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F. Güttler

Veröffentlichungen von F. Güttler zu Güttler, F. ->
weitere Veröffentlichungen von F. Güttler:
Correlated changes in acid hydrolase activity and membrane lipids of HeLa cells: Changes in activity and subcellular distribution of arylsulphatase and acid phenyl phosphomonoesterase (1971)
Dietary problems of phenylketonuria: Effect on CNS transmitters and their possible role in behaviour and neuropsychological function (1986)
Mutation screening versus gene scanning for genotyping phenylketonuria patients (1994)
The influence of mutations on enzyme activity and phenylalanine tolerance in phenylalanine hydroxylase deficiency (1996)
On the possible localization of a gene for triosephosphate isomerase on the short arm of human chromosome 5 (1973)
Molecular genetics of PKU (1986)
Highly increased levels of serum β-hexosaminidase, arylsulphatase A and β-galactosidase in a patient with sepsis (1988)
Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndrome (1983)
Aberrant phenylalanine metabolism in phenylketonuria heterozygotes (1998)
Molecular Analysis of Phenylketonuria in Denmark: 99% of the Mutations Detected by Denaturing Gradient Gel Electrophoresis (1993)
Combined tetrahydrobiopterin-phenylalanine loading test in the detection of partially defective biopterin synthesis (1984)
A scandinavian case of isovaleric acidaemia (1988)
Genotype-phenotype correlation in 11 Romanian PKU families (1994)
Single molecule spectroscopy: Stark effect of pentacene in p-terphenyl (1992)
Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and α1-antitrypsin deficiencydeficiency (1986)
Veröffentlichungen zu Güttler, F.
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1
Guttler, F. Correlated changes in acid hydrolase activity and membrane lipids of HeLa cells: Changes in activity and subcellular distribution of arylsulphatase and acid phenyl...
in: Biochimica et Biophysica Acta (BBA)/General Subjects, in: Biochimica et Biophysica Acta (BBA)/General Subjects . - Amsterdam : Elsevier, ISSN 0304-4165, ZDB-ID 2209617-6 Vol. 237, No. 1 (1971), p. 43-55
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1971
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2
Güttler, F., Lou, H. Dietary problems of phenylketonuria: Effect on CNS transmitters and their possible role in behaviour and neuropsychological function
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 9 (2. 1986), p. 169-177
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1986
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3
Guldberg, P., Güttler, F. Mutation screening versus gene scanning for genotyping phenylketonuria patients
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 17 (3. 1994), p. 359-361
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1994
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4
Güttler, F., Guldberg, P. The influence of mutations on enzyme activity and phenylalanine tolerance in phenylalanine hydroxylase deficiency
in: European journal of pediatrics , ISSN 1432-1076, Vol. 155 (1. 1996), p. S6
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1996
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5
Güttler, F., Niebuhr, E. On the possible localization of a gene for triosephosphate isomerase on the short arm of human chromosome 5
in: Human genetics , ISSN 1432-1203, Vol. 17 (4. 1973), p. 301-306
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1973
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6
Güttler, F., Woo, S. L. C. Molecular genetics of PKU
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 9 (1. 1986), p. 58-68
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1986
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7
Tønnesen, T., Andersen, P., ... Highly increased levels of serum β-hexosaminidase, arylsulphatase A and β-galactosidase in a patient with sepsis
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 11 (4. 1988), p. 428-429
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1988
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8
Tønnesen, T., Güttler, F., ... Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndrome
in: Human genetics , ISSN 1432-1203, Vol. 64 (4. 1983), p. 371-375
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1983
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9
Guldberg, P., Henriksen, K. F., ... Aberrant phenylalanine metabolism in phenylketonuria heterozygotes
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 21 (4. 1998), p. 365-372
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1998
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10
Guldberg, P., Henriksen, K.F., ... Molecular Analysis of Phenylketonuria in Denmark: 99% of the Mutations Detected by Denaturing Gradient Gel Electrophoresis
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 17, No. 1 (1993), p. 141-146
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1993
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11
Güttler, F., Lou, H., ... Combined tetrahydrobiopterin-phenylalanine loading test in the detection of partially defective biopterin synthesis
in: European journal of pediatrics , ISSN 1432-1076, Vol. 142 (2. 1984), p. 126-129
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1984
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12
Gerdes, A. -M., Gregersen, N., ... A scandinavian case of isovaleric acidaemia
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 11 (2. 1988), p. 219-220
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1988
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13
Popescu, A., Andrian, T., ... Genotype-phenotype correlation in 11 Romanian PKU families
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 17 (3. 1994), p. 374-375
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1994
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14
Wild, U.P., Guttler, F., ... Single molecule spectroscopy: Stark effect of pentacene in p-terphenyl
in: Chemical Physics Letters, in: Chemical Physics Letters . - Amsterdam : Elsevier, ISSN 0009-2614, ZDB-ID 1466293-0 Vol. 193, No. 6 (1992), p. 451-455
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1992
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15
Nielsen, J. B., Güttler, F., ... Normal excretion of urinary acid mucopolysaccharides in a boy with iduronate sulphatase deficiency, Hunter phenotype and α1-antitrypsin deficiencydeficiency
in: European journal of pediatrics , ISSN 1432-1076, Vol. 145 (6. 1986), p. 572-575
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1986
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16
Güttler, F., Guldberg, P., ... Molecular basis for the phenotypical diversity of phenylketonuria and related hyperphenylalaninaemias
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 16 (3. 1993), p. 602-604
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1993
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17
Guldberg, P., Mikkelsen, Ingrid, ... In vivo assessment of mutations in the phenylalanine hydroxylase gene by phenylalanine loading: characterization of seven common mutations
in: European journal of pediatrics , ISSN 1432-1076, Vol. 154 (7. 1995), p. 551-556
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1995
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18
Guldberg, P., Henriksen, K. F., ... Large deletions in the phenylalanine hydroxylase gene as a cause of phenylketonuria in India
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 20 (6. 1997), p. 845-846
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1997
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19
Economou-Petersen, E., Henriksen, K.F., ... Molecular basis for nonphenylketonuria hyperphenylalaninemia
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 14, No. 1 (1992), p. 1-5
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1992
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20
Economou-Petersen, E., Henriksen, K.F., ... Molecular basis for nonphenylketonuria hyperphenylalaninemia
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 14, No. 1 (1992), p. 1-5
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1992