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 *

125 related articles for article (PubMed ID: 34487532)

  • 1. [Clinical and genetic analysis of an infant with aldosterone synthase deficiency].
    Yang H; Chen Q; Zhang L; Cui Y; Wei H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Sep; 38(9):865-868. PubMed ID: 34487532
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of novel heterozygous mutations in the CYP11B2 gene causing congenital aldosterone synthase deficiency and literature review.
    Miao H; Yu Z; Lu L; Zhu H; Auchus RJ; Liu J; Jiang J; Pan H; Gong F; Chen S; Lu Z
    Steroids; 2019 Oct; 150():108448. PubMed ID: 31302112
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular Analysis of the CYP11B2 Gene in 62 Patients with Hypoaldosteronism Due to Aldosterone Synthase Deficiency.
    Merakou C; Fylaktou I; Sertedaki A; Dracopoulou M; Voutetakis A; Efthymiadou A; Christoforidis A; Dacou-Voutetakis C; Chrysis D; Kanaka-Gantenbein C
    J Clin Endocrinol Metab; 2021 Jan; 106(1):e182-e191. PubMed ID: 33098647
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Aldosterone synthase (CYP11B2) deficiency among Palestinian infants: Three novel variants and genetic heterogeneity.
    Faingelernt Y; Hershkovitz E; Abu-Libdeh B; Abedrabbo A; Abu-Rmaileh Amro S; Zarivach R; Zangen D; Lavi E; Haim A; Parvari R; Abu-Libdeh A
    Am J Med Genet A; 2021 Apr; 185(4):1033-1038. PubMed ID: 33438832
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel mutations in the CYP11B2 gene causing aldosterone synthase deficiency.
    Li N; Li J; Ding Y; Yu T; Shen Y; Fu Q; Shen Y; Huang X; Wang J
    Mol Med Rep; 2016 Apr; 13(4):3127-32. PubMed ID: 26936515
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two novel mutations of the CYP11B2 gene in a Japanese patient with aldosterone deficiency type 1.
    Kondo E; Nakamura A; Homma K; Hasegawa T; Yamaguchi T; Narugami M; Hattori T; Aoyagi H; Ishizu K; Tajima T
    Endocr J; 2013; 60(1):51-5. PubMed ID: 23018980
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel CYP11B2 mutation causing aldosterone synthase (P450c11AS) deficiency.
    Klomchan T; Supornsilchai V; Wacharasindhu S; Shotelersuk V; Sahakitrungruang T
    Eur J Pediatr; 2012 Oct; 171(10):1559-62. PubMed ID: 22801770
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Clinical features and genetic analysis of a child with glycogen storage disease type VI].
    Su L; Zhu C; Wu J; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Oct; 39(10):1099-1102. PubMed ID: 36184091
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Corticosterone Methyl Oxidase Deficiency Type 1 with Normokalemia in an Infant.
    Üstyol A; Atabek ME; Taylor N; Yeung MC; Chan AO
    J Clin Res Pediatr Endocrinol; 2016 Sep; 8(3):356-9. PubMed ID: 27125267
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A particular phenotype in a girl with aldosterone synthase deficiency.
    Williams TA; Mulatero P; Bosio M; Lewicka S; Palermo M; Veglio F; Armanini D
    J Clin Endocrinol Metab; 2004 Jul; 89(7):3168-72. PubMed ID: 15240589
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis.
    Papailiou S; Vlachopapadopoulou EA; Sertedaki A; Maritsi D; Syggelos N; Syggelou A
    Endocr Regul; 2020 Jul; 54(3):227-229. PubMed ID: 32857717
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Catch-up Growth and Discontinuation of Fludrocortisone Treatment in Aldosterone Synthase Deficiency.
    Gurpinar Tosun B; Kendir Demirkol Y; Seven Menevse T; Kaygusuz SB; Ozbek MN; Altincik SA; Mammadova J; Cayir A; Doger E; Bayramoglu E; Nalbantoglu O; Yesiltepe Mutlu G; Aghayev A; Turan S; Bereket A; Guran T
    J Clin Endocrinol Metab; 2022 Jan; 107(1):e106-e117. PubMed ID: 34415991
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Clinical and genetic analysis of an infant with isolated 17, 20-lyase deficiency].
    Zhou DY; Qiu WJ; Xu MS; Luo JH; Ye J; Han LS; Zhang HW; Yu YG; Liang LL; Gu XF
    Zhonghua Er Ke Za Zhi; 2016 Aug; 54(8):619-22. PubMed ID: 27510877
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Aldosterone signaling defect in young infants: single-center report and review.
    Wijaya M; Ma H; Zhang J; Du M; Li Y; Chen Q; Guo S
    BMC Endocr Disord; 2021 Jul; 21(1):149. PubMed ID: 34243750
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in
    Turan H; Dağdeviren Çakır A; Özer Y; Tarçın G; Özcabi B; Ceylaner S; Ercan O; Evliyaoğlu SO
    J Clin Res Pediatr Endocrinol; 2021 Jun; 13(2):232-238. PubMed ID: 32539318
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis of a child with mucopolysaccharidoses type I due to compound heterozygous variants of IDUA gene].
    Jia H; Wang C; Liu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Oct; 39(10):1140-1144. PubMed ID: 36184100
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A compound heterozygote case of type II aldosterone synthase deficiency.
    Dunlop FM; Crock PA; Montalto J; Funder JW; Curnow KM
    J Clin Endocrinol Metab; 2003 Jun; 88(6):2518-26. PubMed ID: 12788848
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Clinical features and genetic analysis of a case with Perlman syndrome due to variant of DIS3L2 gene].
    Chen J; Hu C; Ren L; Li J; Lei T; Chen S; Zhao P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jan; 39(1):48-51. PubMed ID: 34964966
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Genetic analysis of a child with combined oxidative phosphorylation deficiency 14 due to variant of FARS2 gene].
    Ma J; Zhang H; Lyu Y; Gao M; Wang D; Gai Z; Liu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Dec; 39(12):1393-1397. PubMed ID: 36453966
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene.
    Wasniewska M; De Luca F; Valenzise M; Lombardo F; De Luca F
    Eur J Endocrinol; 2001 Jan; 144(1):59-62. PubMed ID: 11174838
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.