Literature DB >> 26323081

Hypomagnesemia and progressive chronic kidney disease: thinking of HNF1B and other genetic nephropathies.

Claudio Musetti1, Marco Quaglia1, Piero Stratta1, Mara Giordano2.   

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Year:  2015        PMID： 26323081     DOI： 10.1038/ki.2015.187

Source DB:  PubMed          Journal:  Kidney Int        ISSN： 0085-2538            Impact factor:   10.612


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  4 in total

1.  Chronic renal failure of unknown origin is caused by HNF1B mutations in 9% of adult patients: a single centre cohort analysis.

Authors:  Claudio Musetti; Marco Quaglia; Simona Mellone; Alessia Pagani; Ileana Fusco; Alice Monzani; Mara Giordano; Piero Stratta
Journal:  Nephrology (Carlton)       Date:  2014-04       Impact factor: 2.506

2.  Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseases.

Authors:  Laurence Heidet; Stéphane Decramer; Audrey Pawtowski; Vincent Morinière; Flavio Bandin; Bertrand Knebelmann; Anne-Sophie Lebre; Stanislas Faguer; Vincent Guigonis; Corinne Antignac; Rémi Salomon
Journal:  Clin J Am Soc Nephrol       Date:  2010-04-08       Impact factor: 8.237

3.  Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy.

Authors:  Marco Quaglia; Claudio Musetti; Gian Marco Ghiggeri; Giovanni Battista Fogazzi; Fabio Settanni; Renzo Luciano Boldorini; Elisa Lazzarich; Andrea Airoldi; Cristina Izzo; Mara Giordano; Piero Stratta
Journal:  Clin Transplant       Date:  2014-07-18       Impact factor: 2.863

4.  Results from the Atherosclerosis Risk in Communities study suggest that low serum magnesium is associated with incident kidney disease.

Authors:  Adrienne Tin; Morgan E Grams; Nisa M Maruthur; Brad C Astor; David Couper; Thomas H Mosley; Elizabeth Selvin; Josef Coresh; Wen Hong Linda Kao
Journal:  Kidney Int       Date:  2014-10-01       Impact factor: 10.612
  4 in total

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