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European Journal of Pediatrics|April 23, 2022
Is the fear from insulin tolerance test in the evaluation of short stature justified?Aaron Hanukoglu, Regina Weisglass
Molecular Reproduction and Development|January 18, 2020
High-resolution imaging of the actin cytoskeleton and epithelial sodium channel, CFTR, and aquaporin-9 localization in the vas deferensSachin Sharma, Girishkumar K Kumaran, Israel Hanukoglu
Molecular and Cellular Endocrinology|March 18, 2004
ACTH induces TIMP-1 expression and inhibits collagenase in adrenal cortex cellsMoshe Reichenstein, Reuven Reich, Jean-Guy LeHoux, 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.
Clinical Medicine Insights. Endocrinology and Diabetes|June 10, 2024
Autosomal Dominant, Long-Standing Dysglycemia in 2 Families with Unique Phenotypic FeaturesAaron Hanukoglu, Ehud Banne, Dorit Lev, et al.
Hormone Research in Paediatrics|August 28, 2025
Prenatal diagnosis of autosomal dominant pseudohypoaldosteronism due to NR3C2 gene mutation. Immediate post-natal oral saline therapy prevents the clinical manifestations resulting from impaired salt balanceAaron Hanukoglu, Shirli Abiri, Dana Herzberg, et al.
The Journal of Pediatrics|April 25, 2007
Sulfonylurea-responsive diabetes in childhoodZohar Landau, Julio Wainstein, Aaron Hanukoglu, et al.
The Journal of Pediatrics|November 19, 2008
Hypothyroidism and dyshormonogenesis induced by D-penicillamine in children with Wilson's disease and healthy infants born to a mother with Wilson's diseaseAaron Hanukoglu, Batya Curiel, Drora Berkowitz, et al.
Harefuah|November 25, 2011
[Laparoscopic sleeve gastrectomy (LSG) in adolescents with morbid obesity]Zohar Landau, Gideon Karplus, Aaron Hanukoglu, et al.
The Journal of Steroid Biochemistry and Molecular Biology|October 5, 2020
Renin-aldosterone system evaluation over four decades in an extended family with autosomal dominant pseudohypoaldosteronism due to a deletion in the NR3C2 geneAaron Hanukoglu, Rosa Vargas-Poussou, Zohar Landau, et al.
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