Literature DB >> 30504582

Case of hypomagnesemia with secondary hypocalcemia with a novel TRPM6 mutation.

Naresh Lal1, Swati Bhardwaj2, Saptharishi Lalgudi Ganesan3, Rachna Sharma1, Puneet Jain4.   

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Year:  2018        PMID： 30504582     DOI： 10.4103/0028-3886.246240

Source DB:  PubMed          Journal:  Neurol India        ISSN： 0028-3886            Impact factor:   2.117


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  4 in total

Review 1.  Role of TRPM7 in cardiac fibrosis: A potential therapeutic target (Review).

Authors:  Feng Hu; Meiyong Li; Fengyu Han; Qing Zhang; Yuhao Zeng; Weifang Zhang; Xiaoshu Cheng
Journal:  Exp Ther Med       Date:  2020-12-27       Impact factor: 2.447

2.  Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation

Authors:  Hüsniye Yücel; Çiğdem Genç Sel; Çiğdem Seher Kasapkara; Gülin Karacan Küçükali; Senay Savas Erdeve; Ülkühan Öztoprak; Serdar Ceylaner; Saliha Şenel; Meltem Akçaboy
Journal:  J Clin Res Pediatr Endocrinol       Date:  2020-04-17

3.  Case Report: Novel TRPM6 Mutations Cause Hereditary Hypomagnesemia With Secondary Hypocalcemia in a Chinese Family and a Literature Review.

Authors:  Yiran Han; Yajuan Zhao; Hua Wang; Liang Huo
Journal:  Front Pediatr       Date:  2022-07-12       Impact factor: 3.569

4.  Imaging findings in TRPM6-Related hypomagnesemia with secondary hypocalcemia.

Authors:  Prateek Malik; Sayli Umakant Bidkar; Sangeetha Yoganathan; Sarah Mathai; Sumita Danda; Beena Koshy
Journal:  Ann Indian Acad Neurol       Date:  2021-04-28       Impact factor: 1.383
  4 in total

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