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 *

252 related articles for article (PubMed ID: 10988270)

  • 41. Gitelman's syndrome with vomiting manifested by severe metabolic alkalosis and progressive renal insufficiency.
    Lee JH; Lee J; Han JS
    Tohoku J Exp Med; 2013 Nov; 231(3):165-9. PubMed ID: 24162365
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Non-association of the thiazide-sensitive Na,Cl-cotransporter gene with polygenic hypertension in both rats and humans.
    Song Y; Herrera VL; Filigheddu F; Troffa C; Lopez LV; Glorioso N; Ruiz-Opazo N
    J Hypertens; 2001 Sep; 19(9):1547-51. PubMed ID: 11564973
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [A case of Gitelman's syndrome presenting with the hypokalemic periodic paralysis].
    Saiki S; Yoshioka A; Saiki M; Yamaya Y; Hirose G
    Rinsho Shinkeigaku; 2002 Apr; 42(4):317-9. PubMed ID: 12561088
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Recurrent deep intronic mutations in the SLC12A3 gene responsible for Gitelman's syndrome.
    Lo YF; Nozu K; Iijima K; Morishita T; Huang CC; Yang SS; Sytwu HK; Fang YW; Tseng MH; Lin SH
    Clin J Am Soc Nephrol; 2011 Mar; 6(3):630-9. PubMed ID: 21051746
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure.
    Fava C; Montagnana M; Rosberg L; Burri P; Almgren P; Jönsson A; Wanby P; Lippi G; Minuz P; Hulthèn LU; Aurell M; Melander O
    Hum Mol Genet; 2008 Feb; 17(3):413-8. PubMed ID: 17981812
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Novel mutations in the SLC12A3 gene causing Gitelman's syndrome in Swedes.
    Fava C; Montagnana M; Rosberg L; Burri P; Jönsson A; Wanby P; Wahrenberg H; Hulthén UL; Aurell M; Guidi GC; Melander O
    DNA Seq; 2007 Oct; 18(5):395-9. PubMed ID: 17654016
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Mutational analysis of a thiazide-sensitive Na-Cl cotransporter (SLC12A3) gene in a Japanese population--the Iwaki Health Promotion Project].
    Yasujima M; Tsutaya S
    Rinsho Byori; 2009 Apr; 57(4):391-6. PubMed ID: 19489442
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The pathophysiological and molecular basis of Bartter's and Gitelman's syndromes.
    Bhandari S
    Postgrad Med J; 1999 Jul; 75(885):391-6. PubMed ID: 10474721
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Loss of consciousness and hypokalemia in an elderly man with a mutation of the thiazide-sensitive Na-Cl cotransporter gene.
    Hashida T; Yamada M; Hashimoto K; Satoh T; Okada S; Shibusawa N; Ishizuka T; Mori M
    Endocr J; 2006 Dec; 53(6):859-63. PubMed ID: 16966826
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Quadriparesis due to Gitelman's syndrome diagnosed with thiazide diuretic test response.
    Mukhopadhyay S; Jana S; Chatterjee A; Roy M; Sarkar A; Mukhopadhyay J
    Saudi J Kidney Dis Transpl; 2016 Mar; 27(2):407-10. PubMed ID: 26997401
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Altered renal distal tubule structure and renal Na(+) and Ca(2+) handling in a mouse model for Gitelman's syndrome.
    Loffing J; Vallon V; Loffing-Cueni D; Aregger F; Richter K; Pietri L; Bloch-Faure M; Hoenderop JG; Shull GE; Meneton P; Kaissling B
    J Am Soc Nephrol; 2004 Sep; 15(9):2276-88. PubMed ID: 15339977
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A novel initial codon mutation of the thiazide-sensitive Na-Cl cotransporter gene in a Japanese patient with Gitelman's syndrome.
    Aoki K; Tajima T; Yabushita Y; Nakamura A; Nezu U; Takahashi M; Kimura M; Terauchi Y
    Endocr J; 2008 Jul; 55(3):557-60. PubMed ID: 18520105
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Clinical, biochemical and molecular genetic data in five children with Gitelman's syndrome.
    Schmidt H; Kabesch M; Schwarz HP; Kiess W
    Horm Metab Res; 2001 Jun; 33(6):354-7. PubMed ID: 11456284
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Thiazide-sensitive cotransporter mRNA expression is not altered in three models of hypertension.
    Moreno G; Bobadilla NA; González-Salazar J; Mercado A; Tapia E; Hong E; Herrera-Acosta J; Gamba G
    Kidney Blood Press Res; 2001; 24(1):57-63. PubMed ID: 11174008
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Future considerations based on the information from Barrter's and Gitelman's syndromes.
    Alfandary H; Landau D
    Curr Opin Nephrol Hypertens; 2017 Jan; 26(1):9-13. PubMed ID: 27798456
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Mimicry of surreptitious diuretic ingestion and the ability to make a genetic diagnosis.
    Schepkens H; Hoeben H; Vanholder R; Lameire N
    Clin Nephrol; 2001 Mar; 55(3):233-7. PubMed ID: 11316244
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Spectrum of mutations in Gitelman syndrome.
    Vargas-Poussou R; Dahan K; Kahila D; Venisse A; Riveira-Munoz E; Debaix H; Grisart B; Bridoux F; Unwin R; Moulin B; Haymann JP; Vantyghem MC; Rigothier C; Dussol B; Godin M; Nivet H; Dubourg L; Tack I; Gimenez-Roqueplo AP; Houillier P; Blanchard A; Devuyst O; Jeunemaitre X
    J Am Soc Nephrol; 2011 Apr; 22(4):693-703. PubMed ID: 21415153
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Gitelman's syndrome: towards genotype-phenotype correlations?
    Riveira-Munoz E; Chang Q; Bindels RJ; Devuyst O
    Pediatr Nephrol; 2007 Mar; 22(3):326-32. PubMed ID: 17061123
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Inheritance of an autosomal recessive disorder, Gitelman's syndrome, across two generations in one family.
    Yagi H; Yahata K; Usui T; Hasegawa C; Seta K; Sugawara A
    Intern Med; 2011; 50(11):1211-4. PubMed ID: 21628937
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Clinical significance of thiazide-sensitive Na-Cl cotransporter gene by mutational analysis].
    Yasujima M
    Rinsho Byori; 2007 Apr; 55(4):338-43. PubMed ID: 17511264
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.