TYROSINEMIA WITH AMINOLEVULINIC DEHYDRATASE DEFICIENCY

被引：1

作者：

LAMON, JM

FRYKHOLM, BC

TSCHUDY, DP

机构：

来源：

JOURNAL OF PEDIATRICS | 1978年 / 92卷 / 02期

关键词：

D O I：

10.1016/S0022-3476(78)80053-5

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：346 / 346

页数：1

共 8 条

[1]

BURCH HB, 1971, CLIN CHEM, V17, P1038

[2] EXCRETION OF DELTA-AMINOLEVULINIC ACID IN HEREDITARY TYROSINEMIA [J].

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JOHANSSON, S ;

LINDBLAD, B ;

LINDSTEDT, S ;

ZETTERSTROM, R .

CLINICA CHIMICA ACTA, 1969, 23 (02) :257-+

[3] HEREDITARY TYROSINEMIA AND ABNORMAL PYRROLE METABOLISM [J].

KANG, ES ;

GERALD, PS .

JOURNAL OF PEDIATRICS, 1970, 77 (03) :397-+

[4] RED-CELL ENZYME METHOD FOR DIAGNOSIS OF ACUTE INTERMITTENT PORPHYRIA [J].

MAGNUSSEN, CR ;

LEVINE, JB ;

DOHERTY, JM ;

CHEESMAN, JO ;

TSCHUDY, DP .

BLOOD, 1974, 44 (06) :857-868

[5]

SCRIVER CR, 1967, CAN MED ASSOC J, V97, P1047

[6] TYROSINEMIA WITH ACUTE INTERMITTENT PORPHYRIA - AMINOLEVULINIC ACID DEHYDRATASE DEFICIENCY RELATED TO ELEVATED URINARY AMINOLEVULINIC ACID LEVELS [J].

STRIFE, CF ;

ZUROWESTE, EL ;

EMMETT, EA ;

FINELLI, VN ;

PETERING, HG ;

BERRY, HK .

JOURNAL OF PEDIATRICS, 1977, 90 (03) :400-404

[7] ACUTE INTERMITTENT PORPHYRIA - 1ST OVERPRODUCTION DISEASE LOCALIZED TO A SPECIFIC ENZYME [J].

TSCHUDY, DP ;

PERLROTH, MG ;

MARVER, HS ;

COLLINS, A ;

HUNTER, G ;

RECHCIGL, M .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1965, 53 (04) :841-&

[8]

TSCHUDY DP, 1975, ANN INTERN MED, V83, P851, DOI 10.7326/0003-4819-83-6-851

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