Pages that link to "Q44540762"
Jump to navigation
Jump to search
The following pages link to Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome). (Q44540762):
Displaying 50 items.
- The molecular pathology of primary immunodeficiencies (Q24685932) (← links)
- The adaptor protein Crk in immune response (Q26849320) (← links)
- Mechanism-Based Strategies for the Management of Autoimmunity and Immune Dysregulation in Primary Immunodeficiencies (Q28066193) (← links)
- Unbalanced Immune System: Immunodeficiencies and Autoimmunity (Q28075911) (← links)
- Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes (Q28254095) (← links)
- Functional gene-expression analysis shows involvement of schizophrenia-relevant pathways in patients with 22q11 deletion syndrome (Q28730977) (← links)
- Practice parameter for the diagnosis and management of primary immunodeficiency (Q29042159) (← links)
- Frequency of thrombocytopenia and large platelets correlates neither with conotruncal cardiac anomalies nor immunological features in the chromosome 22q11.2 deletion syndrome (Q33362444) (← links)
- Chromosome 22q11.2 deletion presenting with immune-mediated cytopenias, macrothrombocytopenia and platelet dysfunction (Q33375440) (← links)
- Autoimmune haematological disorders in two Italian children with Kabuki syndrome (Q33412879) (← links)
- Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland (Q33763901) (← links)
- CHARGE (coloboma, heart defect, atresia choanae, retarded growth and development, genital hypoplasia, ear anomalies/deafness) syndrome and chromosome 22q11.2 deletion syndrome: a comparison of immunologic and nonimmunologic phenotypic features (Q33903396) (← links)
- An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome (Q34148921) (← links)
- CHARGE syndrome: a review of the immunological aspects (Q34463345) (← links)
- Relevance of laboratory testing for the diagnosis of primary immunodeficiencies: a review of case-based examples of selected immunodeficiencies (Q34832611) (← links)
- A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders. (Q35009738) (← links)
- Update on primary immunodeficiency: defects of lymphocytes (Q35575327) (← links)
- Aberrant Cortical Morphometry in the 22q11.2 Deletion Syndrome (Q35656086) (← links)
- Psychiatric disorders in 22q11.2 deletion syndrome are prevalent but undertreated. (Q35704408) (← links)
- MALDI-TOF-MS Assay to Detect the Hemizygous 22q11.2 Deletion in DNA from Dried Blood Spots (Q35846619) (← links)
- Regulatory T cells in immunologic self-tolerance and autoimmune disease (Q36203567) (← links)
- Immunodeficiency and autoimmunity in 22q11.2 deletion syndrome (Q36857515) (← links)
- Tolerance and autoimmunity: lessons at the bedside of primary immunodeficiencies (Q36942513) (← links)
- Pulmonary extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue associated with granulomatous inflammation in a child with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome) (Q36979766) (← links)
- DiGeorge syndrome presenting as late onset hypocalcaemia in adulthood. (Q37017894) (← links)
- Unravelling the association of partial T-cell immunodeficiency and immune dysregulation (Q37190443) (← links)
- Intrinsic defect of the immune system in children with Down syndrome: a review. (Q37403728) (← links)
- Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome (Q37566124) (← links)
- Newborn screening programs: should 22q11 deletion syndrome be added? (Q37673851) (← links)
- Thymus transplantation (Q37710840) (← links)
- Immunological aspects of 22q11.2 deletion syndrome (Q37943798) (← links)
- From murine to human nude/SCID: the thymus, T-cell development and the missing link (Q37999788) (← links)
- Genetic basis of altered central tolerance and autoimmune diseases: a lesson from AIRE mutations (Q38053490) (← links)
- Association of thymectomy with infection following congenital heart surgery (Q38117254) (← links)
- Immunodeficiency in DiGeorge Syndrome and Options for Treating Cases with Complete Athymia (Q38160483) (← links)
- ICON: the early diagnosis of congenital immunodeficiencies (Q38195246) (← links)
- Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome (Q38429254) (← links)
- Immunodeficiencies Associated with Abnormal Newborn Screening for T Cell and B Cell Lymphopenia (Q39206354) (← links)
- Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency (Q39328117) (← links)
- CD4(+) CD25(+) T-cell production in healthy humans and in patients with thymic hypoplasia. (Q39626063) (← links)
- Resolution of Primary Immune Defect in 22q11.2 Deletion Syndrome. (Q40242997) (← links)
- Neonatal Levels of T-cell Receptor Excision Circles (TREC) in Patients with 22q11.2 Deletion Syndrome and Later Disease Features (Q41378782) (← links)
- DiGeorge Syndrome Presenting as Hypocalcaemia-Induced Seizures in Adulthood (Q41472009) (← links)
- Evans syndrome and antibody deficiency: an atypical presentation of chromosome 22q11.2 deletion syndrome (Q41972351) (← links)
- Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome). (Q42057283) (← links)
- Deletion of chromosome 22q11.2 and outcome in patients with pulmonary atresia and ventricular septal defect (Q43661765) (← links)
- Maturational alterations of peripheral T cell subsets and cytokine gene expression in 22q11.2 deletion syndrome. (Q44895166) (← links)
- Autoimmunity and regulatory T cells in 22q11.2 deletion syndrome patients. (Q45876679) (← links)
- Age-dependent clinical problems in a Norwegian national survey of patients with the 22q11.2 deletion syndrome (Q46819083) (← links)
- Thymic function and impaired maintenance of peripheral T cell populations in children with congenital heart disease and surgical thymectomy (Q46951356) (← links)