Zespół Liddle’a (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Zespół Liddle’a" in Polish language version.

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8nih.gov

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5doi.org

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1czytelniamedyczna.pl

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1ahajournals.org

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ahajournals.org

circ.ahajournals.org

Aamer Abbass, Jason D’Souza, FNU Asad-Ur-Rahman and Sameen Khalid Aortic Dissection in Association With Liddle Syndrome Circulation.2016;134:A14473.

czytelniamedyczna.pl

Andrzej Ciechanowicz, Stanisław Czekalski Aspekty genetyczne nadciśnienia tętniczego, Postępy Nauk Medycznych, s3/2011, s. 18–30.

doi.org

L. Gao, L. Wang, Y. Liu, X. Zhou i inni. A family with Liddle syndrome caused by a novel missense mutation in the PY motif of the beta-subunit of the epithelial sodium channel. „J Pediatr”. 162 (1), s. 166–170, Jan 2013. DOI: 10.1016/j.jpeds.2012.06.017. PMID: 22809657.
Y. Cui, A. Tong, J. Jiang, F. Wang i inni. Liddle syndrome: clinical and genetic profiles. „J Clin Hypertens (Greenwich)”. 19 (5), s. 524–529, May 2017. DOI: 10.1111/jch.12949. PMID: 27896928.
K.Q. Yang, Y. Xiao, T. Tian, L.G. Gao i inni. Molecular genetics of Liddle’s syndrome. „Clin Chim Acta”. 436, s. 202–206, Sep 2014. DOI: 10.1016/j.cca.2014.05.015. PMID: 24882431.
K.Q. Yang, C.X. Lu, P. Fan, Y. Zhang i inni. Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome. „Clin Exp Hypertens”, s. 1–5, Jul 2017. DOI: 10.1080/10641963.2017.1334799. PMID: 28718682.
P.N. Pichurin, G.L. Schwartz. Genetic testing helps to confirm the diagnosis and initiate appropriate treatment, a case of Liddle syndrome. „J Am Soc Hypertens”. 11 (3), s. 134–135, Mar 2017. DOI: 10.1016/j.jash.2017.01.003. PMID: 28229899.

nih.gov

ncbi.nlm.nih.gov

L. Schild. The ENaC channel as the primary determinant of two human diseases: Liddle syndrome and pseudohypoaldosteronism. „Nephrologie”. 17 (7), s. 395–400, 1996. PMID: 8987044.
L. Gao, L. Wang, Y. Liu, X. Zhou i inni. A family with Liddle syndrome caused by a novel missense mutation in the PY motif of the beta-subunit of the epithelial sodium channel. „J Pediatr”. 162 (1), s. 166–170, Jan 2013. DOI: 10.1016/j.jpeds.2012.06.017. PMID: 22809657.
Y. Cui, A. Tong, J. Jiang, F. Wang i inni. Liddle syndrome: clinical and genetic profiles. „J Clin Hypertens (Greenwich)”. 19 (5), s. 524–529, May 2017. DOI: 10.1111/jch.12949. PMID: 27896928.
P.J. Gao, K.X. Zhang, D.L. Zhu, X. He i inni. Diagnosis of Liddle syndrome by genetic analysis of beta and gamma subunits of epithelial sodium channel--a report of five affected family members. „J Hypertens”. 19 (5), s. 885–889, May 2001. PMID: 11393671.
K.Q. Yang, Y. Xiao, T. Tian, L.G. Gao i inni. Molecular genetics of Liddle’s syndrome. „Clin Chim Acta”. 436, s. 202–206, Sep 2014. DOI: 10.1016/j.cca.2014.05.015. PMID: 24882431.
P.M. Snyder, M.P. Price, F.J. McDonald, C.M. Adams i inni. Mechanism by which Liddle’s syndrome mutations increase activity of a human epithelial Na+ channel. „Cell”. 83 (6), s. 969–978, Dec 1995. PMID: 8521520.
K.Q. Yang, C.X. Lu, P. Fan, Y. Zhang i inni. Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome. „Clin Exp Hypertens”, s. 1–5, Jul 2017. DOI: 10.1080/10641963.2017.1334799. PMID: 28718682.
P.N. Pichurin, G.L. Schwartz. Genetic testing helps to confirm the diagnosis and initiate appropriate treatment, a case of Liddle syndrome. „J Am Soc Hypertens”. 11 (3), s. 134–135, Mar 2017. DOI: 10.1016/j.jash.2017.01.003. PMID: 28229899.