126 related articles for article (PubMed ID: 23535960)
21. [A case of multiple brain calcifications associated with hypoparathyroidism].
Delplace PO; Wery D; Lemort M; Baguet J; Jeanmart L
J Belge Radiol; 1989 Aug; 72(4):263-6. PubMed ID: 2793819
[TBL] [Abstract][Full Text] [Related]
22. [Neonatal hypocalcaemic dilated myocardiopathy due to a 22q11 microdeletion].
Goulet M; Rio M; Jacquette A; Ladouceur M; Bonnet D
Arch Mal Coeur Vaiss; 2006 May; 99(5):520-2. PubMed ID: 16802747
[TBL] [Abstract][Full Text] [Related]
23. Hypocalcemia and chromosome 22q11 microdeletion.
Garabédian M
Genet Couns; 1999; 10(4):389-94. PubMed ID: 10631928
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Chromosome 10p deletion in a patient with hypoparathyroidism, severe mental retardation, autism and basal ganglia calcifications.
Verri A; Maraschio P; Devriendt K; Uggetti C; Spadoni E; Haeusler E; Federico A
Ann Genet; 2004; 47(3):281-7. PubMed ID: 15337474
[TBL] [Abstract][Full Text] [Related]
26. Stridor in a neonate--is it just a floppy larynx?
Naeem KB; Ahmed M
J Pak Med Assoc; 2007 Jun; 57(6):322-3. PubMed ID: 17629238
[TBL] [Abstract][Full Text] [Related]
27. Implementation of Fluorescent in situ hybridization (FISH) as a method for detecting microdeletion syndromes - our first experiences.
Sukarova-Angelovska E; Piperkova K; Sredovska A; Ilieva G; Kocova M
Prilozi; 2007 Dec; 28(2):87-98. PubMed ID: 18356781
[TBL] [Abstract][Full Text] [Related]
28. [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]
29. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
Berend SA; Spikes AS; Kashork CD; Wu JM; Daw SC; Scambler PJ; Shaffer LG
Am J Med Genet; 2000 Apr; 91(4):313-7. PubMed ID: 10766989
[TBL] [Abstract][Full Text] [Related]
30. Congenital primary hypoparathyroidism presented with extensive cutaneous and subcutaneous calcifications.
Aslan Y; Gedik Y; Okten A; Aksoy A; Cimşit G; Ari N
Turk J Pediatr; 1999; 41(2):253-7. PubMed ID: 10770667
[TBL] [Abstract][Full Text] [Related]
31. Recurrent seizures, mental retardation and extensive brain calcinosis related to delayed diagnosis of hypoparathyroidism in an adolescent boy.
Eom TH; Kim YH; Kim JM
J Clin Neurosci; 2015 May; 22(5):894-6. PubMed ID: 25835143
[TBL] [Abstract][Full Text] [Related]
32. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation.
Chen CP; Lin SP; Chern SR; Wu PS; Su JW; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2014 Mar; 53(1):74-8. PubMed ID: 24767651
[TBL] [Abstract][Full Text] [Related]
33. Fahr's Syndrome and Secondary Hypoparathyroidism.
Dos Santos VM; Da Mata AM; Ribeiro KR; Calvo IC
Rom J Intern Med; 2016; 54(1):63-5. PubMed ID: 27141572
[TBL] [Abstract][Full Text] [Related]
34. DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review.
Demczuk S; Aurias A
Ann Genet; 1995; 38(2):59-76. PubMed ID: 7486827
[TBL] [Abstract][Full Text] [Related]
35. DiGeorge syndrome: clinical variability in a family with submicroscopic deletion at 22q11.2.
Tsui KM; Ng YY; Lam TS
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(1):52-6. PubMed ID: 9066191
[TBL] [Abstract][Full Text] [Related]
36. A case of chromosome 22q11 deletion syndrome diagnosed in a 32-year-old man with hypoparathyroidism.
Maalouf NM; Sakhaee K; Odvina CV
J Clin Endocrinol Metab; 2004 Oct; 89(10):4817-20. PubMed ID: 15472168
[TBL] [Abstract][Full Text] [Related]
37. Inherited t(9;22) as the cause of DiGeorge syndrome: a case report.
Shuib S; Abdul Latif Z; Abidin NZ; Akmal SN; Zakaria Z
Malays J Pathol; 2009 Dec; 31(2):133-6. PubMed ID: 20514857
[TBL] [Abstract][Full Text] [Related]
38. Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11).
Faed MJ; Robertson J; Beck JS; Cater JI; Bose B; Madlom MM
J Med Genet; 1987 Apr; 24(4):225-7. PubMed ID: 3585938
[TBL] [Abstract][Full Text] [Related]
39. [DiGeorge syndrome. Velocardiofacial syndrome/chromosome 22q11 deletion syndrome].
Hoffmann MH; Vadstrup S
Ugeskr Laeger; 2000 May; 162(19):2736-9. PubMed ID: 10827540
[TBL] [Abstract][Full Text] [Related]
40. [Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].
Demily C; Rossi M; Schneider M; Edery P; Leleu A; d'Amato T; Franck N; Eliez S
Encephale; 2015 Jun; 41(3):266-73. PubMed ID: 25523123
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
