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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 31030432)

  • 1. [A four-generation pedigree affected with X-linked adrenal hypoplasia congenita due to a novel missense DAX1 mutation].
    Yin Z; Jin W; Xu W; Li H; Zhang S; Peng L; Chen X; Peng G; Han L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 May; 36(5):456-461. PubMed ID: 31030432
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Late-onset X-linked adrenal hypoplasia (DAX-1, NR0B1): two new adult-onset cases from a single center.
    Kyriakakis N; Shonibare T; Kyaw-Tun J; Lynch J; Lagos CF; Achermann JC; Murray RD
    Pituitary; 2017 Oct; 20(5):585-593. PubMed ID: 28741070
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel DAX1/NR0B1 mutation in a patient with adrenal hypoplasia congenita and hypogonadotropic hypogonadism.
    Battistin C; Menezes Filho HC; Domenice S; Nishi MY; Della Manna T; Kuperman H; Steinmetz L; Dichtchekenian V; Setian N; Damiani D
    Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):496-500. PubMed ID: 23295288
    [TBL] [Abstract][Full Text] [Related]  

  • 4. X-linked adrenal hypoplasia congenita: a novel DAX1 missense mutation and challenges for clinical diagnosis in Africa.
    Lumaka A; Mubungu G; Nsibu C; Tady BP; Lukusa T; Devriendt K
    Eur J Pediatr; 2012 Feb; 171(2):267-70. PubMed ID: 21739173
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two novel DAX1 gene mutations in Chinese patients with X-linked adrenal hypoplasia congenita: clinical, hormonal and genetic analysis.
    Wu CM; Zhang HB; Zhou Q; Wan L; Jin J; Ni L; Pan YJ; Wu XY; Ruan LY
    J Endocrinol Invest; 2011 Sep; 34(8):e235-9. PubMed ID: 21270512
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Isolated hypoaldosteronism as first sign of X-linked adrenal hypoplasia congenita caused by a novel mutation in NR0B1/DAX-1 gene: a case report.
    Iughetti L; Lucaccioni L; Bruzzi P; Ciancia S; Bigi E; Madeo SF; Predieri B; Roucher-Boulez F
    BMC Med Genet; 2019 Jun; 20(1):98. PubMed ID: 31164167
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of a novel mutation of NR0B1 in a patient with X-linked adrenal hypoplasia and symptomatic treatment.
    Yang J; Lv Y; Zhou Y; Xiao X
    J Pediatr Endocrinol Metab; 2017 Nov; 30(12):1299-1304. PubMed ID: 29176027
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel mutations of DAX1 (NR0B1) in two Chinese families with X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism.
    Qin G; Ji H; Li X; Ma X; Wang D
    J Pediatr Endocrinol Metab; 2015 Jul; 28(7-8):809-14. PubMed ID: 25968435
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Novel DAX1 mutations in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism.
    Bassett JH; O'Halloran DJ; Williams GR; Beardwell CG; Shalet SM; Thakker RV
    Clin Endocrinol (Oxf); 1999 Jan; 50(1):69-75. PubMed ID: 10341858
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel mutations and spectrum of the disease of NR0B1 (DAX1)-related adrenal insufficiency in Indian children.
    Gupta S; Joshi K; Zaidi G; Sarangi AN; Mandal K; Bhavani N; Pavithran PV; Pillai MG; Singh SK; Godbole T; Bhatia V; Bhatia E
    J Pediatr Endocrinol Metab; 2019 Aug; 32(8):863-869. PubMed ID: 31219797
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Delayed-onset adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by a novel mutation in
    Liu S; Yan L; Zhou X; Chen C; Wang D; Yuan G
    J Int Med Res; 2020 Feb; 48(2):300060519882151. PubMed ID: 31642359
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and molecular characterization of five Spanish kindreds with X-linked adrenal hypoplasia congenita: atypical findings and a novel mutation in NR0B1.
    Rodríguez Estévez A; Pérez-Nanclares G; Fernández-Toral J; Rivas-Crespo F; López-Siguero JP; Díez I; Grau G; Castaño L
    J Pediatr Endocrinol Metab; 2015 Sep; 28(9-10):1129-37. PubMed ID: 26030781
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Dysfunction of hypothalamic-pituitary-testicular axis in patients with adrenal hypoplasia congenita due to DAX-1 gene mutation].
    Zheng JJ; Wu XY; Nie M; Liu ZX; Wang X; Huang BK; Fu Y; Lu L; Duan L; Mao JF
    Zhonghua Yi Xue Za Zhi; 2016 Apr; 96(15):1183-7. PubMed ID: 27117364
    [TBL] [Abstract][Full Text] [Related]  

  • 15. X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism: Identification and in vitro study of a novel small indel in the NR0B1 gene.
    Yu T; Wang J; Yu Y; Huang X; Fu Q; Shen Y; Chen F
    Mol Med Rep; 2016 May; 13(5):4039-45. PubMed ID: 27035099
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Clinical features of 9 patients with X-linked adrenal hypoplasia congenita caused by DAX1/NR0B1 gene mutations].
    Fu Y; Nie M; Xia WB; Lu L; Mao JF; Pan H; Wu XY; Zhao WG
    Zhonghua Yi Xue Za Zhi; 2010 Aug; 90(30):2119-22. PubMed ID: 21029627
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Case Report: A Novel Truncating Variant of
    Zhu F; Zhou M; Deng X; Li Y; Xiong J
    Front Endocrinol (Lausanne); 2022; 13():897069. PubMed ID: 35784540
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel mutation in the NR0B1 (DAX1) gene in a large family with two boys affected by congenital adrenal hypoplasia.
    Rojek A; Flader M; Malecka E; Niedziela M
    Hormones (Athens); 2014; 13(3):413-9. PubMed ID: 25079468
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Spontaneous fertility and variable spectrum of reproductive phenotype in a family with adult-onset X-linked adrenal insufficiency harboring a novel DAX-1/NR0B1 mutation.
    Vargas MCC; Moura FS; Elias CP; Carvalho SR; Rassi N; Kunii IS; Dias-da-Silva MR; Costa-Barbosa FA
    BMC Endocr Disord; 2020 Feb; 20(1):21. PubMed ID: 32028936
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.