BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 28586600)

  • 1. Liddle's Syndrome.
    Aziz DA; Memon F; Rahman A; Ali M
    J Ayub Med Coll Abbottabad; 2016; 28(4):809-811. PubMed ID: 28586600
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Liddle's syndrome variant: a diagnostic and therapeutic conundrum.
    Mandal AK; Mouyis K; Walker IA; Missouris CG
    Br J Hosp Med (Lond); 2019 Sep; 80(9):548-549. PubMed ID: 31498669
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Analysis of the genes involved in Mendelian forms of low-renin hypertension in Chinese early-onset hypertensive patients.
    Liu K; Qin F; Sun X; Zhang Y; Wang J; Wu Y; Ma W; Wang W; Wu X; Qin Y; Zhang H; Zhou X; Wu H; Hui R; Zou Y; Jiang X; Song L
    J Hypertens; 2018 Mar; 36(3):502-509. PubMed ID: 28915228
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A case of Liddle's syndrome; unusual presentation with hypertensive encephalopathy.
    Kota SK; Kota SK; Panda S; Modi KD
    Saudi J Kidney Dis Transpl; 2014 Jul; 25(4):869-71. PubMed ID: 24969204
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Liddle syndrome due to a novel mutation in the γ subunit of the epithelial sodium channel (ENaC) in family from Russia: a case report.
    Kozina AA; Trofimova TA; Okuneva EG; Baryshnikova NV; Obuhova VA; Krasnenko AY; Tsukanov KY; Klimchuk OI; Surkova EI; Shatalov PA; Ilinsky VV
    BMC Nephrol; 2019 Oct; 20(1):389. PubMed ID: 31655555
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The importance of genetic counseling and genetic screening: a case report of a 16-year-old boy with resistant hypertension and severe hypokalemia.
    Kuang ZM; Wang Y; Wang JJ; Liu JH; Zeng R; Zhou Q; Yu ZQ; Jiang L
    J Am Soc Hypertens; 2017 Mar; 11(3):136-139. PubMed ID: 28236585
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Liddle's syndrome in an African male due to a novel frameshift mutation in the beta-subunit of the epithelial sodium channel gene.
    Freercks R; Meldau S; Jones E; Ensor J; Weimers-Willard C; Rayner B
    Cardiovasc J Afr; 2017 Sep; 28(4):e4-e6. PubMed ID: 29144530
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Liddle Syndrome: Review of the Literature and Description of a New Case.
    Tetti M; Monticone S; Burrello J; Matarazzo P; Veglio F; Pasini B; Jeunemaitre X; Mulatero P
    Int J Mol Sci; 2018 Mar; 19(3):. PubMed ID: 29534496
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Liddle's syndrome mechanisms, diagnosis and management.
    Enslow BT; Stockand JD; Berman JM
    Integr Blood Press Control; 2019; 12():13-22. PubMed ID: 31564964
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A Rare Case of Familiar Hypertension Presenting with Hypertensive Encephalopathy in an Elderly Patient: A Diagnostic Dilemma: A Presentation of Liddle's Syndrome due to Novel Mutation in SCNN1G Gene.
    Suman S; Sudhir M; Nitin S; Vikas M; Simran K; Preet SM
    Saudi J Kidney Dis Transpl; 2021; 32(4):1163-1165. PubMed ID: 35229818
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic analysis of the epithelial sodium channel in Liddle's syndrome.
    Uehara Y; Sasaguri M; Kinoshita A; Tsuji E; Kiyose H; Taniguchi H; Noda K; Ideishi M; Inoue J; Tomita K; Arakawa K
    J Hypertens; 1998 Aug; 16(8):1131-5. PubMed ID: 9794716
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Abnormalities of nasal potential difference measurement in Liddle's syndrome.
    Baker E; Jeunemaitre X; Portal AJ; Grimbert P; Markandu N; Persu A; Corvol P; MacGregor G
    J Clin Invest; 1998 Jul; 102(1):10-4. PubMed ID: 9649551
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel mutation in the beta-subunit of the epithelial sodium channel gene (SCNN1B) in a Thai family with Liddle's syndrome.
    Sawathiparnich P; Sumboonnanonda A; Weerakulwattana P; Limwongse C
    J Pediatr Endocrinol Metab; 2009 Jan; 22(1):85-9. PubMed ID: 19344079
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic diagnosis of Liddle's syndrome by mutation analysis of SCNN1B and SCNN1G in a Chinese family.
    Wang LP; Gao LG; Zhou XL; Wu HY; Zhang L; Wen D; Li YH; Liu YX; Tian T; Fan XH; Jiang XJ; Zhang HM; Hui RT
    Chin Med J (Engl); 2012 Apr; 125(8):1401-4. PubMed ID: 22613642
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Expression and regulation of normal and polymorphic epithelial sodium channel by human lymphocytes.
    Bubien JK; Watson B; Khan MA; Langloh AL; Fuller CM; Berdiev B; Tousson A; Benos DJ
    J Biol Chem; 2001 Mar; 276(11):8557-66. PubMed ID: 11113130
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia.
    Fan P; Zhao YM; Zhang D; Liao Y; Yang KQ; Tian T; Lou Y; Luo F; Ma WJ; Zhang HM; Song L; Cai J; Liu YX; Zhou XL
    Am J Hypertens; 2019 Jul; 32(8):752-758. PubMed ID: 30977777
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.