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Page 1
Kidney and urinary tract findings among patients with Kabuki (make-up) syndrome.
Merdler-Rabinowicz R, Pode-Shakked B, Vivante A, Lahav E, Kagan M, Chorin O, Somech R, Raas-Rothschild A. Merdler-Rabinowicz R, et al. Among authors: lahav e. Pediatr Nephrol. 2021 Dec;36(12):4009-4012. doi: 10.1007/s00467-021-05216-3. Epub 2021 Sep 27. Pediatr Nephrol. 2021. PMID: 34570271
Crossed ectopic kidney: prenatal diagnosis and postnatal follow-up.
Zajicek M, Perlman S, Dekel B, Lahav E, Lotan D, Lotan D, Achiron R, Gilboa Y. Zajicek M, et al. Among authors: lahav e. Prenat Diagn. 2017 Jul;37(7):712-715. doi: 10.1002/pd.5070. Epub 2017 Jun 13. Prenat Diagn. 2017. PMID: 28505705
Whole exome sequencing in childhood-onset lupus frequently detects single gene etiologies.
Tirosh I, Spielman S, Barel O, Ram R, Stauber T, Paret G, Rubinsthein M, Pessach IM, Gerstein M, Anikster Y, Shukrun R, Dagan A, Adler K, Pode-Shakked B, Volkov A, Perelman M, Greenberger S, Somech R, Lahav E, Majmundar AJ, Padeh S, Hildebrandt F, Vivante A. Tirosh I, et al. Among authors: lahav e. Pediatr Rheumatol Online J. 2019 Jul 30;17(1):52. doi: 10.1186/s12969-019-0349-y. Pediatr Rheumatol Online J. 2019. PMID: 31362757 Free PMC article.
A multidisciplinary nephrogenetic referral clinic for children and adults-diagnostic achievements and insights.
Pode-Shakked B, Ben-Moshe Y, Barel O, Regev LC, Kagan M, Eliyahu A, Marek-Yagel D, Atias-Varon D, Lahav E, Issler N, Shlomovitz O, Semo Oz R, Kol N, Mor N, Bar-Joseph I, Khavkin Y, Javasky E, Beckerman P, Greenberg M, Volovelsky O, Borovitz Y, Davidovits M, Haskin O, Alfandary H, Levi S, Kaidar M, Katzir Z, Angel-Korman A, Becker-Cohen R, Ben-Shalom E, Leiba A, Mor E, Dagan A, Pessach IM, Lotan D, Shashar M, Anikster Y, Raas-Rothschild A, Rechavi G, Dekel B, Vivante A. Pode-Shakked B, et al. Among authors: lahav e. Pediatr Nephrol. 2022 Jul;37(7):1623-1646. doi: 10.1007/s00467-021-05374-4. Epub 2022 Jan 7. Pediatr Nephrol. 2022. PMID: 34993602
Long-term hematopoietic dysfunction in patients with large-scale mitochondrial DNA deletion syndromes.
Greenberg-Kushnir N, Grossmann LD, Barg AA, Schiby G, Mardoukh C, Varda-Bloom N, Marcu-Malina V, Anikster Y, Gruber N, Lahav E, Bolkier Y, Bar D, Bielorai B, Toren A, Jacoby E. Greenberg-Kushnir N, et al. Among authors: lahav e. Pediatr Blood Cancer. 2025 Jan;72(1):e31383. doi: 10.1002/pbc.31383. Epub 2024 Oct 13. Pediatr Blood Cancer. 2025. PMID: 39397288
Mitochondrial augmentation of hematopoietic stem cells in children with single large-scale mitochondrial DNA deletion syndromes.
Jacoby E, Bar-Yosef O, Gruber N, Lahav E, Varda-Bloom N, Bolkier Y, Bar D, Blumkin MB, Barak S, Eisenstein E, Ahonniska-Assa J, Silberg T, Krasovsky T, Bar O, Erez N, Bielorai B, Golan H, Dekel B, Besser MJ, Pozner G, Khoury H, Jacobs A, Campbell J, Herskovitz E, Sher N, Yivgi-Ohana N, Anikster Y, Toren A. Jacoby E, et al. Among authors: lahav e. Sci Transl Med. 2022 Dec 21;14(676):eabo3724. doi: 10.1126/scitranslmed.abo3724. Epub 2022 Dec 21. Sci Transl Med. 2022. PMID: 36542693
19 results