HEREDITARY DISEASES - CAUSES, CURES, AND PROBLEMS

被引：10

作者：

BRADY, RO ^{[1
]}

机构：

[1] NINDS,DEV & METAB NEUROL BRANCH,BETHESDA,MD 20014

来源：

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH | 1973年 / 12卷 / 01期

关键词：

D O I：

10.1002/anie.197300011

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1 / 11

页数：11

共 114 条

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[2]

AUSTIN JH, 1967, INBORN DISORDERS SPH

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NEUROLOGY, 1970, 20 (01) :52-&

[4]

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[5]

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[6]

BONDY PK, 1969, DUNCANS DISEASES MET

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MEDICAL CLINICS OF NORTH AMERICA, 1969, 53 (04) :827-&

[8] ENZYMATIC DEFECT IN FABRYS DISEASE - CERAMIDETRIHEXOSIDASE DEFICIENCY [J].

BRADY, RO ;

GAL, AE ;

BRADLEY, RM ;

MARTENSS.E ;

WARSHAW, AL ;

LASTER, L .

NEW ENGLAND JOURNAL OF MEDICINE, 1967, 276 (21) :1163-&

[9] SPHINGOLIPID HYDROLASES IN BRAIN TISSUE OF PATIENTS WITH GENERALIZED GANG-LIODOSIS [J].

BRADY, RO ;

OBRIEN, JS ;

BRADLEY, RM ;

GAL, AE .

BIOCHIMICA ET BIOPHYSICA ACTA, 1970, 210 (01) :193-&

[10] IDENTIFICATION OF HETEROZYGOUS CARRIERS OF LIPID STORAGE DISEASES - CURRENT STATUS AND CLINICAL APPLICATIONS [J].

BRADY, RO ;

JOHNSON, WG ;

UHLENDORF, BW .

AMERICAN JOURNAL OF MEDICINE, 1971, 51 (04) :423-+

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