Works matching IS 08853185 AND DT 2022 AND VI 37 AND IP 12

Results: 26

The Glycoprotein GPNMB: A Secret Ingredient for Understanding Parkinson's Disease Etiology?

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2342, doi. 10.1002/mds.29264

By:

Pizarro Galleguillos, Benjamín Matías;
Mohamed, Wael;
Periñan, Maria Teresa

Publication type:

Article

Striatal Development in Early‐Onset Huntington's Disease.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2459, doi. 10.1002/mds.29227

By:

Schultz, Jordan L.;
Epping, Eric A.;
van der Plas, Ellen;
Magnotta, Vincent A.;
Nopoulos, Peggy C.

Publication type:

Article

Brain Atrophy Is Substantially Accelerated in Neurological Wilson's Disease: A Longitudinal Study.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2446, doi. 10.1002/mds.29229

By:

Smolinski, Lukasz;
Ziemssen, Tjalf;
Akgun, Katja;
Antos, Agnieszka;
Skowrońska, Marta;
Kurkowska‐Jastrzębska, Iwona;
Członkowska, Anna;
Litwin, Tomasz

Publication type:

Article

Predictive Modeling of Huntington's Disease Unfolds Thalamic and Caudate Atrophy Dissociation.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2407, doi. 10.1002/mds.29219

By:

Castro, Eduardo;
Polosecki, Pablo;
Pustina, Dorian;
Wood, Andrew;
Sampaio, Cristina;
Cecchi, Guillermo A.

Publication type:

Article

December Infographic.

Published in:: Movement Disorders, 2022, v. 37, n. 12, p. N.PAG, doi. 10.1002/mds.29307
Publication type:: Article

Corticospinal Suppression Underlying Intact Movement Preparation Fades in Parkinson's Disease.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2396, doi. 10.1002/mds.29214

By:

Wilhelm, Emmanuelle;
Quoilin, Caroline;
Derosiere, Gerard;
Paço, Susana;
Jeanjean, Anne;
Duque, Julie

Publication type:

Article

Disentangling the Connection Between Neurodevelopment and Neurodegeneration in Huntington's Disease.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2343, doi. 10.1002/mds.29267

By:

Estevez‐Fraga, Carlos;
Tabrizi, Sarah J.

Publication type:

Article

Corrections to "A Machine‐Learning Derived Huntington's Disease Progression Model: Insights for Clinical Trial Design".

Published in:

2022

By:

Mohan, Amrita;
Sun, Zhaonan;
Ghosh, Soumya;
Li, Ying;
Sathe, Swati;
Hu, Jianying;
Sampaio, Cristina

Publication type:

Correction Notice

Reply to: "GNAO1 Haploinsufficiency Associated with a Mild Delayed‐Onset Dystonia Phenotype".

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2466, doi. 10.1002/mds.29256

By:

Wirth, Thomas;
Garone, Giacomo;
Kurian, Manju A.;
Piton, Amélie;
Roze, Emmanuel;
Lin, Jean Pierre;
Tranchant, Christine;
Cif, Laura;
Doummar, Diane;
Anheim, Mathieu

Publication type:

Article

GNAO1 Haploinsufficiency Associated with a Mild Delayed‐Onset Dystonia Phenotype.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2464, doi. 10.1002/mds.29258

By:

Krenn, Martin;
Sommer, Rudolf;
Sycha, Thomas;
Zech, Michael

Publication type:

Article

Aggregation‐Seeding Forms of α‐Synuclein Are Not Detected in Acute Coronavirus Disease 2019 Cerebrospinal Fluid.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2462, doi. 10.1002/mds.29240

By:

Russo, Marco J.;
MacLeod, Karen;
Lamoureux, Jennifer;
Lebovitz, Russ;
Pleshkevich, Maria;
Steriade, Claude;
Wisniewski, Thomas;
Frontera, Jennifer A.;
Kang, Un Jung

Publication type:

Article

Mendelian Randomization Study Using Dopaminergic Neuron‐Specific eQTL Nominates Potential Causal Genes for Parkinson's Disease.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2451, doi. 10.1002/mds.29239

By:

Dang, Xinglun;
Zhang, Zhijun;
Luo, Xiong‐Jian

Publication type:

Article

Impulse Control Disorder Behaviors in Dystonia.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2460, doi. 10.1002/mds.29230

By:

Huovinen, Annu;
Jaakkola, Elina;
Joutsa, Juho

Publication type:

Article

The Unified Multiple System Atrophy Rating Scale: Status, Critique, and Recommendations.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2336, doi. 10.1002/mds.29215

By:

Krismer, Florian;
Palma, Jose‐Alberto;
Calandra‐Buonaura, Giovanna;
Stankovic, Iva;
Vignatelli, Luca;
Berger, Anna‐Karin;
Falup‐Pecurariu, Cristian;
Foubert‐Samier, Alexandra;
Höglinger, Günter;
Kaufmann, Horacio;
Kellerman, Larry;
Kim, Han‐Joon;
Klockgether, Thomas;
Levin, Johannes;
Martinez‐Martin, Pablo;
Mestre, Tiago A.;
Pellecchia, Maria Teresa;
Perlman, Susan;
Qureshi, Irfan;
Rascol, Olivier

Publication type:

Article

Prevalence and Incidence of Huntington's Disease: An Updated Systematic Review and Meta‐Analysis.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2327, doi. 10.1002/mds.29228

By:

Medina, Alex;
Mahjoub, Yasamin;
Shaver, Larry;
Pringsheim, Tamara

Publication type:

Article

Homozygous CADPS2 Mutations Cause Neurodegenerative Disease with Lewy Body‐like Pathology in Parrots.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2345, doi. 10.1002/mds.29211

By:

Lorenzo‐Betancor, Oswaldo;
Galosi, Livio;
Bonfili, Laura;
Eleuteri, Anna Maria;
Cecarini, Valentina;
Verin, Ranieri;
Dini, Fabrizio;
Attili, Anna‐Rita;
Berardi, Sara;
Biagini, Lucia;
Robino, Patrizia;
Stella, Maria Cristina;
Yearout, Dora;
Dorschner, Michael O.;
Tsuang, Debby W.;
Rossi, Giacomo;
Zabetian, Cyrus P.

Publication type:

Article

Early‐Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2440, doi. 10.1002/mds.29225

By:

Mo, Alisa;
Saffari, Afshin;
Kellner, Melanie;
Döbler‐Neumann, Marion;
Jordan, Catherine;
Srivastava, Siddharth;
Zhang, Bo;
Sahin, Mustafa;
Fink, John K.;
Smith, Linsley;
Posey, Jennifer E.;
Alter, Katharine E.;
Toro, Camilo;
Blackstone, Craig;
Soldatos, Ariane G.;
Christie, Michelle;
Schüle, Rebecca;
Ebrahimi‐Fakhari, Darius

Publication type:

Article

Annonaceae Consumption Worsens Disease Severity and Cognitive Deficits in Degenerative Parkinsonism.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2355, doi. 10.1002/mds.29222

By:

Cleret de Langavant, Laurent;
Roze, Emmanuel;
Petit, Aimée;
Tressières, Benoit;
Gharbi‐Meliani, Amin;
Chaumont, Hugo;
Michel, Patrick Pierre;
Bachoud‐Lévi, Anne‐Catherine;
Remy, Philippe;
Edragas, Régine;
Lannuzel, Annie

Publication type:

Article

Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18‐Year Study.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2427, doi. 10.1002/mds.29221

By:

Rosenbohm, Angela;
Pott, Hendrik;
Thomsen, Mirja;
Rafehi, Haloom;
Kaya, Sabine;
Szymczak, Silke;
Volk, Alexander E.;
Mueller, Kathrin;
Silveira, Isabel;
Weishaupt, Jochen H.;
Tönnies, Holger;
Seibler, Philip;
Zschiedrich, Katja;
Schaake, Susen;
Westenberger, Ana;
Zühlke, Christine;
Depienne, Christel;
Trinh, Joanne;
Ludolph, Albert C.;
Klein, Christine

Publication type:

Article

STN‐DBS in the 1950s? Carl Wilhelm Sem‐Jacobsen's Missing Films Recovered.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2457, doi. 10.1002/mds.29217

By:

Dietrichs, Espen

Publication type:

Article

Diet Quality is Associated with Prodromal Parkinson's Disease Features in Chinese Adults.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2367, doi. 10.1002/mds.29208

By:

Zhang, Xinyuan;
Xu, Jipo;
Liu, Yesong;
Chen, Shuohua;
Wu, Shouling;
Gao, Xiang

Publication type:

Article

Joint Modeling Study Identifies Blood‐Based Transcripts Link to Cognitive Decline in Parkinson's Disease.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2386, doi. 10.1002/mds.29213

By:

Luo, Junfeng;
Wu, Hao;
Li, Jinxia;
Xian, Wenbiao;
Li, Weimin;
Locascio, Joseph J.;
Pei, Zhong;
Liu, Ganqiang

Publication type:

Article

Issue Information.

Published in:: Movement Disorders, 2022, v. 37, n. 12, p. 1, doi. 10.1002/mds.28450
Publication type:: Article

Identifying Protective Drugs for Parkinson's Disease in Health‐Care Databases Using Machine Learning.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2376, doi. 10.1002/mds.29205

By:

Courtois, Émeline;
Nguyen, Thi Thu Ha;
Fournier, Agnès;
Carcaillon‐Bentata, Laure;
Moutengou, Élodie;
Escolano, Sylvie;
Tubert‐Bitter, Pascale;
Elbaz, Alexis;
Thiébaut, Anne C.M.;
Ahmed, Ismaïl

Publication type:

Article

Specific Gait Changes in Prodromal Hereditary Spastic Paraplegia Type 4: preSPG4 Study.

Published in:

Movement Disorders, 2022, v. 37, n. 12, p. 2417, doi. 10.1002/mds.29199

By:

Laßmann, Christian;
Ilg, Winfried;
Schneider, Marc;
Völker, Maximilian;
Haeufle, Daniel F.B.;
Schüle, Rebecca;
Giese, Martin;
Synofzik, Matthis;
Schöls, Ludger;
Rattay, Tim W.

Publication type:

Article

Movement Disorders: Volume 37, Number 12, December 2022.

Published in:: Movement Disorders, 2022, v. 37, n. 12, p. 1, doi. 10.1002/mds.28451
Publication type:: Article