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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
408 results