79 related articles for article (PubMed ID: 18386334)
1. Novel human pathological mutations. Gene Symbol: CYP21A2. Disease: Non-classic 21-hydroxylase deficiency.
Concolino P; Santonocito C; Minucci A; Carrozza C; Zuppi C; Capoluongo E; Giardina B
Hum Genet; 2007 Dec; 122(5):559. PubMed ID: 18386334
[No Abstract] [Full Text] [Related]
2. Gene symbol: CYP21A2. Disease: Non-classic 21-Hydroxylase deficiency.
Capoluongo E; Concolino P; Vendittelli F; Zuppi C
Hum Genet; 2008 Jun; 123(5):553. PubMed ID: 20960659
[No Abstract] [Full Text] [Related]
3. Novel human pathological mutations. Gene symbol: CYP21A2. Disease: adrenal hyperplasia.
Carvalho B; Marques CJ; Carvalho D; Barros A; Carvalho F
Hum Genet; 2010 Apr; 127(4):482-3. PubMed ID: 21488305
[No Abstract] [Full Text] [Related]
4. [From gene to disease: adrenogenital syndrome and the CYP21A2 gene].
Claahsen-van der Grinten HL; Hoefsloot LH
Ned Tijdschr Geneeskd; 2007 May; 151(21):1174-7. PubMed ID: 17557757
[TBL] [Abstract][Full Text] [Related]
5. Gene symbol: CYP21A2. Disease: steroid 21-hydroxylase deficiency.
Tardy V
Hum Genet; 2006 Apr; 119(3):363. PubMed ID: 17230656
[No Abstract] [Full Text] [Related]
6. Gene symbol: CYP21A2. Disease: adrenal hyperplasia, CYP21.
Dain L; Minutolo C; Buzzalino N; Belli S; Oneto A; Charreau E; Alba L
Hum Genet; 2006 Apr; 119(3):363. PubMed ID: 17230657
[No Abstract] [Full Text] [Related]
7. Gene symbol: CYP21A2. Disease: Adrenal hyperplasia.
Capoluongo E; Concolino P; Carrozza C; Santonocito C; Zuppi C
Hum Genet; 2008 Jun; 123(5):550. PubMed ID: 20960642
[No Abstract] [Full Text] [Related]
8. Gene symbol: CYP21A2. Disease: Adrenal hyperplasia.
Capoluongo E; Concolino P; Vendittelli F; Zuppi C
Hum Genet; 2008 Jun; 123(5):549-50. PubMed ID: 20960641
[No Abstract] [Full Text] [Related]
9. Gene symbol: CYP21A2. Disease: Adrenal hyperplasia.
Capoluongo E; Concolino P; Minucci A; Giardina B
Hum Genet; 2008 Jun; 123(5):550. PubMed ID: 20960643
[No Abstract] [Full Text] [Related]
10. Three novel CYP21A2 mutations and their protein modelling in patients with classical 21-hydroxylase deficiency from northeastern Iran.
Baradaran-Heravi A; Vakili R; Robins T; Carlsson J; Ghaemi N; A'rabi A; Abbaszadegan MR
Clin Endocrinol (Oxf); 2007 Sep; 67(3):335-41. PubMed ID: 17573904
[TBL] [Abstract][Full Text] [Related]
11. Glucocorticoid withdrawal - heterozygous carriers of congenital adrenal hyperplasia at risk?
Brackmann F; Dörr HG; Bartram CR; Hinderhofer K; Holter W; Langer T
Klin Padiatr; 2012 Oct; 224(6):392-3. PubMed ID: 22915453
[No Abstract] [Full Text] [Related]
12. [Virilizing congenital adrenogenital syndrome with a de novo I172N mutation: study of a new case].
Díez López I; Rodríguez Estévez A; González Molina E; Martínez Ayucar M; Rodríguez Pérez B; Ezquieta Zubicaray B
An Pediatr (Barc); 2010 Jan; 72(1):72-8. PubMed ID: 19819201
[TBL] [Abstract][Full Text] [Related]
13. [Expression of the human steroid 21-hydroxylase gene and its mutant variant C169R in insect cells and functional analysis of expression products].
Grishchuk IuV; Rubtsov PM; Belzhelarskaia SN
Mol Biol (Mosk); 2007; 41(1):71-8. PubMed ID: 17380893
[TBL] [Abstract][Full Text] [Related]
14. Three novel mutations in Japanese patients with 21-hydroxylase deficiency.
Usui T; Nishisho K; Kaji M; Ikuno N; Yorifuji T; Yasuda T; Kuzuya H; Shimatsu A
Horm Res; 2004; 61(3):126-32. PubMed ID: 14676460
[TBL] [Abstract][Full Text] [Related]
15. Bilateral adrenal myelolipoma associated with adrenogenital syndrome.
Sakaki M; Izaki H; Fukumori T; Taue R; Kishimoto T; Kanayama HO
Int J Urol; 2006 Jun; 13(6):801-2. PubMed ID: 16834664
[TBL] [Abstract][Full Text] [Related]
16. [Congenital adrenal hyperplasia].
Bouvattier C; Chatelain P
Rev Prat; 2008 May; 58(9):990-4. PubMed ID: 18672665
[TBL] [Abstract][Full Text] [Related]
17. Functional studies of CYP21A2 mutants complement structural and clinical predictions of disease severity in CAH.
Barbaro M; Soardi FC; de Mello MP; Wedell A; Lajic S
Clin Endocrinol (Oxf); 2012 May; 76(5):766-8. PubMed ID: 22040027
[No Abstract] [Full Text] [Related]
18. Identification of a novel compound heterozygous mutation of the CYP21A2 gene causing 21‑hydroxylase deficiency in a Chinese pedigree.
Liu J; Zhang X; Zhang H; Fang L; Xu J; Guan Q; Xu C
Mol Med Rep; 2018 Mar; 17(3):4265-4272. PubMed ID: 29328376
[TBL] [Abstract][Full Text] [Related]
19. Nonsense mutation causing steroid 21-hydroxylase deficiency.
Globerman H; Amor M; Parker KL; New MI; White PC
J Clin Invest; 1988 Jul; 82(1):139-44. PubMed ID: 3267225
[TBL] [Abstract][Full Text] [Related]
20. [21 hydroxylase deficiency: new strategies emerging from molecular studies].
Morel Y; Tardy V; Costa JM; Forest MG; David M
Ann Endocrinol (Paris); 2003 Dec; 64(6):456-70. PubMed ID: 15067252
[No Abstract] [Full Text] [Related]
[Next] [New Search]
