233 related articles for article (PubMed ID: 19307681)
1. Symptomatic hypoparathyroidism based on a 22q11 deletion first diagnosed in a 43-year-old woman.
van den Berge K; Diderich K; Poddighe P; Berghout A
Neth J Med; 2009 Mar; 67(3):102-4. PubMed ID: 19307681
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [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]
4. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome].
Muñoz S; Garay F; Flores I; Heusser F; Talesnik E; Aracena M; Mellado C; Méndez C; Arnaiz P; Repetto G
Rev Med Chil; 2001 May; 129(5):515-21. PubMed ID: 11464533
[TBL] [Abstract][Full Text] [Related]
5. Hypoparathyroidism as the major manifestation in two patients with 22q11 deletions.
Scirè G; Dallapiccola B; Iannetti P; Bonaiuto F; Galasso C; Mingarelli R; Boscherini B
Am J Med Genet; 1994 Oct; 52(4):478-82. PubMed ID: 7747762
[TBL] [Abstract][Full Text] [Related]
6. Evolution of latent hypoparathyroidism in familial 22q11 deletion syndrome.
Cuneo BF; Driscoll DA; Gidding SS; Langman CB
Am J Med Genet; 1997 Mar; 69(1):50-5. PubMed ID: 9066883
[TBL] [Abstract][Full Text] [Related]
7. [Microdeletion 22q11: apropos of case of schizophrenia in an adolescent].
Pinquier C; Héron D; de Carvalho W; Lazar G; Mazet P; Cohen D
Encephale; 2001; 27(1):45-50. PubMed ID: 11294038
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. 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]
10. [Epilepsy in an adult with chromosome 22q11 micro-deletion].
Alla P; Philip N; Azulay JP; Attarian S; Pouget J
Rev Neurol (Paris); 1999 Nov; 155(11):967-70. PubMed ID: 10603642
[TBL] [Abstract][Full Text] [Related]
11. DiGeorge syndrome presenting as late onset hypocalcaemia in adulthood.
Johnston PC; Donnelly DE; Morrison PJ; Hunter SJ
Ulster Med J; 2008 Sep; 77(3):201-2. PubMed ID: 18956803
[TBL] [Abstract][Full Text] [Related]
12. [Transient neonatal hypocalcemia. Onset Manifestation of the 22q11.2 deletion syndrome].
Pusceddu M; Bertone A; Campra D; Pontoriero D; Guala A
Minerva Pediatr; 2002 Aug; 54(4):343-5. PubMed ID: 12131871
[No Abstract] [Full Text] [Related]
13. [DiGeorge syndrome diagnosed in a 39-year old woman with chronic hypocalcemia].
Hoffmann MH; Vadstrup S
Ugeskr Laeger; 2000 May; 162(19):2755-6. PubMed ID: 10827545
[TBL] [Abstract][Full Text] [Related]
14. Endocrine manifestations of chromosome 22q11.2 microdeletion syndrome.
Choi JH; Shin YL; Kim GH; Seo EJ; Kim Y; Park IS; Yoo HW
Horm Res; 2005; 63(6):294-9. PubMed ID: 15995343
[TBL] [Abstract][Full Text] [Related]
15. Asymmetric crying facies associated with congenital hypoparathyroidism and 22q11 deletion.
Akçakuş M; Güneş T; Kurtoğlu S; Cetin N; Ozkul Y; Narin N; Atabek ME; Uğraş R
Turk J Pediatr; 2004; 46(2):191-3. PubMed ID: 15214756
[TBL] [Abstract][Full Text] [Related]
16. DiGeorge anomaly in the absence of chromosome 22q11.2 deletion.
Rope AF; Cragun DL; Saal HM; Hopkin RJ
J Pediatr; 2009 Oct; 155(4):560-5. PubMed ID: 19595366
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. A prenatally sonographically diagnosed conotruncal anomaly with mosaic type trisomy 21 and 22q11.2 microdeletion/DiGeorge syndrome.
Balci S; Altugan FS; Alehan D; Aypar E; Baltaci V
Genet Couns; 2009; 20(4):373-7. PubMed ID: 20162873
[TBL] [Abstract][Full Text] [Related]
19. Hypocalcemia and chromosome 22q11 microdeletion.
Garabédian M
Genet Couns; 1999; 10(4):389-94. PubMed ID: 10631928
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
