The hereditary and acquired deficiencies of complement (Q39823067)

14 September 2017

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title

The hereditary and acquired deficiencies of complement (English)

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14 September 2017

Nusinow SR

1

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14 September 2017

Zuraw BL

series ordinal

2

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14 September 2017

Curd JG

series ordinal

3

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14 September 2017

language of work or name

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1 May 1985

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Medical Clinics of North America

14 September 2017

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14 September 2017

69

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14 September 2017

3

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14 September 2017

487-504

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Complement deficiency states

14 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Partial genetic deficiency of the C4 component of complement in discoid lupus erythematosus and urticaria/angioedema

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Detection of active kallikrein in induced blister fluids of hereditary angioedema patients

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

A BIOCHEMICAL ABNORMALITY IN HEREDIATRY ANGIONEUROTIC EDEMA: ABSENCE OF SERUM INHIBITOR OF C' 1-ESTERASE.

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Prevalence of congenital or acquired complement deficiency in patients with sporadic meningococcal disease

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Current concepts in immunology: the alternative pathway of complement--a system for host resistance to microbial infection.

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Hereditary Angioedema: the Clinical Syndrome and Its Management

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Evidence for linkage between HL-A histocompatibility genes and those involved in the synthesis of the second component of complement.

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Replacement therapy in hereditary angioedema: successful treatment of acute episodes of angioedema with partly purified C1 inhibitor

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Inherited deficiency of the second component of complement. Rheumatic disease associations

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Inherited disorders of complement

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Activation of complement by serum-resistant Neisseria gonorrhoeae. Assembly of the membrane attack complex without subsequent cell death

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Hereditary angioneurotic edema. I. Case reports and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Hereditary angioneurotic edema. II. Deficiency of inhibitor for serum globulin permeability factor and/or plasma kallikrein

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Familial deficiency of two subunits of the first component of complement. C1r and C1s associated with a lupus erythematosus-like disease

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Familial carboxypeptidase N deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Hypocomplementemia in chronic idiopathic urticaria

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Familial partial deficiency of the third component of complement (C3) and the hypocomplementemic cutaneous vasculitis syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

A selective and complete absence of C1q in a patient with vasculitis and nephritis

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

1 reference

7 January 2021

Lupus Erythematosus-like Syndrome with Selective Complete Deficiency of C1q

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Linkage between the Gene (or Genes) Controlling Synthesis of the Fourth Component of Complement and the Major Histocompatibility Complex

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Homozygous C2 deficiency, lupus erythematosus, and anti-Ro (SSA) antibodies

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Hereditary deficiency of the third component of complement in two sisters with systemic lupus erythematosus-like symptoms

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Severe systemic lupus erythematosus with nephritis in a boy with deficiency of the fourth component of complement

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Complement and lupus erythematosus

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Complement studies of sera and other biologic fluids

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Systemic lupus erythematosus in hereditary deficiency of the fourth component of complement

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

A genetic defect of the C1q subcomponent of complement associated with childhood (immune complex) nephritis

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

Activation of the alternative pathway of complement: A mechanism in search of diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

A hypocomplementemic vasculitic urticarial syndrome. Report of four new cases and definition of the disease

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7125%2816%2931028-8

7 January 2021

10.1016/S0025-7125(16)31028-8

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