(Q34499693)

2 August 2017

Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: a case-control study (English)

1 reference

2 August 2017

José A Lopez-Escamez

1

1 reference

2 August 2017

Pablo Saenz-Lopez

2

1 reference

2 August 2017

Irene Gazquez

3

1 reference

2 August 2017

Antonia Moreno

4

1 reference

2 August 2017

Carlos Gonzalez-Oller

5

1 reference

2 August 2017

Andrés Soto-Varela

6

1 reference

2 August 2017

Sofía Santos

7

1 reference

2 August 2017

Ismael Aran

8

1 reference

2 August 2017

Herminio Perez-Garrigues

9

1 reference

2 August 2017

Agueda Ibañez

10

1 reference

2 August 2017

Miguel A Lopez-Nevot

11

1 reference

2 August 2017

language of work or name

1 reference

5 January 2011

1 reference

2 August 2017

1 reference

2 August 2017

12

1 reference

2 August 2017

2

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-12-2

2 August 2017

0 references

cites work

Pathogenesis of chronic immune thrombocytopenic purpura

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

HLA , CTLA-4 and PTPN22 : the shared genetic master-key to autoimmunity?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

FcgammaR polymorphisms: Implications for function, disease susceptibility and immunotherapy.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

Regulation of endolymphatic fluid volume

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

IgG receptor polymorphisms: risk factors for disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

A novel polymorphism of FcgammaRIIIa (CD16) alters receptor function and predisposes to autoimmune disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

On the interaction of IgG subclasses with the low affinity Fc gamma RIIa (CD32) on human monocytes, neutrophils, and platelets. Analysis of a functional polymorphism to human IgG2

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

Autoimmune Sensorineural Hearing Loss

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

Antibody reactivity to heat shock protein 70 and inner ear-specific proteins in patients with idiopathic sensorineural hearing loss.

7 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-2

Treatment of corticosteroid-responsive autoimmune inner ear disease with methotrexate: a randomized controlled trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-2

Human leukocyte antigen-DQB1 and -DRB1 associations in patients with idiopathic sudden sensorineural hearing loss from a defined population of Northwest Spain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-2

Autoimmune reactivity in Ménière's disease: a preliminary report.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-2

Presence of autoantibodies in the sera of Meniere's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-2

Possible association between thyroid autoimmunity and Menière's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-2

Absence of COCH mutations in patients with Meniere disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-2

Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

FcgammaRIIa, IIIa and IIIb gene polymorphisms in Behçet's disease: do they have any clinical implications?

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

HLA-DRB1*1101 allele may be associated with bilateral Méniére's disease in southern European population.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

Influence of human leukocyte antigen in the pathogenesis of Ménière's disease in the South Korean population.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3022798

Genetic linkage and association of Fc? receptor IIIA (CD16A) on chromosome 1q23 with human systemic lupus erythematosus

27 October 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-2

HLA Associations with Meniere's Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-2

Involvement of Fcgamma receptor IIIA genotypes in susceptibility to rheumatoid arthritis

21 January 2018

1 reference

12 December 2020

IgG receptor IIa alleles determine susceptibility and severity of Guillain-Barré syndrome

1 reference

12 December 2020

Fcgamma receptor type IIIA is associated with rheumatoid arthritis in two distinct ethnic groups

1 reference

12 December 2020

Fcgamma receptor polymorphisms in systemic lupus erythematosus: association with disease and in vivo clearance of immune complexes

1 reference

12 December 2020

HLA antigens in the pathogenesis of Menière's disease

1 reference

12 December 2020

Circulating immune complexes in Meniere's disease

1 reference

12 December 2020

C3 and C1q complement deposits in the membranous labyrinth of patients with Ménière's disease

1 reference

12 December 2020

Immunofluorescent study of the endolymphatic sac in Menière's disease

1 reference

12 December 2020

Menière's disease: an immune complex-mediated illness?

1 reference

12 December 2020

Committee on Hearing and Equilibrium guidelines for the diagnosis and evaluation of therapy in Menière's disease. American Academy of Otolaryngology-Head and Neck Foundation, Inc

1 reference

12 December 2020

Meniere disease as an autosome dominant hereditary disease

1 reference

12 December 2020

Circulating auto-antibodies in Ménière's disease

1 reference

12 December 2020

FcgammaRIIA and FcgammaRIIIB polymorphisms in myasthenia gravis

1 reference

12 December 2020

Non-specific immunological determinations in Meniere's disease: any role in clinical practice?

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-12-2

1 reference

Dimensions Publication ID

2 August 2017

0 references

1 reference

2 August 2017

1 reference