ENZYMIC DEFECTS IN HEREDITARY TYROSINEMIA

被引:415
作者
LINDBLAD, B [1 ]
LINDSTEDT, S [1 ]
STEEN, G [1 ]
机构
[1] UNIV GOTHENBURG,SAHLGRENS HOSP,DEPT CLIN CHEM,S-41345 GOTHENBURG,SWEDEN
关键词
D O I
10.1073/pnas.74.10.4641
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
引用
收藏
页码:4641 / 4645
页数:5
相关论文
共 40 条
[1]  
BJORKMAN L, 1976, CLIN CHEM, V22, P49
[2]   HEREDITARY TYROSINEMIA .3. ON DIFFERENTIAL DIAGNOSIS AND LACK OF EFFECT OF EARLY DIETARY TREATMENT [J].
BODEGARD, G ;
GENTZ, J ;
LINDBLAD, B ;
LINDSTEDT, S ;
ZETTERSTROM, R .
ACTA PAEDIATRICA SCANDINAVICA, 1969, 58 (01) :37-+
[4]  
EDWARDS SW, 1956, J BIOL CHEM, V220, P79
[5]   ASSAY, PROPERTIES AND TISSUE DISTRIBUTION OF PARA HYDROXYPHENYLPYRUVATE HYDROXYLASE [J].
FELLMAN, JH ;
ROTH, ES ;
FUJITA, TS .
BIOCHIMICA ET BIOPHYSICA ACTA, 1972, 284 (01) :90-&
[6]   EXCRETION OF DELTA-AMINOLEVULINIC ACID IN HEREDITARY TYROSINEMIA [J].
GENTZ, J ;
JOHANSSON, S ;
LINDBLAD, B ;
LINDSTEDT, S ;
ZETTERSTROM, R .
CLINICA CHIMICA ACTA, 1969, 23 (02) :257-+
[7]   TYROSINEMIA - AN INBORN ERROR OF TYROSINE METABOLISM WITH CIRRHOSIS OF LIVER AND MULTIPLE RENAL TUBULAR DEFECTS ( DE TONI-DEBRE-FANCONI SYNDROME ) [J].
GENTZ, J ;
JAGENBURG, R ;
ZETTERSTROEM, R .
JOURNAL OF PEDIATRICS, 1965, 66 (04) :670-+
[8]   ENZYMATIC STUDIES IN A CASE OF HEREDITARY TYROSINEMIA WITH HEPATOMA [J].
GENTZ, J ;
HEINRICH, J ;
LINDBLAD, B ;
LINDSTEDT, S ;
ZETTERSTROM, R .
ACTA PAEDIATRICA SCANDINAVICA, 1969, 58 (04) :393-+
[9]   DIETARY TREATMENT IN TYROSINEMIA (TYROSINOSIS) - WITH A NOTE ON THE POSSIBLE RECOGNITION OF CARRIER STATE [J].
GENTZ, J ;
LINDBLAD, B ;
LINDSTEDT, S ;
LEVY, L ;
SHASTEEN, W ;
ZETTERSTROM, R .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1967, 113 (01) :31-+
[10]   PARA-HYDROXYPHENYLPYRUVATE HYDROXYLASE-ACTIVITY IN FINE-NEEDLE ASPIRATION LIVER BIOPSIES IN HEREDITARY TYROSINEMIA [J].
GENTZ, J ;
LINDBLAD, B .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1972, 29 (01) :115-&