Search research articles
Contact Us
Filters
Showing results (11-20 of 17) with videos related to
Page
of 2
Sort By:
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 phenylketonuria
H 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 disease
I 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 deficiency
J B Nielsen, F Güttler, N Hobolth, et al.
Diabetes
|
June 1, 1991
Possible genetic defects in regulation of glycosaminoglycans in patients with diabetic nephropathy
T 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 tyrosine
C Lykkelund, J B Nielsen, H C Lou, et al.
Lancet (London, England)
|
November 12, 1983
Feasibility of first trimester prenatal diagnosis of Hunter syndrome
C Lykkelund, F Søndergaard, A J Therkelsen, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 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 phenylketonuria
H 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 disease
I 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 deficiency
J B Nielsen, F Güttler, N Hobolth, et al.
Diabetes
|
June 1, 1991
Possible genetic defects in regulation of glycosaminoglycans in patients with diabetic nephropathy
T 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 tyrosine
C Lykkelund, J B Nielsen, H C Lou, et al.
Lancet (London, England)
|
November 12, 1983
Feasibility of first trimester prenatal diagnosis of Hunter syndrome
C Lykkelund, F Søndergaard, A J Therkelsen, et al.
Page
of 2