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Molecular Immunology|June 18, 2017
Demyelination, strokes, and eculizumab: Lessons from the congenital CD59 gene mutationsAdi Tabib, Netanel Karbian, Dror Mevorach
Thrombosis Research|June 22, 2018
Prothrombotic mechanisms in patients with congenital p.Cys89Tyr mutation in CD59Adi Tabib, Issam Hindi, Netanel Karbian, et al.
Free Radical Biology & Medicine|February 10, 2017
Mechanisms of defense against products of cysteine catabolism in the nematode Caenorhabditis elegansLeonid Livshits, Arijit Kumar Chatterjee, Netanel Karbian, et al.
Cell Death & Disease|July 17, 2020
Apoptotic cell therapy for cytokine storm associated with acute severe sepsisNetanel Karbian, Avraham Abutbul, Raja El-Amore, et al.
Rheumatology (Oxford, England)|January 25, 2021
A novel loss-of-function mutation in LACC1 underlies hereditary juvenile arthritis with extended intra-familial phenotypic heterogeneityYonatan Butbul Aviel, Ayala Ofir, Ofer Ben-Izhak, et al.
Neurology. Genetics|December 12, 2018
Molecular pathogenesis of human CD59 deficiencyNetanel Karbian, Yael Eshed-Eisenbach, Adi Tabib, et al.
Journal of Neuroinflammation|October 24, 2023
Complement-membrane regulatory proteins are absent from the nodes of Ranvier in the peripheral nervous systemNetanel Karbian, Yael Eshed-Eisenbach, Marian Zeibak, et al.
Npj Metabolic Health and Disease|June 17, 2026
CD59 drives diet-induced obesity and glucose intolerance, insulin resistance, and metabolic dysfunction-associated steatotic liver diseaseMarian Zeibak, Netanel Karbian, Yael Riahi, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 13, 2018
Eculizumab Is Safe and Effective as a Long-term Treatment for Protein-losing Enteropathy Due to CD55 DeficiencyAlina Kurolap, Orly Eshach Adiv, Tova Hershkovitz, et al.
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