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34 results
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Fabry disease in children: agalsidase-beta enzyme replacement therapy.
Borgwardt L, Feldt-Rasmussen U, Rasmussen AK, Ballegaard M, Meldgaard Lund A. Borgwardt L, et al. Among authors: ballegaard m. Clin Genet. 2013 May;83(5):432-8. doi: 10.1111/j.1399-0004.2012.01947.x. Epub 2012 Sep 27. Clin Genet. 2013. PMID: 22880956
The D313Y variant in the GLA gene - no evidence of a pathogenic role in Fabry disease.
Hasholt L, Ballegaard M, Bundgaard H, Christiansen M, Law I, Lund AM, Norremolle A, Krogh Rasmussen A, Ravn K, Tumer Z, Wibrand F, Feldt-Rasmussen U. Hasholt L, et al. Among authors: ballegaard m. Scand J Clin Lab Invest. 2017 Dec;77(8):617-621. doi: 10.1080/00365513.2017.1390782. Epub 2017 Oct 16. Scand J Clin Lab Invest. 2017. PMID: 29037082
Diagnostic dilemma: a young woman with Fabry disease symptoms, no family history, and a "sequencing cryptic" α-galactosidase a large deletion.
Feldt-Rasmussen U, Dobrovolny R, Nazarenko I, Ballegaard M, Hasholt L, Rasmussen AK, Christensen EI, Sorensen SS, Wibrand F, Desnick RJ. Feldt-Rasmussen U, et al. Among authors: ballegaard m. Mol Genet Metab. 2011 Nov;104(3):314-8. doi: 10.1016/j.ymgme.2011.05.008. Epub 2011 May 14. Mol Genet Metab. 2011. PMID: 21641253
Functional and structural nerve fiber findings in heterozygote patients with Fabry disease.
Torvin Møller A, Winther Bach F, Feldt-Rasmussen U, Rasmussen A, Hasholt L, Lan H, Sommer C, Kølvraa S, Ballegaard M, Staehelin Jensen T. Torvin Møller A, et al. Among authors: ballegaard m. Pain. 2009 Sep;145(1-2):237-45. doi: 10.1016/j.pain.2009.06.032. Epub 2009 Aug 7. Pain. 2009. PMID: 19665302 Clinical Trial.
Mind the gap - Practicing neurophysiology between neurology and cardiology.
Ballegaard M. Ballegaard M. Clin Neurophysiol. 2016 Feb;127(2):985-986. doi: 10.1016/j.clinph.2015.08.017. Epub 2015 Sep 8. Clin Neurophysiol. 2016. PMID: 26410253 No abstract available.
Do you define the limits of normalcy from looking at the patient or the healthy subject?
Ballegaard M. Ballegaard M. Clin Neurophysiol. 2018 Mar;129(3):663-665. doi: 10.1016/j.clinph.2018.01.001. Epub 2018 Jan 16. Clin Neurophysiol. 2018. PMID: 29402575 No abstract available.
Discrepancy between stimulus response and tolerance of pain in Alzheimer disease.
Jensen-Dahm C, Werner MU, Jensen TS, Ballegaard M, Andersen BB, Høgh P, Waldemar G. Jensen-Dahm C, et al. Among authors: ballegaard m. Neurology. 2015 Apr 14;84(15):1575-81. doi: 10.1212/WNL.0000000000001465. Epub 2015 Mar 18. Neurology. 2015. PMID: 25788560 Free PMC article.
Atypical early-onset Alzheimer's disease caused by the Iranian APP mutation.
Lindquist SG, Nielsen JE, Stokholm J, Schwartz M, Batbayli M, Ballegaard M, Erdal J, Krabbe K, Waldemar G. Lindquist SG, et al. Among authors: ballegaard m. J Neurol Sci. 2008 May 15;268(1-2):124-30. doi: 10.1016/j.jns.2007.11.021. Epub 2008 Jan 9. J Neurol Sci. 2008. PMID: 18187157
Autonomic Dysfunction in Patients with Mild to Moderate Alzheimer's Disease.
Jensen-Dahm C, Waldemar G, Staehelin Jensen T, Malmqvist L, Moeller MM, Andersen BB, Høgh P, Ballegaard M. Jensen-Dahm C, et al. Among authors: ballegaard m. J Alzheimers Dis. 2015;47(3):681-9. doi: 10.3233/JAD-150169. J Alzheimers Dis. 2015. PMID: 26401703
Peripheral neuropathy in hereditary spastic paraplegia caused by REEP1 variants.
Toft A, Birk S, Ballegaard M, Dunø M, Hjermind LE, Nielsen JE, Svenstrup K. Toft A, et al. Among authors: ballegaard m. J Neurol. 2019 Mar;266(3):735-744. doi: 10.1007/s00415-019-09196-1. Epub 2019 Jan 12. J Neurol. 2019. PMID: 30637453
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