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C Lykkelund

Showing results (11-20 of 17) with videos related to

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Acta Paediatrica Scandinavica|July 1, 1987
Increased vigilance and dopamine synthesis by large doses of tyrosine or phenylalanine restriction in phenylketonuriaH C Lou, C Lykkelund, A M Gerdes, et al.
Ugeskrift for Laeger|June 18, 1984
[Prenatal diagnosis of chromosomal and hereditary metabolic disease during the 1st trimester]F Søndergaard, N J Secher, M Kristensen, et al.
Acta Neurologica Scandinavica|June 1, 1989
Tetrahydrobiopterin and Parkinson's diseaseI C Dissing, F Güttler, H Pakkenberg, et al.
European Journal of Pediatrics|December 1, 1986
Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and alpha 1-antitrypsin deficiencyJ B Nielsen, F Güttler, N Hobolth, et al.
Diabetes|June 1, 1991
Possible genetic defects in regulation of glycosaminoglycans in patients with diabetic nephropathyT Deckert, I M Horowitz, A Kofoed-Enevoldsen, et al.
European Journal of Pediatrics|December 1, 1988
Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of unrestricted diet with large amounts of tyrosineC Lykkelund, J B Nielsen, H C Lou, et al.
Lancet (London, England)|November 12, 1983
Feasibility of first trimester prenatal diagnosis of Hunter syndromeC Lykkelund, F Søndergaard, A J Therkelsen, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Acta Paediatrica Scandinavica|July 1, 1987
Increased vigilance and dopamine synthesis by large doses of tyrosine or phenylalanine restriction in phenylketonuriaH C Lou, C Lykkelund, A M Gerdes, et al.
Ugeskrift for Laeger|June 18, 1984
[Prenatal diagnosis of chromosomal and hereditary metabolic disease during the 1st trimester]F Søndergaard, N J Secher, M Kristensen, et al.
Acta Neurologica Scandinavica|June 1, 1989
Tetrahydrobiopterin and Parkinson's diseaseI C Dissing, F Güttler, H Pakkenberg, et al.
European Journal of Pediatrics|December 1, 1986
Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and alpha 1-antitrypsin deficiencyJ B Nielsen, F Güttler, N Hobolth, et al.
Diabetes|June 1, 1991
Possible genetic defects in regulation of glycosaminoglycans in patients with diabetic nephropathyT Deckert, I M Horowitz, A Kofoed-Enevoldsen, et al.
European Journal of Pediatrics|December 1, 1988
Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of unrestricted diet with large amounts of tyrosineC Lykkelund, J B Nielsen, H C Lou, et al.
Lancet (London, England)|November 12, 1983
Feasibility of first trimester prenatal diagnosis of Hunter syndromeC Lykkelund, F Søndergaard, A J Therkelsen, et al.
Pageof 2