Publications
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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.
J Chromatogr B Analyt Technol Biomed Life Sci.
2013:
929C
51-55
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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.
Pediatr Transplant.
2013;
17
(2):
158-67
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β-Galactosidosis in Patient with Intermediate GM1 and MBD Phenotype.
Moore T,
Bernstein JA, Casson-Parkin S, Cowan TM.
JIMD Rep.
2013:
7
77-9
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An improved LC-MS/MS method for the detection of classic and low excretor glutaric acidemia type 1.
Moore T,
Le A, Cowan TM.
J Inherit Metab Dis.
2012;
35
(3):
431-5
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Increased incidence of profound biotinidase deficiency among Hispanic newborns in California.
Cowan TM,
Kazerouni NN, Dharajiya N, Lorey F, Roberson M, Hodgkinson C, Schrijver I.
Mol Genet Metab.
2012;
106
(4):
485-7
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Commentary.
Cowan TM,
Clin Chem.
2011;
57
(4):
548-9
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The role of vanin-1 and oxidative stress-related pathways in distinguishing acute and chronic pediatric ITP.
Zhang B,
Lo C, Shen L, Sood R, Jones C, Cusmano-Ozog K, Park-Snyder S, Wong W, Jeng M, Cowan T, Engleman EG, Zehnder JL.
Blood.
2011;
117
(17):
4569-79
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Technical standards and guidelines for the diagnosis of biotinidase deficiency.
Cowan TM,
Blitzer MG, Wolf B.
Genet Med.
2010;
12
(7):
464-70
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Inherited disorders affecting mitochondrial function are associated with glutathione deficiency and hypocitrullinemia.
Atkuri KR,
Cowan TM, Kwan T, Ng A, Herzenberg LA, Herzenberg LA, Enns GM.
Proc Natl Acad Sci U S A.
2009;
106
(10):
3941-5
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Mapping gene associations in human mitochondria using clinical disease phenotypes.
Scharfe C,
Lu HH, Neuenburg JK, Allen EA, Li GC, Klopstock T, Cowan TM, Enns GM, Davis RW.
PLoS Comput Biol.
2009;
5
(4):
e1000374
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Acylcarnitine profile analysis.
Rinaldo P,
Cowan TM, Matern D.
Genet Med.
2008;
10
(2):
151-6
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Management and quality assurance in the biochemical genetics laboratory.
Cowan TM,
Strovel ET.
Curr Protoc Hum Genet.
2008:
Chapter 17
Unit 17.7
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Importance of culturing primary lymphocytes at physiological oxygen levels.
Atkuri KR,
Herzenberg LA, Niemi AK, Cowan T, Herzenberg LA.
Proc Natl Acad Sci U S A.
2007;
104
(11):
4547-52
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Glutaryl-CoA dehydrogenase deficiency and newborn screening: retrospective analysis of a low excretor provides further evidence that some cases may be missed.
Gallagher RC,
Cowan TM, Goodman SI, Enns GM.
Mol Genet Metab.
2005;
86
(3):
417-20
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