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

Year Number of Results
1996 1
2003 2
2005 1
2007 2
2008 2
2009 2
2010 2
2011 6
2012 6
2013 5
2014 4
2015 3
2016 3
2017 4
2018 1
2019 4
2020 3
2021 4
2022 1
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44 results
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Page 1
Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria.
Savige J, Storey H, Watson E, Hertz JM, Deltas C, Renieri A, Mari F, Hilbert P, Plevova P, Byers P, Cerkauskaite A, Gregory M, Cerkauskiene R, Ljubanovic DG, Becherucci F, Errichiello C, Massella L, Aiello V, Lennon R, Hopkinson L, Koziell A, Lungu A, Rothe HM, Hoefele J, Zacchia M, Martic TN, Gupta A, van Eerde A, Gear S, Landini S, Palazzo V, Al-Rabadi L, Claes K, Corveleyn A, Van Hoof E, van Geel M, Williams M, Ashton E, Belge H, Ars E, Bierzynska A, Gangemi C, Lipska-Ziętkiewicz BS. Savige J, et al. Among authors: van hoof e. Eur J Hum Genet. 2021 Aug;29(8):1186-1197. doi: 10.1038/s41431-021-00858-1. Epub 2021 Apr 15. Eur J Hum Genet. 2021. PMID: 33854215 Free PMC article.
Guidelines for Genetic Testing and Management of Alport Syndrome.
Savige J, Lipska-Zietkiewicz BS, Watson E, Hertz JM, Deltas C, Mari F, Hilbert P, Plevova P, Byers P, Cerkauskaite A, Gregory M, Cerkauskiene R, Ljubanovic DG, Becherucci F, Errichiello C, Massella L, Aiello V, Lennon R, Hopkinson L, Koziell A, Lungu A, Rothe HM, Hoefele J, Zacchia M, Martic TN, Gupta A, van Eerde A, Gear S, Landini S, Palazzo V, Al-Rabadi L, Claes K, Corveleyn A, Van Hoof E, van Geel M, Williams M, Ashton E, Belge H, Ars E, Bierzynska A, Gangemi C, Renieri A, Storey H, Flinter F. Savige J, et al. Among authors: van hoof e. Clin J Am Soc Nephrol. 2022 Jan;17(1):143-154. doi: 10.2215/CJN.04230321. Epub 2021 Dec 20. Clin J Am Soc Nephrol. 2022. PMID: 34930753
BCAP31-related syndrome: The first de novo report.
Rinaldi B, Van Hoof E, Corveleyn A, Van Cauter A, de Ravel T. Rinaldi B, et al. Among authors: van hoof e. Eur J Med Genet. 2020 Feb;63(2):103732. doi: 10.1016/j.ejmg.2019.103732. Epub 2019 Jul 19. Eur J Med Genet. 2020. PMID: 31330203
Next-generation sequencing in prenatal setting: Some examples of unexpected variant association.
Rinaldi B, Race V, Corveleyn A, Van Hoof E, Bauters M, Van Den Bogaert K, Denayer E, de Ravel T, Legius E, Baldewijns M, Aertsen M, Lewi L, De Catte L, Breckpot J, Devriendt K. Rinaldi B, et al. Among authors: van hoof e. Eur J Med Genet. 2020 May;63(5):103875. doi: 10.1016/j.ejmg.2020.103875. Epub 2020 Feb 10. Eur J Med Genet. 2020. PMID: 32058062
How to bring residents' psychosocial well-being to the heart of the fight against Covid-19 in Belgian nursing homes-A qualitative study.
Kaelen S, van den Boogaard W, Pellecchia U, Spiers S, De Cramer C, Demaegd G, Fouqueray E, Van den Bergh R, Goublomme S, Decroo T, Quinet M, Van Hoof E, Draguez B. Kaelen S, et al. Among authors: van hoof e. PLoS One. 2021 Mar 26;16(3):e0249098. doi: 10.1371/journal.pone.0249098. eCollection 2021. PLoS One. 2021. PMID: 33770110 Free PMC article.
44 results