TimothyCliftonWoodMD

PubMed

• Expanded newborn screening identifies maternal primary carnitine deficiency.
  Schimmenti, L.A., Crombez, E.A., Schwahn, B.C., Heese, B.A., Wood, T.C., Schroer, R.J., Bentler, K., Cederbaum, S., Sarafoglou, K., McCann, M., Rinaldo, P., Matern, D....> ;Mol Genet Metab. 2007 Apr
• 18 citations
  Teaching the musculoskeletal examination: are patient educators as effective as rheumatology faculty?
  Susan Humphrey-Murto, C. Douglas Smith, Claire Touchie, Timothy C. Wood> ;Teaching and Learning in Medicine. 2004 Jan 1
• 237 citations
  Phenol sulfotransferase pharmacogenetics in humans: association of common SULT1A1 alleles with TS PST phenotype.
  Rebecca B. Raftogianis, Thomas C. Wood, Diane M. Otterness, Jon A. Van Loon, Richard M. Weinshilboum> ;Biochemical and Biophysical Research Communications. 1997 Oct 9
• Accident and emergency services--the ambulant patient.
  Cliff, K. S., Wood, T. C.> ;Hosp Health Serv Rev. 1986 Mar
• Sulfation pharmacogenetics: SULT1A1 and SULT1A2 allele frequencies in Caucasian, Chinese and African-American subjects.
  Carlini, E. J., Raftogianis, R. B., Wood, T. C., Jin, F., Zheng, W., Rebbeck, T. R., Weinshilboum, R. M.> ;Pharmacogenetics. 2001 Feb
• Human liver estrogen sulfotransferase: identification by cDNA cloning and expression.
  Aksoy, I. A., Wood, T. C., Weinshilboum, R.> ;Biochem Biophys Res Commun. 1994 May 16
• Human liver thermolabile phenol sulfotransferase: cDNA cloning, expression and characterization.
  Wood, T. C., Aksoy, I. A., Aksoy, S., Weinshilboum, R. M.> ;Biochem Biophys Res Commun. 1994 Feb 15
• Simultaneous determination of guanidinoacetate, creatine and creatinine in urine and plasma by un-derivatized liquid chromatography-tandem mass spectrometry.
  Carling, R. S., Hogg, S. L., Wood, T. C., Calvin, J.> ;Ann Clin Biochem. 2008 Nov
• Human thiopurine methyltransferase pharmacogenetics. Kindred with a terminal exon splice junction mutation that results in loss of activity.
  Otterness, D. M., Szumlanski, C. L., Wood, T. C., Weinshilboum, R. M.> ;J Clin Invest. 1998 Mar 1
• Human phenol sulfotransferases SULT1A2 and SULT1A1: genetic polymorphisms, allozyme properties, and human liver genotype-phenotype correlations.
  Raftogianis, R. B., Wood, T. C., Weinshilboum, R. M.> ;Biochem Pharmacol. 1999 Aug 15
• Human histamine N-methyltransferase pharmacogenetics: common genetic polymorphisms that alter activity.
  Preuss, C. V., Wood, T. C., Szumlanski, C. L., Raftogianis, R. B., Otterness, D. M., Girard, B., Scott, M. C., Weinshilboum, R. M.> ;Mol Pharmacol. 1998 Apr
• Quantification of total and free carnitine in human plasma by hydrophilic interaction liquid chromatography tandem mass spectrometry.
  Sowell, J., Fuqua, M., Wood, T.> ;J Chromatogr Sci. 2011
• Human hydroxysteroid sulfotransferase SULT2B1: two enzymes encoded by a single chromosome 19 gene.
  Her, C., Wood, T. C., Eichler, E. E., Mohrenweiser, H. W., Ramagli, L. S., Siciliano, M. J., Weinshilboum, R. M.> ;Genomics. 1998 Nov 1
• Towards a selected reaction monitoring mass spectrometry fingerprint approach for the screening of oligosaccharidoses.
  Sowell, J., Wood, T.> ;Anal Chim Acta. 2011 Feb 7
• Tandem mass spectrometry for the direct assay of enzymes in dried blood spots: application to newborn screening for mucopolysaccharidosis II (Hunter disease).
  Wang, D., Wood, T., Sadilek, M., Scott, C. R., Turecek, F., Gelb, M. H.> ;Clin Chem. 2007 Jan
• Structured assessment of minor surgical skills (SAMSS) for clinical clerks.
  Friedlich, M., Wood, T., Regehr, G., Hurst, C., Shamji, F.> ;Acad Med. 2002 Oct
• Two patients with hepatic mtDNA depletion syndromes and marked elevations of S-adenosylmethionine and methionine.
  Mudd, S. H., Wagner, C., Luka, Z., Stabler, S. P., Allen, R. H., Schroer, R., Wood, T., Wang, J., Wong, L. J.> ;Mol Genet Metab. 2012 Feb
• Identification and characterization of a novel homozygous deletion in the alpha-N-acetylglucosaminidase gene in a patient with Sanfilippo type B syndrome (mucopolysacc...
  Champion, K. J., Basehore, M. J., Wood, T., Destrée, A., Vannuffel, P., Maystadt, I.> ;Mol Genet Metab. 2010 May
• Quantification of branched-chain amino acids in blood spots and plasma by liquid chromatography tandem mass spectrometry for the diagnosis of maple syrup urine disease.
  Sowell, J., Pollard, L., Wood, T.> ;J Sep Sci. 2011 Mar
• Early onset alpha-mannosidosis with slow progression in three Hispanic males.
  Lyons, M. J., Wood, T., Espinoza, L., Stensland, H. M., Holden, K. R.> ;Dev Med Child Neurol. 2007 Nov
• Diagnostic screening for spermine synthase deficiency by liquid chromatography tandem mass spectrometry.
  Sowell, J., Norris, J., Jones, K., Schwartz, C., Wood, T.> ;Clin Chim Acta. 2011 Mar 18
• X-linked creatine transporter deficiency presenting as a mitochondrial disorder.
  Hathaway, S. C., Friez, M., Limbo, K., Parker, C., Salomons, G. S., Vockley, J., Wood, T., Abdul-Rahman, O. A.> ;J Child Neurol. 2010 Aug
• Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiency.
  Pollard, L. M., Williams, N. R., Espinoza, L., Wood, T. C., Spector, E. B., Schroer, R. J., Holden, K. R.> ;J Child Neurol. 2010 Aug
• Utilization of blood spot testing for metabolic-genetic disorders in Honduras: is it time for newborn screening?
  Slaughter, J. L., Espinoza, L., Molinero, I., Wood, T. C., Duron, C., Flores, A., Porter, R., Tomashitis, K., Holden, K. R.> ;J Child Neurol. 2010 Mar 01
• Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant.
  Giurgiutiu, D. V., Espinoza, L. M., Wood, T. C., DuPont, B. R., Holden, K. R.> ;J Child Neurol. 2008 Jan
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