Parental Consanguinity is Associated with a Severe Phenotype in Common Variable Immunodeficiency (Q57217495)

12

object named as

Julien Haroche

0 references

Isabelle Durieu

7

object named as

Isabelle Durieu

0 references

author name string

Claire Rivoisy

1

0 references

Laurence Gérard

3

0 references

Marion Malphettes

5

0 references

Claire Fieschi

6

0 references

François Tron

8

0 references

Agathe Masseau

9

0 references

Pierre Bordigoni

10

0 references

Laurent Alric

11

0 references

Cyrille Hoarau

13

0 references

Alice Bérézné

14

0 references

Maryvonnick Carmagnat

15

0 references

Gael Mouillot

16

0 references

Eric Oksenhendler

Journal of Clinical Immunology

17

0 references

publication date

15 October 2011

0 references

published in

0 references

volume

32

0 references

issue

1

0 references

page(s)

98-105

0 references

exact match

https://scigraph.springernature.com/pub.10.1007/s10875-011-9604-9

0 references

cites work

Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

How I treat common variable immune deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Common variable immunodeficiency disorders: division into distinct clinical phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

The EUROclass trial: defining subgroups in common variable immunodeficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

B-cell and T-cell phenotypes in CVID patients correlate with the clinical phenotype of the disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Genetics of hypogammaglobulinemia: what do we really know?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

ICOS deficiency in patients with common variable immunodeficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

An antibody-deficiency syndrome due to mutations in the CD19 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Defects in the CD19 complex predispose to glomerulonephritis, as well as IgG1 subclass deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

CD20 deficiency in humans results in impaired T cell-independent antibody responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Late-onset combined immune deficiency: a subset of common variable immunodeficiency with severe T cell defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Primary B cell immunodeficiencies: comparisons and contrasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Parental Consanguinity and the Risk of Primary Immunodeficiency Disorders: Report from the Kuwait National Primary Immunodeficiency Disorders Registry

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Infections in 252 patients with common variable immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Unravelling the complexity of T cell abnormalities in common variable immunodeficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Common variable immunodeficiency at the end of a prospering decade: towards novel gene defects and beyond

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Individuals with IgA deficiency and common variable immunodeficiency share polymorphisms of major histocompatibility complex class III genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Role for Msh5 in the regulation of Ig class switch recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10875-011-9604-9

Novel mutations in a Japanese patient with CD19 deficiency

21 January 2018

1 reference

12 December 2020

Frequency and Clinical Manifestations of Patients with Primary Immunodeficiency Disorders in Iran: Update from the Iranian Primary Immunodeficiency Registry

1 reference

12 December 2020

The French national registry of primary immunodeficiency diseases.

1 reference

12 December 2020

Correlation between common variable immunodeficiency clinical phenotypes and parental consanguinity in children and adults.

1 reference

12 December 2020

Consanguinity in Primary Immunodeficiency Disorders; the Report from Iranian Primary Immunodeficiency Registry

1 reference

12 December 2020