Genetic variation at the tau locus and clinical syndromes associated with progressive supranuclear palsyWILLIAMS, David R; PITTMAN, Alan M; REVESZ, Tamas et al.Movement disorders. 2007, Vol 22, Num 6, pp 895-897, issn 0885-3185, 3 p.Article

Pallidopyramidal Disease: A Misnomer?HORSTINK, Martin W. I. M; DEKKER, Marieke C; MONTAGNA, Pasquale et al.Movement disorders. 2010, Vol 25, Num 9, pp 1109-1115, issn 0885-3185, 7 p.Article

DJ-1, PINK 1, and Their Effects on Mitochondrial PathwaysCOOKSON, Mark R.Movement disorders. 2010, Vol 25, Num 3, issn 0885-3185, S44-S48, SUP1Conference Paper

Neuropsychiatric and cognitive features in autosomal-recessive early parkinsonism due to PINK1 mutationsEPHRATY, Lilach; PORAT, Omer; ISRAELI, David et al.Movement disorders. 2007, Vol 22, Num 4, pp 566-569, issn 0885-3185, 4 p.Article

PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonismCRISCUOLO, Chiara; VOLPE, Giampiero; DE MICHELE, Giuseppe et al.Movement disorders. 2006, Vol 21, Num 8, pp 1265-1267, issn 0885-3185, 3 p.Article

Frequency of movement disorders in an ethiopian university practiceBOWER, James H; TESHOME, Mesfin; MELAKU, Zenebe et al.Movement disorders. 2005, Vol 20, Num 9, pp 1209-1213, issn 0885-3185, 5 p.Article

C9orf72 repeat expansions are a rare genetic cause of parkinsonismLESAGE, Suzanne; LE BER, Isabelle; ROULEAU, Guy A et al.Brain. 2013, Vol 136, pp 385-391, issn 0006-8950, 7 p., 2Article

Movement disorder emergenciesPOSTON, Kathleen L; FRUCHT, Steven J.Journal of neurology. 2008, Vol 255, pp 2-13, issn 0340-5354, 12 p., SUP4Conference Paper

Pathological tau burden and distribution distinguishes progressive supranuclear palsy-parkinsonism from Richardson's syndromeWILLIAMS, David R; HOLTON, Janice L; STRAND, Catherine et al.Brain. 2007, Vol 130, pp 1566-1576, issn 0006-8950, 11 p., 6Article

Convulsive and postural effects of lesioning the mid-substantia nigra pars reticulata in naïve and 6-hydroxydopamine lesioned ratsHENDERSON, Jasmine M; WATSON, Sophie H.Brain research bulletin. 2003, Vol 60, Num 1-2, pp 179-185, issn 0361-9230, 7 p.Article

Non-motor symptoms in atypical and secondary parkinsonism: the PRIAMO studyCOLOSIMO, Carlo; MORGANTE, Letterio; GAGLIO, Rosa M et al.Journal of neurology. 2010, Vol 257, Num 1, pp 5-14, issn 0340-5354, 10 p.Article

Striatal dopamine function in a family with multiple SCA-3 phenotypesCUBO, Esther; DIEZ LOPEZ, Mateo; CEBERIO, Jon Infante et al.Journal of neurology. 2011, Vol 258, Num 2, pp 308-310, issn 0340-5354, 3 p.Article

Therapeutic strategies in multiple system atrophyWENNING, Gregor K; GESER, Felix; POEWE, Werner et al.Movement disorders. 2005, Vol 20, pp S67-S76, issn 0885-3185, SUP12Conference Paper

Geographical Variation of Medicated Parkinsonism in Finland During 1995 to 2000HAVULINNA, Aki S; TIENARI, Pentti J; MARTTILA, Reijo J et al.Movement disorders. 2008, Vol 23, Num 7, pp 1024-1031, issn 0885-3185, 8 p.Article

G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophyOZELIUS, Laurie J; FOROUD, Tatiana; JANKOVIC, Joseph et al.Movement disorders. 2007, Vol 22, Num 4, pp 546-549, issn 0885-3185, 4 p.Article

Assessment of Quality of Life with the Multiple System Atrophy Health-Related Quality of Life ScaleMEISSNER, Wassilios G; FOUBERT-SAMIER, Alexandra; DUPOUY, Sandrine et al.Movement disorders. 2012, Vol 27, Num 12, pp 1574-1577, issn 0885-3185, 4 p.Article

Shunt-responsive parkinsonism and reversible white matter lesions in patients with idiopathic NPHAKIGUCHI, Ichiro; ISHII, Mitsuaki; WATANABE, Yuko et al.Journal of neurology. 2008, Vol 255, Num 9, pp 1392-1399, issn 0340-5354, 8 p.Article

Clinical, imaging and pathological correlates of a hereditary deficit in verb and action processingBAK, Thomas H; YANCOPOULOU, Despina; NESTOR, Peter J et al.Brain. 2006, Vol 129, pp 321-332, issn 0006-8950, 12 p., 2Article

Anaesthesia for deep brain stimulation and in patients with implanted neurostimulator devicesPOON, C. C. M; IRWIN, M. G.British journal of anaesthesia. 2009, Vol 103, Num 2, pp 152-165, issn 0007-0912, 14 p.Article

Parkin mutations are frequent in patients with isolated early-onset parkinsonismPERIQUET, Magali; LATOUCHE, Morwena; BARONE, Paolo et al.Brain. 2003, Vol 126, pp 1271-1278, issn 0006-8950, 8 p., 6Article

The clinical features of pathologically confirmed vascular ParkinsonismGEORGE GLASS, Philip; LEES, Andrew J; BACELLAR, Aroldo et al.Journal of neurology, neurosurgery and psychiatry. 2012, Vol 83, Num 10, pp 1027-1029, issn 0022-3050, 3 p.Article

Levodopa-Responsive Parkinsonism in Probable Extrapontine Myelinolysis of the MesencephalonTOFT, Mathias; DIETRICHS, Espen.Movement disorders. 2011, Vol 26, Num 12, pp 2180-2181, issn 0885-3185, 2 p.Article

Neuronal Intranuclear Inclusion Disease Presenting as Juvenile ParkinsonismWILTSHIRE, Katie M; DUNHAM, Christopher; REID, Stuart et al.Canadian journal of neurological sciences. 2010, Vol 37, Num 2, pp 213-218, issn 0317-1671, 6 p.Article

Rapidly progressive behavioral changes and parkinsonism in a 68-year-old manKLEINER-FISMAN, Galit; LANG, Anthony E; BERGERON, Catherine et al.Movement disorders. 2004, Vol 19, Num 5, pp 534-543, issn 0885-3185, 10 p.Article

Anomalies of asymmetry of clinical signs in parkinsonismTOTH, Cory; RAJPUT, Michelle; RAJPUT, Ali H et al.Movement disorders. 2004, Vol 19, Num 2, pp 151-157, issn 0885-3185, 7 p.Article