Elective Liver Transplantation for the Treatment of Classical Maple Syrup Urine Disease von Strauss, K. A., Mazariegos, G. V., Sindhi, R., Squires, R., Finegold, D. N., Vockley, G., Robinson, D. L., Hendrickson, C., Virji, M., Cropcho, L., Puffenberger, E. G., McGhee, W., Seward, L. M., Morton, D. H.

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The asymmetry of antimatter in the proton von Dove, J., Kerns, B., McClellan, R. E., Miyasaka, S., Morton, D. H., Nagai, K., Prasad, S., Sanftl, F., Scott, M. B. C., Tadepalli, A. S., Aidala, C. A., Arrington, J., Ayuso, C., Barker, C. L., Brown, C. N., Chang, W. C., Chen, A., Christian, D. C., Dannowitz, B. P., Daugherity, M., Diefenthaler, M., El Fassi, L., Geesaman, D. F., Gilman, R., Goto, Y., Guo, L., Guo, R., Hague, T. J., Holt, R. J., Isenhower, D., Kinney, E. R., Kitts, N., Klein, A., Kleinjan, D. W., Kudo, Y., Leung, C., Lin, P.-J., Liu, K., Liu, M. X., Lorenzon, W., Makins, N. C. R., de Medeiros, M. Mesquita, McGaughey, P. L., Miyachi, Y., Mooney, I., Nakahara, K., Nakano, K., Nara, S., Peng, J.-C., Puckett, A. J., Ramson, B. J., Reimer, P. E., Rubin, J. G., Sawada, S., Sawada, T., Shibata, T.-A., Su, D., Teo, M., Tice, B. G., Towell, R. S., Uemura, S., Watson, S., Wang, S. G., Wickes, A. B., Wu, J., Xi, Z., Ye, Z.

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Cognitive and adaptive functioning after liver transplantation for maple syrup urine disease: A case series von Shellmer, D. A., DeVito Dabbs, A., Dew, M. A., Noll, R. B., Feldman, H., Strauss, K. A., Morton, D. H., Vockley, J., Mazariegos, G. V.

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Recessive Symptomatic Focal Epilepsy and Mutant Contactin-Associated Protein-like 2 von Strauss, Kevin A, Puffenberger, Erik G, Huentelman, Matthew J, Gottlieb, Steven, Dobrin, Seth E, Parod, Jennifer M, Stephan, Dietrich A, Morton, D. Holmes

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Gene structure and mutations of glutaryl-coenzyme A dehydrogenase : Impaired association of enzyme subunits that is due to an A421V substitution causes glutaric acidemia type I in... von BIERY, B. J, STEIN, D. E, MORTON, D. H, GOODMAN, S. I

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Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT von Bull, Laura N, Carlton, Victoria E. H, Harris, Baruch Z, Puffenberger, Erik G, Batta, A. K, Knisely, A. S, Robinson, Donna L, Strauss, Kevin A, Shneider, Benjamin L, Lim, Wendell A, Salen, Gerald, Morton, D. Holmes

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Diagnosis and management of glutaric aciduria type I von Barić, I., Zschocke, J., Christensen, E., Duran, M., Goodman, S. I., Leonard, J. V., Müller, E., Morton, D. H., Superti‐Furga, A., Hoffmann, G. F.

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3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their children von Gibson, K.M., Bennett, M.J., Naylor, E.W., Morton, D.H.

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Elevated Frequency and Allelic Heterogeneity of Congenital Nephrotic Syndrome, Finnish Type, in the Old Order Mennonites von Bolk, Stacey, Puffenberger, Erik G., Hudson, Jim, Morton, D. Holmes, Chakravarti, Aravinda

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Brain magnetic resonance imaging in suspected extrapyramidal cerebral palsy: Observations in distinguishing genetic-metabolic from acquired causes von Hoon, Alexander H., Reinhardt, Elsie M., Kelley, Richard I., Breiter, Steven N., Morton, D.Holmes, Naidu, SakkuBai, Johnston, Michael V.

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A Novel Nemaline Myopathy in the Amish Caused by a Mutation in Troponin T1 von Johnston, Jennifer J., Kelley, Richard I., Crawford, Thomas O., Morton, D. Holmes, Agarwala, Richa, Koch, Thorsten, Schäffer, Alejandro A., Francomano, Clair A., Biesecker, Leslie G.

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Mutant deoxynucleotide carrier is associated with congenital microcephaly von Rosenberg, Marjorie J, Agarwala, Richa, Bouffard, Gerard, Davis, Joie, Fiermonte, Giuseppe, Hilliard, Mark S, Koch, Thorsten, Kalikin, Linda M, Makalowska, Izabela, Morton, D. Holmes, Petty, Elizabeth M, Weber, James L, Palmieri, Ferdinando, Kelley, Richard I, Schäffer, Alejandro A, Biesecker, Leslie G

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Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5 von PUFFENBERGER, Erik G, STRAUSS, Kevin A, HEUER, Gregory G, CRINO, Peter B, MORTON, D. Holmes, RAMSEY, Keri E, CRAIG, David W, STEPHAN, Dietrich A, ROBINSON, Donna L, HENDRICKSON, Christine L, GOTTLIEB, Steven, RAMSAY, David A, SIU, Victoria M

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Abnormal hepatic sinusoidal bile acid transport in an Amish Kindred is not linked to FIC1 and is improved by ursodiol von Morton, D.Holmes, Salen, Gerald, Batta, A.K., Shefer, Sarah, Tint, G.Stephen, Belchis, Deborah, Shneider, Benjamin, Puffenberger, Erik, Bull, Laura, Knisely, A.S.

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Through my window-remarks at the 125th year celebration of children's hospital of Boston von MORTON, D. H

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The SeaQuest spectrometer at Fermilab von Aidala, C.A., Arrington, J.R., Ayuso, C., Bowen, B.M., Bowen, M.L., Bowling, K.L., Brown, A.W., Brown, C.N., Byrd, R., Carlisle, R.E., Chang, T., Chang, W.-C., Chen, A., Chen, J.-Y., Christian, D.C., Chu, X., Dannowitz, B.P., Daugherity, M., Diefenthaler, M., Dove, J., Durandet, C., El Fassi, L., Erdos, E., Fox, D.M., Geesaman, D.F., Gilman, R., Goto, Y., Guo, L., Guo, R., Hague, T., Hicks, C.R., Holt, R.J., Isenhower, D., Jiang, X., Katich, J.M., Kerns, B.M., Kinney, E.R., Kitts, N.D., Klein, A., Kleinjan, D., Kras, J., Kudo, Y., Lin, P.-J., Liu, D., Liu, K., Liu, M.X., Lorenzon, W., Makins, N.C.R., Martinez, J.D., McClellan, R.E., McDonald, B., McGaughey, P.L., McNease, S.E., Medeiros, M.M., Miller, B., Miller, A.J., Miyasaka, S., Miyachi, Y., Mooney, I.A., Morton, D.H., Nadim, B., Nagai, K., Nakahara, K., Nakano, K., Nara, S., Obata, S., Peng, J.C., Prasad, S., Puckett, A.J.R., Ramson, B.J., Raymond, R.S., Reimer, P.E., Rubin, J.G., Salinas, R., Sanftl, F., Sawada, S., Sawada, T., Scott, M.B.C., Selensky, L.E., Shibata, T.-A., Shiu, S., Su, D., Tadepalli, A.S., Teo, M., Tice, B.G., Towell, C.L., Towell, R.S., Uemura, S., Wang, S.G., Watson, S., White, N., Wickes, A.B., Wood, M.R., Wu, J., Xi, Z., Ye, Z., Yin, Y.

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Cardiac phenotype of propionic acidemia in the Amysh community von Lopez Sainz, A, Snyder, C, Rozema, T, Wenger, O, Smith, B, Morton, D H, Ammous, Z, Smith, J, Bijnens, B, Chowdhury, D

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Measurement of flavor asymmetry of the light-quark sea in the proton with Drell-Yan dimuon production in p + p and p + d collisions at 120 GeV von Dove, J., Kerns, B., Leung, C., McClellan, R. E., Miyasaka, S., Morton, D. H., Nagai, K., Prasad, S., Sanftl, F., Scott, M. B. C., Tadepalli, A. S., Aidala, C. A., Arrington, J., Ayuso, C., Barker, C. T., Brown, C. N., Chang, T. H., Chang, W. C., Chen, A., Christian, D. C., Dannowitz, B. P., Daugherity, M., Diefenthaler, M., El Fassi, L., Geesaman, D. F., Gilman, R., Goto, Y., Guo, L., Guo, R., Hague, T. J., Holt, R. J., Isenhower, D., Kinney, E. R., Kitts, N. D., Klein, A., Kleinjan, D. W., Kudo, Y., Lin, P.-J., Liu, K., Liu, M. X., Lorenzon, W., Makins, N. C. R., Mesquita de Medeiros, M., McGaughey, P. L., Miyachi, Y., Mooney, I., Nakahara, K., Nakano, K., Nara, S., Peng, J. C., Puckett, A. J., Ramson, B. J., Reimer, P. E., Rubin, J. G., Sawada, S., Sawada, T., Shibata, T.-A., Shiu, S. H., Su, D., Teo, M., Tice, B. G, Towell, R. S., Uemura, S., Watson, T. S., Wang, S. G., Wickes, A. B., Wu, J., Xi, Z., Ye, Z.

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Measurement of J/ψ and ψ(2S) production in p + p and p + d interactions at 120 GeV von Leung, C.H., Nagai, K., Nakano, K., Nawarathne, D., Dove, J., Prasad, S., Wuerfel, N., Aidala, C.A., Arrington, J., Ayuso, C., Barker, C.L., Brown, C.N., Chang, W.C., Chen, A., Christian, D.C., Dannowitz, B.P., Daugherity, M., El Fassi, L., Geesaman, D.F., Gilman, R., Goto, Y., Guo, R., Hague, T.J., Holt, R.J., Hossain, M.F., Isenhower, D., Kinney, E., Klein, A., Kleinjan, D.W., Kudo, Y., Lin, P.-J., Liu, K., Liu, M.X., Lorenzon, W., McClellan, R.E., McGaughey, P.L., Medeiros, M.M., Miyachi, Y., Miyasaka, S., Morton, D.H., Nakahara, K., Nara, S., Pate, S.F., Peng, J.C., Pun, A., Ramson, B.J., Reimer, P.E., Rubin, J.G., Sanftl, F., Sawada, S., Sawada, T., Scott, M.B.C., Shibata, T.-A., Tadepalli, A.S., Teo, M., Towell, R.S., Uemura, S., Wang, S.G., Wickes, A.B., Wu, J., Ye, Z.H.

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Posterior column ataxia with retinitis pigmentosa (AXPC1) maps to chromosome 1q31-q32 von HIGGINS, J. J, MORTON, D. H, LOVELESS, J. M

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