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Flemming G�ttler
Observed names:
F. G�ttler,
Flemming Gttler
Institution:
University of Bergen
Observed institutions:
University of Southern California,
Baylor College of Medicine,
Kennedy Center,
University of Bergen
OpenAlex ID:
A5111784099
Decreased vigilance and neurotransmitter synthesis after discontinuation of dietary treatment for phenylketonuria in adolescents
1985
·
H. C. Lou
, F. G�ttler
, et al.
·
European Journal of Pediatrics
·
113
Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria
1987
·
Ranaiit Chakraborty
, AlanS. Lidsky
, et al.
·
Human Genetics
·
108
Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of unrestricted diet with large amounts of tyrosine
1988
·
C. Lykkelund
, J. B. Nielsen
, et al.
·
European Journal of Pediatrics
·
75
Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria
1987
·
Flemming Gttler
, Fred D. Ledley
, et al.
·
The Journal of Pediatrics
·
55
Variability in clinical expression of Menkes syndrome
1988
·
A.-M. Gerdes
, T. T�nnesen
, et al.
·
European Journal of Pediatrics
·
48
Molecular characterization of PKU allele prevalent in southern Europe and Ireland
1991
·
M. Dasovich
, D. Konecki
, et al.
·
Somatic Cell and Molecular Genetics
·
28
Combined tetrahydrobiopterin-phenylalanine loading test in the detection of partially defective biopterin synthesis
1984
·
F. G�ttler
, H. Lou
, et al.
·
European Journal of Pediatrics
·
20
The International Collaborative Study of Maternal Phenylketonuria status report 1998
1999
·
R. Koch
, E. Friedman
, et al.
·
Mental Retardation and Developmental Disabilities Research Reviews
·
18
Molecular biology of phenylketonuria
1987
·
F. G�ttler
, A. G. DiLella
, et al.
·
European Journal of Pediatrics
·
17
A Phenylalanine Hydroxylase Amino Acid Polymorphism with Implications for Molecular Diagnostics
2001
·
Torben Gjetting
, Anne Romstad
, et al.
·
Molecular Genetics and Metabolism
·
14
The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuria
1991
·
Jadwiga Jaruzelska
, KarenFriis Henriksen
, et al.
·
Human Genetics
·
14
Diagnosis of Hunter's syndrome carriers; Radioactive sulphate incorporation into fibroblasts in the presence of fructose 1-phosphate
1982
·
T�nne T�nnesen
, Claus Lykkelund
, et al.
·
Human Genetics
·
12
The phenylketonuria G272X haplotype 7 mutation in European populations
1993
·
Jaran Apold
, HansG. Eiken
, et al.
·
Human Genetics
·
7
Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndrome
1983
·
T. T�nnesen
, F. G�ttler
, et al.
·
Human Genetics
·
6
Molecular genetics and outcome in PKU
1999
·
Flemming G�ttler
, Per Guldberg
, et al.
·
Mental Retardation and Developmental Disabilities Research Reviews
·
4
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Works count:
15
Citation count:
539
H-index:
12
I10-index:
12
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