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Results: 1-25 | 26-31 |
Results: 26-31/31

Authors: Swoboda, KJ Hyland, K Goldstein, DS Kuban, KCK Arnold, LA Holmes, CS Levy, HL
Citation: Kj. Swoboda et al., Clinical and therapeutic observations in aromatic L-amino acid decarboxylase deficiency, NEUROLOGY, 53(6), 1999, pp. 1205-1211

Authors: Levy, HL
Citation: Hl. Levy, Phenylketonuria: Old disease, new approach to treatment, P NAS US, 96(5), 1999, pp. 1811-1813

Authors: Khan, SG Levy, HL Legerski, R Quackenbush, E Reardon, JT Emmert, S Sancar, A Li, L Schneider, TD Cleaver, JE Kraemer, KH
Citation: Sg. Khan et al., Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemia (vol 111, pg 791, 1998), J INVES DER, 112(3), 1999, pp. 402-402

Authors: Vargas, JE Mudd, SH Waisbren, SE Levy, HL
Citation: Je. Vargas et al., Maternal gamma-cystathionase deficiency: Absence of both teratogenic effects and pregnancy complications, AM J OBST G, 181(3), 1999, pp. 753-755

Authors: Duran, GP Rohr, FJ Slonim, A Guttler, F Levy, HL
Citation: Gp. Duran et al., Necessity of complete intake of phenylalanine-free amino acid mixture for metabolic control of phenylketonuria, J AM DIET A, 99(12), 1999, pp. 1559-1563

Authors: Levy, HL
Citation: Hl. Levy, Newborn screening by tandem mass spectrometry: A new era, CLIN CHEM, 44(12), 1998, pp. 2401-2402
Risultati: 1-25 | 26-31 |