Similar articles for PMID: 17671655

Year	Number of Results
1976	1
1985	1
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1997	1
1999	1
2001	1
2002	2
2003	1
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2005	3
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2007	5
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2010	6
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2012	6
2013	6
2014	5
2015	6
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2017	2
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2020	3
2021	5
2022	1
2024	0

1

Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia.

Groenestege WM, Thébault S, van der Wijst J, van den Berg D, Janssen R, Tejpar S, van den Heuvel LP, van Cutsem E, Hoenderop JG, Knoers NV, Bindels RJ. Groenestege WM, et al. J Clin Invest. 2007 Aug;117(8):2260-7. doi: 10.1172/JCI31680. J Clin Invest. 2007. PMID: 17671655 Free PMC article. Clinical Trial.

2

When EGF is offside, magnesium is wasted.

Muallem S, Moe OW. Muallem S, et al. J Clin Invest. 2007 Aug;117(8):2086-9. doi: 10.1172/JCI33004. J Clin Invest. 2007. PMID: 17671646 Free PMC article.

3

Disorders of renal magnesium handling explain renal magnesium transport.

Wagner CA. Wagner CA. J Nephrol. 2007 Sep-Oct;20(5):507-10. J Nephrol. 2007. PMID: 17918133 Free article. Review.

4

Insight into the molecular regulation of the epithelial magnesium channel TRPM6.

Cao G, Hoenderop JG, Bindels RJ. Cao G, et al. Curr Opin Nephrol Hypertens. 2008 Jul;17(4):373-8. doi: 10.1097/MNH.0b013e328303e184. Curr Opin Nephrol Hypertens. 2008. PMID: 18660673 Review.

5

Magnesium Absorption in Intestinal Cells: Evidence of Cross-Talk between EGF and TRPM6 and Novel Implications for Cetuximab Therapy.

Pietropaolo G, Pugliese D, Armuzzi A, Guidi L, Gasbarrini A, Rapaccini GL, Wolf FI, Trapani V. Pietropaolo G, et al. Nutrients. 2020 Oct 26;12(11):3277. doi: 10.3390/nu12113277. Nutrients. 2020. PMID: 33114586 Free PMC article.

6

Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia.

Schlingmann KP, Sassen MC, Weber S, Pechmann U, Kusch K, Pelken L, Lotan D, Syrrou M, Prebble JJ, Cole DE, Metzger DL, Rahman S, Tajima T, Shu SG, Waldegger S, Seyberth HW, Konrad M. Schlingmann KP, et al. J Am Soc Nephrol. 2005 Oct;16(10):3061-9. doi: 10.1681/ASN.2004110989. Epub 2005 Aug 17. J Am Soc Nephrol. 2005. PMID: 16107578

7

Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes.

Guran T, Akcay T, Bereket A, Atay Z, Turan S, Haisch L, Konrad M, Schlingmann KP. Guran T, et al. Nephrol Dial Transplant. 2012 Feb;27(2):667-73. doi: 10.1093/ndt/gfr300. Epub 2011 Jun 9. Nephrol Dial Transplant. 2012. PMID: 21669885

8

Primary familial hypomagnesemia syndrome: a new approach in treatment.

Nesibe A, Sinasi O. Nesibe A, et al. J Pediatr Endocrinol Metab. 2012;25(5-6):599-602. J Pediatr Endocrinol Metab. 2012. PMID: 22876566

9

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.

Schlingmann KP, Weber S, Peters M, Niemann Nejsum L, Vitzthum H, Klingel K, Kratz M, Haddad E, Ristoff E, Dinour D, Syrrou M, Nielsen S, Sassen M, Waldegger S, Seyberth HW, Konrad M. Schlingmann KP, et al. Nat Genet. 2002 Jun;31(2):166-70. doi: 10.1038/ng889. Epub 2002 May 28. Nat Genet. 2002. PMID: 12032568

10

[Analysis of Factors Influencing the Development of Hypomagnesemia in Patients Receiving Cetuximab Therapy for Head and Neck Cancer].

Inose R, Takahashi K, Nishikawa T, Nagayama K. Inose R, et al. Yakugaku Zasshi. 2015;135(12):1403-7. doi: 10.1248/yakushi.15-00210. Yakugaku Zasshi. 2015. PMID: 26632157 Free article. Japanese.

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