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

Year Number of Results
1942 1
1945 1
1975 2
1976 1
1977 3
1978 1
1980 1
1981 3
1982 2
1983 1
1985 2
1986 5
1987 3
1988 7
1989 7
1990 5
1991 9
1992 7
1993 9
1994 10
1995 10
1996 5
1997 3
1998 6
1999 3
2000 6
2001 3
2003 3
2004 3
2005 6
2006 9
2007 9
2008 10
2009 12
2010 8
2011 10
2012 12
2013 14
2014 13
2015 12
2016 7
2017 2
2018 8
2019 6
2020 2
2021 2
2022 0
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Article type
Publication date

Search Results

250 results
Results by year
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Page 1
Marinus van den Ende.
van den Ende J. van den Ende J. S Afr Med J. 2009 Jan;99(1):29-32. S Afr Med J. 2009. PMID: 19374083
Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype-phenotype study in neurofibromatosis type 1.
Koczkowska M, Callens T, Chen Y, Gomes A, Hicks AD, Sharp A, Johns E, Uhas KA, Armstrong L, Bosanko KA, Babovic-Vuksanovic D, Baker L, Basel DG, Bengala M, Bennett JT, Chambers C, Clarkson LK, Clementi M, Cortés FM, Cunningham M, D'Agostino MD, Delatycki MB, Digilio MC, Dosa L, Esposito S, Fox S, Freckmann ML, Fauth C, Giugliano T, Giustini S, Goetsch A, Goldberg Y, Greenwood RS, Griffis C, Gripp KW, Gupta P, Haan E, Hachen RK, Haygarth TL, Hernández-Chico C, Hodge K, Hopkin RJ, Hudgins L, Janssens S, Keller K, Kelly-Mancuso G, Kochhar A, Korf BR, Lewis AM, Liebelt J, Lichty A, Listernick RH, Lyons MJ, Maystadt I, Martinez Ojeda M, McDougall C, McGregor LK, Melis D, Mendelsohn N, Nowaczyk MJM, Ortenberg J, Panzer K, Pappas JG, Pierpont ME, Piluso G, Pinna V, Pivnick EK, Pond DA, Powell CM, Rogers C, Ruhrman Shahar N, Rutledge SL, Saletti V, Sandaradura SA, Santoro C, Schatz UA, Schreiber A, Scott DA, Sellars EA, Sheffer R, Siqveland E, Slopis JM, Smith R, Spalice A, Stockton DW, Streff H, Theos A, Tomlinson GE, Tran G, Trapane PL, Trevisson E, Ullrich NJ, Van den Ende J, Schrier Vergano SA, Wallace SE, Wangler MF, Weaver DD, Yohay KH, Zackai E, Zonana J, Zurcher V, Claes KBM, Eoli M, Martin Y, Wimmer K, De Luca A, Legius E, Messiaen LM. Koczkowska M, et al. Among authors: van den ende j. Hum Mutat. 2020 Jan;41(1):299-315. doi: 10.1002/humu.23929. Epub 2019 Oct 26. Hum Mutat. 2020. PMID: 31595648 Free PMC article.
DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System.
Sommen M, Schrauwen I, Vandeweyer G, Boeckx N, Corneveaux JJ, van den Ende J, Boudewyns A, De Leenheer E, Janssens S, Claes K, Verstreken M, Strenzke N, Predöhl F, Wuyts W, Mortier G, Bitner-Glindzicz M, Moser T, Coucke P, Huentelman MJ, Van Camp G. Sommen M, et al. Among authors: van den ende j. Hum Mutat. 2016 Aug;37(8):812-9. doi: 10.1002/humu.22999. Epub 2016 May 6. Hum Mutat. 2016. PMID: 27068579
The threshold model revisited.
Djulbegovic B, Hozo I, Mayrhofer T, van den Ende J, Guyatt G. Djulbegovic B, et al. Among authors: van den ende j. J Eval Clin Pract. 2019 Apr;25(2):186-195. doi: 10.1111/jep.13091. Epub 2018 Dec 21. J Eval Clin Pract. 2019. PMID: 30575227 Free PMC article.
Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy.
Duerinckx S, Désir J, Perazzolo C, Badoer C, Jacquemin V, Soblet J, Maystadt I, Tunca Y, Blaumeiser B, Ceulemans B, Courtens W, Debray FG, Destree A, Devriendt K, Jansen A, Keymolen K, Lederer D, Loeys B, Meuwissen M, Moortgat S, Mortier G, Nassogne MC, Sekhara T, Van Coster R, Van Den Ende J, Van der Aa N, Van Esch H, Vanakker O, Verhelst H, Vilain C, Weckhuysen S, Passemard S, Verloes A, Aeby A, Deconinck N, Van Bogaert P, Pirson I, Abramowicz M. Duerinckx S, et al. Among authors: van den ende j. Mol Genet Genomic Med. 2021 Sep;9(9):e1768. doi: 10.1002/mgg3.1768. Epub 2021 Aug 17. Mol Genet Genomic Med. 2021. PMID: 34402213 Free PMC article.
The predicament of patients with suspected Ebola.
Mayrhofer T, Hamm RM, Van den Ende J, Hozo I, Djulbegovic B. Mayrhofer T, et al. Among authors: van den ende j. Lancet Glob Health. 2017 Jul;5(7):e657. doi: 10.1016/S2214-109X(17)30215-2. Lancet Glob Health. 2017. PMID: 28619222 Free article. No abstract available.
Rapid diagnostic tests for malaria.
Bisoffi Z, Gobbi F, Van den Ende J. Bisoffi Z, et al. Among authors: van den ende j. BMJ. 2014 Jun 19;348:g3846. doi: 10.1136/bmj.g3846. BMJ. 2014. PMID: 24948696 No abstract available.
Obituary.
van den Ende JE. van den Ende JE. In Silico Biol. 2011-2012;11(3-4):95. doi: 10.3233/ISB-2012-0450. In Silico Biol. 2011. PMID: 22935963 No abstract available.
Severe strongyloidiasis: a systematic review of case reports.
Buonfrate D, Requena-Mendez A, Angheben A, Muñoz J, Gobbi F, Van Den Ende J, Bisoffi Z. Buonfrate D, et al. Among authors: van den ende j. BMC Infect Dis. 2013 Feb 8;13:78. doi: 10.1186/1471-2334-13-78. BMC Infect Dis. 2013. PMID: 23394259 Free PMC article. Review.
Prevalence of Germline Pathogenic Variants in Cancer Predisposing Genes in Czech and Belgian Pancreatic Cancer Patients.
Wieme G, Kral J, Rosseel T, Zemankova P, Parton B, Vocka M, Van Heetvelde M, Kleiblova P, Blaumeiser B, Soukupova J, van den Ende J, Nehasil P, Tejpar S, Borecka M, Gómez García EB, Blok MJ, Safarikova M, Kalousova M, Geboes K, De Putter R, Poppe B, De Leeneer K, Kleibl Z, Janatova M, Claes KBM. Wieme G, et al. Among authors: van den ende j. Cancers (Basel). 2021 Sep 2;13(17):4430. doi: 10.3390/cancers13174430. Cancers (Basel). 2021. PMID: 34503238 Free PMC article.
250 results