ATYPICAL PHENYLKETONURIA WITH DEFECTIVE BIOPTERIN METABOLISM - MONOTHERAPY WITH TETRAHYDROBIOPTERIN OR SEPIAPTERIN, SCREENING AND STUDY OF BIOSYNTHESIS IN MAN

被引:82
作者
NIEDERWIESER, A [1 ]
CURTIUS, HC [1 ]
WANG, M [1 ]
LEUPOLD, D [1 ]
机构
[1] UNIV ULM,DEPT PEDIAT,D-7900 ULM,FED REP GER
关键词
D O I
10.1007/BF00441135
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:110 / 112
页数:3
相关论文
共 26 条
  • [1] BARTHOLOME K, 1974, LANCET, V2, P1580
  • [2] BARTHOLOME K, 1975, LANCET, V2, P1042
  • [3] BECK B, COMMUNICATION
  • [4] BERLOW S, COMMUNICATION
  • [5] DISORDER OF BIOGENIC-AMINES IN DIHYDROPTERIDINE REDUCTASE DEFICIENCY
    BUTLER, IJ
    KOSLOW, SH
    KRUMHOLZ, A
    HOLTZMAN, NA
    KAUFMAN, S
    [J]. ANNALS OF NEUROLOGY, 1978, 3 (03) : 224 - 230
  • [6] ATYPICAL PHENYLKETONURIA DUE TO TETRAHYDROBIOPTERIN DEFICIENCY - DIAGNOSIS AND TREATMENT WITH TETRAHYDROBIOPTERIN, DIHYDROBIOPTERIN AND SEPIAPTERIN
    CURTIUS, HC
    NIEDERWIESER, A
    VISCONTINI, M
    OTTEN, A
    SCHAUB, J
    SCHEIBENREITER, S
    SCHMIDT, H
    [J]. CLINICA CHIMICA ACTA, 1979, 93 (02) : 251 - 262
  • [7] PATHOGENESIS OF PHENYLKETONURIA - INHIBITION OF DOPA AND CATECHOLAMINE SYNTHESIS IN PATIENTS WITH PHENYLKETONURIA
    CURTIUS, HC
    BAERLOCHER, K
    VOLLMIN, JA
    [J]. CLINICA CHIMICA ACTA, 1972, 42 (01) : 235 - +
  • [8] Danks D M, 1978, J Inherit Metab Dis, V1, P49, DOI 10.1007/BF01801843
  • [9] DANKS DM, 1975, LANCET, V2, P1043
  • [10] ENDRES W, 1982, HELV PAED ACTA