Deep Brain Stimulation for the Treatment of Atypical ParkinsonismSHIH, Ludy C; TARSY, Daniel.Movement disorders. 2007, Vol 22, Num 15, pp 2149-2155, issn 0885-3185, 7 p.Article

Progression of parkinsonism in multiple system atrophySEPPI, Klaus; YEKHLEF, Farid; DIEM, Anja et al.Journal of neurology. 2005, Vol 252, Num 1, pp 91-96, issn 0340-5354, 6 p.Article

Olfactory Heterogeneity in LRRK2 Related ParkinsonismSILVEIRA-MORIYAMA, Laura; PUPI MUNHOZ, Renato; CHIEN, Hsin F et al.Movement disorders. 2010, Vol 25, Num 16, pp 2879-2883, issn 0885-3185, 5 p.Article

Tau gene mutations and their effectsGOEDERT, Michel.Movement disorders. 2005, Vol 20, pp S45-S52, issn 0885-3185, SUP12Conference Paper

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

Clinical Spectrum of Kufor-Rakeb Syndrome in the Chilean Kindred with ATP13A2 MutationsBEHRENS, Maria I; BRÜGGEMANN, Norbert; HAHNEN, Eric et al.Movement disorders. 2010, Vol 25, Num 12, pp 1929-1937, issn 0885-3185, 9 p.Article

Smoking-responsive juvenile-onset ParkinsonismAYHAN HANAGASI, Hasmet; LEES, Andrew; JOHNSON, Janel O et al.Movement disorders. 2007, Vol 22, Num 1, pp 115-118, issn 0885-3185, 4 p.Article

Atypical Parkinsonism and Cerebrotendinous Xanthomatosis: Report of a Family With Corticobasal Syndrome and a Literature ReviewRUBIO-AGUSTI, Ignacio; KOJOVIC, Maja; EDWARDS, Mark J et al.Movement disorders. 2012, Vol 27, Num 14, pp 1769-1774, issn 0885-3185, 6 p.Article

Early-Onset L-dopa-Responsive Parkinsonism with Pyramidal Signs Due to ATP13A2, PLA2G6, FBX07 and Spatacsin MutationsPAISAN-RUIZ, Coro; GUEVARA, Rocio; SINGLETON, Andrew B et al.Movement disorders. 2010, Vol 25, Num 12, pp 1791-1800, issn 0885-3185, 10 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

The differential diagnoses of parkinsonism: Findings from a cohort of 1528 patients and a 10 years comparison in tertiary movement disorders clinicsMUNHOZ, Renato P; WERNECK, Lineu C; TEIVE, Hélio A. G et al.Clinical neurology and neurosurgery (Dutch-Flemish ed.). 2010, Vol 112, Num 5, pp 431-435, issn 0303-8467, 5 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

Atypical Parkinsonism combining α-synuclein inclusions and polyglucosan body diseaseKRIM, Elsa; VITAL, Anne; MACIA, Frederic et al.Movement disorders. 2005, Vol 20, Num 2, pp 200-204, issn 0885-3185, 5 p.Article

Genetic analysis of parkin co-regulated gene (PACRG) in patients with early-onset parkinsonismHAO DENG; LE, Wei-Dong; XIE, Wen-Jie et al.Neuroscience letters. 2005, Vol 382, Num 3, pp 297-299, issn 0304-3940, 3 p.Article

Atypical unclassifiable parkinsonism on guadeloupe : An environmental toxic hypothesisCAPARROS-LEFEBVRE, Dominique; LEES, Andrew J.Movement disorders. 2005, Vol 20, pp S114-S118, issn 0885-3185, SUP12Conference Paper

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