Ammonia control and neurocognitive outcome among urea cycle disorder patients treated with glycerol phenylbutyrate von Diaz, George A., Krivitzky, Lauren S., Mokhtarani, Masoud, Rhead, William, Bartley, James, Feigenbaum, Annette, Longo, Nicola, Berquist, William, Berry, Susan A., Gallagher, Renata, Lichter‐Konecki, Uta, Bartholomew, Dennis, Harding, Cary O., Cederbaum, Stephen, McCandless, Shawn E., Smith, Wendy, Vockley, Gerald, Bart, Stephen A., Korson, Mark S., Kronn, David, Zori, Roberto, Merritt, J. Lawrence, C.S. Nagamani, Sandesh, Mauney, Joseph, LeMons, Cynthia, Dickinson, Klara, Moors, Tristen L., Coakley, Dion F., Scharschmidt, Bruce F., Lee, Brendan

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Clinical approach to genetic cardiomyopathy in children von SCHWARTZ, M. L, COX, G. F, LIN, A. E, KORSON, M. S, PEREZ-ATAYDE, A, LACRO, R. V, LIPSHULTZ, S. E

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Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorder von Lee, Brendan, Diaz, George A., Rhead, William, Lichter-Konecki, Uta, Feigenbaum, Annette, Berry, Susan A., Le Mons, Cindy, Bartley, James A., Longo, Nicola, Nagamani, Sandesh C., Berquist, William, Gallagher, Renata, Bartholomew, Dennis, Harding, Cary O., Korson, Mark S., McCandless, Shawn E., Smith, Wendy, Cederbaum, Stephen, Wong, Derek, Merritt, J. Lawrence, Schulze, Andreas, Vockley, Gerard, Kronn, David, Zori, Roberto, Summar, Marshall, Milikien, Douglas A., Marino, Miguel, Coakley, Dion F., Mokhtarani, Masoud, Scharschmidt, Bruce F.

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Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges von Parikh, Sumit, Goldstein, Amy, Koenig, Mary Kay, Scaglia, Fernando, Enns, Gregory M, Saneto, Russell, Anselm, Irina, Collins, Abigail, Cohen, Bruce H, DeBrosse, Suzanne D, Dimmock, David, Falk, Marni J, Ganesh, Jaya, Greene, Carol, Gropman, Andrea L, Haas, Richard, Kahler, Stephen G, Kamholz, John, Kendall, Fran, Korson, Mark S, Mattman, Andre, Milone, Margherita, Niyazov, Dmitriy, Pearl, Phillip L, Reimschisel, Tyler, Salvarinova-Zivkovic, Ramona, Sims, Katherine, Tarnopolsky, Mark, Tsao, Chang-Yong, van Hove, Johan, Walsh, Laurence, Wolfe, Lynne A

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Practice patterns of mitochondrial disease physicians in North America. Part 2: treatment, care and management von Parikh, Sumit, Goldstein, Amy, Koenig, Mary Kay, Scaglia, Fernando, Enns, Gregory M, Saneto, Russell

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Self-reported treatment-associated symptoms among patients with urea cycle disorders participating in glycerol phenylbutyrate clinical trials von Nagamani, Sandesh C S, Diaz, George A, Rhead, William, Berry, Susan A, Le Mons, Cynthia, Lichter-Konecki, Uta, Bartley, James, Feigenbaum, Annette, Schulze, Andreas, Longo, Nicola, Berquist, William, Gallagher, Renata, Bartholomew, Dennis, Harding, Cary O, Korson, Mark S, McCandless, Shawn E, Smith, Wendy, Vockley, Jerry, Kronn, David, Zori, Robert, Cederbaum, Stephen, Merritt, 2nd, J Lawrence, Wong, Derek, Coakley, Dion F, Scharschmidt, Bruce F, Dickinson, Klara, Marino, Miguel, Lee, Brendan H, Mokhtarani, Masoud

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Quality of Life Assessment in Adults with Type 1 Gaucher Disease von Bruce J. Masek, Katherine B. Sims, Catherine M. Bove, Mark S. Korson, Priscilla Short, Norman, Dennis K.

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Newborn screening for hepatorenal tyrosinemia by tandem mass spectrometry: analysis of succinylacetone extracted from dried blood spots von Allard, Pierre, Grenier, André, Korson, Mark S., Zytkovicz, Thomas H.

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The importance of gut motility in the metabolic control of propionic acidemia von Prasad, Chitra, Nurko, Samuel, Borovoy, Jacob, Korson, Mark S.

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Determination of phenylalanine and tyrosine in dried blood specimens by ion-exchange chromatography using the Hitachi L-8800 analyzer von Allard, Pierre, Cowell, Lurley D., Zytkovicz, Thomas H., Korson, Mark S., Ampola, Mary G.

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A GC/MS/MS screening method for multiple organic acidemias from urine specimens von Hagen, Thilo, Korson, Mark S., Sakamoto, Masayuki, Evans, James E.

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Clinical genetic testing for patients with autism spectrum disorders von Shen, Yiping, Dies, Kira A, Holm, Ingrid A, Bridgemohan, Carolyn, Sobeih, Magdi M, Caronna, Elizabeth B, Miller, Karen J, Frazier, Jean A, Silverstein, Iris, Picker, Jonathan, Weissman, Laura, Raffalli, Peter, Jeste, Shafali, Demmer, Laurie A, Peters, Heather K, Brewster, Stephanie J, Kowalczyk, Sara J, Rosen-Sheidley, Beth, McGowan, Caroline, Duda, 3rd, Andrew W, Lincoln, Sharyn A, Lowe, Kathryn R, Schonwald, Alison, Robbins, Michael, Hisama, Fuki, Wolff, Robert, Becker, Ronald, Nasir, Ramzi, Urion, David K, Milunsky, Jeff M, Rappaport, Leonard, Gusella, James F, Walsh, Christopher A, Wu, Bai-Lin, Miller, David T

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Tyrosine supplementation in phenylketonuria: Diurnal blood tyrosine levels and presumptive brain influx of tyrosine and other large neutral amino acids von Kalsner, Louisa R., Rohr, Frances J., Strauss, Kevin A., Korson, Mark S., Levy, Harvey L.

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Neuropsychiatric Illness in a Patient with Cobalamin G Disease, an Inherited Disorder of Vitamin B12 Metabolism von Hill, Kevin P., Lukonis, Christopher J., Korson, Mark S., Weinstein, Cheryl, Thall, Mark, Schwartz, Jane T.

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Perioperative white matter degeneration and death in a patient with a defect in mitochondrial oxidative phosphorylation von CASTA, A, QUACKENBUSH, E. J, HOUCK, C. S, KORSON, M. S

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Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorder von Lee, Brendan, Diaz, George A, Rhead, William, Lichter-Konecki, Uta, Feigenbaum, Annette, Berry, Susan A, Le Mons, Cindy, Bartley, James A, Longo, Nicola, Nagamani, Sandesh C, Berquist, William, Gallagher, Renata, Bartholomew, Dennis, Harding, Cary O, Korson, Mark S, McCandless, Shawn E, Smith, Wendy, Cederbaum, Stephen, Wong, Derek, Merritt, J Lawrence, Schulze, Andreas, Vockley, Jerry, Vockley, Gerard, Kronn, David, Zori, Roberto, Summar, Marshall, Milikien, Douglas A, Marino, Miguel, Coakley, Dion F, Mokhtarani, Masoud, Scharschmidt, Bruce F

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Treatment-related signs and symptoms among patients with urea cycle disorders (UCDs) during treatment with sodium phenylbutyrate and glycerol phenylbutyrate von Nagamani, Sandesh C., Diaz, George A., Rhead, William J., Berry, Sue A., Le Mons, Cindy, Lichter-Konecki, Uta, Bartley, James A., Feigenbaum, Annette, Schulze, Andreas, Longo, Nicola, Berquist, William E., Gallagher, Renata, Bartholomew, Dennis W., Harding, Cary O., Korson, Mark S., McCandless, Shawn E., Smith, Wendy E., Vockley, Gerard, Kronn, David, Zori, Robert, Coakley, Dion F., Scharschmidt, Bruce F., Mokhtarani, Masoud, Lee, Brendan H.

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BLOOD AMMONIA AND GLUTAMINE AS PREDICTORS OF HYPERAMMONEMIC CRISES IN UREA CYCLE DISORDER PATIENTS von Lee, Brendan, Diaz, George A., Rhead, William, Lichter-Konecki, U., Feigenbaum, Annette, Berry, Susan A., Le Mons, C., Bartley, James A, Longo, Nicola, Nagamani, Sandesh C., Berquist, William, Gallagher, Renata, Bartholomew, Dennis, Harding, Cary O., Korson, Mark S., McCandless, Shawn E., Smith, Wendy, Cederbaum, Stephen, Wong, Derek, Merritt, J. Lawrence, Schulze, A., Vockley, Gerard, Kronn, David, Zori, Roberto, Summar, Marshall, Milikien, D.A., Marino, M., Coakley, D.F., Mokhtarani, M., Scharschmidt, B.F.

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Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiency von Cox, Gerald F., Souri, Masayoshi, Aoyama, Toshifumi, Rockenmacher, Sol, Varvogli, Liza, Rohr, Frances, Hashimoto, Takashi, Korson, Mark S.

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Pitfalls in Diagnosing Galactosemia: False Negative Newborn Screening Following Red Blood Cell Transfusion von Korson, Mark S, Levy, Harvey L

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