INBORN-ERRORS OF TRACE-ELEMENT METABOLISM

被引:9
作者
DANKS, DM
机构
[1] ROYAL CHILDRENS HOSP, DEFECTS RES INST, PARKVILLE, VIC 3052, AUSTRALIA
[2] ROYAL CHILDRENS HOSP, DEPT GENET, PARKVILLE, VIC 3052, AUSTRALIA
来源
CLINICS IN ENDOCRINOLOGY AND METABOLISM | 1985年 / 14卷 / 03期
关键词
D O I
10.1016/S0300-595X(85)80008-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:591 / 615
页数:25
相关论文
共 58 条
[1]   SYMPTOMATIC ZINC-DEFICIENCY IN A BREAST-FED, PRETERM INFANT [J].
AGGETT, PJ ;
ATHERTON, DJ ;
MORE, J ;
DAVEY, J ;
DELVES, HT ;
HARRIES, JT .
ARCHIVES OF DISEASE IN CHILDHOOD, 1980, 55 (07) :547-550
[2]   DEFECT IN ZINC UPTAKE BY JEJUNAL BIOPSIES IN ACRODERMATITIS-ENTEROPATHICA [J].
ATHERTON, DJ ;
MULLER, DPR ;
AGGETT, PJ ;
HARRIES, JT .
CLINICAL SCIENCE, 1979, 56 (05) :505-507
[3]  
BEARN AG, 1960, ANN HUM GENET, V24, P33
[4]  
BRENTON DP, 1981, LANCET, V2, P500
[5]   X-LINKED CUTIS LAXA - DEFECTIVE CROSS-LINK FORMATION IN COLLAGEN DUE TO DECREASED LYSYL OXIDASE ACTIVITY [J].
BYERS, PH ;
SIEGEL, RC ;
HOLBROOK, KA ;
NARAYANAN, AS ;
BORNSTEIN, P ;
HALL, JG .
NEW ENGLAND JOURNAL OF MEDICINE, 1980, 303 (02) :61-65
[6]   ALTERED COPPER-METABOLISM IN CULTURED-CELLS FROM HUMAN MENKES SYNDROME AND MOTTLED MOUSE MUTANTS [J].
CAMAKARIS, J ;
DANKS, DM ;
ACKLAND, L ;
CARTWRIGHT, E ;
BORGER, P ;
COTTON, RGH .
BIOCHEMICAL GENETICS, 1980, 18 (1-2) :117-131
[7]  
Camakaris J, 1980, J Inherit Metab Dis, V3, P155, DOI 10.1007/BF02312550
[8]   GENETIC EXPRESSION OF WILSONS-DISEASE IN CELL-CULTURE - A DIAGNOSTIC MARKER [J].
CHAN, WY ;
CUSHING, W ;
COFFMAN, MA ;
RENNERT, OM .
SCIENCE, 1980, 208 (4441) :299-300
[9]  
Danks D M, 1980, Ciba Found Symp, V79, P209
[10]   DIAGNOSIS OF TRACE-METAL DEFICIENCY - WITH EMPHASIS ON COPPER AND ZINC [J].
DANKS, DM .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1981, 34 (02) :278-280