To the Editor von BERLOW, STANLEY

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Neonatal Screening for Phenylketonuria von BERLOW, STANLEY

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Progress in phenylketonuria: defects in the metabolism of biopterin von Berlow, S

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Glutaric acidemia type II: A form with deleterious intrauterine effects von Goodman, Stephen I., Reale, Mario, Berlow, Stanley

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Reply von Goodman, Stephen I., Reale, Mario, Berlow, Stanley

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TREATMENT OF HYPERPHENYLALANINEMIA SECONDARY TO A DEFICIENCY OF BIOPTERIN WITH REDUCED PTERINS von Muenzer, Joseph, Milstein, Sheldon, Sidbury, James, Berlow, Stanley, Kaufman, Seymour

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Diet discontinuation in phenylketonuria von Williamson, M, Koch, R, Berlow, S

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Biotin-responsive in vivo carboxylase deficiency in two siblings with secretory diarrhea receiving total parenteral nutrition von Kien, Craig L., Kohler, Elaine, Goodman, Stephen I., Berlow, Stanley, Hong, Richard, Horowitz, Sheldon P., Baker, Herman

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IDENTIFICATION OF SHORT CHAIN ACYL-CARNITINE ESTERS (SCAC) IN ORGANIC ACIDURIAS von Hoganson, George E, Paulson, Dennis J, Berlow, Stanley, Shug, Austin L

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Studies in cystathioninuria von Berlow, Stanley, Efron, Mary, Peterson, J.C.

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New Developments in Hyperphenylalaninemia von O'Brien, Donough, Berlow, Stanley, Donnell, George, Justice, Parvin, Kaufman, Seymour, Levy, Harvey L., McCabe, Edward R. B., Snyderman, Selma

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Problems in the outpatient management of phenylketonuria von Berlow, Stanley, Arends, Robert, Barsch, Ray

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HYPERPHENYLALANINEMIA DUE TO PHENYLALANINE HYDROXYLASE COFACTOR DEFICIENCY von Milstien, Sheldon, Orloff, Sheldon, Spielberg, Stephen, Berlow, Stanley, Schulman, Joseph D, Kaufman, Seymour

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Folate Distribution in Cultured Human Cells von Rosenblatt, David S., Cooper, Bernard A., Lue-Shing, Sally, Wong, Paul W. K., Berlow, Stanley, Narisawa, Kuniaka, Baumgartner, Regula

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Folate Distribution in Cultured Human Cells: STUDIES ON 5,10-CH von Rosenblatt, David S., Cooper, Bernard A., Lue-Shing, Sally, Wong, Paul W. K., Berlow, Stanley, Narisawa, Kuniaka, Baumgartner, Regula

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The Basic Trypsin Inhibitor of Bovine Pancreas von Kassell, Beatrice, Radicevic, Milka, Berlow, Stanley, Peanasky, R.J., Laskowski, M.

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YY SYNDROME IN AN AMERICAN NEGRO von Pergament, Eugene, Sato, Hideo, Berlow, Stanley, Mintzer, Richard

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A ring chromosome No. 16 in an infant with primary hypoparathyroidism von Pergament, Eugene, Pietra, Giuseppe C., Kadotani, Tetsuji, Sato, Hideo, Berlow, Stanley

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A three-month-old infant with seizures, hypoglycemia, and apnea von Chesney, Russell W., Sveum, Richard J., Lacey, Michael, Arya, Sunita, Shug, Austin, Saari, Thomas, Berlow, Stanley, Ellefson, Ralph, Gilbert, Enid F., Odell, Gerard B., Opitz, John M., Opitz, John M.

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