Homocysteine, MTHFR 677C→T polymorphism, and risk of ischemic stroke: Results of a meta-analysis von KELLY, P. J, ROSAND, J, KISTLER, J. P, SHIH, V. E, SILVEIRA, S, PLOMARITOGLOU, A, FURIE, K. L

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Argininosuccinate lyase deficiency: Longterm outcome of 13 patients detected by newborn screening von Ficicioglu, C., Mandell, R., Shih, V.E.

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Tandem Mass Spectrometric Analysis for Amino, Organic, and Fatty Acid Disorders in Newborn Dried Blood Spots: A Two-Year Summary from the New England Newborn Screening Program von Zytkovicz, Thomas H, Fitzgerald, Eileen F, Marsden, Deborah, Larson, Cecilia A, Shih, Vivian E, Johnson, Donna M, Strauss, Arnold W, Comeau, Anne Marie, Eaton, Roger B, Grady, George F

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Inflammation, homocysteine, and vitamin B6 status after ischemic stroke von KELLY, P. J, KISTLER, J. P, SHIH, V. E, MANDELL, R, ATASSI, N, BARRON, M, LEE, H, SILVEIRA, S, FURIE, K. L

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Stroke in young patients with hyperhomocysteinemia due to cystathionine beta-synthase deficiency von KELLY, P. J, FURIE, K. L, KISTLER, J. P, BARRON, M, PICARD, E. H, MANDELL, R, SHIH, V. E

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Ornithine aminotransferase deficiency: Diagnostic difficulties in neonatal presentation von Cleary, M. A., Dorland, L., Koning, T. J., Poll‐The, B. T., Duran, M., Mandell, R., Shih, V. E., Berger, R., Olpin, S. E., Besley, G. T. N.

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Novel Possibilities in Pharmacotherapy of Patients With Chronic Heart Failure von Zhuravleva, M V, Prokofiev, A B, Shih, E V, Serebrova, S Y, Gorodetskaya, G I

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Successful long‐term treatment of hepatic carnitine palmitoyltransferase I deficiency and a novel mutation von Stoler, J. M., Sabry, M. A., Hanley, C., Hoppel, C. L., Shih, V. E.

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Reproductive fitness in maternal homocystinuria due to cystathionine β‐synthase deficiency von Levy, H. L., Vargas, J. E., Waisbren, S. E., Kurczynski, T. W., Roeder, E. R., Schwartz, R. S., Rosengren, S., Prasad, C., Greenberg, C. R., Gilfix, B. M., MacGregor, D., Shih, V. E., Bao, L., Kraus, J. P.

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COMPLEX ASSESSMENT OF EFFICACY OF STATINS PRESCRIBED AT MOST BY CLINICIANS von Sivkov, A. S., Shih, E. V., Osadchuk, M. A., Sivkova, S. K., Kireeva, N. V., Chernus, N. P.

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A missense mutation (1278T) in the cystathionine β-synthase gene prevalent in pyridoxine-responsive homocystinuria and associated with mild clinical phenotype von SHIH, V. E, FRINGER, J. M, MANDELL, R, KRAUS, J. P, BERRY, G. T, HEIDENREICH, R. A, KORSON, M. S, LEVY, H. L, RAMESH, V

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Molecular basis of cystathionine β-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuria von Hu, Frances L., Gu, Zen, Kožich, Viktor, Kraus, Jan P., Ramesh, Vijay, Shih, Vivian E.

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Neonatal onset of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with favorable outcome von ZAMMARCHI, E, CIANI, F, PASQUINI, E, BONOCORE, G, SHIH, V. E, DONATI, M. A

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New England Consortium: A model for medical evaluation of expanded newborn screening with tandem mass spectrometry von Albers, S., Waisbren, S. E., Ampola, M. G., Brewster, T. G., Burke, L. W., Demmer, L. A., Filiano, J., Greenstein, R. M. G., Ingham, C. L., Korson, M. S., Marsden, D., Schwartz, R. C., Seashore, M. R., Shih, V. E., Levy, H. L.

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Newborn screening compared to clinical identification of biochemical genetic disorders von Waisbren, S. E., Read, C. Y., Ampola, M., Brewster, T. G., Demmer, L., Greenstein, R., Ingham, C. L., Korson, M., Msall, M., Pueschel, S., Seashore, M., Shih, E., Levy, H. L.

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Ornithine carbamoyltransferase deficiency: Unusual clinical findings and novel mutation von Shih, V. E., Safran, A. P., Ropper, A. H., Tuchman, M.

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The results of the use of a combined probiotic ( Lactobacillus rhamnosus GG and Bifidobacterium animalis spp. lactis ВB-12) in children with gastrointestinal and skin manifestation... von Vorobieva, O A, Shih, E V, Drozdov, V N, Shikh, N V

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Molecular Basis of Ornithine Aminotransferase Deficiency in B-6-Responsive and -Nonresponsive Forms of Gyrate Atrophy von Ramesh, Vijaya, McClatchey, Andrea I., Ramesh, Narayanaswamy, Benoit, Lynne A., Berson, Eliot L., Shih, Vivian E., Gusella, James F.

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Vascular endothelial function in cyclosporine and tacrolimus treated renal transplant recipients von Ovuworie, C A, Fox, E R, Chow, C M, Pascual, M, Shih, V E, Picard, M H, Tolkoff-Rubin, N E

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Organ donation by a maple syrup urine disease patient von Shih, V. E., Stewart, B.

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