Misdiagnosis of hereditary angio-oedema type 1 and type 2.
about
C1 inhibitor deficiency: consensus documentDiagnosis and screening of patients with hereditary angioedema in primary careC1 inhibitor deficiency: diagnosis.Recent advances in cardiorespiratory medicine: management of pulmonary embolism and prevention of venous thromboembolism, recent treatment strategies in childhood asthma, and dermatological adverse reactions to cardiovascular drugs."Nuts and Bolts" of Laboratory Evaluation of Angioedema.Acquired C1 esterase inhibitor deficiency or serendipity? The chance finding of a paraprotein after an apparently low C1 esterase inhibitor concentration.
P2860
Misdiagnosis of hereditary angio-oedema type 1 and type 2.
description
2003 nî lūn-bûn
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2003 թուականի Ապրիլին հրատարակուած գիտական յօդուած
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2003 թվականի ապրիլին հրատարակված գիտական հոդված
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2003年の論文
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年學術文章
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name
Misdiagnosis of hereditary angio-oedema type 1 and type 2.
@ast
Misdiagnosis of hereditary angio-oedema type 1 and type 2.
@en
type
label
Misdiagnosis of hereditary angio-oedema type 1 and type 2.
@ast
Misdiagnosis of hereditary angio-oedema type 1 and type 2.
@en
prefLabel
Misdiagnosis of hereditary angio-oedema type 1 and type 2.
@ast
Misdiagnosis of hereditary angio-oedema type 1 and type 2.
@en
P2093
P2860
P1476
Misdiagnosis of hereditary angio-oedema type 1 and type 2.
@en
P2093
P2860
P304
P356
10.1046/J.1365-2133.2003.05231.X
P407
P577
2003-04-01T00:00:00Z