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Pathophysiology of the renal acidification defect present in the syndrome of familial hypomagnesaemia-hypercalciuria
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Pediatric nephrology (Berlin, West), 1994, Vol.8 (4), p.431-435
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Magnesium deficiency in two hypertensive patient groups
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Southern medical journal (Birmingham, Ala.), 1990, Vol.83 (7), p.739-742
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Effects of vitamin D on magnesium metabolism in rats
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Magnesium metabolism in health and disease
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International urology and nephrology, 2009, Vol.41 (2), p.357-362
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Mechanisms and regulation of renal magnesium transport
by Houillier, Pascal
Annual review of physiology, 2014, Vol.76 (1), p.411-430
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Magnesium wasting associated with epidermal-growth-factor receptor-targeting antibodies in colorectal cancer: a prospective study
by Tejpar, Sabine, Prof
The lancet oncology, 2007, Vol.8 (5), p.387-394
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Utilization of magnesium during hypokinesia and magnesium supplementation in healthy subjects
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Genetic causes of hypercalciuric nephrolithiasis
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Pediatric nephrology (Berlin, West), 2008, Vol.24 (12), p.2321-2332
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Phenotype and Genotype Analysis in Chinese Patients with Gitelman’s Syndrome
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The journal of clinical endocrinology and metabolism, 2005, Vol.90 (5), p.2500-2507
12.
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations
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Pediatric nephrology (Berlin, West), 2005, Vol.20 (10), p.1490-1493
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Unusual Clinical Presentation and Possible Rescue of a Novel Claudin-16 Mutation
by Müller, Dominik
The journal of clinical endocrinology and metabolism, 2006, Vol.91 (8), p.3076-3079
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Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman syndrome
by MASTROIANNI, N
American journal of human genetics, 1996, Vol.59 (5), p.1019-1026
15.
Hereditary Isolated Renal Magnesium Loss Maps to Chromosome 11q23
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American journal of human genetics, 1999, Vol.64 (1), p.180-188
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The effect of losartan and losartan/hydrochlorothiazide fixed-combination on magnesium, zinc, and nitric oxide metabolism in hypertensive patients: A prospective open-label study
by Koren-Michowitz, Maya
American journal of hypertension, 2005, Vol.18 (3), p.358-363
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Hypomagnesemia with hypercalciuria and nephrocalcinosis: case report and a family study
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Transient Receptor Potential Melastatin 6 Knockout Mice Are Lethal whereas Heterozygous Deletion Results in Mild Hypomagnesemia
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Mutations in the chloride channel gene, CLCNKB, leading to a mixed bartter-gitelman phenotype
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20.
Clinical Symptoms of Mitral Valve Prolapse Are Related to Hypomagnesemia and Attenuated by Magnesium Supplementation
by Lichodziejewska, Barbara
The American journal of cardiology, 1997, Vol.79 (6), p.768-772
