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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1958 1
1967 2
1986 1
1988 2
1989 1
1992 1
1993 1
1996 1
1997 2
1998 1
2000 1
2008 1
2009 3
2010 6
2011 2
2012 3
2013 6
2014 3
2016 3
2017 3
2018 7
2019 5
2020 8
2021 8
2022 3
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68 results
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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: rudas g. 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: rudas g. Orv Hetil. 2010 Aug 1;151(31):1243-51. doi: 10.1556/OH.2010.28796. Orv Hetil. 2010. PMID: 20656661 Review. Hungarian.
[Ultrasound diagnosis of fetal adrenal hemorrhage].
Szabó G, Szarka A, Rudas G, Rigó J Jr. Szabó G, et al. Among authors: rudas g. Orv Hetil. 2019 Dec;160(52):2073-2078. doi: 10.1556/650.2019.31578. Orv Hetil. 2019. PMID: 31868009 Hungarian.
Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis.
Balogh E, Chandler JC, Varga M, Tahoun M, Menyhárd DK, Schay G, Goncalves T, Hamar R, Légrádi R, Szekeres Á, Gribouval O, Kleta R, Stanescu H, Bockenhauer D, Kerti A, Williams H, Kinsler V, Di WL, Curtis D, Kolatsi-Joannou M, Hammid H, Szőcs A, Perczel K, Maka E, Toldi G, Sava F, Arrondel C, Kardos M, Fintha A, Hossain A, D'Arco F, Kaliakatsos M, Koeglmeier J, Mifsud W, Moosajee M, Faro A, Jávorszky E, Rudas G, Saied MH, Marzouk S, Kelen K, Götze J, Reusz G, Tulassay T, Dragon F, Mollet G, Motameny S, Thiele H, Dorval G, Nürnberg P, Perczel A, Szabó AJ, Long DA, Tomita K, Antignac C, Waters AM, Tory K. Balogh E, et al. Among authors: rudas g. Proc Natl Acad Sci U S A. 2020 Jun 30;117(26):15137-15147. doi: 10.1073/pnas.2002328117. Epub 2020 Jun 17. Proc Natl Acad Sci U S A. 2020. PMID: 32554502 Free PMC article.
Wernicke-Korsakoff syndrome associated with mtDNA disease.
Jimoh IJ, Sebe B, Balicza P, Fedor M, Pataky I, Rudas G, Gal A, Inczedy-Farkas G, Nemeth G, Molnar MJ. Jimoh IJ, et al. Among authors: rudas g. Ther Adv Neurol Disord. 2020 Jul 30;13:1756286420938972. doi: 10.1177/1756286420938972. eCollection 2020. Ther Adv Neurol Disord. 2020. PMID: 32821290 Free PMC article.
[Cervical artery dissection - retrospective analysis of 19 cases].
Forró C, Mészáros Z, Sipos M, Kerényi RZ, Barsi P, Rudas G, Bereczki D, Vastagh I. Forró C, et al. Among authors: rudas g. Orv Hetil. 2019 Jun;160(22):861-868. doi: 10.1556/650.2019.31333. Orv Hetil. 2019. PMID: 31131609 Hungarian.
[Association of acute retinal necrosis with ischemic stroke].
Magyar M, Gunda B, Rudas G, Resch M, Nagy ZZ, Dohán J. Magyar M, et al. Among authors: rudas g. Orv Hetil. 2021 Nov 28;162(48):1940-1945. doi: 10.1556/650.2021.32260. Orv Hetil. 2021. PMID: 34839275 Hungarian.
68 results