Works matching AU Susan B. Bressman

Results: 64

Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease Progression.

Published in:

JAMA Network Open, 2021, v. 4, n. 4, p. e215845, doi. 10.1001/jamanetworkopen.2021.5845

By:

Ortega, Roberto A.;
Wang, Cuiling;
Raymond, Deborah;
Bryant, Nicole;
Scherzer, Clemens R.;
Thaler, Avner;
Alcalay, Roy N.;
West, Andrew B.;
Mirelman, Anat;
Kuras, Yuliya;
Marder, Karen S.;
Giladi, Nir;
Ozelius, Laurie J.;
Bressman, Susan B.;
Saunders-Pullman, Rachel

Publication type:

Article

Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism.

Published in:

Movement Disorders, 2023, v. 38, n. 4, p. 714, doi. 10.1002/mds.29353

By:

Ortega, Roberto A.;
Bressman, Susan B.;
Raymond, Deborah;
Ozelius, Laurie J.;
Wang, Cuiling;
Bennett, Steffany A.L.;
Saunders‐Pullman, Rachel

Publication type:

Article

Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism.

Published in:

Movement Disorders, 2022, v. 37, n. 11, p. 2217, doi. 10.1002/mds.29197

By:

Ortega, Roberto A.;
Bressman, Susan B.;
Raymond, Deborah;
Ozelius, Laurie J.;
Katsnelson, Viktoriya;
Leaver, Katherine;
Swan, Matthew C.;
Shanker, Vicki;
Miravite, Joan;
Wang, Cuiling;
Bennett, Steffany A.L.;
Saunders‐Pullman, Rachel

Publication type:

Article

Assessment of Glucocerebrosidase Enzyme Activity in Parkinson Disease Using Multiple Approaches.

Published in:

Movement Disorders, 2022, v. 37, n. 3, p. 655, doi. 10.1002/mds.28951

By:

Ortega, Roberto A.;
Bodamer, Olaf;
Peake, Roy W.A.;
Raymond, Deborah;
Bressman, Susan B.;
Saunders‐Pullman, Rachel

Publication type:

Article

Deep Brain Stimulation in Isolated Dystonia With a GNAL Mutation.

Published in:

2019

By:

Sarva, Harini;
Trosch, Richard;
Kiss, Zelma H.T.;
Furtado, Sarah;
Luciano, Marta San;
Glickman, Amanda;
Raymond, Deborah;
Ozelius, Laurie J.;
Bressman, Susan B.;
Saunders‐Pullman, Rachel;
Saunders-Pullman, Rachel

Publication type:

Letter

Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers.

Published in:

2018

By:

Mirelman, Anat;
Saunders‐Pullman, Rachel;
Alcalay, Roy N.;
Shustak, Shiran;
Thaler, Avner;
Gurevich, Tanya;
Raymond, Deborah;
Mejia‐Santana, Helen;
Orbe Reilly, Martha;
Ozelius, Laurie;
Clark, Lorraine;
Gana‐Weisz, Mali;
Bar‐Shira, Anat;
Orr‐Utreger, Avi;
Bressman, Susan B.;
Marder, Karen;
Giladi, Nir;
the AJ LRRK2 Consortium;
Saunders-Pullman, Rachel;
Mejia-Santana, Helen

Publication type:

journal article

Arm swing as a potential new prodromal marker of Parkinson's disease.

Published in:

2016

By:

Mirelman, Anat;
Bernad‐Elazari, Hagar;
Thaler, Avner;
Giladi‐Yacobi, Eytan;
Gurevich, Tanya;
Gana‐Weisz, Mali;
Saunders‐Pullman, Rachel;
Raymond, Deborah;
Doan, Nancy;
Bressman, Susan B.;
Marder, Karen S.;
Alcalay, Roy N.;
Rao, Ashwini K.;
Berg, Daniela;
Brockmann, Kathrin;
Aasly, Jan;
Waro, Bjørg Johanne;
Tolosa, Eduardo;
Vilas, Dolores;
Pont‐Sunyer, Claustre

Publication type:

journal article

REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers.

Published in:

2015

By:

Saunders‐Pullman, Rachel;
Alcalay, Roy N.;
Mirelman, Anat;
Wang, Cuiling;
Luciano, Marta San;
Ortega, Roberto A.;
Glickman, Amanda;
Raymond, Deborah;
Mejia‐Santana, Helen;
Doan, Nancy;
Johannes, Brooke;
Yasinovsky, Kira;
Ozelius, Laurie;
Clark, Lorraine;
Orr‐Utreger, Avi;
Marder, Karen;
Giladi, Nir;
Bressman, Susan B.

Publication type:

journal article

Low-variance RNAs identify Parkinson's disease molecular signature in blood.

Published in:

Movement Disorders, 2015, v. 30, n. 6, p. 813, doi. 10.1002/mds.26205

By:

Chikina, Maria D.;
Gerald, Christophe P.;
Li, Xianting;
Ge, Yongchao;
Pincas, Hanna;
Nair, Venugopalan D.;
Wong, Aaron K.;
Krishnan, Arjun;
Troyanskaya, Olga G.;
Raymond, Deborah;
Saunders‐Pullman, Rachel;
Bressman, Susan B.;
Yue, Zhenyu;
Sealfon, Stuart C.

Publication type:

Article

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

Published in:

Movement Disorders, 2014, v. 29, n. 6, p. 812, doi. 10.1002/mds.25818

By:

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

Publication type:

Article

Reply: Dystonia after severe head injuries.

Published in:

Movement Disorders, 2014, v. 29, n. 4, p. 578, doi. 10.1002/mds.25861

By:

Albanese, Alberto;
Bhatia, Kailash;
Bressman, Susan B.;
DeLong, Mahlon R.;
Fahn, Stanley;
Fung, Victor S.C.;
Hallett, Mark;
Jankovic, Joseph;
Jinnah, H.A.;
Klein, Christine;
Lang, Anthony E.;
Mink, Jonathan W.;
Teller, Jan K.

Publication type:

Article

Phenomenology and classification of dystonia: A consensus update.

Published in:

Movement Disorders, 2013, v. 28, n. 7, p. 863, doi. 10.1002/mds.25475

By:

Albanese, Alberto;
Bhatia, Kailash;
Bressman, Susan B.;
DeLong, Mahlon R.;
Fahn, Stanley;
Fung, Victor S.C.;
Hallett, Mark;
Jankovic, Joseph;
Jinnah, Hyder A.;
Klein, Christine;
Lang, Anthony E.;
Mink, Jonathan W.;
Teller, Jan K.

Publication type:

Article

Primary dystonia: Moribund or viable.

Published in:

Movement Disorders, 2013, v. 28, n. 7, p. 906, doi. 10.1002/mds.25528

By:

Bressman, Susan B.;
Saunders-Pullman, Rachel

Publication type:

Article

LRRK2 G2019S mutations may be increased in Puerto Ricans.

Published in:

Movement Disorders, 2011, v. 26, n. 9, p. 1771, doi. 10.1002/mds.23632

By:

Saunders-Pullman, Rachel;
Cabassa, Jose;
San Luciano, Marta;
Stanley, Kaili;
Raymond, Deborah;
Ozelius, Laurie J.;
Bressman, Susan B.

Publication type:

Article

Milestones in dystonia.

Published in:

Movement Disorders, 2011, v. 26, n. 6, p. 1106, doi. 10.1002/mds.23775

By:

Ozelius, Laurie J.;
Lubarr, Naomi;
Bressman, Susan B.

Publication type:

Article

Phenotypic spectrum of musician's dystonia: A task-specific disorder?

Published in:

Movement Disorders, 2011, v. 26, n. 3, p. 546, doi. 10.1002/mds.23526

By:

Schmidt, Alexander;
Jabusch, Hans-Christian;
Altenmüller, Eckart;
Enders, Leonie;
Saunders-Pullman, Rachel;
Bressman, Susan B.;
Münchau, Alexander;
Klein, Christine;
Hagenah, Johann

Publication type:

Article

LRRK2 G2019S mutations are associated with an increased cancer risk in Parkinson disease.

Published in:

Movement Disorders, 2010, v. 25, n. 15, p. 2536, doi. 10.1002/mds.23314

By:

Saunders-Pullman, Rachel;
Barrett, Matthew J.;
Stanley, Kaili M.;
Luciano, Marta San;
Shanker, Vicki;
Severt, Lawrence;
Hunt, Ann;
Raymond, Deborah;
Ozelius, Laurie J.;
Bressman, Susan B.

Publication type:

Article

Clinical expression of LRRK2 G2019S mutations in the elderly.

Published in:

Movement Disorders, 2010, v. 25, n. 15, p. 2571, doi. 10.1002/mds.23330

By:

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

Publication type:

Article

Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia.

Published in:

Movement Disorders, 2010, v. 25, n. 13, p. 2183, doi. 10.1002/mds.23225

By:

Sharma, Nutan;
Franco, Ramon A.;
Kuster, John K.;
Mitchell, Adele A.;
Fuchs, Tania;
Saunders-Pullman, Rachel;
Raymond, Deborah;
Brin, Mitchell F.;
Blitzer, Andrew;
Bressman, Susan B.;
Ozelius, Laurie J.

Publication type:

Article

Distribution, type, and origin of Parkin mutations: Review and case studies.

Published in:

Movement Disorders, 2004, v. 19, n. 10, p. 1146, doi. 10.1002/mds.20234

By:

Hedrich, Katja;
Eskelson, Cordula;
Wilmot, Beth;
Marder, Karen;
Harris, Juliette;
Garrels, Jennifer;
Meija-Santana, Helen;
Vieregge, Peter;
Jacobs, Helfried;
Bressman, Susan B.;
Lang, Anthony E.;
Kann, Martin;
Abbruzzese, Giovanni;
Martinelli, Paolo;
Schwinger, Eberhard;
Ozelius, Laurie J.;
Pramstaller, Peter P.;
Klein, Christine;
Kramer, Patricia

Publication type:

Article

Progression in the LRRK2-Asssociated Parkinson Disease Population.

Published in:

JAMA Neurology, 2018, v. 75, n. 3, p. 312, doi. 10.1001/jamaneurol.2017.4019

By:

Saunders-Pullman, Rachel;
Mirelman, Anat;
Alcalay, Roy N.;
Wang, Cuiling;
Ortega, Roberto A.;
Raymond, Deborah;
Mejia-Santana, Helen;
Orbe-Reilly, Martha;
Johannes, Brooke A.;
Thaler, Avner;
Ozelius, Laurie;
Orr-Urtreger, Avi;
Marder, Karen S.;
Giladi, Nir;
Bressman, Susan B.

Publication type:

Article

Complex and Dynamic Chromosomal Rearrangements in a Family With Seemingly Non-Mendelian Inheritance of Dopa-Responsive Dystonia.

Published in:

JAMA Neurology, 2017, v. 74, n. 7, p. 806, doi. 10.1001/jamaneurol.2017.0666

By:

Lohmann, Katja;
Redin, Claire;
Tönnies, Holger;
Bressman, Susan B.;
Subero, Jose Ignacio Martin;
Wiegers, Karin;
Hinrichs, Frauke;
Hellenbroich, Yorck;
Rakovic, Aleksandar;
Raymond, Deborah;
Ozelius, Laurie J.;
Schwinger, Eberhard;
Siebert, Reiner;
Talkowski, Michael E.;
Saunders-Pullman, Rachel;
Klein, Christine

Publication type:

Article

Cognitive and Motor Function in Long-Duration PARKIN-Associated Parkinson Disease.

Published in:

JAMA Neurology, 2014, v. 71, n. 1, p. 62, doi. 10.1001/jamaneurol.2013.4498

By:

Alcalay, Roy N.;
Caccappolo, Elise;
Mejia-Santana, Helen;
Ming Xin Tang;
Rosado, Llency;
Reilly, Martha Orbe;
Ruiz, Diana;
Louis, Elan D.;
Comella, Cynthia L.;
Nance, Martha A.;
Bressman, Susan B.;
Scott, William K.;
Tanner, Caroline M.;
Mickel, Susan H.;
Waters, Cheryl H.;
Fahn, Stanley;
Cote, Lucien J.;
Frucht, Steven J.;
Ford, Blair;
Rezak, Michael

Publication type:

Article

Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia.

Published in:

Nature Genetics, 2009, v. 41, n. 3, p. 286, doi. 10.1038/ng.304

By:

Fuchs, Tania;
Gavarini, Sophie;
Saunders-Pullman, Rachel;
Raymond, Deborah;
Ehrlich, Michelle E.;
Bressman, Susan B.;
Ozelius, Laurie J.

Publication type:

Article

Digitized Spiral Drawing: A Possible Biomarker for Early Parkinson’s Disease.

Published in:

PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0162799

By:

San Luciano, Marta;
Wang, Cuiling;
Ortega, Roberto A.;
Yu, Qiping;
Boschung, Sarah;
Soto-Valencia, Jeannie;
Bressman, Susan B.;
Lipton, Richard B.;
Pullman, Seth;
Saunders-Pullman, Rachel

Publication type:

Article

Mutations in GNAL cause primary torsion dystonia.

Published in:

Nature Genetics, 2013, v. 45, n. 1, p. 88, doi. 10.1038/ng.2496

By:

Fuchs, Tania;
Saunders-Pullman, Rachel;
Masuho, Ikuo;
Luciano, Marta San;
Raymond, Deborah;
Factor, Stewart;
Lang, Anthony E;
Liang, Tsao-Wei;
Trosch, Richard M;
White, Sierra;
Ainehsazan, Edmond;
Hervé, Denis;
Sharma, Nutan;
Ehrlich, Michelle E;
Martemyanov, Kirill A;
Bressman, Susan B;
Ozelius, Laurie J

Publication type:

Article

Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?

Published in:

Annals of Clinical & Translational Neurology, 2014, v. 1, n. 9, p. 670, doi. 10.1002/acn3.95

By:

Saunders‐Pullman, Rachel;
Mirelman, Anat;
Wang, Cuiling;
Alcalay, Roy N.;
San Luciano, Marta;
Ortega, Robert;
Raymond, Deborah;
Mejia‐Santana, Helen;
Ozelius, Laurie;
Clark, Lorraine;
Orr‐Utreger, Avi;
Marder, Karen;
Giladi, Nir;
Bressman, Susan B.

Publication type:

Article

De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 7, p. 1133, doi. 10.1093/hmg/7.7.1133

By:

Klein, Christine;
Brin, Mitchell F.;
de Leon, Deborah;
Limborska, Svetlana A.;
Ivanova‐Smolenskaya, Irina A.;
Bressman, Susan B.;
Friedman, Andrzej;
Markova, Elena D.;
Risch, Neil J.;
Breakefield, Xandra O.;
Ozelius, Laurie J.

Publication type:

Article

Multiple sclerosis in LRRK2 G2019S Parkinson's disease and isolated nigral degeneration in a homozygous variant carrier.

Published in:

Frontiers in Neurology, 2024, p. 01, doi. 10.3389/fneur.2024.1450654

By:

Wise, Adina;
Ortega, Roberto A.;
Raymond, Deborah;
Cervera, Alessandra;
Thorn, Emma;
Leaver, Katherine;
Russell, David S.;
Bressman, Susan B.;
Crary, John F.;
Saunders-Pullman, Rachel

Publication type:

Article

Research priorities in spasmodic dysphonia

Published in:

Otolaryngology-Head & Neck Surgery, 2008, v. 139, n. 4, p. 495, doi. 10.1016/j.otohns.2008.05.624

By:

Ludlow, Christy L.;
Adler, Charles H.;
Berke, Gerald S.;
Bielamowicz, Steven A.;
Blitzer, Andrew;
Bressman, Susan B.;
Hallett, Mark;
Jinnah, H.A.;
Juergens, Uwe;
Martin, Sandra B.;
Perlmutter, Joel S.;
Sapienza, Christine;
Singleton, Andrew;
Tanner, Caroline M.;
Woodson, Gayle E.

Publication type:

Article

Cerebellothalamocortical Connectivity Regulates Penetrance in Dystonia.

Published in:

Journal of Neuroscience, 2009, v. 29, n. 31, p. 9740, doi. 10.1523/JNEUROSCI.2300-09.2009

By:

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

Publication type:

Article

The metabolic pathology of dopa‐responsive dystonia.

Published in:

Annals of Neurology, 2005, v. 57, n. 4, p. 596

By:

Kotaro Asanuma;
Yilong Ma;
Chaorui Huang;
Maren Carbon‐Correll;
Christine Edwards;
Deborah Raymond;
Susan B. Bressman;
James R. Moeller;
David Eidelberg

Publication type:

Article

The R98Q variation in DJ-1 represents a rare polymorphism.

Published in:

Annals of Neurology, 2004, v. 55, n. 1, p. 145

By:

Katja Hedrich;
Nora Schäfer;
Robert Hering;
Johann Hagenah;
Andrea J. Lanthaler;
Eberhard Schwinger;
Patricia L. Kramer;
Laurie J. Ozelius;
Susan B. Bressman;
Giovanni Abbruzzese;
Paolo Martinelli;
Vladimir Kostic;
Peter P. Pramstaller;
Peter Vieregge;
Olaf Riess

Publication type:

Article

Primary dystonia: Is abnormal functional brain architecture linked to genotype?

Published in:

Annals of Neurology, 2002, v. 52, n. 6, p. 853, doi. 10.1002/ana.10418

By:

Tros̆t, Maja;
Carbon, Maren;
Edwards, Christine;
Ma, Yilong;
Raymond, Deborah;
Mentis, Marc J.;
Moeller, James R.;
Bressman, Susan B.;
Eidelberg, David

Publication type:

Article

ε-sarcoglycan mutations found in combination with other dystonia gene mutations.

Published in:

Annals of Neurology, 2002, v. 52, n. 5, p. 675, doi. 10.1002/ana.10358

By:

Klein, Christine;
Liu, Liu;
Doheny, Dana;
Kock, Norman;
Müller, Birgitt;
De Carvalho Aguiar, Patricia;
Leung, Joanne;
De Leon, Deborah;
Bressman, Susan B.;
Silverman, Jeremy;
Smith, Christopher;
Danisi, Fabio;
Morrison, Chris;
Walker, Ruth H.;
Velickovic, Miodrag;
Schwinger, Eberhard;
Kramer, Patricia L.;
Breakefield, Xandra O.;
Brin, Mitchell F.;
Ozelius, Laurie J.

Publication type:

Article

Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31.

Published in:

1999

By:

Nygaard, Torbjoern G.;
Raymond, Deborah;
Chen, Caiping;
Nishino, Ichizo;
Greene, Paul E.;
Jennings, Danna;
Heiman, Gary A.;
Klein, Christine;
Saunders-Pullman, Rachel J.;
Kramer, Patricia;
Ozelius, Laurie J.;
Bressman, Susan B.;
Nygaard, T G;
Raymond, D;
Chen, C;
Nishino, I;
Greene, P E;
Jennings, D;
Heiman, G A;
Klein, C

Publication type:

journal article

Rapid-onset dystonia-parkinsonism: linkage to chromosome 19q13.

Published in:

1999

By:

Kramer, Patricia L.;
Mineta, Mari;
Klein, Christine;
Schilling, Karla;
De Leon, Deborah;
Farlow, Martin R.;
Breakefield, Xandra O.;
Bressman, Susan B.;
Dobyns, William B.;
Ozelius, Laurie J.;
Brashear, Allison;
Kramer, P L;
Mineta, M;
Klein, C;
Schilling, K;
de Leon, D;
Farlow, M R;
Breakefield, X O;
Bressman, S B;
Dobyns, W B

Publication type:

journal article

Functional brain networks in DYT1 dystonia.

Published in:

Annals of Neurology, 1998, v. 44, n. 3, p. 303, doi. 10.1002/ana.410440304

By:

Eidelberg, David;
Moeller, James R.;
Antonini, Angelo;
Kazumata, Ken;
Nakamura, Toshitaka;
Dhawan, Vijay;
Spetsieris, Phoebe;
DeLeon, Deborah;
Bressman, Susan B.;
Fahn, Stanley

Publication type:

Article

Dystonia in Ashkenazi Jews: Clinical characterization of a founder mutation.

Published in:

Annals of Neurology, 1994, v. 36, n. 5, p. 771, doi. 10.1002/ana.410360514

By:

Bressman, Susan B.;
de Leon, Deborah;
Kramer, Patricia L.;
Ozelius, Laurie J.;
Brin, Mitchell F.;
Greene, Paul E.;
Fahn, Stanley;
Breakefield, Xandra O.;
Risch, Neil J.

Publication type:

Article

Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34.

Published in:

Annals of Neurology, 1990, v. 27, n. 2, p. 114, doi. 10.1002/ana.410270203

By:

Kramer, Patricia L.;
De Leon, Deborah;
Ozelius, Laurie;
Risch, Neil;
Bressman, Susan B.;
Brin, Mitchell F.;
Schuback, Deborah E.;
Burke, Robert E.;
Kwiatkowski, David J.;
Shale, Heidi;
Gusella, James F.;
Breakefield, Xandra O.;
Fahn, Stanley

Publication type:

Article

Idiopathic dystonia among ashkenazi jews: Evidence for autosomal dominant inheritance.

Published in:

Annals of Neurology, 1989, v. 26, n. 5, p. 612, doi. 10.1002/ana.410260505

By:

Bressman, Susan B.;
De Leon, Deborah;
Brin, Mitchell F.;
Risch, Neil;
Burke, Robert E.;
Greene, Paul E.;
Shale, Heidi;
Fahn, Stanley

Publication type:

Article

Linkage Analysis in a Family with Dominantly Inherited Torsion Dystonia: Exclusion of the Pro-Opiomelanocortin and Glutamic Acid Decarboxylase Genes and Other Chromosomal Regions Using DNA Polymorphisms.

Published in:

Journal of Neurogenetics, 1986, v. 3, n. 3, p. 159, doi. 10.3109/01677068609106846

By:

Breakefield, Xandra O.;
Bressman, Susan B.;
Kramer, Patricia L.;
Ozelius, Laurie;
Moskowitz, Carol;
Tanzi, Rudolph;
Brin, Mitchell F.;
Hobbs, Wendy;
Kaufman, Daniel;
Tobin, Allan;
Kidd, Kenneth K.;
Fahn, Stanley;
Gusella, James F.

Publication type:

Article

Parkinsonism, dystonia, and hemiatrophy.

Published in:

2000

By:

Greene, Paul E.;
Bressman, Susan B.;
Ford, Blair;
Hyland, Keith;
Greene, P E;
Bressman, S B;
Ford, B;
Hyland, K

Publication type:

journal article

Analysis of blink rate patterns in normal subjects.

Published in:

1997

By:

Bentivoglio, Anna Rita;
Bressman, Susan B.;
Cassetta, Emanuele;
Carretta, Donatella;
Tonali, Pietro;
Albanese, Alberto;
Bentivoglio, A R;
Bressman, S B;
Cassetta, E;
Carretta, D;
Tonali, P;
Albanese, A

Publication type:

journal article

Teaching tape for the motor section of the toronto western spasmodic torticollis scale.

Published in:

Movement Disorders, 1997, v. 12, n. 4, p. 570, doi. 10.1002/mds.870120414

By:

Comella, Cynthia L.;
Stebbins, Glenn T.;
Goetz, Christopher G.;
Chmura, Teresa A.;
Bressman, Susan B.;
Lang, Anthony E.

Publication type:

Article

A case of tetrabenazine-induced neuroleptic malignant syndrome after prolonged treatment.

Published in:

Movement Disorders, 1997, v. 12, n. 2, p. 246, doi. 10.1002/mds.870120219

By:

Petzinger, Giselle M.;
Bressman, Susan B.

Publication type:

Article

Speech dysfunction in early Parkinson's disease.

Published in:

Movement Disorders, 1995, v. 10, n. 5, p. 562, doi. 10.1002/mds.870100506

By:

Stewart, Celia;
Winfield, Linda;
Hunt, Ann;
Bressman, Susan B.;
Fahn, Stanley;
Blitzer, Andrew;
Brin, Mitchell F.

Publication type:

Article

Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystonia.

Published in:

Movement Disorders, 1994, v. 9, n. 6, p. 626, doi. 10.1002/mds.870090608

By:

Bressman, Susan B.;
Hunt, Ann L.;
Heiman, Gary A.;
Brin, Mitchell F.;
Burke, Robert E.;
Fahn, Stanley;
Trugman, Joel M.;
de Leon, Deborah;
Kramer, Patricia L.;
Wilhelmsen, Kirk C.;
Nygaard, Torbjoern G.

Publication type:

Article

Analysis of the clinical course of non-Jewish, autosomal dominant torsion dystonia.

Published in:

Movement Disorders, 1986, v. 1, n. 3, p. 163, doi. 10.1002/mds.870010302

By:

Burke, Robert E.;
Brin, Mitchell F.;
Fahn, Stanley;
Bressman, Susan B.;
Moskowitz, Carol

Publication type:

Article

Thalamocortical Connectivity Correlates with Phenotypic Variability in Dystonia.

Published in:

Cerebral Cortex, 2015, v. 25, n. 9, p. 3086, doi. 10.1093/cercor/bhu104

By:

An Vo;
Wataru Sako;
Niethammer, Martin;
Carbon, Maren;
Bressman, Susan B.;
Uluğ, Aziz M.;
Eidelberg, David

Publication type:

Article