. PMID: 12483296.
      View in: PubMed