Dystonia updateBRESSMAN, Susan B.Clinical neuropharmacology. 2000, Vol 23, Num 5, pp 239-251, issn 0362-5664Article

Milestones in DystoniaOZELIUS, Laurie J; LUBARR, Naomi; BRESSMAN, Susan B et al.Movement disorders. 2011, Vol 26, Num 6, pp 1106-1126, issn 0885-3185, 21 p.Article

Diagnosis and Referral Delay in Women With Parkinson's DiseaseSAUNDERS-PULLMAN, Rachel; CUILING WANG; STANLEY, Kaili et al.Gender medicine. 2011, Vol 8, Num 3, pp 209-217, issn 1550-8579, 9 p.Article

Inclusion and Exclusion Criteria for DBS in DystoniaBRONTE-STEWART, Helen; TAIRA, Takaomi; VALLDEORIOLA, Francesc et al.Movement disorders. 2011, Vol 26, Num 7, issn 0885-3185, S5-S16, SUPArticle

Increased frequency of the LRRK2 G2019S mutation in an elderly Ashkenazi Jewish population is not associated with dementiaSAUNDERS-PULLMAN, Rachel; LIPTON, Richard B; SENTHIL, Geetha et al.Neuroscience letters. 2006, Vol 402, Num 1-2, pp 92-96, issn 0304-3940, 5 p.Article

Lower cognitive performance in healthy G₂019S LRRK2 mutation carriersTHALER, Avner; MIRELMAN, Anat; GUREVICH, Tanya et al.Neurology. 2012, Vol 79, Num 10, pp 1027-1032, issn 0028-3878, 6 p.Article

Pre-operative Evaluations for DBS in DystoniaTHOBOIS, Stephane; TAIRA, Takaomi; COMELLA, Cynthia et al.Movement disorders. 2011, Vol 26, Num 7, issn 0885-3185, S17-S26, SUPArticle

Microstructural white matter changes in carriers of the DYT1 gene mutationCARBON, Maren; KINGSLEY, Peter B; SU, Sherwin et al.Annals of neurology. 2004, Vol 56, Num 2, pp 283-286, issn 0364-5134, 4 p.Article

Intragenic cis and trans modification of genetic susceptibility in DYT1 torsion dystoniaRISCH, Neil J; BRESSMAN, Susan B; SENTHIL, Geetha et al.American journal of human genetics. 2007, Vol 80, Num 6, pp 1188-1193, issn 0002-9297, 6 p.Article

Occupation and Risk of Parkinsonism: A Multicenter Case-Control StudyTANNER, Caroline M; WEBSTER ROSS, G; BHUDHIKANOK, Grace S et al.Archives of neurology (Chicago). 2009, Vol 66, Num 9, pp 1106-1113, issn 0003-9942, 8 p.Article

Phenotypic Spectrum and Sex Effects in Eleven Myoclonus-Dystonia Families with ε-Sarcoglycan MutationsRAYMOND, Deborah; SAUNDERS-PULLMAN, Rachel; JENNINGS, Danna et al.Movement disorders. 2008, Vol 23, Num 4, pp 588-592, issn 0885-3185, 5 p.Article

Validity of Spiral Analysis in Early Parkinson's DiseaseSAUNDERS-PULLMAN, Rachel; DERBY, Carol; PULLMAN, Seth L et al.Movement disorders. 2008, Vol 23, Num 4, pp 531-537, issn 0885-3185, 7 p.Article

Impaired sequence learning in carriers of the DYT1 dystonia mutationGHILARDI, Maria-Felice; CARBON, Maren; SILVESTRI, Giulia et al.Annals of neurology. 2003, Vol 54, Num 1, pp 102-109, issn 0364-5134, 8 p.Article

Microstructural White Matter Changes in Primary Torsion DystoniaCARBON, Maren; KINGSLEY, Peter B; CHENGKE TANG et al.Movement disorders. 2008, Vol 23, Num 2, pp 234-239, issn 0885-3185, 6 p.Article

Molecular diagnosis of inherited movement disorders. Movement disorders Society Task Force on Molecular DiagnosisGASSER, Thomas; BRESSMAN, Susan; DÜRR, Alexandra et al.Movement disorders. 2003, Vol 18, Num 1, pp 3-18, issn 0885-3185, 16 p.Article

Increased cerebellar activation during sequence learning in DYTI carriers : an equiperformance studyCARBON, Maren; GHILARDI, Maria Felice; ARGYELAN, Miklos et al.Brain. 2008, Vol 131, pp 146-154, issn 0006-8950, 9 p., 1Article

Head Injury, Alpha-Synuclein Rep1, and Parkinson's DiseaseGOLDMAN, Samuel M; KAMEL, Freya; BRESSMAN, Susan et al.Annals of neurology. 2012, Vol 71, Num 1, pp 40-48, issn 0364-5134, 9 p.Article

Cerebral pathological and compensatory mechanisms in the premotor phase of leucine-rich repeat kinase 2 parkinsonismNUENEN, Bart F. L. Van; HELMICH, Rick C; VAN DE WARRENBURG, Bart P. C et al.Brain. 2012, Vol 135, pp 3687-3698, issn 0006-8950, 12 p., 12Article

Predictors of Parkin Mutations in Early-Onset Parkinson Disease: The Consortium on Risk for Early-Onset Parkinson Disease StudyMARDER, Karen S; TANG, Ming X; BRESSMAN, Susan et al.Archives of neurology (Chicago). 2010, Vol 67, Num 6, pp 731-738, issn 0003-9942, 8 p.Article

Impaired sequence learning in dystonia mutation carriers: a genotypic effectCARBON, Maren; ARGYELAN, Miklos; FELICE GHILARDI, Maria et al.Brain. 2011, Vol 134, pp 1416-1427, issn 0006-8950, 12 p., 5Article

Mood and Cognition in Leucine-Rich Repeat Kinase 2 G2019S Parkinson's DiseaseSHANKER, Vicki; GROVES, Mark; HEIMAN, Gary et al.Movement disorders. 2011, Vol 26, Num 10, pp 1875-1880, issn 0885-3185, 6 p.Article

Motor Phenotype of LRRK2 G2019S Carriers in Early-Onset Parkinson DiseaseALCALAY, Roy N; MEJIA-SANTANA, Helen; JENNINGS, Danna et al.Archives of neurology (Chicago). 2009, Vol 66, Num 12, pp 1517-1522, issn 0003-9942, 6 p.Article

Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the amish-mennonitesSAUNDERS-PULLMAN, Rachel; RAYMOND, Deborah; TAGLIATI, Michele et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 18, pp 2098-2105, issn 1552-4825, 8 p.Article

A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathyTHYAGARAJAN, Dominic; BRESSMAN, Susan; BRUNO, Claudio et al.Annals of neurology. 2000, Vol 48, Num 5, pp 730-736, issn 0364-5134Article

Metabolic changes in DYT11 myoclonus-dystoniaCARBON, Maren; RAYMOND, Deborah; OZELIUS, Laurie et al.Neurology. 2013, Vol 80, Num 4, pp 385-391, issn 0028-3878, 7 p.Article