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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1961 4
1962 2
1963 1
1964 1
1973 1
1975 1
1979 1
1982 1
1984 1
1990 1
1994 2
1995 1
1997 1
1998 2
1999 1
2000 2
2001 4
2002 2
2003 3
2004 4
2005 1
2006 3
2008 2
2009 3
2010 7
2011 4
2013 1
2014 7
2015 5
2016 3
2017 3
2018 7
2019 3
2020 13
2021 8
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Publication date

Similar articles for PMID: 34045298

97 results
Results by year
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Page 1
The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies.
Nozu K, Iijima K, Kanda K, Nakanishi K, Yoshikawa N, Satomura K, Kaito H, Hashimura Y, Ninchoji T, Komatsu H, Kamei K, Miyashita R, Kugo M, Ohashi H, Yamazaki H, Mabe H, Otsubo A, Igarashi T, Matsuo M. Nozu K, et al. J Clin Endocrinol Metab. 2010 Dec;95(12):E511-8. doi: 10.1210/jc.2010-0392. Epub 2010 Sep 1. J Clin Endocrinol Metab. 2010. PMID: 20810575
Outcome of primary tubular tubulopathies diagnosed in pediatric age.
Blázquez Gómez CJ, Gil-Peña H, Ordóñez Álvarez FA, Santos Rodríguez F. Blázquez Gómez CJ, et al. Nefrologia (Engl Ed). 2021 Mar-Apr;41(2):182-190. doi: 10.1016/j.nefro.2020.07.015. Epub 2020 Dec 22. Nefrologia (Engl Ed). 2021. PMID: 33358363 Free article. English, Spanish.
High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults.
Hureaux M, Ashton E, Dahan K, Houillier P, Blanchard A, Cormier C, Koumakis E, Iancu D, Belge H, Hilbert P, Rotthier A, Del Favero J, Schaefer F, Kleta R, Bockenhauer D, Jeunemaitre X, Devuyst O, Walsh SB, Vargas-Poussou R. Hureaux M, et al. Kidney Int. 2019 Dec;96(6):1408-1416. doi: 10.1016/j.kint.2019.08.027. Epub 2019 Sep 16. Kidney Int. 2019. PMID: 31672324
Potassium-related inherited tubulopathies.
Landau D. Landau D. Cell Mol Life Sci. 2006 Sep;63(17):1962-8. doi: 10.1007/s00018-006-6011-0. Cell Mol Life Sci. 2006. PMID: 16810456 Review.
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