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Searching for the Molecular Basis of Partial Deafness.
Int J Mol Sci. 2022 May 27;23(11):6029. doi: 10.3390/ijms23116029.
Int J Mol Sci. 2022.
PMID: 35682719
Free PMC article.
Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss.
Oziębło D, Lee SY, Leja ML, Sarosiak A, Bałdyga N, Skarżyński H, Kim Y, Han JH, Yoo HS, Park MH, Choi BY, Ołdak M.
Oziębło D, et al. Among authors: baldyga n.
Hum Genet. 2022 Apr;141(3-4):445-453. doi: 10.1007/s00439-022-02443-y. Epub 2022 Mar 7.
Hum Genet. 2022.
PMID: 35254497
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Hearing Loss as the Main Clinical Presentation in NLRP3-Associated Autoinflammatory Disease.
Oziębło D, Leja ML, Jeznach A, Orzechowska M, Skirecki T, Więsik-Szewczyk E, Furmanek M, Bałdyga N, Skarżyński H, Ołdak M.
Oziębło D, et al. Among authors: baldyga n.
Front Immunol. 2022 May 26;13:904632. doi: 10.3389/fimmu.2022.904632. eCollection 2022.
Front Immunol. 2022.
PMID: 35720340
Free PMC article.
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Complex Phenotypic Presentation of Syndromic Hearing Loss Deciphered as Three Separate Clinical Entities: How Genetic Testing Guides Final Diagnosis.
Bałdyga N, Sarosiak A, Oziębło D, Furmanek M, Szulborski K, Szaflik JP, Skarżyński H, Ołdak M.
Bałdyga N, et al.
Audiol Neurootol. 2021;26(4):226-235. doi: 10.1159/000510695. Epub 2020 Dec 22.
Audiol Neurootol. 2021.
PMID: 33352548
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The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation.
Bałdyga N, Oziębło D, Gan N, Furmanek M, Leja ML, Skarżyński H, Ołdak M.
Bałdyga N, et al.
Genes (Basel). 2023 Jan 28;14(2):335. doi: 10.3390/genes14020335.
Genes (Basel). 2023.
PMID: 36833263
Free PMC article.
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