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Results 1 - 10 of 148  for Great Falls College MSU

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SNCA: Major genetic modifier of age at onset of Parkinson's disease

Brockmann, Kathrin ; Schulte, Claudia ; Hauser, Ann - Kathrin ; Lichtner, Peter ; Huber, Heiko ; Maetzler, Walter ; Berg, Daniela ; Gasser, Thomas

Movement Disorders, August, 2013, Vol.28(9), p.1217(5) [Peer Reviewed Journal]

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Primary familial brain calcification: Genetic analysis and clinical spectrum.(Report)

Taglia, I ; Mignarri, A ; Olgiati, S ; Menci, E ; Petrocelli, Pl ; Breedveld, Gj ; Scaglione, C ; Martinelli, P ; Federico, A ; Bonifati, V ; Dutti, Mt;

Movement Disorders, June, 2015, Vol.30(7), p.1010(1) [Peer Reviewed Journal]

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Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain.(Report)

Mata, Ignacio F. ; Alvarez, Victoria ; Ribacoba, Renee ; Infante, Jon ; Sierra, María ; Gómez-Garre, Pilar ; Mir, Pablo ; Waldherr, Sarah ; Yearout, Dora ; Zabetian, Cyrus P.;

Movement Disorders, Feb, 2013, Vol.28(2), p.248(1) [Peer Reviewed Journal]

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Families with Wilson's disease in subsequent generations: Clinical and genetic analysis.(Clinical report)

Dziea1 ; Litwin, Tomasz ; Chabik, Grzegorz ; Gramza, Karolina ; Czaonkowska, Anna

Movement Disorders, 2014, Vol.29(14), p.1828(6) [Peer Reviewed Journal]

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Nigral anatomy and striatal denervation in genetic Parkinsonism: A family report.(Report)

Ceravolo, Roberto ; Antonini, Angelo ; Frosini, Daniela ; De Iuliis, Angela ; Weis, Luca ; Cecchin, Diego ; Tosetti, Michela ; Bonuccelli, Ubaldo ; Cosottini, Mirco

Movement Disorders, July, 2015, Vol.30(8), p.1148(3) [Peer Reviewed Journal]

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Two different genetic diseases in the same patient: Coincident, concomitant, or causally related?(Report)

Graf, Julia ; Hellenbroich, Yorck ; Veelken, Norbert ; Figueroa, Karla P. ; Wolff, Simone ; Pulst, Stefan ; Bruggemann, Norbert

Movement Disorders, 2016, Vol.31(4), p.491(2) [Peer Reviewed Journal]

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Disease-causing or benign? challenges in genetic variant interpretation and limitations of ClinVar.(Report)

Petkovic, Sonja ; Lohmann, Katja

Movement Disorders, 2018, Vol.33(8), p.1271(2) [Peer Reviewed Journal]

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Tor1a gene in GABApre interneurons: The new player in the "impaired inhibition" game of dystonia?(Report)

Monje, Mariana H.G. ; Sanchez-Ferro, Alvaro

Movement Disorders, 2018, Vol.33(9), p.1408(1) [Peer Reviewed Journal]

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Motor progression of Parkinson's disease with the leucine-rich repeat kinase 2 G2019S mutation.(Report)

Yahalom, Gilad ; Orlev, Yael ; Cohen, Oren S. ; Kozlova, Evgenia ; Friedman, Eitan ; Inzelberg, Rivka ; Hassin-Baer, Sharon

Movement Disorders, 2014, Vol.29(8), p.1057(4) [Peer Reviewed Journal]

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Pseudo-heterozygous rearrangement mutation of parkin.(Report)

Funayama, Manabu ; Yoshino, Hiroyo ; Li, Yuanzhe ; Kusaka, Hiromichi ; Tomiyama, Hiroyuki ; Hattori, Nobutaka

Movement Disorders, 2012, Vol.27(4), p.552(5) [Peer Reviewed Journal]

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