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Page 1
Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.
Malone AF, Phelan PJ, Hall G, Cetincelik U, Homstad A, Alonso AS, Jiang R, Lindsey TB, Wu G, Sparks MA, Smith SR, Webb NJ, Kalra PA, Adeyemo AA, Shaw AS, Conlon PJ, Jennette JC, Howell DN, Winn MP, Gbadegesin RA. Malone AF, et al. Among authors: alonso as. Kidney Int. 2014 Dec;86(6):1253-9. doi: 10.1038/ki.2014.305. Epub 2014 Sep 17. Kidney Int. 2014. PMID: 25229338 Free PMC article.
Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS.
Gbadegesin RA, Hall G, Adeyemo A, Hanke N, Tossidou I, Burchette J, Wu G, Homstad A, Sparks MA, Gomez J, Jiang R, Alonso A, Lavin P, Conlon P, Korstanje R, Stander MC, Shamsan G, Barua M, Spurney R, Singhal PC, Kopp JB, Haller H, Howell D, Pollak MR, Shaw AS, Schiffer M, Winn MP. Gbadegesin RA, et al. Among authors: alonso a. J Am Soc Nephrol. 2014 Sep;25(9):1991-2002. doi: 10.1681/ASN.2013090976. Epub 2014 Mar 27. J Am Soc Nephrol. 2014. PMID: 24676636 Free PMC article.
Central retinal vein occlusion in young population: risk factors and outcomes.
Berguig J, Abdelmassih Y, Azar G, Lafolie J, Alonso AS, Bonnin S, Vasseur V, Mauget-Faysse M. Berguig J, et al. Among authors: alonso as. Front Med (Lausanne). 2023 Aug 4;10:1180234. doi: 10.3389/fmed.2023.1180234. eCollection 2023. Front Med (Lausanne). 2023. PMID: 37601780 Free PMC article.
Atypical Foveal Hypoplasia in Best Disease.
Moret E, Lejoyeux R, Bonnin S, Azar G, Guillaume J, Le Cossec C, Lafolie J, Alonso AS, Favard C, Meunier I, Vasseur V, Mauget-Faÿsse M. Moret E, et al. Among authors: alonso as. J Pers Med. 2023 Feb 15;13(2):337. doi: 10.3390/jpm13020337. J Pers Med. 2023. PMID: 36836571 Free PMC article.
"En Face" Spectral-Domain Optical Coherence Tomography versus Multifocal Electroretinogram in Hydroxychloroquine Retinopathy Screening.
Mauget-Faÿsse M, Sukkarieh G, Jebrane H, Lafolie J, Alonso AS, Laumonier E, Derrien S, Le Guern V, Behar Cohen F, Thevenin S, Auge E, Guillaume J, Vasseur V, Costedoat-Chalumean N. Mauget-Faÿsse M, et al. Among authors: alonso as. Ophthalmologica. 2023;246(1):14-23. doi: 10.1159/000528146. Epub 2022 Dec 2. Ophthalmologica. 2023. PMID: 36463860
[Moyamoya disease in children].
Frič R, Sorteberg A, Wallace S, Alonso AS, Due-Tønnessen BJ, Wiedmann M. Frič R, et al. Among authors: alonso as. Tidsskr Nor Laegeforen. 2022 Sep 26;142(13). doi: 10.4045/tidsskr.21.0776. Print 2022 Sep 27. Tidsskr Nor Laegeforen. 2022. PMID: 36164799 Free article. Norwegian.
Foveal hypoplasia in parents of patients with albinism.
Lejoyeux R, Alonso AS, Lafolie J, Michaud V, Lasseaux E, Vasseur V, Derrien S, Robert MP, Le Mer Y, Tadayoni R, Arveiler B, Mauget-Faÿsse M. Lejoyeux R, et al. Among authors: alonso as. Ophthalmic Genet. 2022 Dec;43(6):817-823. doi: 10.1080/13816810.2022.2121841. Epub 2022 Sep 13. Ophthalmic Genet. 2022. PMID: 36098180
18 results