Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome.
about
Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndromeMechanism-Based Strategies for the Management of Autoimmunity and Immune Dysregulation in Primary ImmunodeficienciesGraves' Disease in Pediatric and Elderly Patients with 22q11.2 Deletion Syndrome.Autoimmune haematological disorders in two Italian children with Kabuki syndromeTowards a safety net for management of 22q11.2 deletion syndrome: guidelines for our times2013 IDSA clinical practice guideline for vaccination of the immunocompromised host.CHARGE syndrome: a review of the immunological aspects.Immunodeficiency and autoimmunity in 22q11.2 deletion syndrome.22q11.2 deletion syndromeNewborn screening programs: should 22q11 deletion syndrome be added?Immunological aspects of 22q11.2 deletion syndrome.New frontiers in primary immunodeficiency disorders: immunology and beyond….Genetic basis of altered central tolerance and autoimmune diseases: a lesson from AIRE mutations.Autoimmunity in immunodeficiency.Primary selective IgM deficiency: an ignored immunodeficiency.Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete AthymiaICON: the early diagnosis of congenital immunodeficiencies.Immunodeficiencies Associated with Abnormal Newborn Screening for T Cell and B Cell Lymphopenia.Resolution of Primary Immune Defect in 22q11.2 Deletion Syndrome.Selective IgM Deficiency-An Underestimated Primary Immunodeficiency.DiGeorge Syndrome Presenting as Hypocalcaemia-Induced Seizures in Adulthood.Evans syndrome and antibody deficiency: an atypical presentation of chromosome 22q11.2 deletion syndrome.Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).Retrospective analysis of TREC based newborn screening results and clinical phenotypes in infants with the 22q11 deletion syndrome.Maturational alterations of peripheral T cell subsets and cytokine gene expression in 22q11.2 deletion syndrome.Elevated homocysteine and N-methyl-d-aspartate-receptor antibodies as a cause of behavioural and cognitive decline in 22q11.2 deletion syndrome.Development of an anti-Salmonella typhi Vi ELISA: assessment of immunocompetence in healthy donors.Immunodeficiency in CHARGE syndrome.A 13-Year-Old Child with Lupus-Like Nephritis and 22q11 Microduplication Syndrome.Autoimmunity and primary immunodeficiency: two sides of the same coin?Post-childhood Presentation and Diagnosis of DiGeorge Syndrome.A prospective study of influenza vaccination and a comparison of immunologic parameters in children and adults with chromosome 22q11.2 deletion syndrome (digeorge syndrome/velocardiofacial syndrome).Autoimmune disorders in Kabuki syndrome.Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome.The immune deficiency of chromosome 22q11.2 deletion syndrome.Persistent low thymic activity and non-cardiac mortality in children with chromosome 22q11.2 microdeletion and partial DiGeorge syndrome.
P2860
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P2860
Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
2002年论文
@zh
2002年论文
@zh-cn
name
Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome.
@ast
Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome.
@en
type
label
Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome.
@ast
Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome.
@en
prefLabel
Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome.
@ast
Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome.
@en
P2093
P2860
P356
P1476
Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome.
@en
P2093
P2860
P304
P356
10.1136/ADC.86.6.422
P407
P577
2002-06-01T00:00:00Z