Works matching IS 08853185 AND DT 2012 AND VI 27 AND IP 14

Results: 33

Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.

Published in:

2012

By:

Kojovic M;
Sheerin UM;
Rubio-Agusti I;
Saha A;
Bras J;
Gibbons V;
Palmer R;
Houlden H;
Hardy J;
Wood NW;
Bhatia KP;
Kojovic, Maja;
Sheerin, Una-Marie;
Rubio-Agusti, Ignacio;
Saha, Anirban;
Bras, Jose;
Gibbons, Vaneesha;
Palmer, Rodger;
Houlden, Henry;
Hardy, John

Publication type:

Case Study

Meningioma with intense I(123) FP-CIT uptake.

Published in:

2012

By:

Cilia R;
Allegra R;
Pezzoli G;
Cilia, Roberto;
Allegra, Roberta;
Pezzoli, Gianni

Publication type:

journal article

Comparison of dysphagia before and after deep brain stimulation in Parkinson's disease.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1763, doi. 10.1002/mds.25259

By:

Silbergleit, Alice K.;
LeWitt, Peter;
Junn, Fred;
Schultz, Lonni R.;
Collins, Denise;
Beardsley, Tausha;
Hubert, Meghan;
Trosch, Richard;
Schwalb, Jason M.

Publication type:

Article

Respiratory disorders associated with dystonia.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1816, doi. 10.1002/mds.25269

By:

Mehanna, Raja;
Jankovic, Joseph

Publication type:

Article

Color discrimination deficits in Parkinson's disease are related to cognitive impairment and white-matter alterations.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1781, doi. 10.1002/mds.25272

By:

Bertrand, Josie-Anne;
Bedetti, Christophe;
Postuma, Ronald B.;
Monchi, Oury;
Génier Marchand, Daphné;
Jubault, Thomas;
Gagnon, Jean-François

Publication type:

Article

The prevalence of primary dystonia: A systematic review and meta-analysis.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1789, doi. 10.1002/mds.25244

By:

Steeves, Thomas D.;
Day, Lundy;
Dykeman, Jonathan;
Jette, Nathalie;
Pringsheim, Tamara

Publication type:

Article

Meningioma with intense I<sup>123</sup> FP-CIT uptake.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1744, doi. 10.1002/mds.25277

By:

Cilia, Roberto;
Allegra, Roberta;
Pezzoli, Gianni

Publication type:

Article

DYT7 gene locus for cervical dystonia on chromosome 18p is questionable.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1820, doi. 10.1002/mds.25219

By:

Winter, Pia;
Kamm, Christoph;
Biskup, Saskia;
Köhler, Angelika;
Leube, Barbara;
Auburger, Georg;
Gasser, Thomas;
Benecke, Rainer;
Müller, Ulrich

Publication type:

Article

Oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1741, doi. 10.1002/mds.25295

By:

Ushe, Mwiza;
Perlmutter, Joel S.

Publication type:

Article

Common variation in the LRRK2 gene is a risk factor for Parkinson's disease.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1823, doi. 10.1002/mds.25226

By:

Mata, Ignacio F.;
Checkoway, Harvey;
Hutter, Carolyn M.;
Samii, Ali;
Roberts, John W.;
Kim, Hojoong M.;
Agarwal, Pinky;
Alvarez, Victoria;
Ribacoba, Renee;
Pastor, Pau;
Lorenzo-Betancor, Oswaldo;
Infante, Jon;
Sierra, María;
Gómez-Garre, Pilar;
Mir, Pablo;
Ritz, Beate;
Rhodes, Shannon L.;
Colcher, Amy;
Van Deerlin, Vivianna;
Chung, Kathryn A.

Publication type:

Article

Seizures in juvenile Huntington's disease: Frequency and characterization in a multicenter cohort.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1797, doi. 10.1002/mds.25237

By:

Cloud, Leslie J.;
Rosenblatt, Adam;
Margolis, Russel L.;
Ross, Christopher A.;
Pillai, Jagan A.;
Corey-Bloom, Jody;
Tully, Hannah M.;
Bird, Thomas;
Panegyres, Peter K.;
Nichter, Charles A.;
Higgins, Donald S.;
Helmers, Sandra L.;
Factor, Stewart A.;
Jones, Randi;
Testa, Claudia M.

Publication type:

Article

Long-term outcomes of surgical therapies for Parkinson's disease.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1718, doi. 10.1002/mds.25214

By:

Rodriguez-Oroz, Maria C.;
Moro, Elena;
Krack, Paul

Publication type:

Article

Weak detrusor contractility correlates with motor disorders in Parkinson's disease.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1775, doi. 10.1002/mds.25225

By:

Terayama, Keiichiro;
Sakakibara, Ryuji;
Ogawa, Akihiro;
Haruta, Hiroyuki;
Akiba, Takashi;
Nagao, Takeki;
Takahashi, Osamu;
Sugiyama, Megumi;
Tateno, Akihiko;
Tateno, Fuyuki;
Yano, Masashi;
Kishi, Masahiko;
Tsuyusaki, Yohei;
Uchiyama, Tomoyuki;
Yamamoto, Tatsuya

Publication type:

Article

Atypical parkinsonism and cerebrotendinous xanthomatosis: Report of a family with corticobasal syndrome and a literature review.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1769, doi. 10.1002/mds.25229

By:

Rubio-Agusti, Ignacio;
Kojovic, Maja;
Edwards, Mark J.;
Murphy, Elaine;
Chandrashekar, Hoskote S.;
Lachmann, Robin H.;
Bhatia, Kailash P.

Publication type:

Article

Toward magnetic resonance imaging biomarkers for progressive supranuclear palsy and multisystem atrophy.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1711, doi. 10.1002/mds.25196

By:

Sauvaget, Frederic;
Litvan, Irene

Publication type:

Article

Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1829, doi. 10.1002/mds.25199

By:

Kojovic, Maja;
Sheerin, Una-Marie;
Rubio-Agusti, Ignacio;
Saha, Anirban;
Bras, Jose;
Gibbons, Vaneesha;
Palmer, Rodger;
Houlden, Henry;
Hardy, John;
Wood, Nicholas W.;
Bhatia, Kailash P.

Publication type:

Article

Myoclonus and dystonia in cerebrotendinous xanthomatosis.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1805, doi. 10.1002/mds.25206

By:

Lagarde, Julien;
Roze, Emmanuel;
Apartis, Emmanuelle;
Pothalil, Deepa;
Sedel, Frédéric;
Couvert, Philippe;
Vidailhet, Marie;
Degos, Bertrand

Publication type:

Article

Huntington's disease: How intermediate are intermediate repeat lengths?

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1714, doi. 10.1002/mds.25172

By:

Squitieri, Ferdinando;
Jankovic, Joseph

Publication type:

Article

Arkypallidal neuron: A new player in the basal ganglia circuitry.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1740, doi. 10.1002/mds.25257

By:

Baufreton, Jérôme

Publication type:

Article

A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1827, doi. 10.1002/mds.25114

By:

Guerrero-López, Rosa;
García-Ruiz, Pedro J.;
Giráldez, Beatriz G.;
Durán-Herrera, Carmen;
Querol-Pascual, Maria Rosa;
Ramírez-Moreno, José María;
Más, Sebastián;
Serratosa, José M.

Publication type:

Article

Mutations in the phospholipid remodeling gene SERAC1 cause MEGDEL syndrome.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1738, doi. 10.1002/mds.25228

By:

Alexoudi, Athanasia;
Schneider, Susanne A.

Publication type:

Article

Book review: Marsden's Book of Movement Disorders.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1841, doi. 10.1002/mds.25268

By:

Obeso, José A.

Publication type:

Article

Conventional magnetic resonance imaging in confirmed progressive supranuclear palsy and multiple system atrophy.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1754, doi. 10.1002/mds.24968

By:

Massey, Luke A.;
Micallef, Caroline;
Paviour, Dominic C.;
O'Sullivan, Sean S.;
Ling, Helen;
Williams, David R.;
Kallis, Constantinos;
Holton, Janice L.;
Revesz, Tamas;
Burn, David J.;
Yousry, Tarek;
Lees, Andrew J.;
Fox, Nick C.;
Jäger, Hans R.

Publication type:

Article

Tremor-ataxia with central hypomyelination (TACH): Dystonia as a new clinical feature.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1831, doi. 10.1002/mds.25270

By:

Osterman, Bradley;
Sylvain, Michel;
Chouinard, Sylvain;
Bernard, Geneviève

Publication type:

Article

Is it all about timing?

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1739, doi. 10.1002/mds.25252

By:

Hernández, Ledia F.

Publication type:

Article

C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1835, doi. 10.1002/mds.25245

By:

Fogel, Brent L.;
Pribadi, Mochtar;
Pi, Sarah;
Perlman, Susan L.;
Geschwind, Daniel H.;
Coppola, Giovanni

Publication type:

Article

Multiple system atrophy with prolonged survival.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1837, doi. 10.1002/mds.25289

By:

Kim, Han-Joon;
Jeon, Beom S.

Publication type:

Article

Supranuclear gaze palsy in glycine receptor antibody-positive progressive encephalomyelitis with rigidity and myoclonus.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1833, doi. 10.1002/mds.25239

By:

Peeters, Elke;
Vanacker, Peter;
Woodhall, Mark;
Vincent, Angela;
Schrooten, Maarten;
Vandenberghe, Wim

Publication type:

Article

Sleep and Parkinson's disease: A review of case-control polysomnography studies.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1729, doi. 10.1002/mds.25197

By:

Peeraully, Tasneem;
Yong, Ming-Hui;
Chokroverty, Sudhansu;
Tan, Eng-King

Publication type:

Article

Commentary for 'oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8'.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1743, doi. 10.1002/mds.25332

By:

Frucht, Steven

Publication type:

Article

Progression of cortical thinning in early Parkinson's disease.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1746, doi. 10.1002/mds.25240

By:

Ibarretxe-Bilbao, Naroa;
Junque, Carme;
Segura, Barbara;
Baggio, Hugo C.;
Marti, Maria J.;
Valldeoriola, Francesc;
Bargallo, Nuria;
Tolosa, Eduardo

Publication type:

Article

Imaging measures predict progression in progressive supranuclear palsy.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1801, doi. 10.1002/mds.24970

By:

Whitwell, Jennifer L.;
Xu, Jia;
Mandrekar, Jay;
Gunter, Jeffrey L.;
Jack, Clifford R.;
Josephs, Keith A.

Publication type:

Article

An electromyographic study of parkinsonian swallowing and its response to levodopa.

Published in:

Movement Disorders, 2012, v. 27, n. 14, p. 1811, doi. 10.1002/mds.25262

By:

Tawadros, Paul B.;
Cordato, Dennis;
Cathers, Ian;
Burne, John A.

Publication type:

Article