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Page 1
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: krabbe k. 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: krabbe k. 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
MRI of autosomal dominant pure spastic paraplegia.
Krabbe K, Nielsen JE, Fallentin E, Fenger K, Herning M. Krabbe K, et al. Neuroradiology. 1997 Oct;39(10):724-7. doi: 10.1007/s002340050495. Neuroradiology. 1997. PMID: 9351110
Increased intracranial volume in Parkinson's disease.
Krabbe K, Karlsborg M, Hansen A, Werdelin L, Mehlsen J, Larsson HB, Paulson OB. Krabbe K, et al. J Neurol Sci. 2005 Dec 15;239(1):45-52. doi: 10.1016/j.jns.2005.07.013. Epub 2005 Oct 11. J Neurol Sci. 2005. PMID: 16225890
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: krabbe k. 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
Structural brain abnormalities in early onset first-episode psychosis.
Pagsberg AK, Baaré WF, Raabjerg Christensen AM, Fagerlund B, Hansen MB, Labianca J, Krabbe K, Aarkrog T, Paulson OB, Hemmingsen RP. Pagsberg AK, et al. Among authors: krabbe k. J Neural Transm (Vienna). 2007;114(4):489-98. doi: 10.1007/s00702-006-0573-8. Epub 2006 Oct 6. J Neural Transm (Vienna). 2007. PMID: 17024324
67 results