DETERMINATION OF PHENYLALANINE-HYDROXYLASE IN PATIENTS WITH PHENYLKETONURIA AND HYPERPHENYLALANINEMIA

被引：0

作者：

BARTHOLOME, K ^{[1
]}

LUTZ, P ^{[1
]}

机构：

[1] UNIV HEIDELBERG,KINDER KLIN,D-6900 HEIDELBERG,FED REP GER

来源：

MONATSSCHRIFT KINDERHEILKUNDE | 1976年 / 124卷 / 05期

关键词：

D O I：

暂无

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：421 / 422

页数：2

共 50 条

[1] DETERMINATION OF PHENYLALANINE HYDROXYLASE-ACTIVITY IN PATIENTS WITH PHENYLKETONURIA AND HYPERPHENYLALANINEMIA
BARTHOLOME, K
LUTZ, P
BICKEL, H
[J]. PEDIATRIC RESEARCH, 1975, 9 (12) : 899 - 903
[2] SEVERITY OF MUTATION IN THE PHENYLALANINE-HYDROXYLASE GENE INFLUENCES PHENYLALANINE METABOLISM IN PHENYLKETONURIA AND HYPERPHENYLALANINEMIA HETEROZYGOTES
SVENSSON, E
ISELIUS, L
HAGENFELDT, L
[J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1994, 17 (02) : 215 - 222
[3] STUDIES ON THE MOLECULAR DEFECT IN PHENYLKETONURIA AND HYPERPHENYLALANINEMIA USING ANTIBODIES AGAINST PHENYLALANINE-HYDROXYLASE
BARTHOLOME, K
DRESEL, HA
[J]. EUROPEAN JOURNAL OF PEDIATRICS, 1981, 135 (03) : 331 - 331
[4] STUDIES ON THE MOLECULAR DEFECT IN PHENYLKETONURIA AND HYPERPHENYLALANINEMIA USING ANTIBODIES AGAINST PHENYLALANINE-HYDROXYLASE
BARTHOLOME, K
DRESEL, A
[J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1982, 5 (01) : 7 - 10
[5] PHENYLKETONURIA AND THE PHENYLALANINE-HYDROXYLASE GENE
EISENSMITH, RC
WOO, SLC
[J]. MOLECULAR BIOLOGY & MEDICINE, 1991, 8 (01) : 3 - 18
[6] HEPATIC PHENYLALANINE-HYDROXYLASE ACTIVITY IN HYPERPHENYLALANINEMIA
DHONDT, JL
FARRIAUX, JP
[J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1981, 4 (02) : 59 - 60
[7] DIAGNOSIS OF PHENYLALANINE-HYDROXYLASE DEFICIENCY (PHENYLKETONURIA)
BERRY, HK
HSIEH, MH
BOFINGER, MK
SCHUBERT, WK
[J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1982, 136 (02): : 111 - 114
[8] DISTRIBUTIONS OF PHENYLALANINE-HYDROXYLASE MUTATIONS AND HAPLOTYPES IN LITHUANIAN PHENYLKETONURIA PATIENTS
KUCINSKAS, V
JURGELEVICIUS, V
CIMBALISTIENE, L
HOLMGREN, G
[J]. HUMAN HEREDITY, 1994, 44 (02) : 110 - 113
[9] PHENYLALANINE-HYDROXYLASE EXPRESSION IN LIVER OF A FETUS WITH PHENYLKETONURIA
LEDLEY, FD
KOCH, R
JEW, K
BEAUDET, A
OBRIEN, WE
BARTOS, DP
WOO, SLC
[J]. JOURNAL OF PEDIATRICS, 1988, 113 (03): : 463 - 468
[10] MOLECULAR-BIOLOGY OF PHENYLALANINE-HYDROXYLASE AND PHENYLKETONURIA
LEDLEY, FD
DILELLA, AG
WOO, SLC
[J]. TRENDS IN GENETICS, 1985, 1 (11) : 309 - 313

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