Genetic and clinical features of primary torsion dystonia

di Ozelius, Laurie J., Bressman, Susan B.
Pubblicazione 2010

Primary Dystonia: Moribund or Viable?

di Bressman, Susan B., Saunders-Pullman, Rachel
Pubblicazione 2013

Diagnosis and Referral Delay in Women With Parkinson’s Disease

di Saunders-Pullman, Rachel, Wang, Cuiling, Stanley, Kaili, Bressman, Susan B.
Pubblicazione 2011

Disruption of network for visual perception of natural motion in primary dystonia

di Fujita, Koji, Sako, Wataru, Vo, An, Bressman, Susan B., Eidelberg, David
Pubblicato in Hum Brain Mapp (2017)

Intragenic Cis and Trans Modification of Genetic Susceptibility in DYT1 Torsion Dystonia

di Risch, Neil J. , Bressman, Susan B. , Senthil, Geetha , Ozelius, Laurie J. 
Pubblicazione 2007

Functional electrical stimulation for the treatment of lower extremity dystonia

di Barrett, Matthew J., Levy, Oren A., Fahn, Stanley, O'Dell, Michael, Bressman, Susan B.
Pubblicazione 2011

Increased cerebellar activation during sequence learning in DYT1 carriers: an equiperformance study

di Carbon, Maren, Ghilardi, Maria Felice, Argyelan, Miklos, Dhawan, Vijay, Bressman, Susan B., Eidelberg, David
Pubblicato in Brain (2007)

Thalamocortical Connectivity Correlates with Phenotypic Variability in Dystonia

di Vo, An, Sako, Wataru, Niethammer, Martin, Carbon, Maren, Bressman, Susan B., Uluğ, Aziz M., Eidelberg, David
Pubblicato in Cereb Cortex (2015)

DYT1 dystonia increases risk taking in humans

di Arkadir, David, Radulescu, Angela, Raymond, Deborah, Lubarr, Naomi, Bressman, Susan B, Mazzoni, Pietro, Niv, Yael
Pubblicato in eLife (2016)

THAP1 (DYT6) mutations in early-onset primary dystonia

di Bressman, Susan B., Raymond, Deborah, Fuchs, Tania, Heiman, Gary A., Ozelius, Laurie J., Saunders-Pullman, Rachel
Pubblicazione 2009

Benign SLC39A14 Course of Dystonia‐Parkinsonism Secondary to Inherited Manganese Accumulation

di Namnah, Montaser, Bauer, Max, Mor‐Shaked, Hagar, Bressman, Susan B., Raymond, Deborah, Ozelius, Laurie J., Arkadir, David
Pubblicato in Mov Disord Clin Pract (2020)

Obsessive-Compulsive Disorder is not a Clinical Manifestation of the DYT1 Dystonia Gene

di Heiman, Gary A., Ottman, Ruth, Saunders-Pullman, Rachel J., Ozelius, Laurie J., Risch, Neil J., Bressman, Susan B.
Pubblicazione 2007

Cerebellothalamocortical Connectivity Regulates Penetrance in Dystonia

di Argyelan, Miklos, Carbon, Maren, Niethammer, Martin, Uluğ, Aziz M., Voss, Henning U., Bressman, Susan B., Dhawan, Vijay, Eidelberg, David
Pubblicazione 2009

Increased sensorimotor network activity in DYT1 dystonia: a functional imaging study

di Carbon, Maren, Argyelan, Miklos, Habeck, Christian, Ghilardi, M. Felice, Fitzpatrick, Toni, Dhawan, Vijay, Pourfar, Michael, Bressman, Susan B., Eidelberg, David
Pubblicazione 2010

Spatial Discrimination Threshold Abnormalities are not Detected in a Pilot Study of DYT6 Dystonia Mutation Carriers

di Deik, Andres F., O'Riordan, Sean, Luciano, Marta San, Shanker, Vicki L., Raymond, Deborah, Bressman, Susan B., Saunders-Pullman, Rachel
Pubblicazione 2012

Heterogeneity in primary dystonia: lessons from THAP1, GNAL and TOR1A in Amish-Mennonites

di Saunders-Pullman, Rachel, Fuchs, Tania, San Luciano, Marta, Raymond, Deborah, Brashear, Alison, Ortega, Robert, Deik, Andres, Ozelius, Laurie J., Bressman, Susan B.
Pubblicazione 2014

The visual perception of natural motion: abnormal task-related neural activity in DYT1 dystonia

di Sako, Wataru, Fujita, Koji, Vo, An, Rucker, Janet C., Rizzo, John-Ross, Niethammer, Martin, Carbon, Maren, Bressman, Susan B., Uluğ, Aziz M., Eidelberg, David
Pubblicato in Brain (2015)

LRRK2 and GBA Variants Exert Distinct Influences on Parkinson’s Disease-Specific Metabolic Networks

di Schindlbeck, Katharina A, Vo, An, Nguyen, Nha, Tang, Chris C, Niethammer, Martin, Dhawan, Vijay, Brandt, Vicky, Saunders-Pullman, Rachel, Bressman, Susan B, Eidelberg, David
Pubblicato in Cereb Cortex (2020)

Substantia Nigra Hyperechogenicity in DYT6 Dystonia: A Pilot Study

di Saunders-Pullman, Rachel, Stanley, Kaili, Brüggemann, Norbert, Raymond, Deborah, Luciano, Marta San, Wang, Cuiling, Klein, Christine, Lubarr, Naomi, Ozelius, Laurie, Bressman, Susan B, Hagenah, Johann
Pubblicazione 2010

Clinical Expression of LRRK2 G2019S Mutations in the Elderly

di Luciano, Marta San, Lipton, Richard B., Wang, Cuiling, Katz, Mindy, Zimmerman, Molly E., Sanders, Amy E., Ozelius, Laurie J., Bressman, Susan B., Saunders-Pullman, Rachel
Pubblicazione 2010