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Page 1
[Fabry disease--diagnostic guideline].
Constantin T, Rákóczi E, Ponyi A, Ambrus C, Kádár K, Vastagh I, Dajnoki A, Tóth B, Bokrétás G, Müller V, Katona M, Csikós M, Fiedler O, Széchey R, Varga E, Rudas G, Kertész A, Molnár S, Kárpáti S, Nagy V, Magyar P, Mahdi M, Németh K, Bereczki D, Garami M, Erdos M, Maródi L, Fekete G; Fabry Disease Work Group. Constantin T, et al. Among authors: marodi l. Orv Hetil. 2010 Feb 14;151(7):243-9. doi: 10.1556/OH.2010.28795. Orv Hetil. 2010. PMID: 20133243 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: marodi l. Orv Hetil. 2007 Jun 10;148(23):1087-94. doi: 10.1556/OH.2007.28086. Orv Hetil. 2007. PMID: 17545117 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: marodi l. Orv Hetil. 2010 Aug 1;151(31):1243-51. doi: 10.1556/OH.2010.28796. Orv Hetil. 2010. PMID: 20656661 Review. Hungarian.
[WHIM syndrome].
Erdos M, Maródi L. Erdos M, et al. Among authors: marodi l. Orv Hetil. 2007 Jun 24;148(25):1173-9. doi: 10.1556/OH.2007.28074. Orv Hetil. 2007. PMID: 17573253 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: marodi l. 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
213 results