DEFICIENCY OF ALPHA-1 ANTITRYPSIN

被引：8

作者：

ALPER, CA ^{[1
]}

机构：

[1] HARVARD UNIV, MED SCH, DEPT PEDIAT, BOSTON, MA 02115 USA

来源：

ANNALS OF INTERNAL MEDICINE | 1973年 / 78卷 / 02期

关键词：

D O I：

10.7326/0003-4819-78-2-298

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：298 / 299

页数：2

共 7 条

[1]

FAGERHOL MK, 1970, PROG MED GENET, V7, P96

[2] QUANTITATIVE STUDIES ON INHERITED VARIANTS OF SERUM ALPHA1-ANTITRYPSIN [J].

FAGERHOL, MK .

SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1969, 23 (01) :97-&

[3] ALPHA1 ANTITRYPSIN (AT) DEFICIENCY WITH BOTH CIRRHOSIS AND CHRONIC OBSTRUCTIVE LUNG DISEASE IN 2 SIBS [J].

GLASGOW, JFT ;

HERCZ, A ;

LEVISON, H ;

LYNCH, MJ ;

SASSKORT.A .

PEDIATRIC RESEARCH, 1971, 5 (08) :427-&

[4] CHRONIC PULMONARY DISEASE ASSOCIATED WITH AN UNUSUAL GENETIC TYPE OF ALPHA1-ANTITRYPSIN DEFICIENCY IN CHILDHOOD [J].

JOHNSON, AM ;

GOTTOVI, D ;

BARNETT, TB ;

FERNALD, GW .

PEDIATRIC RESEARCH, 1971, 5 (08) :427-&

[5] ELECTROPHORETIC ALPHA1-GLOBULIN PATTERN OF SERUM IN ALPHA1-ANTITRYPSIN DEFICIENCY [J].

LAURELL, CB ;

ERIKSSON, S .

SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1963, 15 (02) :132-+

[6] ALPHA-1-ANTITRYPSIN DEFICIENCY AND NEONATAL HEPATITIS [J].

PORTER, CA ;

WILLIAMS, R ;

SHILKIN, KB ;

HAYNES, DWG ;

COOK, PJL ;

MOWAT, AP .

BMJ-BRITISH MEDICAL JOURNAL, 1972, 3 (5824) :435-+

[7]

SHARP HL, 1969, J LAB CLIN MED, V73, P934

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