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

Year Number of Results
2002 1
2003 4
2004 1
2005 3
2007 3
2008 6
2009 6
2010 10
2011 9
2012 7
2013 4
2014 3
2015 3
2016 3
2017 10
2018 12
2019 5
2020 6
2021 4
2022 4
2024 0

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91 results

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Page 1
A Unique Microglia Type Associated with Restricting Development of Alzheimer's Disease.
Keren-Shaul H, Spinrad A, Weiner A, Matcovitch-Natan O, Dvir-Szternfeld R, Ulland TK, David E, Baruch K, Lara-Astaiso D, Toth B, Itzkovitz S, Colonna M, Schwartz M, Amit I. Keren-Shaul H, et al. Among authors: toth b. Cell. 2017 Jun 15;169(7):1276-1290.e17. doi: 10.1016/j.cell.2017.05.018. Epub 2017 Jun 8. Cell. 2017. PMID: 28602351 Free article.
Single-cell spatial reconstruction reveals global division of labour in the mammalian liver.
Halpern KB, Shenhav R, Matcovitch-Natan O, Toth B, Lemze D, Golan M, Massasa EE, Baydatch S, Landen S, Moor AE, Brandis A, Giladi A, Avihail AS, David E, Amit I, Itzkovitz S. Halpern KB, et al. Among authors: toth b. Nature. 2017 Feb 16;542(7641):352-356. doi: 10.1038/nature21065. Epub 2017 Feb 6. Nature. 2017. PMID: 28166538 Free PMC article.
[Autoinflammatory diseases].
Mosdósi B, Tóth B. Mosdósi B, et al. Among authors: toth b. Orv Hetil. 2018 Jun;159(23):898-907. doi: 10.1556/650.2018.31068. Orv Hetil. 2018. PMID: 29860887 Review. Hungarian.
Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype.
Toubiana J, Okada S, Hiller J, Oleastro M, Lagos Gomez M, Aldave Becerra JC, Ouachée-Chardin M, Fouyssac F, Girisha KM, Etzioni A, Van Montfrans J, Camcioglu Y, Kerns LA, Belohradsky B, Blanche S, Bousfiha A, Rodriguez-Gallego C, Meyts I, Kisand K, Reichenbach J, Renner ED, Rosenzweig S, Grimbacher B, van de Veerdonk FL, Traidl-Hoffmann C, Picard C, Marodi L, Morio T, Kobayashi M, Lilic D, Milner JD, Holland S, Casanova JL, Puel A; International STAT1 Gain-of-Function Study Group. Toubiana J, et al. Blood. 2016 Jun 23;127(25):3154-64. doi: 10.1182/blood-2015-11-679902. Epub 2016 Apr 25. Blood. 2016. PMID: 27114460 Free PMC article.
[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: toth b. Orv Hetil. 2010 Feb 14;151(7):243-9. doi: 10.1556/OH.2010.28795. Orv Hetil. 2010. PMID: 20133243 Review. Hungarian.
[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.
Fifteen Years of the J Project.
Maródi L; J Project study group. Maródi L, et al. J Clin Immunol. 2019 May;39(4):363-369. doi: 10.1007/s10875-019-00633-4. Epub 2019 May 17. J Clin Immunol. 2019. PMID: 31102035 No abstract available.
[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.
[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.
91 results