TETRAHYDROBIOPTERIN BIOSYNTHETIC-PATHWAY AND DEFICIENCY

[11] PHENYLKETONURIA DUE TO A DEFICIENCY OF DIHYDROPTERIDINE REDUCTASE [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1975, 293 (16) : 785 - 790

[12] DYSPROPTERIN, AN INTERMEDIATE FORMED FROM DIHYDRONEOPTERIN TRIPHOSPHATE IN THE BIOSYNTHETIC-PATHWAY OF TETRAHYDROBIOPTERIN [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 840 (02) : 235 - 244

[13] BIOSYNTHESIS OF TETRAHYDROBIOTERIN - CONVERSION OF DIHYDRONEOPTERIN TRIPHOSPHATE TO TETRAHYDROPTERIN INTERMEDIATES [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1985, 128 (03) : 1099 - 1107

[14] GTP CYCLOHYDROLASE-I DEFICIENCY, A NEW ENZYME DEFECT CAUSING HYPERPHENYLALANINEMIA WITH NEOPTERIN, BIOPTERIN, DOPAMINE, AND SEROTONIN DEFICIENCIES AND MUSCULAR HYPOTONIA [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1984, 141 (04) : 208 - 214

[15] PRENATAL-DIAGNOSIS OF DIHYDROBIOPTERIN SYNTHETASE DEFICIENCY, A VARIANT FORM OF PHENYLKETONURIA [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1986, 145 (03) : 176 - 178

[16] HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH COLUMN SWITCHING FOR THE ANALYSIS OF BIOGENIC-AMINE METABOLITES AND PTERINS [J]. JOURNAL OF CHROMATOGRAPHY, 1984, 290 (MAY): : 237 - 246

[17] NIEDERWIESER A, 1980, HELV PAEDIATR ACTA, V35, P335

[18] ATYPICAL PHENYLKETONURIA WITH DIHYDROBIOPTERIN SYNTHETASE DEFICIENCY - ABSENCE OF PHOSPHATE-ELIMINATING ENZYME-ACTIVITY DEMONSTRATED IN LIVER [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1985, 144 (01) : 13 - 16

[19] NIEDERWIESER A, 1987, UNCONJUGATED PTERINS, P107

[20] PONZONE A, 1987, LANCET, V1, P512

[11] PHENYLKETONURIA DUE TO A DEFICIENCY OF DIHYDROPTERIDINE REDUCTASE [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1975, 293 (16) : 785 - 790

[12] DYSPROPTERIN, AN INTERMEDIATE FORMED FROM DIHYDRONEOPTERIN TRIPHOSPHATE IN THE BIOSYNTHETIC-PATHWAY OF TETRAHYDROBIOPTERIN [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 840 (02) : 235 - 244

[13] BIOSYNTHESIS OF TETRAHYDROBIOTERIN - CONVERSION OF DIHYDRONEOPTERIN TRIPHOSPHATE TO TETRAHYDROPTERIN INTERMEDIATES [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1985, 128 (03) : 1099 - 1107

[14] GTP CYCLOHYDROLASE-I DEFICIENCY, A NEW ENZYME DEFECT CAUSING HYPERPHENYLALANINEMIA WITH NEOPTERIN, BIOPTERIN, DOPAMINE, AND SEROTONIN DEFICIENCIES AND MUSCULAR HYPOTONIA [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1984, 141 (04) : 208 - 214

[15] PRENATAL-DIAGNOSIS OF DIHYDROBIOPTERIN SYNTHETASE DEFICIENCY, A VARIANT FORM OF PHENYLKETONURIA [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1986, 145 (03) : 176 - 178

[16] HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH COLUMN SWITCHING FOR THE ANALYSIS OF BIOGENIC-AMINE METABOLITES AND PTERINS [J]. JOURNAL OF CHROMATOGRAPHY, 1984, 290 (MAY): : 237 - 246

[17] NIEDERWIESER A, 1980, HELV PAEDIATR ACTA, V35, P335

[18] ATYPICAL PHENYLKETONURIA WITH DIHYDROBIOPTERIN SYNTHETASE DEFICIENCY - ABSENCE OF PHOSPHATE-ELIMINATING ENZYME-ACTIVITY DEMONSTRATED IN LIVER [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1985, 144 (01) : 13 - 16

[19] NIEDERWIESER A, 1987, UNCONJUGATED PTERINS, P107

[20] PONZONE A, 1987, LANCET, V1, P512