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[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: fekete g. Orv Hetil. 2010 Aug 1;151(31):1243-51. doi: 10.1556/OH.2010.28796. Orv Hetil. 2010. PMID: 20656661 Review. Hungarian.
[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: fekete g. Orv Hetil. 2010 Feb 14;151(7):243-9. doi: 10.1556/OH.2010.28795. Orv Hetil. 2010. PMID: 20133243 Review. Hungarian.
[Neurological complications of Fabry-disease].
Vastagh I, Constantin T, Kéri A, Rudas G, Fekete G, Bereczki D. Vastagh I, et al. Among authors: fekete g. Ideggyogy Sz. 2011 Jan 30;64(1-2):29-35. Ideggyogy Sz. 2011. PMID: 21428036 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: fekete g. 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
[Clinical characteristics of juvenile dermatomyositis].
Constantin T, Ponyi A, Garami M, Gergely L, Fekete G, Dankó K. Constantin T, et al. Among authors: fekete g. Orv Hetil. 2003 Jun 22;144(25):1245-50. Orv Hetil. 2003. PMID: 12901181 Hungarian.
363 results