Cutaneous manifestations of complement deficiencies (Q37778649)

23 August 2017

1 reference

title

Cutaneous manifestations of complement deficiencies (English)

1 reference

23 August 2017

D Lipsker

1

1 reference

PubMed ID

20693203

23 August 2017

G Hauptmann

series ordinal

2

1 reference

23 August 2017

1 August 2010

1 reference

23 August 2017

1 reference

23 August 2017

19

1 reference

23 August 2017

9

1 reference

23 August 2017

1096-1106

1 reference

Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond

23 August 2017

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

Deficiencies of C1 inhibitor

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

Clinical practice. Hereditary angioedema

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

C1 inhibitor deficiency: consensus document

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

A hierarchical role for classical pathway complement proteins in the clearance of apoptotic cells in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

Systemic lupus erythematosus, complement deficiency, and apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

Molecular basis of a new type of C1q-deficiency associated with a non-functional low molecular weight (LMW) C1q: parallels and differences to other known genetic C1q-defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

Homozygous single nucleotide polymorphism of the complement C1QA gene is associated with decreased levels of C1q in patients with subacute cutaneous lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

Molecular basis of a selective C1s deficiency associated with early onset multiple autoimmune diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

The intricate role of complement component C4 in human systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

Immunoglobulin deficiencies and susceptibility to infection among homozygotes and heterozygotes for C2 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

Clinical aspects and molecular basis of primary deficiencies of complement component C3 and its regulatory proteins factor I and factor H.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

Mannose binding lectin: genetics and autoimmune disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

The mannose-binding lectin gene polymorphisms and systemic lupus erythematosus: two case-control studies and a meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

Consumption of erythrocyte CR1 (CD35) is associated with protection against systemic lupus erythematosus renal flare.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

Functional analysis of the classical, alternative, and MBL pathways of the complement system: standardization and validation of a simple ELISA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

Clinical and laboratory evaluation of complement deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0961203310373370

21 January 2018

Identifiers

DOI

10.1177/0961203310373370

1 reference

23 August 2017

1 reference

PubMed ID

20693203