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Page 1
Pathogenic variants in glutamyl-tRNAGln amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder.
Friederich MW, Timal S, Powell CA, Dallabona C, Kurolap A, Palacios-Zambrano S, Bratkovic D, Derks TGJ, Bick D, Bouman K, Chatfield KC, Damouny-Naoum N, Dishop MK, Falik-Zaccai TC, Fares F, Fedida A, Ferrero I, Gallagher RC, Garesse R, Gilberti M, González C, Gowan K, Habib C, Halligan RK, Kalfon L, Knight K, Lefeber D, Mamblona L, Mandel H, Mory A, Ottoson J, Paperna T, Pruijn GJM, Rebelo-Guiomar PF, Saada A, Sainz B Jr, Salvemini H, Schoots MH, Smeitink JA, Szukszto MJ, Ter Horst HJ, van den Brandt F, van Spronsen FJ, Veltman JA, Wartchow E, Wintjes LT, Zohar Y, Fernández-Moreno MA, Baris HN, Donnini C, Minczuk M, Rodenburg RJ, Van Hove JLK. Friederich MW, et al. Among authors: fedida a. Nat Commun. 2018 Oct 3;9(1):4065. doi: 10.1038/s41467-018-06250-w. Nat Commun. 2018. PMID: 30283131 Free PMC article.
COG6-CDG: Expanding the phenotype with emphasis on glycosylation defects involved in the causation of male disorders of sex development.
Mandel H, Cohen Kfir N, Fedida A, Shuster Biton E, Odeh M, Kalfon L, Ben-Harouch S, Fleischer Sheffer V, Hoffman Y, Goldberg Y, Dinwiddie A, Dumin E, Eran A, Apel-Sarid L, Tiosano D, Falik-Zaccai TC. Mandel H, et al. Among authors: fedida a. Clin Genet. 2020 Oct;98(4):402-407. doi: 10.1111/cge.13816. Epub 2020 Aug 4. Clin Genet. 2020. PMID: 32683677
A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness.
Issler N, Afonso S, Weissman I, Jordan K, Cebrian-Serrano A, Meindl K, Dahlke E, Tziridis K, Yan G, Robles-López JM, Tabernero L, Patel V, Kesselheim A, Klootwijk ED, Stanescu HC, Dumitriu S, Iancu D, Tekman M, Mozere M, Jaureguiberry G, Outtandy P, Russell C, Forst AL, Sterner C, Heinl ES, Othmen H, Tegtmeier I, Reichold M, Schiessl IM, Limm K, Oefner P, Witzgall R, Fu L, Theilig F, Schilling A, Shuster Biton E, Kalfon L, Fedida A, Arnon-Sheleg E, Ben Izhak O, Magen D, Anikster Y, Schulze H, Ziegler C, Lowe M, Davies B, Böckenhauer D, Kleta R, Falik Zaccai TC, Warth R. Issler N, et al. Among authors: fedida a. J Am Soc Nephrol. 2022 Apr;33(4):732-745. doi: 10.1681/ASN.2021101312. Epub 2022 Feb 11. J Am Soc Nephrol. 2022. PMID: 35149593 Free PMC article.
Long term ophthalmic complications of distal arthrogryposis type 5D.
Cohen D, Sloma R, Pizem H, Fedida A, Kalfon L, Ovadia R, Segal Z, Kassif Y, Falik Zaccai T. Cohen D, et al. Among authors: fedida a. Ophthalmic Genet. 2023 Feb;44(1):28-34. doi: 10.1080/13816810.2022.2141791. Epub 2022 Dec 2. Ophthalmic Genet. 2023. PMID: 36459431
Transcriptome dynamics of a broad host-range cyanophage and its hosts.
Doron S, Fedida A, Hernández-Prieto MA, Sabehi G, Karunker I, Stazic D, Feingersch R, Steglich C, Futschik M, Lindell D, Sorek R. Doron S, et al. Among authors: fedida a. ISME J. 2016 Jun;10(6):1437-55. doi: 10.1038/ismej.2015.210. Epub 2015 Dec 1. ISME J. 2016. PMID: 26623542 Free PMC article.
Salmonella Group B Ileitis Mimicking Crohn's Disease: A Case Report.
Tewoldemedhin B, Pati S, Atiyat R, Fedida A, Suleiman A, Abu Ruman Y, Muhanna A, Iheagwara C, Szabela M, Slim J, Boghossian J. Tewoldemedhin B, et al. Among authors: fedida a. Cureus. 2024 Jan 18;16(1):e52495. doi: 10.7759/cureus.52495. eCollection 2024 Jan. Cureus. 2024. PMID: 38371045 Free PMC article.
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