Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
My NCBI Filters
Results by year

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

Year Number of Results
1963 1
1975 2
1979 1
1985 1
1986 1
1987 3
1990 1
1992 1
1993 1
1994 1
1997 1
1998 2
1999 2
2000 3
2001 1
2002 3
2003 2
2005 2
2006 3
2007 1
2008 5
2009 5
2010 7
2011 10
2012 5
2013 10
2014 10
2015 16
2016 13
2017 14
2018 13
2019 10
2020 14
Text availability
Article attribute
Article type
Publication date

Similar Articles for PMID: 19389850

143 results
Results by year
Filters applied: . Clear all
Page 1
HNF1B mutations associate with hypomagnesemia and renal magnesium wasting.
Adalat S, Woolf AS, Johnstone KA, Wirsing A, Harries LW, Long DA, Hennekam RC, Ledermann SE, Rees L, van't Hoff W, Marks SD, Trompeter RS, Tullus K, Winyard PJ, Cansick J, Mushtaq I, Dhillon HK, Bingham C, Edghill EL, Shroff R, Stanescu H, Ryffel GU, Ellard S, Bockenhauer D. Adalat S, et al. J Am Soc Nephrol. 2009 May;20(5):1123-31. doi: 10.1681/ASN.2008060633. Epub 2009 Apr 23. J Am Soc Nephrol. 2009. PMID: 19389850 Free PMC article.
Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseases.
Heidet L, Decramer S, Pawtowski A, Morinière V, Bandin F, Knebelmann B, Lebre AS, Faguer S, Guigonis V, Antignac C, Salomon R. Heidet L, et al. Clin J Am Soc Nephrol. 2010 Jun;5(6):1079-90. doi: 10.2215/CJN.06810909. Epub 2010 Apr 8. Clin J Am Soc Nephrol. 2010. PMID: 20378641 Free PMC article.
Hypomagnesemia as First Clinical Manifestation of ADTKD-HNF1B: A Case Series and Literature Review.
van der Made CI, Hoorn EJ, de la Faille R, Karaaslan H, Knoers NV, Hoenderop JG, Vargas Poussou R, de Baaij JH. van der Made CI, et al. Am J Nephrol. 2015;42(1):85-90. doi: 10.1159/000439286. Am J Nephrol. 2015. PMID: 26340261 Free article. Review.
Mutations in PCBD1 cause hypomagnesemia and renal magnesium wasting.
Ferrè S, de Baaij JH, Ferreira P, Germann R, de Klerk JB, Lavrijsen M, van Zeeland F, Venselaar H, Kluijtmans LA, Hoenderop JG, Bindels RJ. Ferrè S, et al. J Am Soc Nephrol. 2014 Mar;25(3):574-86. doi: 10.1681/ASN.2013040337. Epub 2013 Nov 7. J Am Soc Nephrol. 2014. PMID: 24204001 Free PMC article.
[Clinical phenotypes of hepatocyte nuclear factor 1 homeobox b-associated disease].
Wang F, Yao Y, Yang HX, Shi CY, Zhang XX, Xiao HJ, Zhang HW, Su BG, Zhang YQ, Guo JF, Ding J. Wang F, et al. Zhonghua Er Ke Za Zhi. 2017 Sep 2;55(9):658-662. doi: 10.3760/cma.j.issn.0578-1310.2017.09.006. Zhonghua Er Ke Za Zhi. 2017. PMID: 28881510 Chinese.
[HNF1B-related disease: paradigm of a developmental gene and unexpected recognition of a new renal disease].
Chauveau D, Faguer S, Bandin F, Guigonis V, Chassaing N, Decramer S. Chauveau D, et al. Nephrol Ther. 2013 Nov;9(6):393-7. doi: 10.1016/j.nephro.2013.05.004. Epub 2013 Oct 9. Nephrol Ther. 2013. PMID: 24119877 French.
HNF1B Mutations Are Associated With a Gitelman-like Tubulopathy That Develops During Childhood.
Adalat S, Hayes WN, Bryant WA, Booth J, Woolf AS, Kleta R, Subtil S, Clissold R, Colclough K, Ellard S, Bockenhauer D. Adalat S, et al. Kidney Int Rep. 2019 May 29;4(9):1304-1311. doi: 10.1016/j.ekir.2019.05.019. eCollection 2019 Sep. Kidney Int Rep. 2019. PMID: 31517149 Free PMC article.
Chronic renal failure of unknown origin is caused by HNF1B mutations in 9% of adult patients: a single centre cohort analysis.
Musetti C, Quaglia M, Mellone S, Pagani A, Fusco I, Monzani A, Giordano M, Stratta P. Musetti C, et al. Nephrology (Carlton). 2014 Apr;19(4):202-9. doi: 10.1111/nep.12199. Nephrology (Carlton). 2014. PMID: 24387224
Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations.
Oram RA, Edghill EL, Blackman J, Taylor MJ, Kay T, Flanagan SE, Ismail-Pratt I, Creighton SM, Ellard S, Hattersley AT, Bingham C. Oram RA, et al. Am J Obstet Gynecol. 2010 Oct;203(4):364.e1-5. doi: 10.1016/j.ajog.2010.05.022. Epub 2010 Jul 15. Am J Obstet Gynecol. 2010. PMID: 20633866
Expression of renal cystic genes in patients with HNF1B mutations.
Faguer S, Decramer S, Devuyst O, Lengelé JP, Fournié GJ, Chauveau D. Faguer S, et al. Nephron Clin Pract. 2012;120(2):c71-8. doi: 10.1159/000334954. Epub 2012 Jan 21. Nephron Clin Pract. 2012. PMID: 22269832 Free article.
143 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page
Feedback