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1.

Genetic causes of hypomagnesemia, a clinical overview
by Viering, D.H

Pediatric nephrology (Berlin, West), 2017, Vol.32 (7), p.1123-1135

5.

Genetic causes of hypercalciuric nephrolithiasis
by Stechman, Michael J

Pediatric nephrology (Berlin, West), 2008, Vol.24 (12), p.2321-2332

8.

Phenotype and Genotype Analysis in Chinese Patients with Gitelman’s Syndrome
by Lin, Shih-Hua

The journal of clinical endocrinology and metabolism, 2005, Vol.90 (5), p.2500-2507

9.

Inherited forms of renal hypomagnesemia: an update
by Knoers, N.V.A.M

Pediatric nephrology (Berlin, West), 2009, Vol.24 (4), p.697-705

11.

Tight junctions and human diseases
by Sawada, Norimasa

Medical electron microscopy, 2003, Vol.36 (3), p.147-156

14.

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

19.

Ocular involvement in a child with medullary nephrocalcinosis
by Kasap, Belde

Pediatric nephrology (Berlin, West), 2013, Vol.28 (4), p.627-630

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