PHENYLALANINE-HYDROXYLASE ACTIVITY AND THE PATTERN OF SERUM PHENYLALANINE CHANGES IN PHENYLKETONURIA (PKU)

被引：0
|
作者：
HSIEH, MC [1 ]
BERRY, HK [1 ]
机构：
[1] CHILDRENS HOSP RES FDN,CINCINNATI,OH 45229
来源：
FEDERATION PROCEEDINGS | 1981年 / 40卷 / 03期
关键词：
D O I：
暂无
中图分类号：
Q [生物科学];
学科分类号：
07 ; 0710 ; 09 ;
摘要：
引用
收藏
页码：861 / 861
页数：1
相关论文
共 50 条
  • [1] PHENYLKETONURIA AND THE PHENYLALANINE-HYDROXYLASE GENE
    EISENSMITH, RC
    WOO, SLC
    MOLECULAR BIOLOGY & MEDICINE, 1991, 8 (01) : 3 - 18
  • [2] ABSENT PHENYLALANINE-HYDROXYLASE ACTIVITY WITHOUT PHENYLKETONURIA
    YUDKOFF, M
    SEGAL, S
    EUROPEAN JOURNAL OF PEDIATRICS, 1980, 134 (01) : 85 - 86
  • [3] ANALYSIS OF CLASSICAL PHENYLKETONURIA (PKU) BY MAPPING OF THE HUMAN PHENYLALANINE-HYDROXYLASE GENE
    ROBSON, KJH
    LIDSKY, A
    STACKHOUSE, R
    CHANDRA, T
    WOO, SLC
    JOURNAL OF CELL BIOLOGY, 1982, 95 (02): : A219 - A219
  • [4] ANALYSIS OF PHENYLKETONURIA (PKU) BY CLONING AND CHARACTERIZATION OF THE HUMAN PHENYLALANINE-HYDROXYLASE GENE
    WOO, SLC
    CHANDRA, T
    STACKHOUSE, R
    ROBSON, KJH
    AMERICAN JOURNAL OF HUMAN GENETICS, 1982, 34 (06) : A168 - A168
  • [5] COMPARATIVE DIAGNOSTIC-VALUE OF PHENYLALANINE CHALLENGE AND PHENYLALANINE-HYDROXYLASE ACTIVITY IN PHENYLKETONURIA
    HSIEH, MC
    BERRY, HK
    BOFINGER, MK
    PHILLIPS, PJ
    GUILFOILE, MB
    HUNT, MM
    CLINICAL GENETICS, 1983, 23 (06) : 415 - 421
  • [6] DIAGNOSIS OF PHENYLALANINE-HYDROXYLASE DEFICIENCY (PHENYLKETONURIA)
    BERRY, HK
    HSIEH, MH
    BOFINGER, MK
    SCHUBERT, WK
    AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1982, 136 (02): : 111 - 114
  • [7] PHENYLALANINE-HYDROXYLASE ACTIVITY
    DANKS, DM
    COTTON, RGH
    AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1983, 137 (04): : 409 - 409
  • [8] POLYMORPHIC DNA HAPLOTYPES AT THE PHENYLALANINE-HYDROXYLASE (PAH) LOCUS IN ASIAN FAMILIES WITH PHENYLKETONURIA (PKU)
    DAIGER, SP
    REED, L
    HUANG, SS
    ZENG, YT
    WANG, T
    LO, WHY
    OKANO, Y
    HASE, Y
    FUKUDA, Y
    OURA, T
    TADA, K
    WOO, SLC
    AMERICAN JOURNAL OF HUMAN GENETICS, 1989, 45 (02) : 319 - 324
  • [9] PHENYLKETONURIA IN THE GREEK POPULATION - HAPLOTYPE ANALYSIS OF THE PHENYLALANINE-HYDROXYLASE GENE AND IDENTIFICATION OF A PKU MUTATION
    HOFMAN, KJ
    ANTONARAKIS, SE
    MISSIOUTSANGARAKI, S
    BOEHM, CD
    VALLE, D
    MOLECULAR BIOLOGY & MEDICINE, 1989, 6 (03) : 245 - 250
  • [10] POLYMORPHIC DNA HAPLOTYPES AT THE PHENYLALANINE-HYDROXYLASE (PAH) LOCUS IN EUROPEAN FAMILIES WITH PHENYLKETONURIA (PKU)
    DAIGER, SP
    CHAKRABORTY, R
    REED, L
    FEKETE, G
    SCHULER, D
    BERENSSI, G
    NASZ, I
    BRDICKA, R
    KAMARYT, J
    PIJACKOVA, A
    MOORE, S
    SULLIVAN, S
    WOO, SLC
    AMERICAN JOURNAL OF HUMAN GENETICS, 1989, 45 (02) : 310 - 318
12345