Niemi AK - Search Results

1

McClafferty H, Vohra S, Bailey M, Brown M, Esparham A, Gerstbacher D, Golianu B, Niemi AK, Sibinga E, Weydert J, Yeh AM; SECTION ON INTEGRATIVE MEDICINE. McClafferty H, et al. Among authors: niemi ak. Pediatrics. 2017 Sep;140(3):e20171961. doi: 10.1542/peds.2017-1961. Epub 2017 Aug 28. Pediatrics. 2017. PMID: 28847978

2

Reply: To PMID 25771389.

Niemi AK, Enns GM. Niemi AK, et al. J Pediatr. 2015 Nov;167(5):1173-4. doi: 10.1016/j.jpeds.2015.08.031. Epub 2015 Sep 9. J Pediatr. 2015. PMID: 26362093 No abstract available.

3

Near-Infrared Spectroscopy in the Diagnostic Evaluation of Mitochondrial Disorders: A Neonatal Intensive Care Unit Case Series.

Niemi AK, Chock VY. Niemi AK, et al. J Pediatr. 2019 May;208:282-286. doi: 10.1016/j.jpeds.2019.01.022. Epub 2019 Mar 8. J Pediatr. 2019. PMID: 30853194

4

Treatment of methylmalonic acidemia by liver or combined liver-kidney transplantation.

Niemi AK, Kim IK, Krueger CE, Cowan TM, Baugh N, Farrell R, Bonham CA, Concepcion W, Esquivel CO, Enns GM. Niemi AK, et al. J Pediatr. 2015 Jun;166(6):1455-61.e1. doi: 10.1016/j.jpeds.2015.01.051. Epub 2015 Mar 11. J Pediatr. 2015. PMID: 25771389

5

Liver transplantation for urea cycle disorders in pediatric patients: a single-center experience.

Kim IK, Niemi AK, Krueger C, Bonham CA, Concepcion W, Cowan TM, Enns GM, Esquivel CO. Kim IK, et al. Among authors: niemi ak. Pediatr Transplant. 2013 Mar;17(2):158-67. doi: 10.1111/petr.12041. Epub 2013 Jan 24. Pediatr Transplant. 2013. PMID: 23347504

6

Abnormal hepatocellular mitochondria in methylmalonic acidemia.

Wilnai Y, Enns GM, Niemi AK, Higgins J, Vogel H. Wilnai Y, et al. Among authors: niemi ak. Ultrastruct Pathol. 2014 Oct;38(5):309-14. doi: 10.3109/01913123.2014.921657. Epub 2014 Jun 16. Ultrastruct Pathol. 2014. PMID: 24933007

7

Impaired Health-Related Quality of Life in Children and Families Affected by Methylmalonic Acidemia.

Splinter K, Niemi AK, Cox R, Platt J, Shah M, Enns GM, Kasahara M, Bernstein JA. Splinter K, et al. Among authors: niemi ak. J Genet Couns. 2016 Oct;25(5):936-44. doi: 10.1007/s10897-015-9921-x. Epub 2015 Dec 14. J Genet Couns. 2016. PMID: 26667650

8

Expanding the phenotype of hawkinsinuria: new insights from response to N-acetyl-L-cysteine.

Gomez-Ospina N, Scott AI, Oh GJ, Potter D, Goel VV, Destino L, Baugh N, Enns GM, Niemi AK, Cowan TM. Gomez-Ospina N, et al. Among authors: niemi ak. J Inherit Metab Dis. 2016 Nov;39(6):821-829. doi: 10.1007/s10545-016-9963-8. Epub 2016 Aug 3. J Inherit Metab Dis. 2016. PMID: 27488560

9

A new LC-MS/MS method for the clinical determination of reduced and oxidized glutathione from whole blood.

Moore T, Le A, Niemi AK, Kwan T, Cusmano-Ozog K, Enns GM, Cowan TM. Moore T, et al. Among authors: niemi ak. J Chromatogr B Analyt Technol Biomed Life Sci. 2013 Jun 15;929:51-5. doi: 10.1016/j.jchromb.2013.04.004. Epub 2013 Apr 12. J Chromatogr B Analyt Technol Biomed Life Sci. 2013. PMID: 23660247

10

Degree of glutathione deficiency and redox imbalance depend on subtype of mitochondrial disease and clinical status.

Enns GM, Moore T, Le A, Atkuri K, Shah MK, Cusmano-Ozog K, Niemi AK, Cowan TM. Enns GM, et al. Among authors: niemi ak. PLoS One. 2014 Jun 18;9(6):e100001. doi: 10.1371/journal.pone.0100001. eCollection 2014. PLoS One. 2014. PMID: 24941115 Free PMC article.

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