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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Daniella Magen

Pediatric Nephrology Unit

Rambam Health Care Campus

Haifa

Israel

[email]@tx.technion.ac.il

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Affiliations

Pediatric Nephrology Unit, Rambam Health Care Campus, Haifa, Israel. 2005 - 2010
Pediatric Nephrology Unit, Meyer Children's Hospital, Rambam Medical Center and Faculty of Medicine, Technion-Israel Institute of Technology, Israel. 2004

References

A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome. Magen, D., Berger, L., Coady, M.J., Ilivitzki, A., Militianu, D., Tieder, M., Selig, S., Lapointe, J.Y., Zelikovic, I., Skorecki, K. N. Engl. J. Med. (2010) [Pubmed]
A novel missense mutation in SLC5A2 encoding SGLT2 underlies autosomal-recessive renal glucosuria and aminoaciduria. Magen, D., Sprecher, E., Zelikovic, I., Skorecki, K. Kidney Int. (2005) [Pubmed]
Autosomal recessive renal proximal tubulopathy and hypercalciuria: a new syndrome. Magen, D., Adler, L., Mandel, H., Efrati, E., Zelikovic, I. Am. J. Kidney Dis. (2004) [Pubmed]