Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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
2023 0

Text availability

Article attribute

Article type

Publication date

Search Results

44 results

Results by year

Filters applied: . Clear all
Page 1
[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.
[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.
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
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
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.
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
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
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
44 results