These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
92 related articles for article (PubMed ID: 27843055)
1. Abnormal premotor-motor interaction in heterozygous Parkin- and Pink1 mutation carriers. Weissbach A; Bäumer T; Pramstaller PP; Brüggemann N; Tadic V; Chen R; Klein C; Münchau A Clin Neurophysiol; 2017 Jan; 128(1):275-280. PubMed ID: 27843055 [TBL] [Abstract][Full Text] [Related]
2. Influence of L-dopa on subtle motor signs in heterozygous Parkin- and PINK1 mutation carriers. Weissbach A; König IR; Hückelheim K; Pramstaller PP; Werner E; Brüggemann N; Tadic V; Lohmann K; Bäumer T; Münchau A; Kasten M; Klein C Parkinsonism Relat Disord; 2017 Sep; 42():95-99. PubMed ID: 28716427 [TBL] [Abstract][Full Text] [Related]
3. Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype. van Nuenen BF; Weiss MM; Bloem BR; Reetz K; van Eimeren T; Lohmann K; Hagenah J; Pramstaller PP; Binkofski F; Klein C; Siebner HR Neurology; 2009 Mar; 72(12):1041-7. PubMed ID: 19038850 [TBL] [Abstract][Full Text] [Related]
4. Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia. Binkofski F; Reetz K; Gaser C; Hilker R; Hagenah J; Hedrich K; van Eimeren T; Thiel A; Büchel C; Pramstaller PP; Siebner HR; Klein C Neurology; 2007 Aug; 69(9):842-50. PubMed ID: 17724286 [TBL] [Abstract][Full Text] [Related]
5. Motor cortical physiology in patients and asymptomatic carriers of parkin gene mutations. Schneider SA; Talelli P; Cheeran BJ; Khan NL; Wood NW; Rothwell JC; Bhatia KP Mov Disord; 2008 Oct; 23(13):1812-9. PubMed ID: 18759365 [TBL] [Abstract][Full Text] [Related]
6. Sensorimotor integration is abnormal in asymptomatic Parkin mutation carriers: a TMS study. Bäumer T; Pramstaller PP; Siebner HR; Schippling S; Hagenah J; Peller M; Gerloff C; Klein C; Münchau A Neurology; 2007 Nov; 69(21):1976-81. PubMed ID: 18025391 [TBL] [Abstract][Full Text] [Related]
7. Compensatory premotor activity during affective face processing in subclinical carriers of a single mutant Parkin allele. Anders S; Sack B; Pohl A; Münte T; Pramstaller P; Klein C; Binkofski F Brain; 2012 Apr; 135(Pt 4):1128-40. PubMed ID: 22434215 [TBL] [Abstract][Full Text] [Related]
8. Responsiveness to distracting stimuli, though increased in Parkinson's disease, is decreased in asymptomatic PINK1 and Parkin mutation carriers. Verleger R; Hagenah J; Weiss M; Ewers T; Heberlein I; Pramstaller PP; Siebner HR; Klein C Neuropsychologia; 2010 Jan; 48(2):467-76. PubMed ID: 19822161 [TBL] [Abstract][Full Text] [Related]
9. Abnormal excitability of premotor-motor connections in de novo Parkinson's disease. Buhmann C; Gorsler A; Bäumer T; Hidding U; Demiralay C; Hinkelmann K; Weiller C; Siebner HR; Münchau A Brain; 2004 Dec; 127(Pt 12):2732-46. PubMed ID: 15509619 [TBL] [Abstract][Full Text] [Related]
10. [Molecular genetics of PINK1]. Funayama M; Hattori N Brain Nerve; 2007 Aug; 59(8):831-8. PubMed ID: 17713119 [TBL] [Abstract][Full Text] [Related]
11. Motor reorganization in asymptomatic carriers of a single mutant Parkin allele: a human model for presymptomatic parkinsonism. Buhmann C; Binkofski F; Klein C; Büchel C; van Eimeren T; Erdmann C; Hedrich K; Kasten M; Hagenah J; Deuschl G; Pramstaller PP; Siebner HR Brain; 2005 Oct; 128(Pt 10):2281-90. PubMed ID: 15947065 [TBL] [Abstract][Full Text] [Related]
12. Nigrostriatal dysfunction in homozygous and heterozygous parkin gene carriers: an 18F-dopa PET progression study. Pavese N; Khan NL; Scherfler C; Cohen L; Brooks DJ; Wood NW; Bhatia KP; Quinn NP; Lees AJ; Piccini P Mov Disord; 2009 Nov; 24(15):2260-6. PubMed ID: 19845000 [TBL] [Abstract][Full Text] [Related]
13. Mapping preclinical compensation in Parkinson's disease: an imaging genomics approach. van Nuenen BF; van Eimeren T; van der Vegt JP; Buhmann C; Klein C; Bloem BR; Siebner HR Mov Disord; 2009; 24 Suppl 2():S703-10. PubMed ID: 19877238 [TBL] [Abstract][Full Text] [Related]
14. Bilateral subthalamic stimulation in Parkin and PINK1 parkinsonism. Moro E; Volkmann J; König IR; Winkler S; Hiller A; Hassin-Baer S; Herzog J; Schnitzler A; Lohmann K; Pinsker MO; Voges J; Djarmatic A; Seibler P; Lozano AM; Rogaeva E; Lang AE; Deuschl G; Klein C Neurology; 2008 Apr; 70(14):1186-91. PubMed ID: 18378882 [TBL] [Abstract][Full Text] [Related]
15. Deciphering the role of heterozygous mutations in genes associated with parkinsonism. Klein C; Lohmann-Hedrich K; Rogaeva E; Schlossmacher MG; Lang AE Lancet Neurol; 2007 Jul; 6(7):652-62. PubMed ID: 17582365 [TBL] [Abstract][Full Text] [Related]
16. Premotor-motor excitability is altered in dopa-responsive dystonia. Weissbach A; Bäumer T; Brüggemann N; Tadic V; Zittel S; Cheng B; Thomalla G; Klein C; Münchau A Mov Disord; 2015 Oct; 30(12):1705-9. PubMed ID: 26230973 [TBL] [Abstract][Full Text] [Related]
17. Mutation analysis of the parkin and PINK1 genes in American Caucasian early-onset Parkinson disease families. Deng H; Le W; Shahed J; Xie W; Jankovic J Neurosci Lett; 2008 Jan; 430(1):18-22. PubMed ID: 18068301 [TBL] [Abstract][Full Text] [Related]
18. Familial Parkinsonism with digenic parkin and PINK1 mutations. Funayama M; Li Y; Tsoi TH; Lam CW; Ohi T; Yazawa S; Uyama E; Djaldetti R; Melamed E; Yoshino H; Imamichi Y; Takashima H; Nishioka K; Sato K; Tomiyama H; Kubo S; Mizuno Y; Hattori N Mov Disord; 2008 Jul; 23(10):1461-5. PubMed ID: 18546294 [TBL] [Abstract][Full Text] [Related]
19. Motor cortex excitability in seizure-free STX1B mutation carriers with a history of epilepsy and febrile seizures. Stefanou MI; Desideri D; Marquetand J; Belardinelli P; Zrenner C; Lerche H; Ziemann U Clin Neurophysiol; 2017 Dec; 128(12):2503-2509. PubMed ID: 29101845 [TBL] [Abstract][Full Text] [Related]
20. Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. Ibáñez P; Lesage S; Lohmann E; Thobois S; De Michele G; Borg M; Agid Y; Dürr A; Brice A; Brain; 2006 Mar; 129(Pt 3):686-94. PubMed ID: 16401616 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]