TYPE-III GLYCOGENOSIS PRESENTING AS LIVER-DISEASE IN ADULTS WITH ATYPICAL HISTOLOGICAL FEATURES

被引:21
作者
FELLOWS, IW
LOWE, JS
OGILVIE, AL
STEVENS, A
TOGHILL, PJ
ATKINSON, M
机构
关键词
D O I
10.1136/jcp.36.4.431
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
引用
收藏
页码:431 / 434
页数:4
相关论文
共 9 条
[1]   HEPATIC PHOSPHORYLASE DEFICIENCY - ITS DIFFERENTIATION FROM OTHER HEPATIC GLYCOGENOSES [J].
FERNANDES, J ;
KOSTER, JF ;
GROSE, WFA ;
SORGEDRAGER, N .
ARCHIVES OF DISEASE IN CHILDHOOD, 1974, 49 (03) :186-191
[2]  
GARANCIS J, 1970, LAB INVEST, V22, P268
[3]  
HOWELL RR, 1978, METABOLIC BASIS INHE, P137
[4]  
Hug G, 1976, Birth Defects Orig Artic Ser, V12, P145
[5]  
LEVIN S, 1967, ISRAEL J MED SCI, V3, P397
[6]   GLYCOGEN-STORAGE DISEASE, TYPES I TO X - CRITERIA FOR MORPHOLOGIC DIAGNOSIS [J].
MCADAMS, AJ ;
HUG, G ;
BOVE, KE .
HUMAN PATHOLOGY, 1974, 5 (04) :463-487
[7]  
Senior B, 1976, Clin Perinatol, V3, P79
[8]   PORTAL DIVERSION FOR TREATMENT OF GLYCOGEN-STORAGE DISEASE IN HUMANS [J].
STARZL, TE ;
PUTNAM, CW ;
PORTER, KA ;
HALGRIMS.CG ;
CORMAN, J ;
BROWN, BI ;
GOTLIN, RW ;
RODGERSO.DO ;
GREENE, HL .
ANNALS OF SURGERY, 1973, 178 (04) :525-539
[9]  
VANCREVELD S, 1928, MANDSCHR NEDER GENEE, V15, P349