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[Cartilage-hair hypoplasia].
Erdos M, Tóth B, Almássy Z, Tímár L, Maródi L. Erdos M, et al. Among authors: toth b. Orv Hetil. 2008 Feb 3;149(5):209-17. doi: 10.1556/OH.2008.28256. Orv Hetil. 2008. PMID: 18218588 Review. Hungarian.
[Molecular pathology and clinical manifestations of Fabry disease].
Rákóczi E, Görögh S, Grubits J, Erdos M, Garzuly F, Hahn K, Bencsik K, Vécsei L, Trinn C, Kristóf E, Mogyorósy G, Tóth B, Maródi L. Rákóczi E, et al. Among authors: toth b. Orv Hetil. 2007 Jun 10;148(23):1087-94. doi: 10.1556/OH.2007.28086. Orv Hetil. 2007. PMID: 17545117 Hungarian.
[Nijmegen Breakage syndrome].
Erdos M, Tóth B, Juhász P, Mahdi M, Maródi L. Erdos M, et al. Among authors: toth b. Orv Hetil. 2010 Apr 18;151(16):665-73. doi: 10.1556/OH.2010.28851. Orv Hetil. 2010. PMID: 20353920 Review. Hungarian.
[Management of Fabry disease].
Constantin T, Székely A, Ponyi A, Gulácsy V, Ambrus C, Kádár K, Vastagh I, Dajnoki A, Tóth B, Bokrétás G, Müller V, Katona M, Medvecz M, Fiedler O, Széchey R, Varga E, Rudas G, Kertész A, Molnár S, Kárpáti S, Nagy V, Magyar P, Mahdi M, Rákóczi E, Németh K, Bereczki D, Garami M, Erdos M, Maródi L, Fekete G. Constantin T, et al. Among authors: toth b. Orv Hetil. 2010 Aug 1;151(31):1243-51. doi: 10.1556/OH.2010.28796. Orv Hetil. 2010. PMID: 20656661 Review. Hungarian.
Novel sequence variants of the alpha-galactosidase A gene in patients with Fabry disease.
Erdos M, Németh K, Tóth B, Constantin T, Rákóczi E, Ponyi A, Dajnoki A, Grubits J, Pintér I, Garzuly F, Hahn K, Bencsik K, Vécsei L, Fekete G, Maródi L. Erdos M, et al. Among authors: toth b. Mol Genet Metab. 2008 Dec;95(4):224-8. doi: 10.1016/j.ymgme.2008.09.002. Epub 2008 Oct 11. Mol Genet Metab. 2008. PMID: 18849176
Association of renal ectopia with Fabry's disease in 3 patients.
Rákóczi E, Tóth B, Görögh S, Erdos M, Sümegi J, Maródi L. Rákóczi E, et al. Among authors: toth b. J Urol. 2009 Apr;181(4):1949-54. doi: 10.1016/j.juro.2008.11.091. Epub 2009 Feb 23. J Urol. 2009. PMID: 19237168
1,086 results