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Medical College of Wisconsin

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William Rhead MD, PhD

Adjunct Professor

Institution: Medical College of Wisconsin
Department: Pediatrics
Division: Genetics

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Publications (121)

Identification of Urine Organic Acids for the Detection of Inborn Errors of Metabolism Using Urease and Gas Chromatography-Mass Spectrometry (GC/MS). (Lo SF, Pierzchalski K, Young V, Rhead WJ) Methods Mol Biol 2022;2546:335-350 PMID: 36127602 SCOPUS ID: 2-s2.0-85138168219 09/21/2022 3 Citations

Long-term safety and efficacy of glycerol phenylbutyrate for the management of urea cycle disorder patients. (Diaz GA, Schulze A, Longo N, Rhead W, Feigenbaum A, Wong D, Merritt JL 2nd, Berquist W, Gallagher RC, Bartholomew D, McCandless SE, Smith WE, Harding CO, Zori R, Lichter-Konecki U, Vockley J, Canavan C, Vescio T, Holt RJ, Berry SA) Mol Genet Metab 2019 Aug;127(4):336-345 PMID: 31326288 SCOPUS ID: 2-s2.0-85068992352 07/22/2019 23 Citations

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (Redin C, Brand H, Collins RL, Kammin T, Mitchell E, Hodge JC, Hanscom C, Pillalamarri V, Seabra CM, Abbott MA, Abdul-Rahman OA, Aberg E, Adley R, Alcaraz-Estrada SL, Alkuraya FS, An Y, Anderson MA, Antolik C, Anyane-Yeboa K, Atkin JF, Bartell T, Bernstein JA, Beyer E, Blumenthal I, Bongers EM, Brilstra EH, Brown CW, Brüggenwirth HT, Callewaert B, Chiang C, Corning K, Cox H, Cuppen E, Currall BB, Cushing T, David D, Deardorff MA, Dheedene A, D'Hooghe M, de Vries BB, Earl DL, Ferguson HL, Fisher H, FitzPatrick DR, Gerrol P, Giachino D, Glessner JT, Gliem T, Grady M, Graham BH, Griffis C, Gripp KW, Gropman AL, Hanson-Kahn A, Harris DJ, Hayden MA, Hill R, Hochstenbach R, Hoffman JD, Hopkin RJ, Hubshman MW, Innes AM, Irons M, Irving M, Jacobsen JC, Janssens S, Jewett T, Johnson JP, Jongmans MC, Kahler SG, Koolen DA, Korzelius J, Kroisel PM, Lacassie Y, Lawless W, Lemyre E, Leppig K, Levin AV, Li H, Li H, Liao EC, Lim C, Lose EJ, Lucente D, Macera MJ, Manavalan P, Mandrile G, Marcelis CL, Margolin L, Mason T, Masser-Frye D, McClellan MW, Mendoza CJ, Menten B, Middelkamp S, Mikami LR, Moe E, Mohammed S, Mononen T, Mortenson ME, Moya G, Nieuwint AW, Ordulu Z, Parkash S, Pauker SP, Pereira S, Perrin D, Phelan K, Aguilar RE, Poddighe PJ, Pregno G, Raskin S, Reis L, Rhead W, Rita D, Renkens I, Roelens F, Ruliera J, Rump P, Schilit SL, Shaheen R, Sparkes R, Spiegel E, Stevens B, Stone MR, Tagoe J, Thakuria JV, van Bon BW, van de Kamp J, van Der Burgt I, van Essen T, van Ravenswaaij-Arts CM, van Roosmalen MJ, Vergult S, Volker-Touw CM, Warburton DP, Waterman MJ, Wiley S, Wilson A, Yerena-de Vega MC, Zori RT, Levy B, Brunner HG, de Leeuw N, Kloosterman WP, Thorland EC, Morton CC, Gusella JF, Talkowski ME) Nat Genet 2017 Jan;49(1):36-45 PMID: 27841880 PMCID: PMC5307971 SCOPUS ID: 2-s2.0-84995436852 11/15/2016 238 Citations

Characteristic Pulvinar Sign in Pseudo-α-galactosidase Deficiency Syndrome. (Farooq S, Hiner BC, Rhead WJ, Kirschner AL, Chelimsky TC) JAMA Neurol 2016 Aug 01;73(8):1020-1 PMID: 27323002 SCOPUS ID: 2-s2.0-84981274404 06/21/2016 2 Citations

Glutamine and hyperammonemic crises in patients with urea cycle disorders. (Lee B, Diaz GA, Rhead W, Lichter-Konecki U, Feigenbaum A, Berry SA, Le Mons C, Bartley J, Longo N, Nagamani SC, Berquist W, Gallagher RC, Harding CO, McCandless SE, Smith W, Schulze A, Marino M, Rowell R, Coakley DF, Mokhtarani M, Scharschmidt BF) Mol Genet Metab 2016 Jan;117(1):27-32 PMID: 26586473 PMCID: PMC4915945 SCOPUS ID: 2-s2.0-84951762877 11/21/2015 18 Citations

Self-reported treatment-associated symptoms among patients with urea cycle disorders participating in glycerol phenylbutyrate clinical trials. (Nagamani SC, Diaz GA, Rhead W, Berry SA, Le Mons C, Lichter-Konecki U, Bartley J, Feigenbaum A, Schulze A, Longo N, Berquist W, Gallagher R, Bartholomew D, Harding CO, Korson MS, McCandless SE, Smith W, Vockley J, Kronn D, Zori R, Cederbaum S, Merritt JL 2nd, Wong D, Coakley DF, Scharschmidt BF, Dickinson K, Marino M, Lee BH, Mokhtarani M) Mol Genet Metab 2015;116(1-2):29-34 PMID: 26296711 PMCID: PMC4804346 SCOPUS ID: 2-s2.0-84940895916 08/25/2015 18 Citations

Long-term velaglucerase alfa treatment in children with Gaucher disease type 1 naïve to enzyme replacement therapy or previously treated with imiglucerase. (Smith L, Rhead W, Charrow J, Shankar SP, Bavdekar A, Longo N, Mardach R, Harmatz P, Hangartner T, Lee HM, Crombez E, Pastores GM) Mol Genet Metab 2016 Feb;117(2):164-71 PMID: 26043810 SCOPUS ID: 2-s2.0-84957842180 06/06/2015 35 Citations

Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance. (Russell B, Johnston JJ, Biesecker LG, Kramer N, Pickart A, Rhead W, Tan WH, Brownstein CA, Kate Clarkson L, Dobson A, Rosenberg AZ, Vergano SA, Helm BM, Harrison RE, Graham JM Jr) Am J Med Genet A 2015 Sep;167A(9):2122-31 PMID: 25921057 PMCID: PMC4760347 SCOPUS ID: 2-s2.0-84939467262 04/30/2015 59 Citations

Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorder. (Lee B, Diaz GA, Rhead W, Lichter-Konecki U, Feigenbaum A, Berry SA, Le Mons C, Bartley JA, Longo N, Nagamani SC, Berquist W, Gallagher R, Bartholomew D, Harding CO, Korson MS, McCandless SE, Smith W, Cederbaum S, Wong D, Merritt JL 2nd, Schulze A, Vockley J, Kronn D, Zori R, Summar M, Milikien DA, Marino M, Coakley DF, Mokhtarani M, UCD Consortium, Scharschmidt BF) Genet Med 2015 Jul;17(7):561-8 PMID: 25503497 PMCID: PMC4465427 SCOPUS ID: 2-s2.0-84942804923 12/17/2014 29 Citations

Mutation Update for UBE3A variants in Angelman syndrome. (Sadikovic B, Fernandes P, Zhang VW, Ward PA, Miloslavskaya I, Rhead W, Rosenbaum R, Gin R, Roa B, Fang P) Hum Mutat 2014 Dec;35(12):1407-17 PMID: 25212744 SCOPUS ID: 2-s2.0-84911442598 09/13/2014 62 Citations

Glycerol phenylbutyrate treatment in children with urea cycle disorders: pooled analysis of short and long-term ammonia control and outcomes. (Berry SA, Lichter-Konecki U, Diaz GA, McCandless SE, Rhead W, Smith W, Lemons C, Nagamani SC, Coakley DF, Mokhtarani M, Scharschmidt BF, Lee B) Mol Genet Metab 2014 May;112(1):17-24 PMID: 24630270 PMCID: PMC4382922 SCOPUS ID: 2-s2.0-84899632831 03/19/2014 39 Citations

Elevated phenylacetic acid levels do not correlate with adverse events in patients with urea cycle disorders or hepatic encephalopathy and can be predicted based on the plasma PAA to PAGN ratio. (Mokhtarani M, Diaz GA, Rhead W, Berry SA, Lichter-Konecki U, Feigenbaum A, Schulze A, Longo N, Bartley J, Berquist W, Gallagher R, Smith W, McCandless SE, Harding C, Rockey DC, Vierling JM, Mantry P, Ghabril M, Brown RS Jr, Dickinson K, Moors T, Norris C, Coakley D, Milikien DA, Nagamani SC, Lemons C, Lee B, Scharschmidt BF) Mol Genet Metab 2013 Dec;110(4):446-53 PMID: 24144944 PMCID: PMC4108288 SCOPUS ID: 2-s2.0-84897089628 10/23/2013 35 Citations

Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes. (Weh E, Reis LM, Tyler RC, Bick D, Rhead WJ, Wallace S, McGregor TL, Dills SK, Chao MC, Murray JC, Semina EV) Clin Genet 2014 Aug;86(2):142-8 PMID: 23889335 PMCID: PMC4103962 SCOPUS ID: 2-s2.0-84904703878 07/31/2013 43 Citations

Population pharmacokinetic modeling and dosing simulations of nitrogen-scavenging compounds: disposition of glycerol phenylbutyrate and sodium phenylbutyrate in adult and pediatric patients with urea cycle disorders. (Monteleone JP, Mokhtarani M, Diaz GA, Rhead W, Lichter-Konecki U, Berry SA, Lemons C, Dickinson K, Coakley D, Lee B, Scharschmidt BF) J Clin Pharmacol 2013 Jul;53(7):699-710 PMID: 23775211 PMCID: PMC3923458 SCOPUS ID: 2-s2.0-84880285317 06/19/2013 35 Citations

Prevalence and mutation analysis of short/branched chain acyl-CoA dehydrogenase deficiency (SBCADD) detected on newborn screening in Wisconsin. (Van Calcar SC, Baker MW, Williams P, Jones SA, Xiong B, Thao MC, Lee S, Yang MK, Rice GM, Rhead W, Vockley J, Hoffman G, Durkin MS) Mol Genet Metab 2013;110(1-2):111-5 PMID: 23712021 PMCID: PMC5006389 SCOPUS ID: 2-s2.0-84882895521 05/29/2013 27 Citations

Changes in plasma and urine globotriaosylceramide levels do not predict Fabry disease progression over 1 year of agalsidase alfa. (Schiffmann R, Ries M, Blankenship D, Nicholls K, Mehta A, Clarke JT, Steiner RD, Beck M, Barshop BA, Rhead W, West M, Martin R, Amato D, Nair N, Huertas P) Genet Med 2013 Dec;15(12):983-9 PMID: 23680766 SCOPUS ID: 2-s2.0-84890084688 05/18/2013 23 Citations

Safety and efficacy of velaglucerase alfa in Gaucher disease type 1 patients previously treated with imiglucerase. (Zimran A, Pastores GM, Tylki-Szymanska A, Hughes DA, Elstein D, Mardach R, Eng C, Smith L, Heisel-Kurth M, Charrow J, Harmatz P, Fernhoff P, Rhead W, Longo N, Giraldo P, Ruiz JA, Zahrieh D, Crombez E, Grabowski GA) Am J Hematol 2013 Mar;88(3):172-8 PMID: 23339116 PMCID: PMC3586535 SCOPUS ID: 2-s2.0-84874303983 01/23/2013 52 Citations

Ammonia control and neurocognitive outcome among urea cycle disorder patients treated with glycerol phenylbutyrate. (Diaz GA, Krivitzky LS, Mokhtarani M, Rhead W, Bartley J, Feigenbaum A, Longo N, Berquist W, Berry SA, Gallagher R, Lichter-Konecki U, Bartholomew D, Harding CO, Cederbaum S, McCandless SE, Smith W, Vockley G, Bart SA, Korson MS, Kronn D, Zori R, Merritt JL 2nd, C S Nagamani S, Mauney J, Lemons C, Dickinson K, Moors TL, Coakley DF, Scharschmidt BF, Lee B) Hepatology 2013 Jun;57(6):2171-9 PMID: 22961727 PMCID: PMC3557606 SCOPUS ID: 2-s2.0-84879118512 09/11/2012 87 Citations

Urinary phenylacetylglutamine as dosing biomarker for patients with urea cycle disorders. (Mokhtarani M, Diaz GA, Rhead W, Lichter-Konecki U, Bartley J, Feigenbaum A, Longo N, Berquist W, Berry SA, Gallagher R, Bartholomew D, Harding CO, Korson MS, McCandless SE, Smith W, Vockley J, Bart S, Kronn D, Zori R, Cederbaum S, Dorrani N, Merritt JL 2nd, Sreenath-Nagamani S, Summar M, Lemons C, Dickinson K, Coakley DF, Moors TL, Lee B, Scharschmidt BF) Mol Genet Metab 2012 Nov;107(3):308-14 PMID: 22958974 PMCID: PMC3608516 SCOPUS ID: 2-s2.0-84867901846 09/11/2012 44 Citations

Pancreatic insufficiency in Toriello-Carey syndrome: report of a second patient. (El-Chammas KI, Venkatasubramani N, Veith R, Sekhri N, Rhead W, Toriello HV, Goday PS) Am J Med Genet A 2012 May;158A(5):1208-11 PMID: 22496049 SCOPUS ID: 2-s2.0-84859991434 04/13/2012 2 Citations

Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndrome. (Campeau PM, Kim JC, Lu JT, Schwartzentruber JA, Abdul-Rahman OA, Schlaubitz S, Murdock DM, Jiang MM, Lammer EJ, Enns GM, Rhead WJ, Rowland J, Robertson SP, Cormier-Daire V, Bainbridge MN, Yang XJ, Gingras MC, Gibbs RA, Rosenblatt DS, Majewski J, Lee BH) Am J Hum Genet 2012 Feb 10;90(2):282-9 PMID: 22265014 PMCID: PMC3276659 SCOPUS ID: 2-s2.0-84862803991 01/24/2012 119 Citations

Successful immune tolerance induction to enzyme replacement therapy in CRIM-negative infantile Pompe disease. (Messinger YH, Mendelsohn NJ, Rhead W, Dimmock D, Hershkovitz E, Champion M, Jones SA, Olson R, White A, Wells C, Bali D, Case LE, Young SP, Rosenberg AS, Kishnani PS) Genet Med 2012 Jan;14(1):135-42 PMID: 22237443 PMCID: PMC3711224 SCOPUS ID: 2-s2.0-84855542158 01/13/2012 200 Citations

Ammonia control in children with urea cycle disorders (UCDs); phase 2 comparison of sodium phenylbutyrate and glycerol phenylbutyrate. (Lichter-Konecki U, Diaz GA, Merritt JL 2nd, Feigenbaum A, Jomphe C, Marier JF, Beliveau M, Mauney J, Dickinson K, Martinez A, Mokhtarani M, Scharschmidt B, Rhead W) Mol Genet Metab 2011 Aug;103(4):323-9 PMID: 21612962 PMCID: PMC4880058 SCOPUS ID: 2-s2.0-79960848652 05/27/2011 65 Citations

Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B. (Ho G, Yonezawa A, Masuda S, Inui K, Sim KG, Carpenter K, Olsen RK, Mitchell JJ, Rhead WJ, Peters G, Christodoulou J) Hum Mutat 2011 Jan;32(1):E1976-84 PMID: 21089064 SCOPUS ID: 2-s2.0-78650443606 11/23/2010 106 Citations

Novel ETF dehydrogenase mutations in a patient with mild glutaric aciduria type II and complex II-III deficiency in liver and muscle. (Wolfe LA, He M, Vockley J, Payne N, Rhead W, Hoppel C, Spector E, Gernert K, Gibson KM) J Inherit Metab Dis 2010 Dec;33 Suppl 3(0 3):S481-7 PMID: 21088898 PMCID: PMC3970109 SCOPUS ID: 2-s2.0-84897954933 11/20/2010 23 Citations

Phase 2 comparison of a novel ammonia scavenging agent with sodium phenylbutyrate in patients with urea cycle disorders: safety, pharmacokinetics and ammonia control. (Lee B, Rhead W, Diaz GA, Scharschmidt BF, Mian A, Shchelochkov O, Marier JF, Beliveau M, Mauney J, Dickinson K, Martinez A, Gargosky S, Mokhtarani M, Berry SA) Mol Genet Metab 2010 Jul;100(3):221-8 PMID: 20382058 PMCID: PMC2905228 SCOPUS ID: 2-s2.0-77953019684 04/13/2010 82 Citations

Identification of urine organic acids for the detection of inborn errors of metabolism using urease and gas chromatography-mass spectrometry (GC-MS). (Lo SF, Young V, Rhead WJ) Methods Mol Biol 2010;603:433-43 PMID: 20077095 SCOPUS ID: 2-s2.0-77950354711 01/16/2010 10 Citations

National academy of clinical biochemistry laboratory medicine practice guidelines: follow-up testing for metabolic disease identified by expanded newborn screening using tandem mass spectrometry; executive summary. (Dietzen DJ, Rinaldo P, Whitley RJ, Rhead WJ, Hannon WH, Garg UC, Lo SF, Bennett MJ) Clin Chem 2009 Sep;55(9):1615-26 PMID: 19574465 SCOPUS ID: 2-s2.0-69549118945 07/04/2009 74 Citations

Agalsidase alfa and kidney dysfunction in Fabry disease. (West M, Nicholls K, Mehta A, Clarke JT, Steiner R, Beck M, Barshop BA, Rhead W, Mensah R, Ries M, Schiffmann R) J Am Soc Nephrol 2009 May;20(5):1132-9 PMID: 19357250 PMCID: PMC2678048 SCOPUS ID: 2-s2.0-65649096032 04/10/2009 164 Citations

Tetrahydrobiopterin deficiency in human rabies. (Willoughby RE, Opladen T, Maier T, Rhead W, Schmiedel S, Hoyer J, Drosten C, Rupprecht CE, Hyland K, Hoffmann GF) J Inherit Metab Dis 2009 Feb;32(1):65-72 PMID: 18949578 SCOPUS ID: 2-s2.0-59749105128 10/25/2008 34 Citations

Creating genetics-based infusion centers: a case study of two models. (Laney DJ, White AL, Rhead WJ, Fernhoff P) Genet Med 2008 Aug;10(8):626-32 PMID: 18641514 SCOPUS ID: 2-s2.0-55849153560 07/22/2008 2 Citations

Rescue from neonatal death in the murine model of hereditary tyrosinemia by glutathione monoethylester and vitamin C treatment. (Langlois C, Jorquera R, Orejuela D, Bergeron A, Finegold MJ, Rhead WJ, Tanguay RM) Mol Genet Metab 2008 Mar;93(3):306-13 PMID: 18023223 SCOPUS ID: 2-s2.0-38849168252 11/21/2007 7 Citations

Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency. (Chiong MA, Sim KG, Carpenter K, Rhead W, Ho G, Olsen RK, Christodoulou J) Mol Genet Metab 2007;92(1-2):109-14 PMID: 17689999 SCOPUS ID: 2-s2.0-34548472017 08/11/2007 44 Citations

Survival after treatment with phenylacetate and benzoate for urea-cycle disorders. (Enns GM, Berry SA, Berry GT, Rhead WJ, Brusilow SW, Hamosh A) N Engl J Med 2007 May 31;356(22):2282-92 PMID: 17538087 SCOPUS ID: 2-s2.0-34249803312 06/01/2007 303 Citations

2-methylbutyryl-CoA dehydrogenase deficiency in Hmong infants identified by expanded newborn screen. (van Calcar SC, Gleason LA, Lindh H, Hoffman G, Rhead W, Vockley G, Wolff JA, Durkin MS) WMJ 2007 Feb;106(1):12-5 PMID: 17393751 SCOPUS ID: 2-s2.0-33847168609 03/31/2007 33 Citations

'Classical' organic acidurias, propionic aciduria, methylmalonic aciduria and isovaleric aciduria: long-term outcome and effects of expanded newborn screening using tandem mass spectrometry. (Dionisi-Vici C, Deodato F, Röschinger W, Rhead W, Wilcken B) J Inherit Metab Dis 2006;29(2-3):383-9 PMID: 16763906 SCOPUS ID: 2-s2.0-33745098400 06/10/2006 211 Citations

Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: a global perspective. (Rhead WJ) J Inherit Metab Dis 2006;29(2-3):370-7 PMID: 16763904 SCOPUS ID: 2-s2.0-33745098087 06/10/2006 84 Citations

Urea cycle disorders: clinical presentation outside the newborn period. (Smith W, Kishnani PS, Lee B, Singh RH, Rhead WJ, Sniderman King L, Smith M, Summar M) Crit Care Clin 2005 Oct;21(4 Suppl):S9-17 PMID: 16227115 SCOPUS ID: 2-s2.0-26844455345 10/18/2005 85 Citations

Genetic counseling issues in urea cycle disorders. (Sniderman King L, Singh RH, Rhead WJ, Smith W, Lee B, Summar ML) Crit Care Clin 2005 Oct;21(4 Suppl):S37-44 PMID: 16227114 SCOPUS ID: 2-s2.0-26844487848 10/18/2005 20 Citations

Nutritional management of urea cycle disorders. (Singh RH, Rhead WJ, Smith W, Lee B, Sniderman King L, Summar M) Crit Care Clin 2005 Oct;21(4 Suppl):S27-35 PMID: 16227113 SCOPUS ID: 2-s2.0-26844432821 10/18/2005 46 Citations

Considerations in the difficult-to-manage urea cycle disorder patient. (Lee B, Singh RH, Rhead WJ, Sniderman King L, Smith W, Summar ML) Crit Care Clin 2005 Oct;21(4 Suppl):S19-25 PMID: 16227112 SCOPUS ID: 2-s2.0-26844482679 10/18/2005 14 Citations

Unmasked adult-onset urea cycle disorders in the critical care setting. (Summar ML, Barr F, Dawling S, Smith W, Lee B, Singh RH, Rhead WJ, Sniderman King L, Christman BW) Crit Care Clin 2005 Oct;21(4 Suppl):S1-8 PMID: 16227111 SCOPUS ID: 2-s2.0-26844529765 10/18/2005 118 Citations

Ascorbate decreases Fabry cerebral hyperperfusion suggesting a reactive oxygen species abnormality: an arterial spin tagging study. (Moore DF, Ye F, Brennan ML, Gupta S, Barshop BA, Steiner RD, Rhead WJ, Brady RO, Hazen SL, Schiffmann R) J Magn Reson Imaging 2004 Oct;20(4):674-83 PMID: 15390234 SCOPUS ID: 2-s2.0-4744344117 09/25/2004 68 Citations

The call from the newborn screening laboratory: frustration in the afternoon. (Rhead WJ, Irons M) Pediatr Clin North Am 2004 Jun;51(3):803-18, xii PMID: 15157599 SCOPUS ID: 2-s2.0-2442587371 05/26/2004 9 Citations

Genitopatellar syndrome: expanding the phenotype. (Lifchez CA, Rhead WJ, Leuthner SR, Lubinsky MS) Am J Med Genet A 2003 Sep 15;122A(1):80-3 PMID: 12949978 SCOPUS ID: 2-s2.0-0042819648 09/02/2003 18 Citations

Phenylketonuria in adulthood: a collaborative study. (Koch R, Burton B, Hoganson G, Peterson R, Rhead W, Rouse B, Scott R, Wolff J, Stern AM, Guttler F, Nelson M, de la Cruz F, Coldwell J, Erbe R, Geraghty MT, Shear C, Thomas J, Azen C) J Inherit Metab Dis 2002 Sep;25(5):333-46 PMID: 12408183 SCOPUS ID: 2-s2.0-0036744719 11/01/2002 178 Citations

Evaluation of liver fatty acid oxidation in the leptin-deficient obese mouse. (Brix AE, Elgavish A, Nagy TR, Gower BA, Rhead WJ, Wood PA) Mol Genet Metab 2002 Mar;75(3):219-26 PMID: 11914033 SCOPUS ID: 2-s2.0-0036353136 03/27/2002 33 Citations

Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse. (Cox KB, Hamm DA, Millington DS, Matern D, Vockley J, Rinaldo P, Pinkert CA, Rhead WJ, Lindsey JR, Wood PA) Hum Mol Genet 2001 Sep 15;10(19):2069-77 PMID: 11590124 SCOPUS ID: 2-s2.0-0034782503 10/09/2001 112 Citations

Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency. (Corydon MJ, Vockley J, Rinaldo P, Rhead WJ, Kjeldsen M, Winter V, Riggs C, Babovic-Vuksanovic D, Smeitink J, De Jong J, Levy H, Sewell AC, Roe C, Matern D, Dasouki M, Gregersen N) Pediatr Res 2001 Jan;49(1):18-23 PMID: 11134486 SCOPUS ID: 2-s2.0-0035193285 01/03/2001 112 Citations

US newborn screening system guidelines II: follow-up of children, diagnosis, management, and evaluation. Statement of the Council of Regional Networks for Genetic Services (CORN). (Pass KA, Lane PA, Fernhoff PM, Hinton CF, Panny SR, Parks JS, Pelias MZ, Rhead WJ, Ross SI, Wethers DL, Elsas LJ 2nd) J Pediatr 2000 Oct;137(4 Suppl):S1-46 PMID: 11044838 SCOPUS ID: 2-s2.0-0033785508 10/25/2000 133 Citations

Lessons learned from the mouse model of short-chain acyl-CoA dehydrogenase deficiency. (Wood PA, Kelly-Kurtz CL, Hinsdale ME, Hamm DA, Rhead WJ) Adv Exp Med Biol 1999;466:395-402 PMID: 10709668 SCOPUS ID: 2-s2.0-0034469096 03/10/2000 4 Citations

Undiagnosed maternal phenylketonuria: the need for prenatal selective screening or case finding. (Hanley WB, Platt LD, Bachman RP, Buist N, Geraghty MT, Isaacs J, O'Flynn ME, Rhead WJ, Seidlitz G, Tishler B) Am J Obstet Gynecol 1999 Apr;180(4):986-94 PMID: 10203668 SCOPUS ID: 2-s2.0-0032937137 04/16/1999 27 Citations

Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy. (Tein I, Haslam RH, Rhead WJ, Bennett MJ, Becker LE, Vockley J) Neurology 1999 Jan 15;52(2):366-72 PMID: 9932958 SCOPUS ID: 2-s2.0-0033555567 02/05/1999 76 Citations

Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation. (Kurtz DM, Rinaldo P, Rhead WJ, Tian L, Millington DS, Vockley J, Hamm DA, Brix AE, Lindsey JR, Pinkert CA, O'Brien WE, Wood PA) Proc Natl Acad Sci U S A 1998 Dec 22;95(26):15592-7 PMID: 9861014 PMCID: PMC28088 SCOPUS ID: 2-s2.0-13044277575 12/23/1998 211 Citations

Carbohydrate-deficient glycoprotein syndrome type 1 with profound thrombocytopenia and normal phosphomannomutase and phosphomannose isomerase activities. (Acarregui MJ, George TN, Rhead WJ) J Pediatr 1998 Nov;133(5):697-700 PMID: 9821433 SCOPUS ID: 2-s2.0-0031743493 11/20/1998 21 Citations

Analysis of carnitine esters by radio-high performance liquid chromatography in cultured skin fibroblasts from patients with mitochondrial fatty acid oxidation disorders. (Schmidt-Sommerfeld E, Bobrowski PJ, Penn D, Rhead WJ, Wanders RJ, Bennett MJ) Pediatr Res 1998 Aug;44(2):210-4 PMID: 9702916 SCOPUS ID: 2-s2.0-0031821935 08/14/1998 17 Citations

Stridor as the major presenting symptom in riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency. (Sperl W, Geiger R, Lehnert W, Rhead W) Eur J Pediatr 1997 Oct;156(10):800-2 PMID: 9365073 SCOPUS ID: 2-s2.0-0030759186 11/19/1997 8 Citations

Deficient muscle carnitine transport in primary carnitine deficiency. (Pons R, Carrozzo R, Tein I, Walker WF, Addonizio LJ, Rhead W, Miranda AF, Dimauro S, De Vivo DC) Pediatr Res 1997 Nov;42(5):583-7 PMID: 9357927 SCOPUS ID: 2-s2.0-0030772205 11/14/1997 48 Citations

Functional correction of short-chain acyl-CoA dehydrogenase deficiency in transgenic mice: implications for gene therapy of human mitochondrial enzyme deficiencies. (Kelly CL, Rhead WJ, Kutschke WK, Brix AE, Hamm DA, Pinkert CA, Lindsey JR, Wood PA) Hum Mol Genet 1997 Sep;6(9):1451-5 PMID: 9285781 SCOPUS ID: 2-s2.0-0030774807 09/01/1997 18 Citations

Mutations in the glutathione synthetase gene cause 5-oxoprolinuria. (Shi ZZ, Habib GM, Rhead WJ, Gahl WA, He X, Sazer S, Lieberman MW) Nat Genet 1996 Nov;14(3):361-5 PMID: 8896573 SCOPUS ID: 2-s2.0-0030292360 11/01/1996 79 Citations

Prenatal ultrasound findings in hydrolethalus: continuing difficulties in diagnosis. (Norgard M, Yankowitz J, Rhead W, Kanis AB, Hall BD) Prenat Diagn 1996 Feb;16(2):173-9 PMID: 8650130 SCOPUS ID: 2-s2.0-0030020468 02/01/1996 8 Citations

Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its deficiency in two patients. (Aoyama T, Souri M, Ueno I, Kamijo T, Yamaguchi S, Rhead WJ, Tanaka K, Hashimoto T) Am J Hum Genet 1995 Aug;57(2):273-83 PMID: 7668252 PMCID: PMC1801555 SCOPUS ID: 2-s2.0-0029073089 08/01/1995 76 Citations

Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients. (Aoyama T, Souri M, Ushikubo S, Kamijo T, Yamaguchi S, Kelley RI, Rhead WJ, Uetake K, Tanaka K, Hashimoto T) J Clin Invest 1995 Jun;95(6):2465-73 PMID: 7769092 PMCID: PMC295925 SCOPUS ID: 2-s2.0-0029078041 06/01/1995 159 Citations

Formation of a novel arachidonic acid metabolite in peroxisomes. (Gordon JA, Heller SK, Rhead WJ, Watkins PA, Spector AA) Prostaglandins Leukot Essent Fatty Acids 1995;52(2-3):77-81 PMID: 7540307 SCOPUS ID: 2-s2.0-0028883254 02/01/1995 8 Citations

Evidence for intermediate channeling in mitochondrial beta-oxidation. (Nada MA, Rhead WJ, Sprecher H, Schulz H, Roe CR) J Biol Chem 1995 Jan 13;270(2):530-5 PMID: 7822275 SCOPUS ID: 2-s2.0-0028950214 01/13/1995 100 Citations

Transient improvement of congenital lactic acidosis in a male infant with pyruvate decarboxylase deficiency treated with dichloroacetate. (Tóth PP, el-Shanti H, Eivins S, Rhead WJ, Klein JM) J Pediatr 1993 Sep;123(3):427-30 PMID: 8355121 SCOPUS ID: 2-s2.0-0027170619 09/01/1993 22 Citations

A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase. (Aoyama T, Uchida Y, Kelley RI, Marble M, Hofman K, Tonsgard JH, Rhead WJ, Hashimoto T) Biochem Biophys Res Commun 1993 Mar 31;191(3):1369-72 PMID: 8466512 SCOPUS ID: 2-s2.0-0027295763 03/31/1993 151 Citations

Multiple acyl-coenzyme A dehydrogenation disorder responsive to riboflavin: substrate oxidation, flavin metabolism, and flavoenzyme activities in fibroblasts. (Rhead W, Roettger V, Marshall T, Amendt B) Pediatr Res 1993 Feb;33(2):129-35 PMID: 8433888 SCOPUS ID: 2-s2.0-0027400923 02/01/1993 44 Citations

Glutaric acidemia type II. Heterogeneity in beta-oxidation flux, polypeptide synthesis, and complementary DNA mutations in the alpha subunit of electron transfer flavoprotein in eight patients. (Freneaux E, Sheffield VC, Molin L, Shires A, Rhead WJ) J Clin Invest 1992 Nov;90(5):1679-86 PMID: 1430199 PMCID: PMC443224 SCOPUS ID: 2-s2.0-0026454729 11/01/1992 50 Citations

Short-chain acyl-coenzyme A dehydrogenase activity, antigen, and biosynthesis are absent in the BALB/cByJ mouse. (Amendt BA, Freneaux E, Reece C, Wood PA, Rhead WJ) Pediatr Res 1992 Jun;31(6):552-6 PMID: 1635815 SCOPUS ID: 2-s2.0-0026602820 06/01/1992 25 Citations

Neuropsychiatric manifestations of defect in mitochondrial beta oxidation response to riboflavin. (Triggs WJ, Roe CR, Rhead WJ, Hanson SK, Lin SN, Willmore LJ) J Neurol Neurosurg Psychiatry 1992 Mar;55(3):209-11 PMID: 1564483 PMCID: PMC1014728 SCOPUS ID: 2-s2.0-0026562538 03/01/1992 24 Citations

Multiple acyl-coenzyme A dehydrogenation disorders (MAD) responsive to riboflavin: biochemical studies in fibroblasts. (Roettger V, Marshall T, Amendt B, Rhead WJ) Prog Clin Biol Res 1992;375:317-26 PMID: 1438377 SCOPUS ID: 2-s2.0-0026620040 01/01/1992 8 Citations

An atypical case of cytochrome c oxidase deficiency with biochemical heterogeneity in fibroblasts. (Lutz R, Garnica A, Shires A, Freneaux E, De Vivo D, Neuhoff P, Rhead WJ) Neurology 1991 Dec;41(12):1957-60 PMID: 1660571 SCOPUS ID: 2-s2.0-0026327060 12/01/1991

A case of glutaric acidemia type II (severe multiple acyl-CoA dehydrogenation disorder) with subsequent prenatal exclusion in a sibling. (Medlock MD, Rhead WJ, Pollack L, Meredith JT, Pearl G, Reece C) J Perinatol 1991 Sep;11(3):227-30 PMID: 1919819 SCOPUS ID: 2-s2.0-0026229584 09/01/1991 2 Citations

The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene. (Kølvraa S, Gregersen N, Blakemore AI, Schneidermann AK, Winter V, Andresen BS, Curtis D, Engel PC, Pricille D, Rhead W) Hum Genet 1991 Aug;87(4):425-8 PMID: 1679031 SCOPUS ID: 2-s2.0-0025781068 08/01/1991 22 Citations

Inborn errors of fatty acid oxidation in man. (Rhead WJ) Clin Biochem 1991 Aug;24(4):319-29 PMID: 1959223 SCOPUS ID: 2-s2.0-0025814952 08/01/1991 20 Citations

Defect in fatty acid oxidation: laboratory and pathologic findings in a patient. (Tonsgard JH, Stephens JK, Rhead WJ, Penn D, Horwitz AL, Kirschner BS, Whitington PF, Berger S, Tripp ME) Pediatr Neurol 1991;7(2):125-30 PMID: 2059253 SCOPUS ID: 2-s2.0-0025851939 03/01/1991 6 Citations

Species variation in organellar location and activity of L-pipecolic acid oxidation in mammals. (Mihalik SJ, Rhead WJ) J Comp Physiol B 1991;160(6):671-6 PMID: 2045546 SCOPUS ID: 2-s2.0-0026101107 01/01/1991 16 Citations

Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency. (Matsubara Y, Narisawa K, Miyabayashi S, Tada K, Coates PM, Bachmann C, Elsas LJ 2nd, Pollitt RJ, Rhead WJ, Roe CR) Biochem Biophys Res Commun 1990 Aug 31;171(1):498-505 PMID: 2393404 SCOPUS ID: 2-s2.0-0025183418 08/31/1990 111 Citations

Juvenile multiple sclerosis-like episodes associated with a defect of mitochondrial beta oxidation. (Powell BR, Kennaway NG, Rhead WJ, Reece CJ, Burlingame TG, Buist NR) Neurology 1990 Mar;40(3 Pt 1):487-91 PMID: 2314592 SCOPUS ID: 2-s2.0-0025239837 03/01/1990 22 Citations

Riboflavin responsive glutaric aciduria type II. (Gregersen N, Rhead W, Christensen E) Prog Clin Biol Res 1990;321:477-94 PMID: 2183240 SCOPUS ID: 2-s2.0-0025034913 01/01/1990 27 Citations

Screening for inborn errors of fatty acid oxidation in cultured fibroblasts: an overview. (Rhead WJ) Prog Clin Biol Res 1990;321:365-82 PMID: 2183237 SCOPUS ID: 2-s2.0-0025177610 01/01/1990 17 Citations

A murine model for short-chain acyl-CoA dehydrogenase deficiency. (Wood PA, Amendt BA, Rhead WJ, Armstrong D, Millington DS, Inoue F) Prog Clin Biol Res 1990;321:427-34 PMID: 2326304 SCOPUS ID: 2-s2.0-0025105439 01/01/1990 3 Citations

Purified U5 small nuclear ribonucleoprotein can relieve the inhibition of spliceosome assembly and splicing by snRNP-free nuclear proteins. (Tazi J, Temsamani J, Alibert C, Rhead W, Khellil S, Cathala G, Brunel C, Jeanteur P) Nucleic Acids Res 1989 Jul 11;17(13):5223-43 PMID: 2527352 PMCID: PMC318107 SCOPUS ID: 2-s2.0-0024342728 07/11/1989 10 Citations

Mitochondrial encephalomyopathy with associated aminoacidopathy in a male sibship. (Booth FA, Haworth JC, Dilling LA, Perry TL, Greenberg CR, Seargeant LE, Penn AM, Rhead WJ) J Pediatr 1989 Jul;115(1):81-8 PMID: 2738799 SCOPUS ID: 2-s2.0-0024411172 07/01/1989 5 Citations

Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patients. (Mihalik SJ, Moser HW, Watkins PA, Danks DM, Poulos A, Rhead WJ) Pediatr Res 1989 May;25(5):548-52 PMID: 2717271 SCOPUS ID: 2-s2.0-0024580930 05/01/1989 36 Citations

L-pipecolic acid oxidation in the rabbit and cynomolgus monkey. Evidence for differing organellar locations and cofactor requirements in each species. (Mihalik SJ, Rhead WJ) J Biol Chem 1989 Feb 15;264(5):2509-17 PMID: 2914918 SCOPUS ID: 2-s2.0-0024501676 02/15/1989 46 Citations

Short-chain acyl-coenzyme A dehydrogenase deficiency in mice. (Wood PA, Amendt BA, Rhead WJ, Millington DS, Inoue F, Armstrong D) Pediatr Res 1989 Jan;25(1):38-43 PMID: 2919115 SCOPUS ID: 2-s2.0-0024496544 01/01/1989 86 Citations

Long-chain acyl-coenzyme A dehydrogenase deficiency: biochemical studies in fibroblasts from three patients. (Amendt BA, Moon A, Teel L, Rhead WJ) Pediatr Res 1988 Jun;23(6):603-5 PMID: 3393393 SCOPUS ID: 2-s2.0-0023918710 06/01/1988 18 Citations

Trisomy 2q and monosomy 11q in the same individual: the importance of considering the deleted segment. (Ardinger HH, Patil SR, Rhead WJ) Clin Genet 1987 Jun;31(6):381-5 PMID: 3621640 SCOPUS ID: 2-s2.0-0023236084 06/01/1987 10 Citations

Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patients. (Amendt BA, Greene C, Sweetman L, Cloherty J, Shih V, Moon A, Teel L, Rhead WJ) J Clin Invest 1987 May;79(5):1303-9 PMID: 3571488 PMCID: PMC424368 SCOPUS ID: 2-s2.0-0023248335 05/01/1987 157 Citations

Clinical and biochemical variation and family studies in the multiple acyl-CoA dehydrogenation disorders. (Rhead WJ, Wolff JA, Lipson M, Falace P, Desai N, Fritchman K, Moon A, Sweetman L) Pediatr Res 1987 Apr;21(4):371-6 PMID: 3574988 SCOPUS ID: 2-s2.0-0023179086 04/01/1987 37 Citations

Complementation analysis of fatty acid oxidation disorders. (Moon A, Rhead WJ) J Clin Invest 1987 Jan;79(1):59-64 PMID: 3793932 PMCID: PMC423985 SCOPUS ID: 2-s2.0-0023155640 01/01/1987 92 Citations

Multiple congenital anomalies syndrome with myopathy in chromosome 16 abnormality. (Ionasescu V, Patil S, Hart M, Rhead W, Smith W) Am J Med Genet 1987 Jan;26(1):189-94 PMID: 3812561 SCOPUS ID: 2-s2.0-0023232098 01/01/1987 14 Citations

Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency. (Duran M, Hofkamp M, Rhead WJ, Saudubray JM, Wadman SK) Pediatrics 1986 Dec;78(6):1052-7 PMID: 3786030 SCOPUS ID: 2-s2.0-0022991503 12/01/1986 108 Citations

The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts. (Amendt BA, Rhead WJ) J Clin Invest 1986 Jul;78(1):205-13 PMID: 3722376 PMCID: PMC329551 SCOPUS ID: 2-s2.0-0022474628 07/01/1986 54 Citations

14C-labeled substrate catabolism by human diploid fibroblasts derived from infants and adults. (Rhead WJ, Moon A, Roettger V, Henkle K) Biochem Med 1985 Oct;34(2):182-8 PMID: 3936490 SCOPUS ID: 2-s2.0-0022273039 10/01/1985 6 Citations

Catalytic defect of medium-chain acyl-coenzyme A dehydrogenase deficiency. Lack of both cofactor responsiveness and biochemical heterogeneity in eight patients. (Amendt BA, Rhead WJ) J Clin Invest 1985 Sep;76(3):963-9 PMID: 3840178 PMCID: PMC423960 SCOPUS ID: 2-s2.0-0022359510 09/01/1985 14 Citations

Fatal infantile cardiac glycogenosis without acid maltase deficiency presenting as congenital hydrops. (Atkin J, Snow JW Jr, Zellweger H, Rhead WJ) Eur J Pediatr 1984 Jun;142(2):150 PMID: 6590305 SCOPUS ID: 2-s2.0-0021238722 06/01/1984 12 Citations

Electron-transferring flavoprotein deficiency in the multiple acyl-CoA dehydrogenation disorders, glutaric aciduria type II and ethylmalonic--adipic aciduria. (Rhead WJ, Amendt BA) J Inherit Metab Dis 1984;7 Suppl 2:99-100 PMID: 6434879 SCOPUS ID: 2-s2.0-0021142012 01/01/1984 9 Citations

Abetalipoproteinemia. Report of an unusual patient. (Judisch GF, Rhead WJ, Miller DK) Ophthalmologica 1984;189(1-2):73-9 PMID: 6472810 SCOPUS ID: 2-s2.0-0021211592 01/01/1984 11 Citations

Dicarboxylic aciduria: deficient [1-14C]octanoate oxidation and medium-chain acyl-CoA dehydrogenase in fibroblasts. (Rhead WJ, Amendt BA, Fritchman KS, Felts SJ) Science 1983 Jul 01;221(4605):73-5 PMID: 6857268 SCOPUS ID: 2-s2.0-0020570022 07/01/1983 87 Citations

An intraoral nighttime feeding attachment for patients with glycogen storage disease, types I and III. (LaVelle WE, Rhead W) J Prosthet Dent 1983 May;49(5):687-9 PMID: 6406667 SCOPUS ID: 2-s2.0-0020756710 05/01/1983

Novel tritium release assays for isovaleryl-CoA and butyryl-CoA dehydrogenases. (Rhead WJ, Hall CL, Tanaka K) J Biol Chem 1981 Feb 25;256(4):1616-24 PMID: 7007368 SCOPUS ID: 2-s2.0-0019500393 02/25/1981 19 Citations

Glutaric aciduria type II: in vitro studies on substrate oxidation, acyl-CoA dehydrogenases, and electron-transferring flavoprotein in cultured skin fibroblasts. (Rhead W, Mantagos S, Tanaka K) Pediatr Res 1980 Dec;14(12):1339-42 PMID: 7208150 SCOPUS ID: 2-s2.0-0019137391 12/01/1980 30 Citations

Isovaleryl-CoA dehydrogenase: demonstration in rat liver mitochondria by ion exchange chromatography and isoelectric focusing. (Noda C, Rhead WJ, Tanaka K) Proc Natl Acad Sci U S A 1980 May;77(5):2646-50 PMID: 6930657 PMCID: PMC349459 SCOPUS ID: 2-s2.0-0019016567 05/01/1980 22 Citations

Demonstration of a specific mitochondrial isovaleryl-CoA dehydrogenase deficiency in fibroblasts from patients with isovaleric acidemia. (Rhead WJ, Tanaka K) Proc Natl Acad Sci U S A 1980 Jan;77(1):580-3 PMID: 6928646 PMCID: PMC348317 SCOPUS ID: 2-s2.0-0018833720 01/01/1980 62 Citations

Smoking and SIDS. (Rhead WJ) Pediatrics 1977 May;59(5):791-2 PMID: 558578 SCOPUS ID: 2-s2.0-0017493086 05/01/1977 3 Citations

A final note on the lack of relationship of selenium, other trace elements, and vitamin E in the causation of SIDS. (Rhead WJ) J Pediatr 1977 Mar;90(3):500 PMID: 839357 SCOPUS ID: 2-s2.0-0017582804 03/01/1977 2 Citations

Cystine metabolism in human fibroblasts. Comparison of normal, cystinotic, and gamma-glutamylcysteine synethetase-deficient cells. (Oshima RG, Rhead WJ, Thoene JG, Schneider JA) J Biol Chem 1976 Jul 25;251(14):4287-93 PMID: 932033 SCOPUS ID: 2-s2.0-0017115242 07/25/1976 43 Citations

Effect of selenium compounds on selenium content, growth and 35S-cystine metabolism of skin fibroblasts from normal and cystinotic individuals. (Rhead WJ, Schneider JA) Bioinorg Chem 1976;6(3):187-202 PMID: 1053514 SCOPUS ID: 2-s2.0-0017025868 01/01/1976 2 Citations

Sudden infant death syndrome: plasma vitamin E levels and dietary factors. (Schrauzer GN, Rhead WJ, Saltzstein SL) Ann Clin Lab Sci 1975;5(1):31-7 PMID: 1111439 SCOPUS ID: 2-s2.0-0016632097 01/01/1975 17 Citations

Letter: Determinants of ascorbic acid levels. (Rhead WJ) N Engl J Med 1974 May 02;290(18):1024-5 PMID: 4818904 SCOPUS ID: 2-s2.0-0016383009 05/02/1974

Selenium in human plasma: levels in blood proteins and behavior upon dialysis, acidification, and reduction. (Rhead WJ, Evans GA, Schrauzer GN) Bioinorg Chem 1974 Apr;3(3):217-23 PMID: 4214146 SCOPUS ID: 2-s2.0-0016224110 04/01/1974 9 Citations

The selenium catalyzed reduction of methylene blue by thiols. (Rhead WJ, Schrauzer GN) Bioinorg Chem 1974 Apr;3(3):225-42 PMID: 4424135 SCOPUS ID: 2-s2.0-0016169675 04/01/1974 24 Citations

Letter: Sudden death in infancy and vitamin E deficiency. (Rhead WJ, Schrauzer GN, Saltzstein SL) Br Med J 1973 Dec 01;4(5891):548-9 PMID: 4796619 PMCID: PMC1587486 SCOPUS ID: 2-s2.0-0015827231 12/01/1973 13 Citations

Letter: Sudden infant deaths and deficiencies in diet. (Saltzstein SL, Schrauzer GN, Rhead WJ) JAMA 1973 Oct 22;226(4):466 PMID: 4800242 SCOPUS ID: 2-s2.0-0015933042 10/22/1973 5 Citations

Ascorbic acid abuse: effects on long term ingestion of excessive amounts on blood levels and urinary excretion. (Schrauzer GN, Rhead WJ) Int J Vitam Nutr Res 1973;43(2):201-11 PMID: 4716569 SCOPUS ID: 2-s2.0-0015836248 01/01/1973 34 Citations

Vitamin E, selenium, and the sudden infant death syndrome. (Rhead WJ, Schrauzer GN, Saltzstein SL, Cary EE, Allaway WH) J Pediatr 1972 Aug;81(2):415-6 PMID: 5042504 SCOPUS ID: 2-s2.0-0015386374 08/01/1972 13 Citations

Risks of long-term ascorbic acid overdosage. (Rhead WJ, Schrauzer GN) Nutr Rev 1971 Nov;29(11):262-3 PMID: 5127162 SCOPUS ID: 2-s2.0-0015151725 11/01/1971 36 Citations

Interpretation of the methylene blue reduction test of human plasma and the possible cancer protecting effect of selenium. (Schrauzer GN, Rhead WJ) Experientia 1971 Sep 15;27(9):1069-71 PMID: 5116139 SCOPUS ID: 2-s2.0-0015226742 09/15/1971 35 Citations

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Profiles for MCW, MU, MSOE, UWM, BCW, CW, Froedtert, and VA Faculty

William Rhead MD, PhD

Adjunct Professor

Publications (121)