FAMILIAL EMPHYSEMA ASSOCIATED WITH ANTITRYPSIN DEFICIENCY

被引：24

作者：

KOWALYSHYN, T

SATALINE, LR

机构：

来源：

DISEASES OF THE CHEST | 1969年 / 55卷 / 04期

关键词：

D O I：

10.1378/chest.55.4.285

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：285 / +

页数：1

共 14 条

[1]

AXELSSON U, 1965, AM J HUM GENET, V17, P466

[2]

BRISCOE WA, 1966, AM REV RESPIR DIS, V94, P529

[3]

ERIKSSON S, 1965, ACTA MED SCAND, VS177, P5

[4]

ERIKSSON S, 1964, ACTA MED SCAND, V175, P197

[5] POLYMORPHISM OF PREALBUMINS AND ALPHA1-ANTITRYPSIN IN HUMAN SERA [J].

FAGERHOL, MK ;

LAURELL, CB .

CLINICA CHIMICA ACTA, 1967, 16 (02) :199-&

[6] OBSTRUCTIVE LUNG DISEASE AND TRYPSIN INHIBITORS IN ALPHA1-ANTITRYPSIN DEFICIENCY [J].

GANROT, PO ;

LAURELL, CB ;

ERIKSSON, S .

SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1967, 19 (03) :205-&

[7] ALPHA1-ANTITRYPSIN DEFICIENCY [J].

HUNTER, CC ;

PIERCE, JA ;

LABORDE, JB .

JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1968, 205 (01) :23-&

[8]

KUEPPERS F, 1966, P SOC EXP BIOL MED, V121, P1207

[9] HEREDITARY DEFICIENCY OF SERUM ALPHA1-ANTITRYPSIN [J].

KUEPPERS, F ;

BEARN, AG ;

BRISCOE, WA .

SCIENCE, 1964, 146 (365) :1678-&

[10] 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-+

← 1 2 →