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Induction of retinopathy by fibrillar oxalate assemblies.
Zaguri D, Shaham-Niv S, Naaman E, Mimouni M, Magen D, Pollack S, Kreiser T, Leibu R, Rencus-Lazar S, Adler-Abramovich L, Perlman I, Gazit E, Zayit-Soudry S. Zaguri D, et al. Among authors: magen d. Commun Chem. 2020 Jan 3;3(1):2. doi: 10.1038/s42004-019-0247-8. Commun Chem. 2020. PMID: 36703385 Free PMC article.
A broad spectrum of developmental delay in a large cohort of prolidase deficiency patients demonstrates marked interfamilial and intrafamilial phenotypic variability.
Falik-Zaccai TC, Khayat M, Luder A, Frenkel P, Magen D, Brik R, Gershoni-Baruch R, Mandel H. Falik-Zaccai TC, et al. Among authors: magen d. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):46-56. doi: 10.1002/ajmg.b.30945. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19308961
A Novel Homozygous In-Frame Deletion in Complement Factor 3 Underlies Early-Onset Autosomal Recessive Atypical Hemolytic Uremic Syndrome - Case Report.
Pollack S, Eisenstein I, Mory A, Paperna T, Ofir A, Baris-Feldman H, Weiss K, Veszeli N, Csuka D, Shemer R, Glaser F, Prohászka Z, Magen D. Pollack S, et al. Among authors: magen d. Front Immunol. 2021 Jun 24;12:608604. doi: 10.3389/fimmu.2021.608604. eCollection 2021. Front Immunol. 2021. PMID: 34248927 Free PMC article.
Acute hemodialysis therapy in neonates with inborn errors of metabolism.
Eisenstein I, Pollack S, Hadash A, Eytan D, Attias O, Halberthal M, Ben-Ari J, Bar-Joseph G, Zelikovic I, Mandel H, Tal G, Magen D. Eisenstein I, et al. Among authors: magen d. Pediatr Nephrol. 2022 Nov;37(11):2725-2732. doi: 10.1007/s00467-022-05507-3. Epub 2022 Mar 3. Pediatr Nephrol. 2022. PMID: 35239033
52 results