case report | Q2782326 |
scholarly article | Q13442814 |
P50 | author | Hiroto Furuta | Q90443925 |
Hiroshi Iwakura | Q42852704 | ||
P2093 | author name string | Hiroyuki Ariyasu | |
Takashi Akamizu | |||
Takayuki Ota | |||
Yoko Ueda | |||
Hidefumi Inaba | |||
Masahiro Nishi | |||
Shinsuke Uraki | |||
Sakiko Nakashima | |||
P2860 | cites work | 22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features | Q26798055 |
Aire regulates negative selection of organ-specific T cells | Q28213185 | ||
Hassall's corpuscles instruct dendritic cells to induce CD4+CD25+ regulatory T cells in human thymus | Q28268867 | ||
Autoimmune polyendocrine syndrome type 1 and NALP5, a parathyroid autoantigen | Q33322653 | ||
Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles | Q33816981 | ||
Graves' hyperthyroidism is antibody-mediated but is predominantly a Th1-type cytokine disease | Q34468100 | ||
Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome | Q35571176 | ||
Graves' disease in DiGeorge syndrome: patient report with a review of endocrine autoimmunity associated with 22q11.2 deletion | Q35967082 | ||
22q11.2 deletion syndrome | Q36988231 | ||
Epidemiology and Health-Related Quality of Life in Hypoparathyroidism in Norway | Q37147509 | ||
Immunological aspects of 22q11.2 deletion syndrome | Q37943798 | ||
T regulatory (Treg) and T helper 17 (Th17) lymphocytes in thyroid autoimmunity | Q38609536 | ||
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 antibodies | Q41702375 | ||
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 syndrome | Q47587653 | ||
Endocrine manifestations of chromosome 22q11.2 microdeletion syndrome. | Q53619205 | ||
T cell tolerance by clonal elimination in the thymus | Q56922465 | ||
Graves' disease in patients with 22q11.2 deletion | Q62111826 | ||
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 disease | Q69801924 | ||
DiGeorge syndrome with Graves' disease: A case report | Q73793467 | ||
Immunologic defects in 22q11.2 deletion syndrome | Q81292579 | ||
Helios expression in T-regulatory cells in patients with di George Syndrome | Q87375140 | ||
P433 | issue | 10 | |
P921 | main subject | Graves' disease | Q50357588 |
P304 | page(s) | 1169-1173 | |
P577 | publication date | 2017-05-15 | |
P1433 | published in | Internal Medicine | Q6047666 |
P1476 | title | Graves' Disease in Pediatric and Elderly Patients with 22q11.2 Deletion Syndrome | |
P478 | volume | 56 |
Q99711424 | Autoimmune Thyroid Disease in Specific Genetic Syndromes in Childhood and Adolescence | cites work | P2860 |
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