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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 1
1989 2
1992 1
1993 1
1996 2
1998 2
1999 1
2000 3
2003 1
2004 2
2005 2
2006 2
2007 2
2008 3
2009 4
2010 3
2011 2
2012 1
2013 5
2014 5
2015 2
2016 1
2018 1
2022 0
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44 results
Results by year
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Page 1
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
[From gene to diseases; hypokalemic periodic paralysis].
Links TP, Ginjaar HB, van der Hoeven JH. Links TP, et al. Among authors: ginjaar hb. Ned Tijdschr Geneeskd. 2004 May 22;148(21):1035-8. Ned Tijdschr Geneeskd. 2004. PMID: 15185439 Review. Dutch.
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
Diagnosis of becker muscular dystrophy: Results of Re-analysis of DNA samples.
Straathof CS, Van Heusden D, Ippel PF, Post JG, Voermans NC, De Visser M, Brusse E, Van Den Bergen JC, Van Der Kooi AJ, Verschuuren JJ, Ginjaar HB. Straathof CS, et al. Among authors: ginjaar hb. Muscle Nerve. 2016 Jan;53(1):44-8. doi: 10.1002/mus.24691. Epub 2015 Jun 3. Muscle Nerve. 2016. PMID: 25900853
Forty-Five Years of Duchenne Muscular Dystrophy in The Netherlands.
van den Bergen JC, Ginjaar HB, van Essen AJ, Pangalila R, de Groot IJ, Wijkstra PJ, Zijnen MP, Cobben NA, Kampelmacher MJ, Wokke BH, de Coo IF, Fock JM, Horemans AM, van Tol M, Vroom E, Rijlaarsdam ME, Straathof CS, Niks EH, Verschuuren JJ. van den Bergen JC, et al. Among authors: ginjaar hb. J Neuromuscul Dis. 2014;1(1):99-109. J Neuromuscul Dis. 2014. PMID: 27858664
Calpainopathy-a survey of mutations and polymorphisms.
Richard I, Roudaut C, Saenz A, Pogue R, Grimbergen JE, Anderson LV, Beley C, Cobo AM, de Diego C, Eymard B, Gallano P, Ginjaar HB, Lasa A, Pollitt C, Topaloglu H, Urtizberea JA, de Visser M, van der Kooi A, Bushby K, Bakker E, Lopez de Munain A, Fardeau M, Beckmann JS. Richard I, et al. Among authors: ginjaar hb. Am J Hum Genet. 1999 Jun;64(6):1524-40. doi: 10.1086/302426. Am J Hum Genet. 1999. PMID: 10330340 Free PMC article.
Dystrophin levels and clinical severity in Becker muscular dystrophy patients.
van den Bergen JC, Wokke BH, Janson AA, van Duinen SG, Hulsker MA, Ginjaar HB, van Deutekom JC, Aartsma-Rus A, Kan HE, Verschuuren JJ. van den Bergen JC, et al. Among authors: ginjaar hb. J Neurol Neurosurg Psychiatry. 2014 Jul;85(7):747-53. doi: 10.1136/jnnp-2013-306350. Epub 2013 Nov 29. J Neurol Neurosurg Psychiatry. 2014. PMID: 24292997
Redefining the clinical phenotypes of non-dystrophic myotonic syndromes.
Trip J, Drost G, Ginjaar HB, Nieman FH, van der Kooi AJ, de Visser M, van Engelen BG, Faber CG. Trip J, et al. Among authors: ginjaar hb. J Neurol Neurosurg Psychiatry. 2009 Jun;80(6):647-52. doi: 10.1136/jnnp.2008.162396. Epub 2009 Feb 11. J Neurol Neurosurg Psychiatry. 2009. PMID: 19211598
CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.
Stam AH, Vanmolkot KR, Kremer HP, Gärtner J, Brown J, Leshinsky-Silver E, Gilad R, Kors EE, Frankhuizen WS, Ginjaar HB, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM, Terwindt GM. Stam AH, et al. Among authors: ginjaar hb. Clin Genet. 2008 Nov;74(5):481-5. doi: 10.1111/j.1399-0004.2008.00996.x. Epub 2008 Apr 8. Clin Genet. 2008. PMID: 18400034
44 results