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Clinics and Research in Hepatology and Gastroenterology|August 28, 2025
Multiorgan fibrosis in Gaucher disease type I: an unmet goal of enzyme replacement therapyZufit Hexner-Erlichman, Nimer Assy, Nayaf Habashi, et al.
Internal Medicine Journal|May 21, 2025
Hyperuricaemia in type 1 Gaucher disease: is uric acid a biomarker for disease severity?Zufit Hexner-Erlichman, Salmas Watad, Jeff Szer, et al.
International Journal of Molecular Sciences|April 14, 2026
Glomerular Injury Findings in Patients with Thalassemia MinorZufit Hexner-Erlichman, Erez Shamir, Basem Hijazi, et al.
Scientific Reports|April 4, 2020
Campylobacter gastroenteritis in children in north-eastern Israel comparison with other common pathogensWaheeb Sakran, Zufit Hexner-Erlichman, Ronen Spiegel, et al.
Ejhaem|July 18, 2022
Primary autoimmune myelofibrosis: A case report in a childZufit Hexner-Erlichman, Joanne Yacobovich, Philippe Trougouboff, et al.
Frontiers in Pediatrics|December 12, 2022
Favorable outcome of empagliflozin treatment in two pediatric glycogen storage disease type 1b patientsZufit Hexner-Erlichman, Maria Veiga-da-Cunha, Yoav Zehavi, et al.
Frontiers in Pediatrics|June 3, 2022
A Novel Homozygous Missense Variant in the <i>LRRC32</i> Gene Is Associated With a New Syndrome of Cleft Palate, Progressive Vitreoretinopathy, Growth Retardation, and Developmental DelayZufit Hexner-Erlichman, Boris Fichtman, Yoav Zehavi, et al.
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