PERSISTENT PROTOPORPHYRINEMIA IN HEREDITARY PORPHOBILINOGEN SYNTHASE (DELTA-AMINOLEVULINIC-ACID DEHYDRASE) DEFICIENCY UNDER LOW LEAD-EXPOSURE - A NEW MOLECULAR-BASIS FOR THE PATHOGENESIS OF LEAD-INTOXICATION

被引：27

作者：

DOSS, M

BECKER, U

SIXEL, F

GEISSE, S

SOLCHER, H

SCHNEIDER, J

KUFNER, G

SCHLEGEL, H

STOEPPLER, M

机构：

[1] UNIV MARBURG, DEPT NEUROL, D-3550 MARBURG, FED REP GER

[2] UNIV MARBURG, FAC MED, MED POLYCLIN, D-3550 MARBURG, FED REP GER

[3] DAIMLER BENZ AG, OCCUPAT MED SERV, D-7000 STUTTGART, FED REP GER

[4] FORSCHUNGSZENTRUM JULICH, NUCL RES CTR, INST CHEM, D-5170 JULICH 1, FED REP GER

来源：

KLINISCHE WOCHENSCHRIFT | 1982年 / 60卷 / 12期

关键词：

D O I：

10.1007/BF01711435

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

收藏

页码：599 / 606

页数：8

相关论文

共 38 条

[1] INCREASED ERYTHROCYTE UROPORPHYRINOGEN-I-SYNTHETASE, DELTA-AMINOLEVULINIC-ACID DEHYDRATASE AND PROTOPORPHYRIN IN HEMOLYTIC-ANEMIAS
ANDERSON, KE
SASSA, S
PETERSON, CM
KAPPAS, A
[J]. AMERICAN JOURNAL OF MEDICINE, 1977, 63 (03) : 359 - 364
[2] CHARACTERIZATION OF THE PORPHOBILINOGEN DEAMINASE DEFICIENCY IN ACUTE INTERMITTENT PORPHYRIA - IMMUNOLOGICAL EVIDENCE FOR HETEROGENEITY OF THE GENETIC-DEFECT
ANDERSON, PM
REDDY, RM
ANDERSON, KE
DESNICK, RJ
[J]. JOURNAL OF CLINICAL INVESTIGATION, 1981, 68 (01) : 1 - 12
[3] THE MOLECULAR-BASIS OF THE HETEROGENEITY IN PHENYLKETONURIA
BARTHOLOME, K
[J]. NATURWISSENSCHAFTEN, 1980, 67 (10) : 495 - 498
[4] BERK PD, 1970, AM J MED, V48, P139
[5] BERLIN A, 1974, Z KLIN CHEM KLIN BIO, V12, P389
[6] BEVAN DR, 1980, J BIOL CHEM, V255, P2030
[7] BIRD TD, 1979, AM J HUM GENET, V31, P662
[8] HEREDITARY PORPHOBILINOGEN SYNTHASE DEFICIENCY IN HUMAN ASSOCIATED WITH ACUTE HEPATIC PORPHYRIA
BRANDT, A
DOSS, M
[J]. HUMAN GENETICS, 1981, 58 (02) : 194 - 197
[9] RELATIONSHIPS BETWEEN ACUTE HEPATIC PORPHYRIAS DUE TO GENETIC-VARIABILITY OF PRIMARY ENZYME DEFECTS AND LIMITING FUNCTION OF UROPORPHYRINOGEN SYNTHASE
DOSS, M
[J]. INTERNATIONAL JOURNAL OF BIOCHEMISTRY, 1978, 9 (12): : 911 - 916
[10] NEW TYPE OF HEPATIC PORPHYRIA WITH PORPHOBILINOGEN SYNTHASE DEFECT AND INTERMITTENT ACUTE CLINICAL MANIFESTATION
DOSS, M
TIEPERMANN, RV
SCHNEIDER, J
SCHMID, H
[J]. KLINISCHE WOCHENSCHRIFT, 1979, 57 (20): : 1123 - 1127

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