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

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Sixty hertz pallidal deep brain stimulation for primary torsion dystonia von ALTERMAN, R. L, MIRAVITE, J, WEISZ, D, SHILS, J. L, BRESSMAN, S. B, TAGLIATI, M

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Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites von SAUNDERS-PULLMAN, R, RAYMOND, D, STANLEY, K, LUCIANO, M. San, HAGENAH, J, GATTI, R, OZELIUS, L. J, BRESSMAN, S. B, STOESSL, A. J, HOBSON, D, NAKAMURA, T, PULLMAN, S, LEFTON, D, OKUN, M. S, UITTI, R, SACHDEV, R

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Etiology of musician's dystonia : Familial or environmental? von SCHMIDT, A, JABUSCH, H.-C, MÜNCHAU, A, KLEIN, C, ALTENMÜLLER, E, HAGENAH, J, BRÜGGEMANN, N, LOHMANN, K, ENDERS, L, KRAMER, P. L, SAUNDERS-PULLMAN, R, BRESSMAN, S. B

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Olfactory dysfunction in LRRK2 G2019S mutation carriers von SAUNDERS-PULLMAN, R, STANLEY, K, BRESSMAN, S. B, WANG, C, SAN LUCIANO, M, SHANKER, V, HUNT, A, SEVERT, L, RAYMOND, D, OZELIUS, L. J, LIPTON, R. B

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Cognitive performance of GBA mutation carriers with early-onset PD: The CORE-PD study von ALCALAY, R. N, CACCAPPOLO, E, LOUIS, E, COMELLA, C, COLCHER, A, JENNINGS, D, NANCE, M, BRESSMAN, S, SCOTT, W. K, TANNER, C, MICKEL, S, ANDREWS, H, MEJIA-SANTANA, H, WATERS, C, FAHN, S, COTE, L, FRUCHT, S, FORD, B, REZAK, M, NOVAK, K, FRIEDMAN, J. H, PFEIFFER, R, MARSH, L, TANG, M.-X, HINER, B, SIDEROWF, A, PAYAMI, H, MOLHO, E, FACTOR, S, OTTMAN, R, CLARK, L. N, MARDER, K, ROSADO, L, ORBE REILLY, M, RUIZ, D, ROSS, B, VERBITSKY, M, KISSELEV, S

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Decreased striatal D2 receptor binding in non-manifesting carriers of the DYT1 dystonia mutation von ASANUMA, K, MA, Y, OKULSKI, J, DHAWAN, V, CHALY, T, CARBON, M, BRESSMAN, S. B, EIDELBERG, D

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Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia von CARBON, M, NIETHAMMER, M, PENG, S, RAYMOND, D, DHAWAN, V, CHALY, T, MA, Y, BRESSMAN, S, EIDELBERG, D

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Gender differences in the risk of familial parkinsonism: Beyond LRRK2? von Saunders-Pullman, R., Stanley, K., Luciano, M. San, Barrett, M.J., Shanker, V., Raymond, D., Ozelius, L.J., Bressman, S.B.

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The DYT1 phenotype and guidelines for diagnostic testing von BRESSMAN, S. B, SABATTI, C, RISCH, N. J, RAYMOND, D, DE LEON, D, KLEIN, C, KRAMER, P. L, BRIN, M. F, FAHN, S, BREAKEFIELD, X, OZELIUS, L. J

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DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease von HEDRICH, K, DJARMATI, A, BONIFATI, V, SCHWINGER, E, LANG, A. E, NOTH, J, BRESSMAN, S. B, PRAMSTALLER, P. P, RIESS, O, KLEIN, C, SCHÄFER, N, HERING, R, WELLENBROCK, C, WEISS, P. H, HILKER, R, VIEREGGE, P, OZELIUS, L. J, HEUTINK, P

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Impaired sequence learning in dystonia mutation carriers: a genotypic effect von CARBON, Maren, ARGYELAN, Miklos, FELICE GHILARDI, Maria, MATTIS, Paul, DHAWAN, Vijay, BRESSMAN, Susan, EIDELBERG, David

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Age at onset as a factor in determining the phenotype of primary torsion dystonia von O'RIORDAN, S, RAYMOND, D, LYNCH, T, SAUNDERS-PULLMAN, R, BRESSMAN, S. B, DALY, L, HUTCHINSON, M

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Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations von HEDRICH, K, MARDER, K, KLEIN, C, HARRIS, J, KANN, M, LYNCH, T, MEIJA-SANTANA, H, PRAMSTALLER, P. P, SCHWINGER, E, BRESSMAN, S. B, FAHN, S

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Increased risk for recurrent major depression in DYT1 dystonia mutation carriers von HEIMAN, G. A, OTTMAN, R, SAUNDERS-PULLMAN, R. J, OZELIUS, L. J, RISCH, N. J, BRESSMAN, S. B

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Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers von HESS, C. W, RAYMOND, D, SAUNDERS-PULLMAN, R, DE CARVALHO AGUIAR, P, FRUCHT, S, SHRIBERG, J, HEIMAN, G. A, KURLAN, R, KLEIN, C, BRESSMAN, S. B, OZELIUS, L. J

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High mutation rate in dopa-responsive dystonia : Detection with comprehensive GCHI screening von HAGENAH, J, SAUNDERS-PULLMAN, R, NYGAARD, T, OZELIUS, L. J, BRESSMAN, S. B, KLEIN, C, HEDRICH, K, KABAKCI, K, HABERMANN, K, WIEGERS, K, MOHRMANN, K, LOHNAU, T, RAYMOND, D, VIEREGGE, P

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The Alzheimer disease BIN1 locus as a modifier of GBA-associated Parkinson disease von Gan-Or, Z., Amshalom, I., Bar-Shira, A., Gana-Weisz, M., Mirelman, A., Marder, K., Bressman, S., Giladi, N., Orr-Urtreger, A.

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The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein von Ozelius, Laurie J., Hewett, Jeffrey W., Page, Curtis E., Bressman, Susan B., Kramer, Patricia L., Shalish, Christo, de Leon, Deborah, Brin, Mitchell F., Raymond, Deborah, Corey, David P., Fahn, Stanley, Risch, Neil J., Buckler, Alan J., Gusella, James F., Breakefield, Xandra O.

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Analysis of blink rate patterns in normal subjects von Bentivoglio, Anna Rita, Bressman, Susan B., Cassetta, Emanuele, Carretta, Donatella, Tonali, Pietro, Albanese, Alberto

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