Wagner C - Search Results

1

Prevention of brain disease from severe 5,10-methylenetetrahydrofolate reductase deficiency.

Strauss KA, Morton DH, Puffenberger EG, Hendrickson C, Robinson DL, Wagner C, Stabler SP, Allen RH, Chwatko G, Jakubowski H, Niculescu MD, Mudd SH. Strauss KA, et al. Among authors: wagner c. Mol Genet Metab. 2007 Jun;91(2):165-75. doi: 10.1016/j.ymgme.2007.02.012. Epub 2007 Apr 3. Mol Genet Metab. 2007. PMID: 17409006

2

Liver transplantation for treatment of severe S-adenosylhomocysteine hydrolase deficiency.

Strauss KA, Ferreira C, Bottiglieri T, Zhao X, Arning E, Zhang S, Zeisel SH, Escolar ML, Presnick N, Puffenberger EG, Vugrek O, Kovacevic L, Wagner C, Mazariegos GV, Mudd SH, Soltys K. Strauss KA, et al. Among authors: wagner c. Mol Genet Metab. 2015 Sep-Oct;116(1-2):44-52. doi: 10.1016/j.ymgme.2015.06.005. Epub 2015 Jun 19. Mol Genet Metab. 2015. PMID: 26095522

3

Enzymatic activity of methionine adenosyltransferase variants identified in patients with persistent hypermethioninemia.

Fernández-Irigoyen J, Santamaría E, Chien YH, Hwu WL, Korman SH, Faghfoury H, Schulze A, Hoganson GE, Stabler SP, Allen RH, Wagner C, Mudd SH, Corrales FJ. Fernández-Irigoyen J, et al. Among authors: wagner c. Mol Genet Metab. 2010 Oct-Nov;101(2-3):172-7. doi: 10.1016/j.ymgme.2010.07.009. Epub 2010 Jul 15. Mol Genet Metab. 2010. PMID: 20675163 Free article.

4

Two patients with hepatic mtDNA depletion syndromes and marked elevations of S-adenosylmethionine and methionine.

Mudd SH, Wagner C, Luka Z, Stabler SP, Allen RH, Schroer R, Wood T, Wang J, Wong LJ. Mudd SH, et al. Among authors: wagner c. Mol Genet Metab. 2012 Feb;105(2):228-36. doi: 10.1016/j.ymgme.2011.11.006. Epub 2011 Nov 12. Mol Genet Metab. 2012. PMID: 22137549 Free PMC article.

5

Progressive cerebral edema associated with high methionine levels and betaine therapy in a patient with cystathionine beta-synthase (CBS) deficiency.

Yaghmai R, Kashani AH, Geraghty MT, Okoh J, Pomper M, Tangerman A, Wagner C, Stabler SP, Allen RH, Mudd SH, Braverman N. Yaghmai R, et al. Among authors: wagner c. Am J Med Genet. 2002 Feb 15;108(1):57-63. doi: 10.1002/ajmg.10186. Am J Med Genet. 2002. PMID: 11857551

6

Elevated plasma total homocysteine in severe methionine adenosyltransferase I/III deficiency.

Stabler SP, Steegborn C, Wahl MC, Oliveriusova J, Kraus JP, Allen RH, Wagner C, Mudd SH. Stabler SP, et al. Among authors: wagner c. Metabolism. 2002 Aug;51(8):981-8. doi: 10.1053/meta.2002.34017. Metabolism. 2002. PMID: 12145770

7

Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap.

Harvey Mudd S, Braverman N, Pomper M, Tezcan K, Kronick J, Jayakar P, Garganta C, Ampola MG, Levy HL, McCandless SE, Wiltse H, Stabler SP, Allen RH, Wagner C, Borschel MW. Harvey Mudd S, et al. Among authors: wagner c. Mol Genet Metab. 2003 May;79(1):6-16. doi: 10.1016/s1096-7192(03)00066-0. Mol Genet Metab. 2003. PMID: 12765841

8

Glycine N -methyltransferase deficiency: a new patient with a novel mutation.

Augoustides-Savvopoulou P, Luka Z, Karyda S, Stabler SP, Allen RH, Patsiaoura K, Wagner C, Mudd SH. Augoustides-Savvopoulou P, et al. Among authors: wagner c. J Inherit Metab Dis. 2003;26(8):745-59. doi: 10.1023/B:BOLI.0000009978.17777.33. J Inherit Metab Dis. 2003. PMID: 14739680

9

Methyl balance and transmethylation fluxes in humans.

Mudd SH, Brosnan JT, Brosnan ME, Jacobs RL, Stabler SP, Allen RH, Vance DE, Wagner C. Mudd SH, et al. Among authors: wagner c. Am J Clin Nutr. 2007 Jan;85(1):19-25. doi: 10.1093/ajcn/85.1.19. Am J Clin Nutr. 2007. PMID: 17209172 Free article.

10

S-adenosylhomocysteine hydrolase deficiency: two siblings with fetal hydrops and fatal outcomes.

Grubbs R, Vugrek O, Deisch J, Wagner C, Stabler S, Allen R, Barić I, Rados M, Mudd SH. Grubbs R, et al. Among authors: wagner c. J Inherit Metab Dis. 2010 Dec;33(6):705-13. doi: 10.1007/s10545-010-9171-x. Epub 2010 Sep 18. J Inherit Metab Dis. 2010. PMID: 20852937

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