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[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: kadar k. Orv Hetil. 2010 Feb 14;151(7):243-9. doi: 10.1556/OH.2010.28795. Orv Hetil. 2010. PMID: 20133243 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: kadar k. Orv Hetil. 2010 Aug 1;151(31):1243-51. doi: 10.1556/OH.2010.28796. Orv Hetil. 2010. PMID: 20656661 Review. Hungarian.
[Genetic diagnosis of Williams syndrome].
Urbán Z, Kiss E, Kádár K, Szabolcs J, Csiszár K, Boyd DC, Fekete G. Urbán Z, et al. Among authors: kadar k. Orv Hetil. 1997 Jul 6;138(27):1749-52. Orv Hetil. 1997. PMID: 9273487 Review. Hungarian.
[Clinical aspects of 22q11.2 microdeletion syndrome].
Szumutku F, Kádár K, Kovács ÁF, Lengyel A, Pinti É, Némethi Z, Abonyi T, Csáky-Szunyogh M, Fekete G, Haltrich I. Szumutku F, et al. Among authors: kadar k. Orv Hetil. 2022 Jan 2;163(1):21-30. doi: 10.1556/650.2022.32299. Print 2022 Jan 2. Orv Hetil. 2022. PMID: 34974426 Hungarian.
106 results