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Literature DB >> 18227801

Hereditary etiologies of hypomagnesemia.

Amir Said Alizadeh Naderi¹, Robert F Reilly.

Abstract

Magnesium ions are essential to all living cells. As the second most abundant intracellular cation, magnesium has a crucial role in fundamental metabolic processes such as DNA and protein synthesis, oxidative phosphorylation, enzyme function, ion channel regulation, and neuromuscular excitability. After presenting an overview of magnesium homeostasis, we review the etiologies of hypomagnesemia, with an emphasis on hereditary causes.

Entities: Chemical Disease

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Year: 2008 PMID： 18227801 DOI： 10.1038/ncpneph0680

Source DB: PubMed Journal: Nat Clin Pract Nephrol ISSN： 1745-8323

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Cited

9 in total

1. Double gene deletion reveals lack of cooperation between claudin 11 and claudin 14 tight junction proteins.

Authors: Liron Elkouby-Naor; Zaid Abassi; Ayala Lagziel; Alexander Gow; Tamar Ben-Yosef
Journal: Cell Tissue Res Date: 2008-07-29 Impact factor: 5.249

2. Alterations in early cytokine-mediated immune responses to Plasmodium falciparum infection in Tanzanian children with mineral element deficiencies: a cross-sectional survey.

Authors: Erasto V Mbugi; Marjolein Meijerink; Jacobien Veenemans; Prescilla V Jeurink; Matthew McCall; Raimos M Olomi; John F Shao; Hans Verhoef; Huub Fj Savelkoul
Journal: Malar J Date: 2010-05-17 Impact factor: 2.979

3. Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.

Authors: Tamra E Meyer; Germaine C Verwoert; Shih-Jen Hwang; Nicole L Glazer; Albert V Smith; Frank J A van Rooij; Georg B Ehret; Eric Boerwinkle; Janine F Felix; Tennille S Leak; Tamara B Harris; Qiong Yang; Abbas Dehghan; Thor Aspelund; Ronit Katz; Georg Homuth; Thomas Kocher; Rainer Rettig; Janina S Ried; Christian Gieger; Hanna Prucha; Arne Pfeufer; Thomas Meitinger; Josef Coresh; Albert Hofman; Mark J Sarnak; Yii-Der Ida Chen; André G Uitterlinden; Aravinda Chakravarti; Bruce M Psaty; Cornelia M van Duijn; W H Linda Kao; Jacqueline C M Witteman; Vilmundur Gudnason; David S Siscovick; Caroline S Fox; Anna Köttgen
Journal: PLoS Genet Date: 2010-08-05 Impact factor: 5.917

4. HNF1B mutations associate with hypomagnesemia and renal magnesium wasting.

Authors: Shazia Adalat; Adrian S Woolf; Karen A Johnstone; Andrea Wirsing; Lorna W Harries; David A Long; Raoul C Hennekam; Sarah E Ledermann; Lesley Rees; William van't Hoff; Stephen D Marks; Richard S Trompeter; Kjell Tullus; Paul J Winyard; Janette Cansick; Imran Mushtaq; Harjeeta K Dhillon; Coralie Bingham; Emma L Edghill; Rukshana Shroff; Horia Stanescu; Gerhart U Ryffel; Sian Ellard; Detlef Bockenhauer
Journal: J Am Soc Nephrol Date: 2009-04-23 Impact factor: 10.121

Hereditary etiologies of hypomagnesemia.

1. Double gene deletion reveals lack of cooperation between claudin 11 and claudin 14 tight junction proteins.

2. Alterations in early cytokine-mediated immune responses to Plasmodium falciparum infection in Tanzanian children with mineral element deficiencies: a cross-sectional survey.

3. Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.

4. HNF1B mutations associate with hypomagnesemia and renal magnesium wasting.

Review 5. The role of transient receptor potential channels in kidney disease.

6. Two novel mutations of the CLDN16 gene cause familial hypomagnesaemia with hypercalciuria and nephrocalcinosis.

Review 7. Magnesium Status and Stress: The Vicious Circle Concept Revisited.

Review 8. Magnesium and osteoporosis: current state of knowledge and future research directions.

9. Primary renal magnesium wasting: an unusual clinical picture of exercise-induced symptoms.