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Clinical Endocrinology|May 29, 2009
Neonatal hyperthyrotropinemia: population characteristics, diagnosis, management and outcome after cessation of therapyAmnon Zung, Yardena Tenenbaum-Rakover, Shiri Barkan, et al.
The Israel Medical Association Journal : IMAJ|December 18, 2013
Association of the M3151 variant in the transient receptor potential vanilloid receptor-1 (TRPV1) gene with type 1 diabetes in an Ashkenazi Jewish populationMenachem Sadeh, Benjamin Glazer, Zohar Landau, et al.
Nephron|May 17, 2017
Familial Hyperkalemia and Hypertension (FHHt) and KLHL3: Description of a Family with a New Recessive Mutation (S553L) Compared to a Family with a Dominant Mutation, Q309R, with Analysis of Urinary Sodium Chloride CotransporterOrit Kliuk-Ben Bassat, Vered Carmon, Aaron Hanukoglu, et al.
Hormone Research|May 31, 2006
Congenital hyperreninemic hypoaldosteronism in Israel: sequence analysis of CYP11B2 geneEsther Leshinsky-Silver, Zohar Landau, Sema Unlubay, et al.
Nephron|May 1, 2015
Hypercalciuria in familial hyperkalemia and hypertension with KLHL3 mutationsHaim Mayan, Vered Carmon, Kira Oleinikov, et al.
Clinical Endocrinology|June 11, 2009
Clinical and genetic heterogeneity of congenital adrenal hypoplasia due to NR0B1 gene mutationsZohar Landau, Aaron Hanukoglu, Joseph Sack, et al.
Diabetes Care|March 29, 2003
Extrapancreatic autoimmune manifestations in type 1 diabetes patients and their first-degree relatives: a multicenter studyAaron Hanukoglu, Avraam Mizrachi, Ilan Dalal, et al.
Pediatric Diabetes|December 14, 2011
Increase in the incidence of type 1 diabetes in Israeli children following the Second Lebanon WarAmnon Zung, Orit Blumenfeld, Naim Shehadeh, et al.
Human Genetics|December 25, 2010
Autosomal recessive hyponatremia due to isolated salt wasting in sweat associated with a mutation in the active site of Carbonic Anhydrase 12Emad Muhammad, Neta Leventhal, Galit Parvari, et al.
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