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Diagnosis and treatment of upper limb apraxia.
Dovern A, Fink GR, Weiss PH. Dovern A, et al. Among authors: weiss ph. J Neurol. 2012 Jul;259(7):1269-83. doi: 10.1007/s00415-011-6336-y. Epub 2012 Jan 4. J Neurol. 2012. PMID: 22215235 Free PMC article. Review.
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.
Hedrich K, Djarmati A, Schäfer N, Hering R, Wellenbrock C, Weiss PH, Hilker R, Vieregge P, Ozelius LJ, Heutink P, Bonifati V, Schwinger E, Lang AE, Noth J, Bressman SB, Pramstaller PP, Riess O, Klein C. Hedrich K, et al. Among authors: weiss ph. Neurology. 2004 Feb 10;62(3):389-94. doi: 10.1212/01.wnl.0000113022.51739.88. Neurology. 2004. PMID: 14872018
Deficient sequencing of pantomimes in apraxia.
Weiss PH, Rahbari NN, Hesse MD, Fink GR. Weiss PH, et al. Neurology. 2008 Mar 11;70(11):834-40. doi: 10.1212/01.wnl.0000297513.78593.dc. Neurology. 2008. PMID: 18332341
119 results