Novel heterozygous mutations in the PGAM2 gene with negative exercise testing von Sidhu, M., Brady, L., Vladutiu, G.D., Tarnopolsky, M.A.

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Compensatory amplification of mtDNA in a patient with a novel deletion/duplication and high mutant load von Wong, L-J C, Perng, C-L, Hsu, C-H, Bai, R-K, Schelley, S, Vladutiu, G D, Vogel, H, Enns, G M

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Statin therapy depresses total body fat oxidation in the absence of genetic limitations to fat oxidation von Fisher, N. M, Meksawan, K, Limprasertkul, A, Isackson, P. J, Pendergast, D. R, Vladutiu, G. D

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Six novel mutations in the myophosphorylase gene in patients with McArdle disease and a family with pseudo-dominant inheritance pattern von Wu, Y., Weber, J.L., Vladutiu, G.D., Tarnopolsky, M.A.

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The distribution of white blood cell fat oxidation in health and disease von Pendergast, D. R., Fisher, N. M., Meksawan, K., Doubrava, M., Vladutiu, G. D.

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Synergistic Heterozygosity: Disease Resulting from Multiple Partial Defects in One or More Metabolic Pathways von Vockley, Jerry, Rinaldo, Piero, Bennett, Michael J., Matern, Dietrich, Vladutiu, Georgirene D.

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Biochemical and molecular correlations in carnitine palmitoyltransferase II deficiency von Vladutiu, Georgirene D.

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Rapid, cost-effective gene mutation screening for carnitine palmitoyltransferase II deficiency using whole blood on filter paper von SMAIL, D, GAMBINO, L, BOLES, C, VLADUTIU, G. D

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Heterozygosity: An Expanding Role in Proteomics von Vladutiu, Georgirene D.

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Novel mutations associated with carnitine palmitoyltransferase II deficiency von Taggart, R. Thomas, Smail, David, Apolito, Christopher, Vladutiu, Georgirene D.

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Mitochondrial Disease in Patients with Exercise Intolerance von Vladutiu, G D, Tabone, E

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A novel mutation in the PYGM gene in a family with pseudo-dominant transmission of McArdle disease von Isackson, Paul J., Tarnopolsky, Mark, Vladutiu, Georgirene D.

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Complex phenotypes in metabolic muscle diseases von Vladutiu, Georgirene D.

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Association between internalized nuclei and mitochondrial enzyme defects in muscle von Vladutiu, Georgirene D., Idiculla, Sebu

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RYR1 and CACNA1S genetic variants identified with statin-associated muscle symptoms von Isackson, Paul J, Wang, Jianxin, Zia, Mohammad, Spurgeon, Paul, Levesque, Adrian, Bard, Jonathan, James, Smitha, Nowak, Norma, Lee, Tae Keun, Vladutiu, Georgirene D

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Carnitine palmitoyl transferase deficiency in malignant hyperthermia von Vladutiu, Georgirene D., Hogan, Kirk, Saponara, Isora, Tassini, Lawrence, Conroy, Jeffrey

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Clinical Spectrum, Morbidity, and Mortality in 113 Pediatric Patients With Mitochondrial Disease von Scaglia, Fernando, Towbin, Jeffrey A, Craigen, William J, Belmont, John W, Smith, E. O'Brian, Neish, Stephen R, Ware, Stephanie M, Hunter, Jill V, Fernbach, Susan D, Vladutiu, Georgirene D, Wong, Lee-Jun C, Vogel, Hannes

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A Variable Myopathy Associated with Heterozygosity for the R503C Mutation in the Carnitine Palmitoyltransferase II Gene von Vladutiu, Georgirene D., Bennett, Michael J., Smail, David, Wong, Lee-Jun, Taggart, R.Thomas, Lindsley, Herbert B.

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Corrigendum to “Six novel mutations in the myophosphorylase gene in patients with McArdle disease and a family with pseudo-dominant inheritance pattern” [Mol. Genet. Metab. 104 (20... von Wu, Y., Weber, J.L., Vladutiu, G.D., Tarnopolsky, M.A.

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Quality improvement of mitochondrial respiratory chain complex enzyme assays using Caenorhabditis elegans von Chen, Xiulian, Thorburn, David R, Wong, Lee-Jun, Vladutiu, Georgirene D, Haas, Richard H, Le, Thuy, Hoppel, Charles, Sedensky, Margaret, Morgan, Philip, Hahn, Si Houn

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