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Page 1
ANO5 mutations in the Dutch limb girdle muscular dystrophy population.
van der Kooi AJ, Ten Dam L, Frankhuizen WS, Straathof CS, van Doorn PA, de Visser M, Ginjaar IB. van der Kooi AJ, et al. Among authors: straathof cs. Neuromuscul Disord. 2013 Jun;23(6):456-60. doi: 10.1016/j.nmd.2013.03.012. Epub 2013 Apr 19. Neuromuscul Disord. 2013. PMID: 23607914
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: straathof cs. Clin Genet. 2019 Aug;96(2):126-133. doi: 10.1111/cge.13544. Epub 2019 May 6. Clin Genet. 2019. PMID: 30919934
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. Muscle Nerve. 2016 Jan;53(1):44-8. doi: 10.1002/mus.24691. Epub 2015 Jun 3. Muscle Nerve. 2016. PMID: 25900853
Clinical characterisation of Becker muscular dystrophy patients predicts favourable outcome in exon-skipping therapy.
van den Bergen JC, Schade van Westrum SM, Dekker L, van der Kooi AJ, de Visser M, Wokke BH, Straathof CS, Hulsker MA, Aartsma-Rus A, Verschuuren JJ, Ginjaar HB. van den Bergen JC, et al. Among authors: straathof cs. J Neurol Neurosurg Psychiatry. 2014 Jan;85(1):92-8. doi: 10.1136/jnnp-2012-304729. Epub 2013 May 10. J Neurol Neurosurg Psychiatry. 2014. PMID: 23667215
[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: straathof cs. Ned Tijdschr Geneeskd. 2009 May 2;153(18):870-5. Ned Tijdschr Geneeskd. 2009. PMID: 19475867 Review. Dutch. No abstract available.
Reduced cerebral gray matter and altered white matter in boys with Duchenne muscular dystrophy.
Doorenweerd N, Straathof CS, Dumas EM, Spitali P, Ginjaar IB, Wokke BH, Schrans DG, van den Bergen JC, van Zwet EW, Webb A, van Buchem MA, Verschuuren JJ, Hendriksen JG, Niks EH, Kan HE. Doorenweerd N, et al. Among authors: straathof cs. Ann Neurol. 2014 Sep;76(3):403-11. doi: 10.1002/ana.24222. Epub 2014 Jul 24. Ann Neurol. 2014. PMID: 25043804
RYR1-related myopathies: a wide spectrum of phenotypes throughout life.
Snoeck M, van Engelen BG, Küsters B, Lammens M, Meijer R, Molenaar JP, Raaphorst J, Verschuuren-Bemelmans CC, Straathof CS, Sie LT, de Coo IF, van der Pol WL, de Visser M, Scheffer H, Treves S, Jungbluth H, Voermans NC, Kamsteeg EJ. Snoeck M, et al. Among authors: straathof cs. Eur J Neurol. 2015 Jul;22(7):1094-112. doi: 10.1111/ene.12713. Epub 2015 May 11. Eur J Neurol. 2015. PMID: 25960145
Decreased cerebral perfusion in Duchenne muscular dystrophy patients.
Doorenweerd N, Dumas EM, Ghariq E, Schmid S, Straathof CS, Roest AA, Wokke BH, van Zwet EW, Webb AG, Hendriksen JG, van Buchem MA, Verschuuren JJ, Asllani I, Niks EH, van Osch MJ, Kan HE. Doorenweerd N, et al. Among authors: straathof cs. Neuromuscul Disord. 2017 Jan;27(1):29-37. doi: 10.1016/j.nmd.2016.10.005. Epub 2016 Oct 17. Neuromuscul Disord. 2017. PMID: 27927595
32 results