These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
242 related articles for article (PubMed ID: 11549627)
1. Adrenocorticotropin-dependent precocious puberty of testicular origin in a boy with X-linked adrenal hypoplasia congenita due to a novel mutation in the DAX1 gene. Domenice S; Latronico AC; Brito VN; Arnhold IJ; Kok F; Mendonca BB J Clin Endocrinol Metab; 2001 Sep; 86(9):4068-71. PubMed ID: 11549627 [TBL] [Abstract][Full Text] [Related]
2. X-linked adrenal hypoplasia congenita: a mutation in DAX1 expands the phenotypic spectrum in males and females. Seminara SB; Achermann JC; Genel M; Jameson JL; Crowley WF J Clin Endocrinol Metab; 1999 Dec; 84(12):4501-9. PubMed ID: 10599709 [TBL] [Abstract][Full Text] [Related]
3. Gonadotropin- and Adrenocorticotropic Hormone-Independent Precocious Puberty of Gonadal Origin in a Patient with Adrenal Hypoplasia Congenita Due to DAX1 Gene Mutation - A Case Report and Review of the Literature: Implications for the Pathomechanism. Nagel SA; Hartmann MF; Riepe FG; Wudy SA; Wabitsch M Horm Res Paediatr; 2019; 91(5):336-345. PubMed ID: 30537713 [TBL] [Abstract][Full Text] [Related]
4. A case of X-linked adrenal hypoplasia congenita, central precocious puberty and absence of the DAX-1 gene: implications for pubertal regulation. Loke KY; Poh LK; Lee WW; Lai PS Horm Res; 2009; 71(5):298-304. PubMed ID: 19339795 [TBL] [Abstract][Full Text] [Related]
5. Identification of novel mutations of the DAX-1 gene in patients with X-linked adrenal hypoplasia congenita. Choi JH; Shin YL; Kim GH; Kim Y; Park S; Park JY; Oh C; Yoo HW Horm Res; 2005; 63(4):200-5. PubMed ID: 15860922 [TBL] [Abstract][Full Text] [Related]
6. Truncation at the C-terminus of the DAX-1 protein impairs its biological actions in patients with X-linked adrenal hypoplasia congenita. Nakae J; Tajima T; Kusuda S; Kohda N; Okabe T; Shinohara N; Kato M; Murashita M; Mukai T; Imanaka K; Fujieda K J Clin Endocrinol Metab; 1996 Oct; 81(10):3680-5. PubMed ID: 8855822 [TBL] [Abstract][Full Text] [Related]
8. Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita. Reutens AT; Achermann JC; Ito M; Ito M; Gu WX; Habiby RL; Donohoue PA; Pang S; Hindmarsh PC; Jameson JL J Clin Endocrinol Metab; 1999 Feb; 84(2):504-11. PubMed ID: 10022408 [TBL] [Abstract][Full Text] [Related]
9. Combined hypothalamic-pituitary-gonadal defect in a hypogonadic man with a novel mutation in the DAX-1 gene. Caron P; Imbeaud S; Bennet A; Plantavid M; Camerino G; Rochiccioli P J Clin Endocrinol Metab; 1999 Oct; 84(10):3563-9. PubMed ID: 10522996 [TBL] [Abstract][Full Text] [Related]
10. X-linked congenital adrenal hypoplasia: new mutations and long-term follow-up in three patients. Binder G; Wollmann H; Schwarze CP; Strom TM; Peter M; Ranke MB Clin Endocrinol (Oxf); 2000 Aug; 53(2):249-55. PubMed ID: 10931108 [TBL] [Abstract][Full Text] [Related]
11. Missense mutations cluster within the carboxyl-terminal region of DAX-1 and impair transcriptional repression. Achermann JC; Ito M; Silverman BL; Habiby RL; Pang S; Rosler A; Jameson JL J Clin Endocrinol Metab; 2001 Jul; 86(7):3171-5. PubMed ID: 11443184 [TBL] [Abstract][Full Text] [Related]
12. Congenital adrenal hypoplasia: clinical spectrum, experience with hormonal diagnosis, and report on new point mutations of the DAX-1 gene. Peter M; Viemann M; Partsch CJ; Sippell WG J Clin Endocrinol Metab; 1998 Aug; 83(8):2666-74. PubMed ID: 9709929 [TBL] [Abstract][Full Text] [Related]
13. Diagnosis of X-linked adrenal hypoplasia congenita by mutation analysis of the DAX1 gene. Guo W; Mason JS; Stone CG; Morgan SA; Madu SI; Baldini A; Lindsay EA; Biesecker LG; Copeland KC; Horlick MN JAMA; 1995 Jul; 274(4):324-30. PubMed ID: 7609262 [TBL] [Abstract][Full Text] [Related]
14. Novel deletion mutations of the DAX1 (NR0B1) gene in two Taiwanese families with X-linked adrenal hypoplasia congenita. Tsai WY; Tung YC J Pediatr Endocrinol Metab; 2005 Oct; 18(10):991-7. PubMed ID: 16355812 [TBL] [Abstract][Full Text] [Related]
15. Novel mutation of the DAX1 gene in a patient with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism. Hamaguchi K; Arikawa M; Yasunaga S; Kakuma T; Fukagawa K; Yanase T; Nawata H; Sakata T Am J Med Genet; 1998 Feb; 76(1):62-6. PubMed ID: 9508067 [TBL] [Abstract][Full Text] [Related]
16. A novel stop-loss DAX1 variant affecting its protein-interaction with SF1 precedes the adrenal hypoplasia congenital with rare spontaneous precocious puberty and elevated hypothalamic-pituitary-gonadal/adrenal axis responses. Yang H; Wei H; Shen L; Kumar C S; Chen Q; Chen Y; Kumar SA Eur J Med Genet; 2021 May; 64(5):104192. PubMed ID: 33766795 [TBL] [Abstract][Full Text] [Related]
17. Three novel mutations and a de novo deletion mutation of the DAX-1 gene in patients with X-linked adrenal hypoplasia congenita. Nakae J; Abe S; Tajima T; Shinohara N; Murashita M; Igarashi Y; Kusuda S; Suzuki J; Fujieda K J Clin Endocrinol Metab; 1997 Nov; 82(11):3835-41. PubMed ID: 9360549 [TBL] [Abstract][Full Text] [Related]
18. Hypogonadotropic hypogonadism as a presenting feature of late-onset X-linked adrenal hypoplasia congenita. Mantovani G; Ozisik G; Achermann JC; Romoli R; Borretta G; Persani L; Spada A; Jameson JL; Beck-Peccoz P J Clin Endocrinol Metab; 2002 Jan; 87(1):44-8. PubMed ID: 11788621 [TBL] [Abstract][Full Text] [Related]
19. ACTH-dependent precocious pseudopuberty in an infant with DAX1 gene mutation. Yeste D; González-Niño C; Pérez de Nanclares G; Pérez-Nanclares G; Audi L; Castaño L; Carrascosa A Eur J Pediatr; 2009 Jan; 168(1):65-9. PubMed ID: 18414894 [TBL] [Abstract][Full Text] [Related]
20. An alternate translation initiation site circumvents an amino-terminal DAX1 nonsense mutation leading to a mild form of X-linked adrenal hypoplasia congenita. Ozisik G; Mantovani G; Achermann JC; Persani L; Spada A; Weiss J; Beck-Peccoz P; Jameson JL J Clin Endocrinol Metab; 2003 Jan; 88(1):417-23. PubMed ID: 12519885 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]