255 related articles for article (PubMed ID: 11228173)
21. Genotype-phenotype analysis of a newly discovered family with Liddle's syndrome.
Jeunemaitre X; Bassilana F; Persu A; Dumont C; Champigny G; Lazdunski M; Corvol P; Barbry P
J Hypertens; 1997 Oct; 15(10):1091-100. PubMed ID: 9350583
[TBL] [Abstract][Full Text] [Related]
22. Liddle's syndrome mutations disrupt cAMP-mediated translocation of the epithelial Na(+) channel to the cell surface.
Snyder PM
J Clin Invest; 2000 Jan; 105(1):45-53. PubMed ID: 10619860
[TBL] [Abstract][Full Text] [Related]
23. A clinical phenotype mimicking essential hypertension in a newly discovered family with Liddle's syndrome.
Rossi E; Farnetti E; Nicoli D; Sazzini M; Perazzoli F; Regolisti G; Grasselli C; Santi R; Negro A; Mazzeo V; Mantero F; Luiselli D; Casali B
Am J Hypertens; 2011 Aug; 24(8):930-5. PubMed ID: 21525970
[TBL] [Abstract][Full Text] [Related]
24. Novel mutations in epithelial sodium channel (ENaC) subunit genes and phenotypic expression of multisystem pseudohypoaldosteronism.
Edelheit O; Hanukoglu I; Gizewska M; Kandemir N; Tenenbaum-Rakover Y; Yurdakök M; Zajaczek S; Hanukoglu A
Clin Endocrinol (Oxf); 2005 May; 62(5):547-53. PubMed ID: 15853823
[TBL] [Abstract][Full Text] [Related]
25. 'Treasure your exceptions': what we can learn from autosomal-dominant inherited forms of hypertension.
Luft FC; Schuster H; Bilginturan N; Wienker T
J Hypertens; 1995 Dec; 13(12 Pt 2):1535-8. PubMed ID: 8903606
[TBL] [Abstract][Full Text] [Related]
26. Conservation of pH sensitivity in the epithelial sodium channel (ENaC) with Liddle's syndrome mutation.
Konstas AA; Mavrelos D; Korbmacher C
Pflugers Arch; 2000 Dec; 441(2-3):341-50. PubMed ID: 11211122
[TBL] [Abstract][Full Text] [Related]
27. Liddle's syndrome: prospective genetic screening and suppressed aldosterone secretion in an extended kindred.
Findling JW; Raff H; Hansson JH; Lifton RP
J Clin Endocrinol Metab; 1997 Apr; 82(4):1071-4. PubMed ID: 9100575
[TBL] [Abstract][Full Text] [Related]
28. Low-renin hypertension: more common than we think?
Pratt JH
Cardiol Rev; 2000; 8(4):202-6. PubMed ID: 11174896
[TBL] [Abstract][Full Text] [Related]
29. Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel.
Shimkets RA; Warnock DG; Bositis CM; Nelson-Williams C; Hansson JH; Schambelan M; Gill JR; Ulick S; Milora RV; Findling JW
Cell; 1994 Nov; 79(3):407-14. PubMed ID: 7954808
[TBL] [Abstract][Full Text] [Related]
30. Mutations and variants of the epithelial sodium channel gene in Liddle's syndrome and primary hypertension.
Melander O; Orho M; Fagerudd J; Bengtsson K; Groop PH; Mattiasson I; Groop L; Hulthén UL
Hypertension; 1998 May; 31(5):1118-24. PubMed ID: 9576123
[TBL] [Abstract][Full Text] [Related]
31. Disorders of the epithelial Na(+) channel in Liddle's syndrome and autosomal recessive pseudohypoaldosteronism type 1.
Oh YS; Warnock DG
Exp Nephrol; 2000; 8(6):320-5. PubMed ID: 11014928
[TBL] [Abstract][Full Text] [Related]
32. Molecular genetics of Liddle's syndrome.
Yang KQ; Xiao Y; Tian T; Gao LG; Zhou XL
Clin Chim Acta; 2014 Sep; 436():202-6. PubMed ID: 24882431
[TBL] [Abstract][Full Text] [Related]
33. Liddle's-like syndrome associated with nephrotic syndrome secondary to membranous nephropathy: the first case report.
Yamaguchi E; Yoshikawa K; Nakaya I; Kato K; Miyasato Y; Nakagawa T; Kakizoe Y; Mukoyama M; Soma J
BMC Nephrol; 2018 May; 19(1):122. PubMed ID: 29792170
[TBL] [Abstract][Full Text] [Related]
34. Liddle's syndrome: genetics and mechanisms of Na+ channel defects.
Warnock DG
Contrib Nephrol; 2001; (136):1-10. PubMed ID: 11688373
[No Abstract] [Full Text] [Related]
35. The epithelial Na+ channel: cell surface insertion and retrieval in Na+ homeostasis and hypertension.
Snyder PM
Endocr Rev; 2002 Apr; 23(2):258-75. PubMed ID: 11943747
[TBL] [Abstract][Full Text] [Related]
36. Mutation analysis of SCNN1B in a family with Liddle's syndrome.
Wang W; Zhou W; Jiang L; Cui B; Ye L; Su T; Wang J; Li X; Ning G
Endocrine; 2006 Jun; 29(3):385-90. PubMed ID: 16943574
[TBL] [Abstract][Full Text] [Related]
37. Inherited sodium avid states.
Achard JM; Hadchouel J; Faure S; Jeunemaitre X
Adv Chronic Kidney Dis; 2006 Apr; 13(2):118-23. PubMed ID: 16580612
[TBL] [Abstract][Full Text] [Related]
38. Identification of a single cytosine base insertion mutation at Arg-597 of the beta subunit of the human epithelial sodium channel in a family with Liddle's disease.
Inoue T; Okauchi Y; Matsuzaki Y; Kuwajima K; Kondo H; Horiuchi N; Nakao K; Iwata M; Yokogoshi Y; Shintani Y; Bando H; Saito S
Eur J Endocrinol; 1998 Jun; 138(6):691-7. PubMed ID: 9678538
[TBL] [Abstract][Full Text] [Related]
39. The molecular basis of hypertension.
Toka HR
Turk J Pediatr; 2002; 44(3):183-93. PubMed ID: 12405428
[TBL] [Abstract][Full Text] [Related]
40. Abnormal membrane sodium transport in Liddle's syndrome.
Gardner JD; Lapey A; Simopoulos P; Bravo EL
J Clin Invest; 1971 Nov; 50(11):2253-8. PubMed ID: 4328882
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
