A. Bargeliotis

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Morita J, Ito Y, Yoshino M, et al (1989) Persistent hyperkataemia in vitamin Bj2-unresponsive methylmalonic acidaemia. J Inher Metab Dis 12: 89-93. Naylor G, Sweetman L, Nyhan WL, et al (t980) Isotope dilution analysis of methylmalonic acidemia. Clin Chim Acta 107: 175-183. Tanaka H, Hine DG, West-Dull A, Lynn TB (1980) Gas chromatographic methods of(More)
Classical phenylketonuria (PKU) (McKusick 261600) is an inborn error of metabolism treated by a controlled low-phenylalanine (Phe) diet started as soon as possible in the first days of life. Such a diet can be achieved with vegetable protein and can be considered non-atherogenic because of the reduction of animal products. Thirty patients with PKU were(More)
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