173 related articles for article (PubMed ID: 10811298)
1. DiGeorge syndrome with Graves' disease: A case report.
Kawamura T; Nimura I; Hanafusa M; Fujikawa R; Okubo M; Egusa G; Amakido M
Endocr J; 2000 Feb; 47(1):91-5. PubMed ID: 10811298
[TBL] [Abstract][Full Text] [Related]
2. Graves' disease in DiGeorge syndrome: patient report with a review of endocrine autoimmunity associated with 22q11.2 deletion.
Brown JJ; Datta V; Browning MJ; Swift PG
J Pediatr Endocrinol Metab; 2004 Nov; 17(11):1575-9. PubMed ID: 15570997
[TBL] [Abstract][Full Text] [Related]
3. Hypocalcemia following treatment for hyperthyroidism.
Meek CL; Kaplan F; Pereira RS; Viljoen A
Clin Chem; 2011 Jun; 57(6):811-4. PubMed ID: 21622923
[No Abstract] [Full Text] [Related]
4. [DiGeorge syndrome. An underdiagnosed disease category with different clinical features].
Graesdal A; Surén P; Vadstrup S
Tidsskr Nor Laegeforen; 2001 Nov; 121(27):3177-9. PubMed ID: 11876140
[TBL] [Abstract][Full Text] [Related]
5. An adult case of 22q11.2 deletion syndrome diagnosed in a 36-year-old woman with hypocalcemia caused by hypoparathyroidism and Hashimoto's thyroiditis.
Nakada Y; Terui K; Kageyama K; Tsushima Y; Murakami H; Soma Y; Nigawara T; Sakihara S
Intern Med; 2013; 52(12):1365-8. PubMed ID: 23774548
[TBL] [Abstract][Full Text] [Related]
6. Hypocalcemia and Graves' disease associated with 22q11.2 deletion syndrome.
Tanaka W; Oyama N; Makimura M; Miyako K
Pediatr Int; 2023; 65(1):e15709. PubMed ID: 37968902
[No Abstract] [Full Text] [Related]
7. DiGeorge syndrome with microdeletion of chromosome 22q11.2: report of one case.
Wang JL; Chen SJ; Chung MY; Niu DM; Lin CY; Hwang BT; Lu JH
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(5):385-9. PubMed ID: 9401184
[TBL] [Abstract][Full Text] [Related]
8. Symptomatic hypocalcemia after treatment for hyperthyroidism in a woman with chromosome 22q11.2 deletion syndrome complicated by Graves' disease: longitudinal changes in the number of subsets of CD4 and CD8 lymphocytes after thyroidectomy.
Iijima T; Jojima T; Hosonuma S; Ohhira E; Tomaru T; Kogai T; Usui I; Aso Y
Endocr J; 2021 Oct; 68(10):1187-1195. PubMed ID: 33980771
[TBL] [Abstract][Full Text] [Related]
9. Hypocalcemia impacts heart failure control in DiGeorge 2 syndrome.
Chao PH; Chao MC; Hwang KP; Chung MY
Acta Paediatr; 2009 Jan; 98(1):195-8. PubMed ID: 18795911
[TBL] [Abstract][Full Text] [Related]
10. FISH investigation of 22q11.2 deletion in patients with immunodeficiency and/or cardiac abnormalities.
Yakut T; Kilic SS; Cil E; Yapici E; Egeli U
Pediatr Surg Int; 2006 Apr; 22(4):380-3. PubMed ID: 16463032
[TBL] [Abstract][Full Text] [Related]
11. Hypoparathyroidism Associated with Benign Thyroid Nodules in DiGeorge-like Syndrome: A Rare Case Report and Literature Review.
Spinelli C; Ghionzoli M; Guglielmo C; Baroncelli G; Tyutyusheva N; Frega A; Patrizio A; Fallahi P; Ferrari SM; Antonelli A
Endocr Metab Immune Disord Drug Targets; 2024; 24(7):850-856. PubMed ID: 37986268
[TBL] [Abstract][Full Text] [Related]
12. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects.
Hou JW; Wang JK; Tsai WY; Chou CC; Wang TR
J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164
[TBL] [Abstract][Full Text] [Related]
13. [An Adult Case of 22q11.2 Deletion Syndrome with Congenital Abnormalities and Neurodevelopmental Disorders, Which Remained Undiagnosed Until Presentation of Auditory Hallucinations].
Tamune H; Nishimura F; Koshiyama D; Yamada K; Kondo S; Kano Y; Kasai K
Seishin Shinkeigaku Zasshi; 2017; 119(1):9-16. PubMed ID: 30629863
[TBL] [Abstract][Full Text] [Related]
14. Endocrine and Growth Disorders in Taiwanese Children With 22q11.2 Deletion Syndrome.
Lin HY; Tsai WY; Tung YC; Liu SY; Lee NC; Chien YH; Hwu WL; Lee CT
Front Endocrinol (Lausanne); 2022; 13():771100. PubMed ID: 35432203
[TBL] [Abstract][Full Text] [Related]
15. DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.
Wilson DI; Cross IE; Goodship JA; Coulthard S; Carey AH; Scambler PJ; Bain HH; Hunter AS; Carter PE; Burn J
Br Heart J; 1991 Oct; 66(4):308-12. PubMed ID: 1747284
[TBL] [Abstract][Full Text] [Related]
16. [Clinical features and molecular diagnosis of three patients with DiGeorge anomaly].
Sun JQ; Wang LS; Qi CH; Ying WJ; Guo XH; Liu DR; Hui XY; Liu F; Cao Y; Luo FH; Wang XC
Zhonghua Er Ke Za Zhi; 2012 Dec; 50(12):944-7. PubMed ID: 23324155
[TBL] [Abstract][Full Text] [Related]
17. Clinical manifestations and frequency of hypocalcemia in 22q11.2 deletion syndrome.
Fujii S; Nakanishi T
Pediatr Int; 2015 Dec; 57(6):1086-9. PubMed ID: 25925264
[TBL] [Abstract][Full Text] [Related]
18. Commentary on: hypocalcemia following treatment for hyperthyroidism.
Endres DB
Clin Chem; 2011 Jun; 57(6):815. PubMed ID: 21622925
[No Abstract] [Full Text] [Related]
19. Commentary on: hypocalcemia following treatment for hyperthyroidism.
Zimmerman D
Clin Chem; 2011 Jun; 57(6):814. PubMed ID: 21622924
[No Abstract] [Full Text] [Related]
20. DiGeorge syndrome and partial monosomy 10p: case report and review.
Schuffenhauer S; Seidel H; Oechsler H; Belohradsky B; Bernsau U; Murken J; Meitinger T
Ann Genet; 1995; 38(3):162-7. PubMed ID: 8540688
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
