Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset von NICHOLS, W. C, PANKRATZ, N, MAREK, D. K, PAUCIULO, M. W, ELSAESSER, V. E, HALTER, C. A, RUDOLPH, A, WOJCIESZEK, J, PFEIFFER, R. F, FOROUD, T

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Novel THAP1 sequence variants in primary dystonia von XIAO, J, ZHAO, Y, VAN GERPEN, J. A, SIMON, D. K, TARSY, D, HEDERA, P, TRUONG, D. D, FREI, K. P, DEV BATISH, S, BLITZER, A, PFEIFFER, R. F, GONG, S, BASTIAN, R. W, LEDOUX, M. S, PERLMUTTER, J. S, RACETTE, B. A, TABBAL, S. D, KARIMI, M, PANIELLO, R. C, WSZOLEK, Z. K, UITTI, R. J

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Autosomal dominant parkinsonism associated with variable synuclein and tau pathology von WSZOLEK, Z. K, PFEIFFER, R. F, GASSER, T, CALNE, D. B, DICKSON, D. W, TSUBOI, Y, UITTI, R. J, MCCOMB, R. D, STOESSL, A. J, STRONGOSKY, A. J, ZIMPRICH, A, MÜLLER-MYHSOK, B, FARRER, M. J

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Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations von PANKRATZ, N, KISSELL, D. K, PAUCIULO, M. W, HALTER, C. A, RUDOLPH, A, PFEIFFER, R. F, MARDER, K. S, FOROUD, T, NICHOLS, W. C

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Variation in GIGYF2 is not associated with Parkinson disease von NICHOLS, W. C, KISSELL, D. K, FOROUD, T, PANKRATZ, N, PAUCIULO, M. W, ELSAESSER, V. E, CLARK, K. A, HALTER, C. A, RUDOLPH, A, WOJCIESZEK, J, PFEIFFER, R. F

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A family with parkinsonism, essential tremor, restless legs syndrome, and depression von PUSCHMANN, A, PFEIFFER, R. F, DICKSON, D. W, WSZOLEK, Z. K, STOESSL, A. J, KURIAKOSE, R, LASH, J. L, SEARCY, J. A, STRONGOSKY, A. J, VILARINO-GÜELL, C, FARRER, M. J, ROSS, O. A

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Autonomic dysfunction in Parkinson's disease: a comprehensive symptom survey von Siddiqui, M.F, Rast, S, Lynn, M.J, Auchus, A.P, Pfeiffer, R.F

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Gastrointestinal involvement in Parkinson's disease: the horse or the cart von Pfeiffer, R. F.

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Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology von Zimprich, Alexander, Biskup, Saskia, Leitner, Petra, Lichtner, Peter, Farrer, Matthew, Lincoln, Sarah, Kachergus, Jennifer, Hulihan, Mary, Uitti, Ryan J., Calne, Donald B., Stoessl, A.Jon, Pfeiffer, Ronald F., Patenge, Nadja, Carbajal, Iria Carballo, Vieregge, Peter, Asmus, Friedrich, Müller-Myhsok, Bertram, Dickson, Dennis W., Meitinger, Thomas, Strom, Tim M., Wszolek, Zbigniew K., Gasser, Thomas

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Constipation in parkinson's disease: Objective assessment and response to psyllium von Ashraf, Waseem, Pfeiffer, Ronald F., Park, Faye, Lof, John, Quigley, Eamonn M. M.

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Gastrointestinal symptoms in Parkinson's disease von Edwards, L. L., Pfeiffer, R. F., Quigley, E. M. M., Hofman, Ruth, Balluff, Mary

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Gastrointestinal symptoms in parkinson disease: 18-month follow-up study von Edwards, L., Quigley, E. M. M., Hofman, R., Pfeiffer, R. F.

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A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation von Markopoulou, K., Wszolek, Z. K., Pfeiffer, R. F.

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Expression and regulation of brain metallothionein von Ebadi, M., Iversen, P.L., Hao, R., Cerutis, D.R., Rojas, P., Happe, H.K., Murrin, L.C., Pfeiffer, R.F.

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Western Nebraska Family (Family D) with Autosomal Dominant Parkinsonism von Wszolek, Z K, Pfeiffer, B, Fulgham, J R, Parisi, J E, Thompson, B M, Uitti, R J, Calne, D B, Pfeiffer, R F

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Localization of the Gene for Rapidly Progressive Autosomal Dominant Parkinsonism and Dementia with Pallido-Ponto-Nigral Degeneration to Chromosome 17q21 von Wijker, Mario, Wszolek, Zbigniew K., Wolters, Eric C. H., Rooimans, Martin A., Pals, Gerard, Pfeiffer, Ronald F., Lynch, Timothy, Rodnitzky, R. L., Wilhelmsen, Kirk C., Arwert, Fré

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Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration von Wszolek, Z. K., Pfeiffer, R. F., Bhatt, M. H., Schelper, R. L., Cordes, M., Snow, B. J., Rodnitzky, R. L., Wolters, E. Ch, Arwert, F., Calne, D. B.

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Reduced expression of the G209A α-synuclein allele in familial parkinsonism von Markopoulou, Katerina, Wszolek, Zbigniew K., Pfeiffer, Ronald F., Chase, Bruce A.

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The PARK8 Locus in Autosomal Dominant Parkinsonism: Confirmation of Linkage and Further Delineation of the Disease-Containing Interval von Zimprich, Alexander, Müller-Myhsok, Bertram, Farrer, Matthew, Leitner, Petra, Sharma, Manu, Hulihan, Mary, Lockhart, Paul, Strongosky, Audrey, Kachergus, Jennifer, Calne, Donald B., Stoessl, Jon, Uitti, Ryan J., Pfeiffer, Ronald F., Trenkwalder, Claudia, Homann, Nikolaus, Ott, Erwin, Wenzel, Karoline, Asmus, Friedrich, Hardy, John, Wszolek, Zbigniew, Gasser, Thomas

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Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonism von WSZOLEK, Z. K, GWINN-HARDY, K, WSZOLEK, E. K, MUENTER, M. D, PFEIFFER, R. F, RODNITZKY, R. L, UITTI, R. J, MCCOMB, R. D, GASSER, T, DICKSON, D. W

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