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Collagen formation, function and role in kidney disease.
De Gregorio V, Barua M, Lennon R. De Gregorio V, et al. Among authors: barua m. Nat Rev Nephrol. 2024 Nov 15. doi: 10.1038/s41581-024-00902-5. Online ahead of print. Nat Rev Nephrol. 2024. PMID: 39548215 Review.
LAMA2 and LOXL4 are candidate FSGS genes.
Vijayan P, Hack S, Yao T, Qureshi MA, Paterson AD, John R, Davenport B, Lennon R, Pei Y, Barua M. Vijayan P, et al. Among authors: barua m. BMC Nephrol. 2021 Sep 26;22(1):320. doi: 10.1186/s12882-021-02524-6. BMC Nephrol. 2021. PMID: 34565340 Free PMC article.
Clinical trial recommendations for potential Alport syndrome therapies.
Weinstock BA, Feldman DL, Fornoni A, Gross O, Kashtan CE, Lagas S, Lennon R, Miner JH, Rheault MN, Simon JF; Workshop Participants. Weinstock BA, et al. Kidney Int. 2020 Jun;97(6):1109-1116. doi: 10.1016/j.kint.2020.02.029. Epub 2020 Apr 6. Kidney Int. 2020. PMID: 32386680 Free PMC article.
The 2019 and 2021 International Workshops on Alport Syndrome.
Daga S, Ding J, Deltas C, Savige J, Lipska-Ziętkiewicz BS, Hoefele J, Flinter F, Gale DP, Aksenova M, Kai H, Perin L, Barua M, Torra R, Miner JH, Massella L, Ljubanović DG, Lennon R, Weinstock AB, Knebelmann B, Cerkauskaite A, Gear S, Gross O, Turner AN, Baldassarri M, Pinto AM, Renieri A. Daga S, et al. Among authors: barua m. Eur J Hum Genet. 2022 May;30(5):507-516. doi: 10.1038/s41431-022-01075-0. Epub 2022 Mar 9. Eur J Hum Genet. 2022. PMID: 35260866 Free PMC article.
Integration of Genetic Testing and Pathology for the Diagnosis of Adults with FSGS.
Yao T, Udwan K, John R, Rana A, Haghighi A, Xu L, Hack S, Reich HN, Hladunewich MA, Cattran DC, Paterson AD, Pei Y, Barua M. Yao T, et al. Among authors: barua m. Clin J Am Soc Nephrol. 2019 Feb 7;14(2):213-223. doi: 10.2215/CJN.08750718. Epub 2019 Jan 15. Clin J Am Soc Nephrol. 2019. PMID: 30647093 Free PMC article.
136 results