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

Year Number of Results
1975 1
1978 1
1987 2
1989 3
1990 4
1991 3
1992 3
1993 5
1995 1
1996 3
1997 1
1998 2
1999 2
2000 4
2001 1
2003 1
2004 5
2005 5
2006 3
2007 4
2008 5
2009 9
2010 4
2011 2
2012 4
2013 10
2014 11
2015 4
2016 2
2018 1
2019 1
2021 1
2024 0

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97 results

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Page 1
Showing results for ginjaar[au]
Your search for Ginja R[au] retrieved no results
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients.
Ten Dam L, Frankhuizen WS, Linssen WHJP, Straathof CS, Niks EH, Faber K, Fock A, Kuks JB, Brusse E, de Coo R, Voermans N, Verrips A, Hoogendijk JE, van der Pol L, Westra D, de Visser M, van der Kooi AJ, Ginjaar I. Ten Dam L, et al. Among authors: ginjaar i. Clin Genet. 2019 Aug;96(2):126-133. doi: 10.1111/cge.13544. Epub 2019 May 6. Clin Genet. 2019. PMID: 30919934
[The heartache of muscular dystrophy].
Hoogerwaard EM, Ginjaar HB, Wilde AA, Leschot NJ, de Voogt WG, de Visser M. Hoogerwaard EM, et al. Among authors: ginjaar hb. Ned Tijdschr Geneeskd. 2000 Nov 11;144(46):2181-4. Ned Tijdschr Geneeskd. 2000. PMID: 11103252 Review. Dutch.
Therapeutic exon skipping for dysferlinopathies?
Aartsma-Rus A, Singh KH, Fokkema IF, Ginjaar IB, van Ommen GJ, den Dunnen JT, van der Maarel SM. Aartsma-Rus A, et al. Among authors: ginjaar ib. Eur J Hum Genet. 2010 Aug;18(8):889-94. doi: 10.1038/ejhg.2010.4. Epub 2010 Feb 10. Eur J Hum Genet. 2010. PMID: 20145676 Free PMC article.
[Experimental therapy in Duchenne muscular dystrophy].
van den Bergen JC, Straathof CS, Aartsma-Rus A, Ginjaar IB, Verschuuren JJ. van den Bergen JC, et al. Among authors: ginjaar ib. Ned Tijdschr Geneeskd. 2009 May 2;153(18):870-5. Ned Tijdschr Geneeskd. 2009. PMID: 19475867 Review. Dutch. No abstract available.
Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands.
Stunnenberg BC, Raaphorst J, Deenen JCW, Links TP, Wilde AA, Verbove DJ, Kamsteeg EJ, van den Wijngaard A, Faber CG, van der Wilt GJ, van Engelen BGM, Drost G, Ginjaar HB. Stunnenberg BC, et al. Among authors: ginjaar hb. Neuromuscul Disord. 2018 May;28(5):402-407. doi: 10.1016/j.nmd.2018.03.006. Epub 2018 Mar 9. Neuromuscul Disord. 2018. PMID: 29606556
Myotonic discharges discriminate chloride from sodium muscle channelopathies.
Drost G, Stunnenberg BC, Trip J, Borm G, McGill KC, Ginjaar IH, van der Kooi AW, Zwarts MJ, van Engelen BG, Faber CG, Stegeman DF, Lateva Z. Drost G, et al. Among authors: ginjaar ih. Neuromuscul Disord. 2015 Jan;25(1):73-80. doi: 10.1016/j.nmd.2014.09.014. Epub 2014 Oct 6. Neuromuscul Disord. 2015. PMID: 25454733
Duplications in the DMD gene.
White SJ, Aartsma-Rus A, Flanigan KM, Weiss RB, Kneppers AL, Lalic T, Janson AA, Ginjaar HB, Breuning MH, den Dunnen JT. White SJ, et al. Among authors: ginjaar hb. Hum Mutat. 2006 Sep;27(9):938-45. doi: 10.1002/humu.20367. Hum Mutat. 2006. PMID: 16917894
97 results