164 related articles for article (PubMed ID: 26807262)
1. Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene.
Nobel YR; Lodish MB; Raygada M; Rivero JD; Faucz FR; Abraham SB; Lyssikatos C; Belyavskaya E; Stratakis CA; Zilbermint M
Endocrinol Diabetes Metab Case Rep; 2016; 2016():150104. PubMed ID: 26807262
[TBL] [Abstract][Full Text] [Related]
2. Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small town.
Serra G; Antona V; D'Alessandro MM; Maggio MC; Verde V; Corsello G
Ital J Pediatr; 2021 Jun; 47(1):138. PubMed ID: 34134742
[TBL] [Abstract][Full Text] [Related]
3. Systemic Pseudohypoaldosteronism Type 1 due to 3 Novel Mutations in SCNN1Aand SCNN1BGenes.
Cayir A; Demirelli Y; Yildiz D; Kahveci H; Yarali O; Kurnaz E; Vuralli D; Demirbilek H
Horm Res Paediatr; 2019; 91(3):175-185. PubMed ID: 31018202
[TBL] [Abstract][Full Text] [Related]
4. Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes.
Jeong HA; Park YK; Jung YS; Nam MH; Nam HK; Lee KH; Rhie YJ
Ann Pediatr Endocrinol Metab; 2015 Dec; 20(4):230-4. PubMed ID: 26817011
[TBL] [Abstract][Full Text] [Related]
5. A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene.
Lee SE; Jung YH; Han KH; Lee HK; Kang HG; Ha IS; Choi Y; Cheong HI
Korean J Pediatr; 2011 Feb; 54(2):90-3. PubMed ID: 21503203
[TBL] [Abstract][Full Text] [Related]
6. A novel splice site mutation of the beta subunit gene of epithelial sodium channel (ENaC) in one Turkish patient with a systemic form of pseudohypoaldosteronism Type 1.
Dogan CS; Erdem D; Mesut P; Merve A; Sema A; Iffet B; Afig B
J Pediatr Endocrinol Metab; 2012; 25(9-10):1035-9. PubMed ID: 23426840
[TBL] [Abstract][Full Text] [Related]
7. Systemic pseudohypoaldosteronism-1 with episodic dyslipidemia in a Sudanese child.
Abdalla A; Alhassan MA; Tawfeeg R; Sanad A; Tawamie H; Abdullah M
Endocrinol Diabetes Metab Case Rep; 2021 Jun; 2021():. PubMed ID: 34165441
[TBL] [Abstract][Full Text] [Related]
8. Novel mutations in the SCNN1A gene causing Pseudohypoaldosteronism type 1.
Wang J; Yu T; Yin L; Li J; Yu L; Shen Y; Yu Y; Shen Y; Fu Q
PLoS One; 2013; 8(6):e65676. PubMed ID: 23762408
[TBL] [Abstract][Full Text] [Related]
9. [Mineralocorticoid resistance: pseudohypoaldosteronism type 1].
Fernandes-Rosa FL; Antonini SR
Arq Bras Endocrinol Metabol; 2007 Apr; 51(3):373-81. PubMed ID: 17546235
[TBL] [Abstract][Full Text] [Related]
10. Phenotypic diversity and correlation with the genotypes of pseudohypoaldosteronism type 1.
Gopal-Kothandapani JS; Doshi AB; Smith K; Christian M; Mushtaq T; Banerjee I; Padidela R; Ramakrishnan R; Owen C; Cheetham T; Dimitri P
J Pediatr Endocrinol Metab; 2019 Sep; 32(9):959-967. PubMed ID: 31301676
[TBL] [Abstract][Full Text] [Related]
11. Compound heterozygous mutations in the gamma subunit gene of ENaC (1627delG and 1570-1G-->A) in one sporadic Japanese patient with a systemic form of pseudohypoaldosteronism type 1.
Adachi M; Tachibana K; Asakura Y; Abe S; Nakae J; Tajima T; Fujieda K
J Clin Endocrinol Metab; 2001 Jan; 86(1):9-12. PubMed ID: 11231969
[TBL] [Abstract][Full Text] [Related]
12. A Neonate with Autosomal Dominant Pseudohypoaldosteronism Type 1 Due to a Novel Microdeletion of the
Kim SJ; Park D; Jang W; Lee J
Children (Basel); 2021 Nov; 8(12):. PubMed ID: 34943285
[TBL] [Abstract][Full Text] [Related]
13. A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1.
Dirlewanger M; Huser D; Zennaro MC; Girardin E; Schild L; Schwitzgebel VM
Am J Physiol Endocrinol Metab; 2011 Sep; 301(3):E467-73. PubMed ID: 21653223
[TBL] [Abstract][Full Text] [Related]
14. Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1.
Welzel M; Akin L; Büscher A; Güran T; Hauffa BP; Högler W; Leonards J; Karges B; Kentrup H; Kirel B; Senses EE; Tekin N; Holterhus PM; Riepe FG
Eur J Endocrinol; 2013 May; 168(5):707-15. PubMed ID: 23416952
[TBL] [Abstract][Full Text] [Related]
15. Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I.
Geller DS; Rodriguez-Soriano J; Vallo Boado A; Schifter S; Bayer M; Chang SS; Lifton RP
Nat Genet; 1998 Jul; 19(3):279-81. PubMed ID: 9662404
[TBL] [Abstract][Full Text] [Related]
16. Failure to thrive, hyponatremia, and hyperkalemia in a neonate.
Sopfe J; Simmons JH
Pediatr Ann; 2013 May; 42(5):74-9. PubMed ID: 23641881
[TBL] [Abstract][Full Text] [Related]
17. Clinical and molecular features of type 1 pseudohypoaldosteronism.
Riepe FG
Horm Res; 2009; 72(1):1-9. PubMed ID: 19571553
[TBL] [Abstract][Full Text] [Related]
18. Severe Salt-Losing Syndrome and Hyperkalemia Induced by Adult Nephron-Specific Knockout of the Epithelial Sodium Channel α-Subunit.
Perrier R; Boscardin E; Malsure S; Sergi C; Maillard MP; Loffing J; Loffing-Cueni D; Sørensen MV; Koesters R; Rossier BC; Frateschi S; Hummler E
J Am Soc Nephrol; 2016 Aug; 27(8):2309-18. PubMed ID: 26701978
[TBL] [Abstract][Full Text] [Related]
19. Pseudohypoaldosteronism in a Neonate Presenting as Life-Threatening Hyperkalemia.
Attia NA; Marzouk YI
Case Rep Endocrinol; 2016; 2016():6384697. PubMed ID: 26904317
[TBL] [Abstract][Full Text] [Related]
20. Autosomal dominant pseudohypoaldosteronism type 1 in an infant with salt wasting crisis associated with urinary tract infection and obstructive uropathy.
Bowden SA; Cozzi C; Hickey SE; Thrush DL; Astbury C; Nuthakki S
Case Rep Endocrinol; 2013; 2013():524647. PubMed ID: 24455331
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
