Decreased vigilance and neurotransmitter synthesis after discontinuation of dietary treatment for phenylketonuria in adolescents von LOU, H. C, GUTTLER, F, LYKKELUND, C, BRUHN, P, NIEDERWIESER, A

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Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of unrestricted diet with large amounts of tyrosine von LYKKELUND, C, NELSEN, J. B, LOU, H. C, RASMUSSEN, V, GERDES, A. M, CHRISTENSEN, E, GUTTLER, F

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Rapid micromethod for flourometric determination of neutral lipids on thin-layer chromatograms von Lykkelund, C., Damgaard-Pedersen, F.

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Plasma glucagon responses to insulin-induced hypoglycaemia and arginine in normal and alloxan diabetic rats von Lykkelund, C., Lund, E. D.

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Detection of hyperlipidemia by semiquantitative fluorometric determinations of serum lipids on thin-layer chromatograms von Damgaard-Pedersen, F., Lykkelund, C.

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Combined tetrahydrobiopterin-phenylalanine loading test in the detection of partially defective biopterin synthesis von GUTTLER, F, LOU, H, LYKKELUND, C, NIEDERWIESER, A

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Biopterin, neopterin and tyrosine responses to combined oral phenylalanine and tetrahydrobiopterin loading tests in two normal children and in a girl with partial biopterin deficie... von Lykkelund, C., Lou, H. C., Rasmussen, V., Güttler, F., Niederwieser, A.

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Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndrome von TONNESEN, T, GÜTTLER, F, LYKKELUND, C

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FEASIBILITY OF FIRST TRIMESTER PRENATAL DIAGNOSIS OF HUNTER SYNDROME von Lykkelund, C., Søndergaard, F., Therkelsen, A.J., Tønnesen, T., Rasmussen, V., Mikkelsen, M., Guttler, F., Nyland, M.H.

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Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and α1-antitrypsin deficiencydeficiency von Nielsen, J. B., Güttler, F., Hobolth, N., Tønnesen, T., Pedersen, O. D., Lykkelund, C., Rosleff, F.

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Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and alpha 1-antitrypsin deficiency von Nielsen, J B, Güttler, F, Hobolth, N, Tønnesen, T, Pedersen, O D, Lykkelund, C, Rosleff, F

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Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphate von Tønnesen, T, Lykkelund, C, Güttler, F

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Feasibility of first trimester prenatal diagnosis of Hunter syndrome von Lykkelund, C, Søndergaard, F, Therkelsen, A J, Tønnesen, T, Rasmussen, V, Mikkelsen, M, Güttler, F, Nyland, M H

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Feasibility of first trimester prenatal diagnosis of Hunter syndrome von Lykkelund, C, Søndergaard, F, Therkelsen, A J, Tønnesen, T, Rasmussen, V, Mikkelsen, M, Güttler, F, Nyland, M H

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