Home About us Current issue Ahead of Print Back issues Submission Instructions Advertise Contact Login   

Search Article 
Advanced search 
Saudi Journal of Kidney Diseases and Transplantation
Users online: 506 Home Bookmark this page Print this page Email this page Small font sizeDefault font size Increase font size 

    Article Cited by others


Resolving basal ganglia calcification in hereditary hypomagnesemia with secondary hypocalcemia due to a novel TRMP6 gene mutation

Habeb Abdelhadi M, Al-Harbi Hanan, Schlingmann Karl P

Year : 2012| Volume: 23| Issue : 5 | Page no: 1038-1042

   This article has been cited by
1 Hypomagnesemia with Secondary Hypoparathyroidism and Hypocalcemia due to Novel Variants in the Transient Receptor Potential Cation Channel Subfamily M Member 6 (TRPM6) Gene
Geetanjali Jain, Gourab Das, Rakhi Malhotra, Sateesh Ramchandran, Nagaraja M. Phani, Giridharan Appaswamy, Upasana Sridharan, Aradhana Dwivedi
Journal of Pediatric Genetics. 2021;
[Pubmed]  [Google Scholar] [DOI]
2 Mg2+ homeostasis
Jenny van der Wijst,René J.M. Bindels,Joost G.J. Hoenderop
Current Opinion in Nephrology and Hypertension. 2014; 23(4): 361
[Pubmed]  [Google Scholar] [DOI]
3 New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia
Sergio Lainez,Karl Peter Schlingmann,Jenny van der Wijst,Bernd Dworniczak,Femke van Zeeland,Martin Konrad,René J Bindels,Joost G Hoenderop
European Journal of Human Genetics. 2013;
[Pubmed]  [Google Scholar] [DOI]


Read this article