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American Journal of Human Genetics|November 2, 2010
Hyperchlorhidrosis caused by homozygous mutation in CA12, encoding carbonic anhydrase XIIMaya Feldshtein, Suliman Elkrinawi, Baruch Yerushalmi, et al.
Harefuah|November 21, 2024
[A NEW TRANSITION PROGRAM FOR KIDNEY TRANSPLANTED YOUNG ADULTS FROM PEDIATRIC TO ADULT CARE SERVICES]Yael Borovitz, Neomi Zanhendler, Noga Katz, et al.
The Journal of Clinical Investigation|October 23, 2019
Hyperuricemia and gout caused by missense mutation in d-lactate dehydrogenaseMax Drabkin, Yuval Yogev, Lior Zeller, et al.
Clinical Journal of the American Society of Nephrology : CJASN|February 1, 2023
Dialysis in Israeli Children between 1990 and 2020: Trends and International ComparisonsLilach C Regev-Epstein, Yaacov Frishberg, Miriam Davidovits, et al.
Nature Genetics|May 29, 2002
Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemiaRoxanne Y Walder, Daniel Landau, Peter Meyer, et al.
Pediatric Nephrology (Berlin, Germany)|September 19, 2008
Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndromeGema Ariceta, Nesrin Besbas, Sally Johnson, et al.
Frontiers in Pediatrics|November 5, 2024
Childhood onset C3 glomerulopathy: recurrence after kidney transplantation-a case seriesYael Borovitz, Daniel Landau, Amit Dagan, et al.
Seminars in Thrombosis and Hemostasis|April 1, 2006
Epidemiology, clinical presentation, and pathophysiology of atypical and recurrent hemolytic uremic syndromeL Bernd Zimmerhackl, Nesir Besbas, Therese Jungraithmayr, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 4, 2011
Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2Dganit Dinour, Nicola K Gray, Liat Ganon, et al.
Frontiers in Pediatrics|December 17, 2024
Nephrocalcinosis tendency does not worsen under burosumab treatment for X-linked hypophosphatemic rickets: a multicenter pediatric studyShelly Levi, Daniel Landau, Miriam Davidovits, et al.
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