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2002 1
2005 1
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2010 1
2011 3
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2020 1
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Page 1
[Genetic revision of the Hungarian Cystic Fibrosis Registry].
Deák A, Koczok K, Bessenyei B, Szűcs Z, Madar L, Csorba G, Orosz O, Laki I, Halász A, Marsal G, Balogh I. Deák A, et al. Among authors: bessenyei b. Orv Hetil. 2022 Dec 18;163(51):2052-2059. doi: 10.1556/650.2022.32655. Print 2022 Dec 18. Orv Hetil. 2022. PMID: 36528828 Review. Hungarian.
Missense MED12 variants in 22 males with intellectual disability: From nonspecific symptoms to complete syndromes.
Maia N, Ibarluzea N, Misra-Isrie M, Koboldt DC, Marques I, Soares G, Santos R, Marcelis CLM, Keski-Filppula R, Guitart M, Gabau Vila E, Lehman A, Hickey S, Mori M, Terhal P, Valenzuela I, Lasa-Aranzasti A, Cueto-González AM, Chhouk BH, Yeh RC, Neil JE, Abu-Libde B, Kleefstra T, Elting MW, Császár A, Kárteszi J, Bessenyei B, van Bokhoven H, Jorge P, van Hagen JM, de Brouwer APM. Maia N, et al. Among authors: bessenyei b. Am J Med Genet A. 2023 Jan;191(1):135-143. doi: 10.1002/ajmg.a.63004. Epub 2022 Oct 22. Am J Med Genet A. 2023. PMID: 36271811 Free PMC article.
MED13L-related intellectual disability due to paternal germinal mosaicism.
Bessenyei B, Balogh I, Mokánszki A, Ujfalusi A, Pfundt R, Szakszon K. Bessenyei B, et al. Cold Spring Harb Mol Case Stud. 2022 Jan 10;8(1):a006124. doi: 10.1101/mcs.a006124. Print 2022 Jan. Cold Spring Harb Mol Case Stud. 2022. PMID: 34654706 Free PMC article.
On the role of aging in the etiology of autoimmunity.
Urbán L, Bessenyei B, Márka M, Semsei I. Urbán L, et al. Among authors: bessenyei b. Gerontology. 2002 May-Jun;48(3):179-84. doi: 10.1159/000052839. Gerontology. 2002. PMID: 11961373 Review.
Clinical and genetic characteristics of craniosynostosis in Hungary.
Bessenyei B, Nagy A, Szakszon K, Mokánszki A, Balogh E, Ujfalusi A, Tihanyi M, Novák L, Bognár L, Oláh É. Bessenyei B, et al. Am J Med Genet A. 2015 Dec;167A(12):2985-91. doi: 10.1002/ajmg.a.37298. Epub 2015 Aug 20. Am J Med Genet A. 2015. PMID: 26289989
21 results