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Year | Number of Results |
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2019 | 1 |
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Page 1
Genetic Spectrum of ABCA4-Associated Retinal Degeneration in Poland.
Genes (Basel). 2019 Nov 21;10(12):959. doi: 10.3390/genes10120959.
Genes (Basel). 2019.
PMID: 31766579
Free PMC article.
Non-syndromic inherited retinal diseases in Poland: Genes, mutations, and phenotypes.
Tracewska AM, Kocyła-Karczmarewicz B, Rafalska A, Murawska J, Jakubaszko-Jabłónska J, Rydzanicz M, Stawiński P, Ciara E, Lipska-Ziętkiewicz BS, Khan MI, Cremers FPM, Płoski R, Chrzanowska KH.
Tracewska AM, et al. Among authors: rafalska a.
Mol Vis. 2021 Jul 16;27:457-465. eCollection 2021.
Mol Vis. 2021.
PMID: 34321860
Free PMC article.
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A Mild Phenotype Caused by Two Novel Compound Heterozygous Mutations in CEP290.
Rafalska A, Tracewska AM, Turno-Kręcicka A, Szafraniec MJ, Misiuk-Hojło M.
Rafalska A, et al.
Genes (Basel). 2020 Oct 22;11(11):1240. doi: 10.3390/genes11111240.
Genes (Basel). 2020.
PMID: 33105651
Free PMC article.
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Stratifying risk for progression in IgA nephropathy: how to predict the future?
Rafalska A, Franczuk J, Franczuk P, Augustyniak-Bartosik H, Krajewska M.
Rafalska A, et al.
Pol Arch Med Wewn. 2014;124(7-8):365-72. doi: 10.20452/pamw.2341. Epub 2014 May 14.
Pol Arch Med Wewn. 2014.
PMID: 24824600
Free article.
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