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Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.
Nielsen JE, Johnsen B, Koefoed P, Scheuer KH, Grønbech-Jensen M, Law I, Krabbe K, Nørremølle A, Eiberg H, Søndergård H, Dam M, Rehfeld JF, Krarup C, Paulson OB, Hasholt L, Sørensen SA. Nielsen JE, et al. Among authors: law i. Eur J Neurol. 2004 Dec;11(12):817-24. doi: 10.1111/j.1468-1331.2004.00888.x. Eur J Neurol. 2004. PMID: 15667412
Motor activation in SPG4-linked hereditary spastic paraplegia.
Scheuer KH, Nielsen JE, Krabbe K, Paulson OB, Law I. Scheuer KH, et al. Among authors: law i. J Neurol Sci. 2006 May 15;244(1-2):31-9. doi: 10.1016/j.jns.2005.12.007. Epub 2006 Mar 29. J Neurol Sci. 2006. PMID: 16571355
Hereditary spastic paraplegia caused by the PLP1 'rumpshaker mutation'.
Svenstrup K, Giraud G, Boespflug-Tanguy O, Danielsen ER, Thomsen C, Rasmussen K, Law I, Vogel A, Stokholm J, Crone C, Hjermind LE, Nielsen JE. Svenstrup K, et al. Among authors: law i. J Neurol Neurosurg Psychiatry. 2010 Jun;81(6):666-72. doi: 10.1136/jnnp.2009.180315. Epub 2009 Dec 1. J Neurol Neurosurg Psychiatry. 2010. PMID: 19955111
[Biomarkers for early diagnosis of Alzheimer's disease].
Frederiksen KS, Hasselbalch S, Law I, Højgaard L, Waldemar G. Frederiksen KS, et al. Among authors: law i. Ugeskr Laeger. 2015 Jun 8;177(24):V12140684. Ugeskr Laeger. 2015. PMID: 26058526 Free article. Review. Danish.
Use of amyloid-PET to determine cutpoints for CSF markers: A multicenter study.
Zwan MD, Rinne JO, Hasselbalch SG, Nordberg A, Lleó A, Herukka SK, Soininen H, Law I, Bahl JM, Carter SF, Fortea J, Blesa R, Teunissen CE, Bouwman FH, van Berckel BN, Visser PJ. Zwan MD, et al. Among authors: law i. Neurology. 2016 Jan 5;86(1):50-8. doi: 10.1212/WNL.0000000000002081. Epub 2015 Oct 14. Neurology. 2016. PMID: 26468410 Free PMC article.
427 results