Digitized Spiral Drawing: A Possible Biomarker for Early Parkinson's Disease von 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

Volltext

Phenomenology and classification of dystonia: A consensus update von 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.

Volltext

Arm swing as a potential new prodromal marker of Parkinson's disease von 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, Orr-Urtreger, Avi, Hausdorff, Jeffrey M., Giladi, Nir

Volltext

Cerebellothalamocortical Connectivity Regulates Penetrance in Dystonia von Argyelan, Miklos, Carbon, Maren, Niethammer, Martin, Ulug, Aziz M, Voss, Henning U, Bressman, Susan B, Dhawan, Vijay, Eidelberg, David

Volltext

Progression in the LRRK2-Asssociated Parkinson Disease Population von 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

Volltext

Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia von Ozelius, Laurie J, Fuchs, Tania, Gavarini, Sophie, Saunders-Pullman, Rachel, Raymond, Deborah, Ehrlich, Michelle E, Bressman, Susan B

Volltext

Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study von Bressman, Susan B, MD, Raymond, Deborah, MS, Fuchs, Tania, PhD, Heiman, Gary A, PhD, Ozelius, Laurie J, PhD, Saunders-Pullman, Rachel, MD

Volltext

Disordered network structure and function in dystonia: pathological connectivity vs. adaptive responses von Vo, An, Nguyen, Nha, Fujita, Koji, Schindlbeck, Katharina A, Rommal, Andrea, Bressman, Susan B, Niethammer, Martin, Eidelberg, David

Volltext

LRRK2 and GBA Variants Exert Distinct Influences on Parkinson’s Disease-Specific Metabolic Networks von Schindlbeck, Katharina A, Vo, An, Nguyen, Nha, Tang, Chris C, Niethammer, Martin, Dhawan, Vijay, Brandt, Vicky, Saunders-Pullman, Rachel, Bressman, Susan B, Eidelberg, David

Volltext

Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition von Arystarkhova, Elena, Haq, Ihtsham U., Luebbert, Timothy, Mochel, Fanny, Saunders-Pullman, Rachel, Bressman, Susan B., Feschenko, Polina, Salazar, Cynthia, Cook, Jared F., Demarest, Scott, Brashear, Allison, Ozelius, Laurie J., Sweadner, Kathleen J.

Volltext

Genetic and clinical features of primary torsion dystonia von Ozelius, Laurie J, Bressman, Susan B

Volltext

Mutations in GNAL cause primary torsion dystonia von 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

Volltext

Metabolomic profiling to develop blood biomarkers for Parkinson's disease von Bogdanov, Mikhail, Matson, Wayne R., Wang, Lei, Matson, Theodore, Saunders-Pullman, Rachel, Bressman, Susan S., Beal, M. Flint

Volltext

The diagnosis of dystonia von Geyer, Howard L, Bressman, Susan B

Volltext

Intragenic Cis and Trans Modification of Genetic Susceptibility in DYT1 Torsion Dystonia von Risch, Neil J., Bressman, Susan B., Senthil, Geetha, Ozelius, Laurie J.

Volltext

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease von Gan-Or, Ziv, Ozelius, Laurie J, Bar-Shira, Anat, Saunders-Pullman, Rachel, Mirelman, Anat, Kornreich, Ruth, Gana-Weisz, Mali, Raymond, Deborah, Rozenkrantz, Liron, Deik, Andres, Gurevich, Tanya, Gross, Susan J, Schreiber-Agus, Nicole, Giladi, Nir, Bressman, Susan B, Orr-Urtreger, Avi

Volltext

Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry von Lee, Annie J., Wang, Yuanjia, Alcalay, Roy N., Mejia‐Santana, Helen, Saunders‐Pullman, Rachel, Bressman, Susan, Corvol, Jean‐Christophe, Brice, Alexis, Lesage, Suzanne, Mangone, Graziella, Tolosa, Eduardo, Pont‐Sunyer, Claustre, Vilas, Dolores, Schüle, Birgitt, Kausar, Farah, Foroud, Tatiana, Berg, Daniela, Brockmann, Kathrin, Goldwurm, Stefano, Siri, Chiara, Asselta, Rosanna, Ruiz‐Martinez, Javier, Mondragón, Elisabet, Marras, Connie, Ghate, Taneera, Giladi, Nir, Mirelman, Anat, Marder, Karen

Volltext

Supplemental ambient lighting intervention to improve sleep in Parkinson's disease: A pilot trial von Yoo, Andrea S., Wise, Adina, Ortega, Roberto A., Raymond, Deborah, Plitnick, Barbara, Brons, Jennifer, Liang, Judy, Bressman, Susan B., Yang, Mengxi, Pedler, David, Figueiro, Mariana G., Saunders-Pullman, Rachel

Volltext

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

Volltext

Application of the Movement Disorder Society prodromal criteria in healthy G2019S‐LRRK2 carriers von 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

Volltext