Ginjaar IB - Search Results

1

Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysis.

Almomani R, van der Stoep N, Bakker E, den Dunnen JT, Breuning MH, Ginjaar IB. Almomani R, et al. Among authors: ginjaar ib. Neuromuscul Disord. 2009 Jun;19(6):383-90. doi: 10.1016/j.nmd.2009.03.004. Epub 2009 May 5. Neuromuscul Disord. 2009. PMID: 19409785

2

A protein truncation test for Emery-Dreifuss muscular dystrophy (EMD): detection of N-terminal truncating mutations.

de Koning Gans PA, Ginjaar I, Bakker E, Yates JR, den Dunnen JT. de Koning Gans PA, et al. Neuromuscul Disord. 1999 Jun;9(4):247-50. doi: 10.1016/s0960-8966(98)00128-x. Neuromuscul Disord. 1999. PMID: 10399752

3

Sarcoglycanopathies and the risk of undetected deletion alleles in diagnosis.

White SJ, Uitte de Willige S, Verbove D, Politano L, Ginjaar I, Breuning MH, den Dunnen JT. White SJ, et al. Hum Mutat. 2005 Jul;26(1):59. doi: 10.1002/humu.9347. Hum Mutat. 2005. PMID: 15954112

4

Theoretic applicability of antisense-mediated exon skipping for Duchenne muscular dystrophy mutations.

Aartsma-Rus A, Fokkema I, Verschuuren J, Ginjaar I, van Deutekom J, van Ommen GJ, den Dunnen JT. Aartsma-Rus A, et al. Hum Mutat. 2009 Mar;30(3):293-9. doi: 10.1002/humu.20918. Hum Mutat. 2009. PMID: 19156838 Review.

5

DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients.

Hofstra RM, Mulder IM, Vossen R, de Koning-Gans PA, Kraak M, Ginjaar IB, van der Hout AH, Bakker E, Buys CH, van Ommen GJ, van Essen AJ, den Dunnen JT. Hofstra RM, et al. Among authors: ginjaar ib. Hum Mutat. 2004 Jan;23(1):57-66. doi: 10.1002/humu.10283. Hum Mutat. 2004. PMID: 14695533

6

Duchenne and Becker muscular dystrophy.

Kneppers AL, Ginjaar IB, Bakker E. Kneppers AL, et al. Among authors: ginjaar ib. Methods Mol Med. 2004;92:311-41. doi: 10.1385/1-59259-432-8:311. Methods Mol Med. 2004. PMID: 14733319 No abstract available.

7

Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophy.

Hoogerwaard EM, Ginjaar IB, Bakker E, de Visser M. Hoogerwaard EM, et al. Among authors: ginjaar ib. Neurology. 2005 Dec 27;65(12):1984-6. doi: 10.1212/01.wnl.0000188909.89849.59. Neurology. 2005. PMID: 16380627

8

Local dystrophin restoration with antisense oligonucleotide PRO051.

van Deutekom JC, Janson AA, Ginjaar IB, Frankhuizen WS, Aartsma-Rus A, Bremmer-Bout M, den Dunnen JT, Koop K, van der Kooi AJ, Goemans NM, de Kimpe SJ, Ekhart PF, Venneker EH, Platenburg GJ, Verschuuren JJ, van Ommen GJ. van Deutekom JC, et al. Among authors: ginjaar ib. N Engl J Med. 2007 Dec 27;357(26):2677-86. doi: 10.1056/NEJMoa073108. N Engl J Med. 2007. PMID: 18160687 Free article. Clinical Trial.

9

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.

10

Immunohistochemical studies show truncated dystrophins in the myotubes of three fetuses at risk for Duchenne muscular dystrophy.

Ginjaar IB, Bakker E, van Paassen MM, den Dunnen JT, Wessels A, Zubrzycka-Gaarn EE, Moorman AF, van Ommen GJ. Ginjaar IB, et al. J Med Genet. 1991 Aug;28(8):505-10. doi: 10.1136/jmg.28.8.505. J Med Genet. 1991. PMID: 1920366 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

51 results

Search Page

Filters