ALPHA-GLUCOSIDASE DEFICIENCY IN A CHILD

被引：1

作者：

GRIFFITHS, RD

HEAF, D

COOPER, A

SARDHARWALLA, IB

机构：

[1] UNIV LIVERPOOL,DEPT CHILD HLTH,LIVERPOOL L69 3BX,ENGLAND

[2] ROYAL MANCHESTER CHILDRENS HOSP,WILLINK BIOCHEM GENET UNIT,MANCHESTER M27 1HA,LANCS,ENGLAND

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1990年 / 13卷 / 03期

关键词：

D O I：

10.1007/BF01799374

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：283 / 284

页数：2

共 3 条

[1] HUMAN BETA-MANNOSIDASE DEFICIENCY - BIOCHEMICAL FINDINGS IN PLASMA, FIBROBLASTS, WHITE CELLS AND URINE [J].

COOPER, A ;

HATTON, C ;

THORNLEY, M ;

SARDHARWALLA, IB .

JOURNAL OF INHERITED METABOLIC DISEASE, 1988, 11 (01) :17-29

[2] SPECTRUM AND DIAGNOSIS OF ACID MALTASE DEFICIENCY [J].

ENGEL, AG ;

GOMEZ, MR ;

SEYBOLD, ME ;

LAMBER, EH .

NEUROLOGY, 1973, 23 (01) :95-106

[3] IMPROVEMENT OF MUSCLE FUNCTION IN ACID MALTASE DEFICIENCY BY HIGH-PROTEIN THERAPY [J].

SLONIM, AE ;

COLEMAN, RA ;

MCELLIGOT, MA ;

NAJJAR, J ;

HIRSCHHORN, K ;

LABADIE, GU ;

MRAK, R ;

EVANS, OB ;

SHIPP, E ;

PRESSON, R .

NEUROLOGY, 1983, 33 (01) :34-38

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