Cortical sensorimotor alterations classify clinical phenotype and putative genotype of spasmodic dysphonia von Battistella, G., Fuertinger, S., Fleysher, L., Ozelius, L. J., Simonyan, K.

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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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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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RAPID-ONSET DYSTONIA-PARKINSONISM IN A CHILD WITH A NOVEL ATP1A3 GENE MUTATION von ANSELM, I. A, SWEADNER, K. J, GOLLAMUDI, S, OZELIUS, L. J, DARRAS, B. T

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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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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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A single nucleotide polymorphism in the matrix metalloproteinase-1 promoter creates an Ets binding site and augments transcription von RUTTER, J. L, MITCHELL, T. I, BUTTICE, G, MEYERS, J, GUSELLA, J. F, OZELIUS, L. J, BRINCKERHOFF, C. E

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Myoclonus dystonia: Possible association with obsessive-compulsive disorder and alcohol dependence von SAUNDERS-PULLMAN, R, SHRIBERG, J, RISCH, N. J, BRESSMAN, S. B, HEIMAN, G, RAYMOND, D, WENDT, K, KRAMER, P, SCHILLING, K, KURLAN, R, KLEIN, C, OZELIUS, L. J

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Mutations in DYT1: Extension of the phenotypic and mutational spectrum von KABAKCI, K, HEDRICH, K, SVETEL, M, FRIEDMAN, J, KOSTIC, V, BRESSMAN, S. B, BREAKEFIELD, X. O, OZELIUS, L. J, PRAMSTALLER, P. P, KLEIN, C, LEUNG, J. C, MITTERER, M, VIEREGGE, P, LENCER, R, HAGENAH, J, GARRELS, J, WITT, K, KLOSTERMANN, F

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The TOR1A (DYT1) Gene Family and Its Role in Early Onset Torsion Dystonia von Ozelius, Laurie J., Page, Curtis E., Klein, Christine, Hewett, Jeffrey W., Mineta, Mari, Leung, Joanne, Shalish, Christo, Bressman, Susan B., de Leon, Deborah, Brin, Mitchell F., Fahn, Stanley, Corey, David P., Breakefield, Xandra O.

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Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease von Barrett, M.J, Hagenah, J, Dhawan, V, Peng, S, Stanley, K, Raymond, D, Deik, A, Gross, S.J, Schreiber-Agus, N, Mirelman, A, Marder, K, Ozelius, L.J, Eidelberg, D, Bressman, S.B, Saunders-Pullman, R

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Genetic heterogeneity in ten families with myoclonus-dystonia von Schüle, B, Kock, N, Svetel, M, Dragasevic, N, Hedrich, K, de Carvalho Aguiar, P, Liu, L, Kabakci, K, Garrels, J, Meyer, E-M, Berisavac, I, Schwinger, E, Kramer, P L, Ozelius, L J, Klein, C, Kostic, V

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Phenotype-genotype correlation in Dutch patients with myoclonus-dystonia von GERRITS, M. C. F, FONCKE, E. M. J, DE HAAN, R, HEDRICH, K, VAN DE LEEMPUT, Y. L. C, BAAS, F, OZELIUS, L. J, SPEELMAN, J. D, KLEIN, C, TIJSSEN, M. A. J

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Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: Expanding the phenotype von Klein, Christine, Pramstaller, Peter P., Kis, Bernhard, Page, Curtis C., Kann, Martin, Leung, Joanne, Woodward, Heather, Castellan, Claudio C., Scherer, Monika, Vieregge, Peter, Breakefield, Xandra O., Kramer, Patricia L., Ozelius, Laurie J.

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The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene von Brashear, Allison, Dobyns, William B., de Carvalho Aguiar, Patricia, Borg, Michel, Frijns, C. J. M., Gollamudi, Seema, Green, Andrew, Guimaraes, João, Haake, Bret C., Klein, Christine, Linazasoro, Gurutz, Münchau, Alexander, Raymond, Deborah, Riley, David, Saunders-Pullman, Rachel, Tijssen, Marina A. J., Webb, David, Zaremba, Jacek, Bressman, Susan B., Ozelius, Laurie J.

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Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new family von Kabakci, K, Isbruch, K, Schilling, K, Hedrich, K, de Carvalho Aguiar, P, Ozelius, L J, Kramer, P L, Schwarz, M H R M, Klein, C

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Phenotypic features of myoclonus-dystonia in three kindreds von DOHENY, D. O, BRIN, M. F, SCHILLING, K, KRAMER, P, DE LEON, D, RAYMOND, D, SAUNDERS-PULLMAN, R, KLEIN, C, BRESSMAN, S. B, SCHMAND, B, TIJSSEN, M. A. J, OZELIUS, L. J, MORRISON, C. E, SILVERMAN, J. M, SMITH, C. J, WALKER, R. H, ABBASI, S, MÜLLER, B, GARRELS, J, LIU, L, DE CARVALHO AGUIAR, P

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