Fetal fatty acid oxidation defects and maternal liver disease in pregnancy von BROWNING, Marsha F, LEVY, Harvey L, WILKINS-HAUG, Louise E, LARSON, Cecilia, SHIH, Vivian E

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Alternative-Pathway Therapy for Hyperammonemia von Shih, Vivian E

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Long-term follow-up of four patients affected by HHH syndrome von Kim, Sook Z., Song, Wung J., Nyhan, William L., Ficicioglu, Can, Mandell, Roseann, Shih, Vivian E.

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Spectrum of Medium-Chain Acyl-CoA Dehydrogenase Deficiency Detected by Newborn Screening von Hsu, Ho-Wen, Zytkovicz, Thomas H, Comeau, Anne Marie, Strauss, Arnold W, Marsden, Deborah, Shih, Vivian E, Grady, George F, Eaton, Roger B

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Vascular endothelial function in cyclosporine and tacrolimus treated renal transplant recipients von OVUWORIE, Cyril A, FOX, Ervin R, CHOW, Chi-Ming, PASCUAL, Manuel, SHIH, Vivian E, PICARD, Michael H, TOLKOFF-RUBIN, Nina E

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Effect of Expanded Newborn Screening for Biochemical Genetic Disorders on Child Outcomes and Parental Stress von Waisbren, Susan E, Albers, Simone, Amato, Steve, Ampola, Mary, Brewster, Thomas G, Demmer, Laurie, Eaton, Roger B, Greenstein, Robert, Korson, Mark, Larson, Cecilia, Marsden, Deborah, Msall, Michael, Naylor, Edwin W, Pueschel, Siegfried, Seashore, Margretta, Shih, Vivian E, Levy, Harvey L

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Isolated Sulfite Oxidase Deficiency: A Case Report With a Novel Mutation and Review of the Literature von Tan, Wen-Hann, Eichler, Florian S, Hoda, Sadaf, Lee, Melissa S, Baris, Hagit, Hanley, Catherine A, Grant, P. Ellen, Krishnamoorthy, Kalpathy S, Shih, Vivian E

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Fumarase deficiency caused by homozygous P131R mutation and paternal partial isodisomy of chromosome 1 von Zeng, Wen‐Qi, Gao, Hanlin, Brueton, Louise, Hutchin, Tim, Gray, George, Chakrapani, Anupam, Olpin, Simon, Shih, Vivian E.

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Low vitamin B6 but not homocyst(e)ine is associated with increased risk of stroke and transient ischemic attack in the era of folic acid grain fortification von Kelly, Peter J, Shih, Vivian E, Kistler, J Philip, Barron, Megan, Lee, Hang, Mandell, Roseann, Furie, Karen L

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Proton Magnetic Resonance Spectroscopy and Diffusion-Weighted Imaging in Isolated Sulfite Oxidase Deficiency von Eichler, Florian, Tan, Wen-Hann, Shih, Vivian E., Grant, P. Ellen, Krishnamoorthy, Kalpathy

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Arginase deficiency with lethal neonatal expression: Evidence for the glutamine hypothesis of cerebral edema von Picker, Jonathan D., Puga, Ana C., Levy, Harvey L., Marsden, Deborah, Shih, Vivian E., DeGirolami, Umberto, Ligon, Keith L., Cederbaum, Stephen D., Kern, Rita M., Cox, Gerald F.

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Pericardial effusion in primary systemic carnitine deficiency von Wattanasirichaigoon, Duangrurdee, Khowsathit, Pongsak, Visudtibhan, Anannit, Suthutvoravut, Umaporn, Charoenpipop, Dussadee, Kim, Sook Z., Levy, Harvey L., Shih, Vivian 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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USE OF AMNIOTIC FLUID AMINO ACIDS IN PRENATAL TESTING FOR ARGININOSUCCINIC ACIDURIA AND CITRULLINAEMIA von MANDELL, ROSEANN, PACKMAN, SEYMOUR, LAFRAMBOISE, RACHEL, GOLBUS, MITCHELL S., SCHMIDT, KATHLEEN, WORKMAN, LAURA, SAUDUBRAY, J. M., SHIH, VIVIAN E.

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Carbamyl phosphate synthetase 1 deficiency: A destructive encephalopathy von Takeoka, Masanori, Soman, Teesta B, Shih, Vivian E, Caviness, Verne S, Krishnamoorthy, Kalpathy S

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Effect of Expanded Newborn Screening for Biochemical Genetic Disorders on Child Outcomes and Parental Stress von Waisbren, Susan E, Albers, Simone, Amato, Steve, Ampola, Mary, Brewster, Thomas G, Demmer, Laurie, Eaton, Roger B, Greenstein, Robert, Korson, Mark, Larson, Cecilia, Marsden, Deborah, Msall, Michael, Naylor, Edwin W, Pueschel, Siegfried, Seashore, Margretta, Shih, Vivian E, Levy, Harvey L

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Tandem Mass Spectrometric Analysis for Amino, Organic, and Fatty Acid Disorders in Newborn Dried Blood Spots 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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Benign Methylmalonic Aciduria von Ledley, Fred D, Levy, Harvey L, Shih, Vivian E, Benjamin, Rachel, Mahoney, Maurice J

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Lysinuric Protein Intolerance Presenting as Childhood Osteoporosis: Clinical and Skeletal Response to Citrulline Therapy von Carpenter, Thomas O, Levy, Harvey L, Holtrop, Marijke E, Shih, Vivian E, Anast, Constantine S

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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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