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SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.
Orlén H, Melberg A, Raininko R, Kumlien E, Entesarian M, Söderberg P, Påhlman M, Darin N, Kyllerman M, Holmberg E, Engler H, Eriksson U, Dahl N. Orlén H, et al. Among authors: engler h. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):984-92. doi: 10.1002/ajmg.b.30928. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19194956
Evidence for astrocytosis in ALS demonstrated by [11C](L)-deprenyl-D2 PET.
Johansson A, Engler H, Blomquist G, Scott B, Wall A, Aquilonius SM, Långström B, Askmark H. Johansson A, et al. Among authors: engler h. J Neurol Sci. 2007 Apr 15;255(1-2):17-22. doi: 10.1016/j.jns.2007.01.057. Epub 2007 Mar 7. J Neurol Sci. 2007. PMID: 17346749
Fluorodeoxyglucose PET in Neurology and Psychiatry.
Schöll M, Damián A, Engler H. Schöll M, et al. Among authors: engler h. PET Clin. 2014 Oct;9(4):371-90, v. doi: 10.1016/j.cpet.2014.07.005. Epub 2014 Aug 12. PET Clin. 2014. PMID: 26050943 Review.
[(11)C]-PIB imaging in patients with Parkinson's disease: preliminary results.
Johansson A, Savitcheva I, Forsberg A, Engler H, Långström B, Nordberg A, Askmark H. Johansson A, et al. Among authors: engler h. Parkinsonism Relat Disord. 2008;14(4):345-7. doi: 10.1016/j.parkreldis.2007.07.010. Epub 2007 Sep 14. Parkinsonism Relat Disord. 2008. PMID: 17855149
342 results