S‐Adenosylhomocysteine hydrolase deficiency: A second patient, the younger brother of the index patient, and outcomes during therapy von Barić, I., Ćuk, M., Fumić, K., Vugrek, O., Allen, R. H., Glenn, B., Maradin, M., Pažanin, L., Pogribny, I., Radoš, M., Sarnavka, V., Schulze, A., Stabler, S., Wagner, C., Zeisel, S. H., Mudd, S. H.

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S‐Adenosylhomocysteine hydrolase deficiency in a 26‐year‐old man von Buist, N. R. M., Glenn, B., Vugrek, O., Wagner, C., Stabler, S., Allen, R. H., Pogribny, I., Schulze, A., Zeisel, S. H., Barić, I., Mudd, S. H.

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Homocysteine and Its Disulfide Derivatives: A Suggested Consensus Terminology von Mudd, S Harvey, Finkelstein, James D, Refsum, Helga, Ueland, Per M, Malinow, M René, Lentz, Steven R, Jacobsen, Donald W, Brattström, Lars, Wilcken, Bridget, Wilcken, David E. L, Blom, Henk J, Stabler, Sally P, Allen, Robert H, Selhub, Jacob, Rosenberg, Irwin H

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Glycine N‐methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia von Mudd, S. H., Cerone, R., Schiaffino, M. C., Fantasia, A. R., Minniti, G., Caruso, U., Lorini, R., Watkins, D., Matiaszuk, N., Rosenblatt, D. S., Schwahn, B., Rozen, R., LeGros, L., Kotb, M., Capdevila, A., Luka, Z., Finkelstein, J. D., Tangerman, A., Stabler, S. P., Allen, R. H., Wagner, C.

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Glycine N‐methyltransferase deficiency: A new patient with a novel mutation von Augoustides‐Savvopoulou, P., Luka, Z., Karyda, S., Stabler, S. P., Allen, R. H., Patsiaoura, K., Wagner, C., Mudd, S. H.

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Consensus nomenclature for the mammalian methionine adenosyltransferase genes and gene products von Kotb, Malak, Mudd, S.Harvey, Mato, Jose M., Geller, Arthur M., Kredich, Nicholas M., Chou, Janice Y., Cantoni, Gulio L.

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Methionine transamination in patients with homocystinuria due to cystathionine β-synthase deficiency von Tangerman, Albert, Wilcken, Bridget, Levy, Harvey L., Boers, Godfried H.J., Mudd, S.Harvey

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Methionine adenosyltransferase I/III deficiency : Novel mutations and clinical variations von CHAMBERLIN, M. E, UBAGAI, T, MUDD, S. H, THOMAS, J, PAO, V. Y, NGUYEN, T. K, LEVY, H. L, GREENE, C, FREEHAUF, C, YANG CHOU, J

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Isolated persistent hypermethioninemia von MUDD, S. H, LEVY, H. L, TANGERMAN, A, BOUJET, C, BUIST, N, DAVIDSON-MUNDT, A, HUDGINS, L, OYANAGI, K, NAGAO, M, WILSON, W. G

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Maternal methionine adenosyltransferase I/III deficiency: Reproductive outcomes in a woman with four pregnancies von Mudd, S. H., Tangerman, A., Stabler, S. P., Allen, R. H., Wagner, C., Zeisel, S. H., Levy, H. L.

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Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene von CHAMBERLIN, M. E, UBAGAI, T, MUDD, S. H, LEVY, H. L, YANG CHOU, J

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Hypermethioninaemia due to methionine adenosyltransferase I/III (MAT I/III) deficiency: Diagnosis in an expanded neonatal screening programme von Couce, M. L., Bóveda, M. D., Castiñeiras, D. E., Corrales, F. J., Mora, M. I., Fraga, J. M., Mudd, S. H.

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Methionine adenosyltransferase I/III deficiency: two Korean compound heterozygous siblings with a novel mutation von KIM, S. Z, SANTAMARIA, E, JEONG, T. E, LEVY, H. L, MATO, J. M, CORRALES, F. J, MUDD, S. H

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Maternal γ-cystathionase deficiency: Absence of both teratogenic effects and pregnancy complications von Vargas, Juan E., Mudd, S.Harvey, Waisbren, Susan E., Levy, Harvey L.

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Enzymes of phosphatidylcholine synthesis in Lemna, soybean, and carrot von Datko, A.H, Mudd, S.H

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Phosphatidylcholine synthesis. Differing patterns in soybean and carrot von Datko, A.H, Mudd, S.H

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The natural history of homocystinura due to cystathionine β-synthase deficiency von MUDD, S. H, SKOVBY, F, FOWLER, B, GROBE, H, SCHMIDT, H, SCHWEITZER, L, LEVY, H. L, PETTIGREW, K. D, WILCKEN, B, PYERITZ, R. E, ANDRIA, G, BOERS, G. H. J, BROMBERG, I. L, CERONE, R

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Quantitative Analysis of Pathways of Methionine Metabolism and Their Regulation in Lemna von Giovanelli, John, Mudd, S. Harvey, Anne H. Datko

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Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency von Chamberlin, M E, Ubagai, T, Mudd, S H, Wilson, W G, Leonard, J V, Chou, J Y

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Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiency von GAHL, W. A, BERNARDINI, I, FINKELSTEIN, J. D, TANGERMAN, A, MARTIN, J. J, BLOM, H. J, MULLEN, K. D, MUDD, S. H

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