Graves' Disease in Pediatric and Elderly Patients with 22q11.2 Deletion Syndrome.

scientific article

Graves' Disease in Pediatric and Elderly Patients with 22q11.2 Deletion Syndrome. is …
instance of (P31):
case reportQ2782326
scholarly articleQ13442814

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P356DOI10.2169/INTERNALMEDICINE.56.7927
P932PMC publication ID5491811
P698PubMed publication ID28502931

P50authorHiroto FurutaQ90443925
Hiroshi IwakuraQ42852704
P2093author name stringHiroyuki Ariyasu
Takashi Akamizu
Takayuki Ota
Yoko Ueda
Hidefumi Inaba
Masahiro Nishi
Shinsuke Uraki
Sakiko Nakashima
P2860cites work22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated FeaturesQ26798055
Aire regulates negative selection of organ-specific T cellsQ28213185
Hassall's corpuscles instruct dendritic cells to induce CD4+CD25+ regulatory T cells in human thymusQ28268867
Autoimmune polyendocrine syndrome type 1 and NALP5, a parathyroid autoantigenQ33322653
Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association allelesQ33816981
Graves' hyperthyroidism is antibody-mediated but is predominantly a Th1-type cytokine diseaseQ34468100
Antibody deficiency and autoimmunity in 22q11.2 deletion syndromeQ35571176
Graves' disease in DiGeorge syndrome: patient report with a review of endocrine autoimmunity associated with 22q11.2 deletionQ35967082
22q11.2 deletion syndromeQ36988231
Epidemiology and Health-Related Quality of Life in Hypoparathyroidism in NorwayQ37147509
Immunological aspects of 22q11.2 deletion syndromeQ37943798
T regulatory (Treg) and T helper 17 (Th17) lymphocytes in thyroid autoimmunityQ38609536
CD4(+) CD25(+) T-cell production in healthy humans and in patients with thymic hypoplasia.Q39626063
Pathogenesis of Graves' disease: molecular analysis of anti-thyrotropin receptor antibodiesQ41702375
Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).Q42057283
Identification of independent susceptible and protective HLA alleles in Japanese autoimmune thyroid disease and their epistasis.Q45306458
T-cell homeostasis in humans with thymic hypoplasia due to chromosome 22q11.2 deletion syndromeQ47587653
Endocrine manifestations of chromosome 22q11.2 microdeletion syndrome.Q53619205
T cell tolerance by clonal elimination in the thymusQ56922465
Graves' disease in patients with 22q11.2 deletionQ62111826
Juvenile rheumatoid arthritis-like polyarthritis in chromosome 22q11.2 deletion syndrome (digeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome)Q62111859
DiGeorge syndrome: long-term survival complicated by Graves diseaseQ69801924
DiGeorge syndrome with Graves' disease: A case reportQ73793467
Immunologic defects in 22q11.2 deletion syndromeQ81292579
Helios expression in T-regulatory cells in patients with di George SyndromeQ87375140
P433issue10
P921main subjectGraves' diseaseQ50357588
P304page(s)1169-1173
P577publication date2017-05-15
P1433published inInternal MedicineQ6047666
P1476titleGraves' Disease in Pediatric and Elderly Patients with 22q11.2 Deletion Syndrome
P478volume56

Reverse relations

Q99711424Autoimmune Thyroid Disease in Specific Genetic Syndromes in Childhood and Adolescencecites workP2860

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