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.
162 related articles for article (PubMed ID: 34130666)
61. Entire DAX1 gene deletion in an Indian boy with adrenal hypoplasia congenita. Khadilkar VV; Mangtani HR; Jahagirdar RR; Khatod KA; Phadke ND; Deepa PS; Khadilkar AV Indian J Pediatr; 2013 Aug; 80(8):631-5. PubMed ID: 23263975 [TBL] [Abstract][Full Text] [Related]
62. Next-Generation Sequencing Identifies Different Genetic Defects in 2 Patients with Primary Adrenal Insufficiency and Gonadotropin-Independent Precocious Puberty. Guzzetti C; Bizzarri C; Pisaneschi E; Mucciolo M; Bellacchio E; Ibba A; Casula L; Novelli A; Loche S; Cappa M Horm Res Paediatr; 2018; 90(3):203-211. PubMed ID: 30179867 [TBL] [Abstract][Full Text] [Related]
63. [A novel mutation of 428delG in DAX-1 gene causing X-linked adrenal congenital hypoplasia]. Xu M; Wang YM; Xing XN; Zhou XH Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb; 26(1):11-5. PubMed ID: 19199243 [TBL] [Abstract][Full Text] [Related]
64. A Novel NR0B1 Gene Mutation Causes Different Phenotypes in Two Male Patients with Congenital Adrenal Hypoplasia. Wu SM; Gao JZ; He B; Long WJ; Luo XP; Chen L Curr Med Sci; 2020 Feb; 40(1):172-177. PubMed ID: 32166680 [TBL] [Abstract][Full Text] [Related]
70. Rarer syndromes characterized by hypogonadotropic hypogonadism. Aminzadeh M; Kim HG; Layman LC; Cheetham TD Front Horm Res; 2010; 39():154-167. PubMed ID: 20389093 [TBL] [Abstract][Full Text] [Related]
71. A novel stop mutation (p.(Gln22*)) of DAX1 (NR0B1) results in late-onset X-linked adrenal hypoplasia congenita. Gerards J; Ritter MM; Kaminsky E; Gal A; Hoeppner W; Quinkler M Endocrinol Diabetes Metab Case Rep; 2017; 2017():. PubMed ID: 28924487 [TBL] [Abstract][Full Text] [Related]
72. A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism. Balsamo A; Antelli A; Baldazzi L; Baronio F; Lazareva D; Cassio A; Cicognani A Am J Med Genet A; 2005 Jun; 135(3):292-6. PubMed ID: 15884018 [TBL] [Abstract][Full Text] [Related]
73. A novel mutation in DAX1 causes delayed-onset adrenal insufficiency and incomplete hypogonadotropic hypogonadism. Tabarin A; Achermann JC; Recan D; Bex V; Bertagna X; Christin-Maitre S; Ito M; Jameson JL; Bouchard P J Clin Invest; 2000 Feb; 105(3):321-8. PubMed ID: 10675358 [TBL] [Abstract][Full Text] [Related]
74. A novel mutation in the NR0B1 gene in a family with monozygotic twin sisters and congenital adrenal hypoplasia affected children. Minari R; Vottero A; Tassi F; Viani I; Neri TM; Street ME; Ghizzoni L; Bernasconi S; Martorana D Hormones (Athens); 2015; 14(1):160-6. PubMed ID: 25402384 [TBL] [Abstract][Full Text] [Related]
75. DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease. Suntharalingham JP; Buonocore F; Duncan AJ; Achermann JC Best Pract Res Clin Endocrinol Metab; 2015 Aug; 29(4):607-19. PubMed ID: 26303087 [TBL] [Abstract][Full Text] [Related]
76. Pleomorphism of the HPG axis with Zhang J; Chen Q; Guo S; Li Y; Ma H; Zheng R; Du M J Pediatr Endocrinol Metab; 2022 Jul; 35(7):962-967. PubMed ID: 35417110 [TBL] [Abstract][Full Text] [Related]
77. DAX1 and X-linked adrenal hypoplasia congenita: clinical and molecular analysis in five patients. Mantovani G; De Menis E; Borretta G; Radetti G; Bondioni S; Spada A; Persani L; Beck-Peccoz P Eur J Endocrinol; 2006 May; 154(5):685-9. PubMed ID: 16645015 [TBL] [Abstract][Full Text] [Related]
78. Adrenal Hypoplasia Congenita-Hypogonadotropic Hypogonadism Syndrome Due to NR0B1 Gene Mutations. Gupta P; Sharma R; Jain V Indian J Pediatr; 2022 Jun; 89(6):587-590. PubMed ID: 35230670 [TBL] [Abstract][Full Text] [Related]
79. CRISPR/Cas9-mediated Dax1 knockout in the monkey recapitulates human AHC-HH. Kang Y; Zheng B; Shen B; Chen Y; Wang L; Wang J; Niu Y; Cui Y; Zhou J; Wang H; Guo X; Hu B; Zhou Q; Sha J; Ji W; Huang X Hum Mol Genet; 2015 Dec; 24(25):7255-64. PubMed ID: 26464492 [TBL] [Abstract][Full Text] [Related]
80. 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] [Previous] [Next] [New Search]