139 related articles for article (PubMed ID: 24027733)
1. Pseudohypoaldosteronism type 1: a rare cause of severe dyselectrolytemia and cardiovascular collapse in neonates.
Saravanapandian N; Paul S; Matthai J
J Clin Neonatol; 2012 Oct; 1(4):224-6. PubMed ID: 24027733
[TBL] [Abstract][Full Text] [Related]
2. Pseudohypoaldosteronism in a neonate presenting as life-threatening arrhythmia.
Rajpoot SK; Maggi C; Bhangoo A
Endocrinol Diabetes Metab Case Rep; 2014; 2014():130077. PubMed ID: 24688761
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Difficulties in the diagnosis and management of eight infants with secondary pseudohypoaldosteronism.
Günay F; Şıklar Z; Berberoğlu M
Turk J Pediatr; 2022; 64(3):490-499. PubMed ID: 35899562
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Cross-reactivity of adrenal steroids with aldosterone may prevent the accurate diagnosis of congenital adrenal hyperplasia.
Tuhan HU; Catli G; Anik A; Onay H; Dundar B; Bober E; Abaci A
J Pediatr Endocrinol Metab; 2015 May; 28(5-6):701-4. PubMed ID: 25503463
[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. Pseudohypoaldosteronism type 1: management issues.
Sharma R; Pandey M; Kanwal SK; Zennaro MC
Indian Pediatr; 2013 Mar; 50(3):331-3. PubMed ID: 23680607
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Pseudohypoaldosteronism type-I: a rare cause of hyperkalemia in neonates.
Bangash AS; Ali NF; Sami S; Iqbal M
J Pak Med Assoc; 2014 Apr; 64(4):484-6. PubMed ID: 24864655
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. A Novel
Huneif MA; Alhazmy ZH; Shoomi AM; Alghofely MA; Heena H; Mushiba AM; AlSaheel A
J Clin Res Pediatr Endocrinol; 2022 Jun; 14(2):244-250. PubMed ID: 33829730
[TBL] [Abstract][Full Text] [Related]
13. High aldosterone and cortisol levels in salt wasting congenital adrenal hyperplasia: a clinical conundrum.
Boddu SK; Madhavan S
J Pediatr Endocrinol Metab; 2017 Nov; 30(12):1327-1331. PubMed ID: 29127765
[TBL] [Abstract][Full Text] [Related]
14. Secondary Pseudohypoaldosteronism Associated With Mild Hydronephrosis in a Newborn.
Kodo K; Goto S; Katsumi Y
Cureus; 2021 Feb; 13(2):e13462. PubMed ID: 33777551
[TBL] [Abstract][Full Text] [Related]
15. Life threatening hyperkalemia in a neonate with pseudo-hypoaldosteronism.
Choudhry S; Najam Y
J Pak Med Assoc; 2012 Mar; 62(3):287-8. PubMed ID: 22764468
[TBL] [Abstract][Full Text] [Related]
16. [Pseudohypoaldosteronism type 1 in an infant with bilateral primary obstructive megaureter : a case report].
Makino Y; Kanematsu A; Imamura M; Yoshimura K; Nishiyama H; Yorifuji T; Ogawa O
Hinyokika Kiyo; 2011 Apr; 57(4):193-7. PubMed ID: 21646850
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. An infant presenting with failure to thrive and hyperkalaemia owing to transient pseudohypoaldosteronism: case report.
De Clerck M; Vande Walle J; Dhont E; Dehoorne J; Keenswijk W
Paediatr Int Child Health; 2018 Nov; 38(4):277-280. PubMed ID: 28557682
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]