CrossRef Text and Data Mining

Result of CrossRef Text and Data Mining Search is the related articles with entitled article. If you click link1 or link2 you will be able to reach the full text site of selected articles; however, some links do not show the full text immediately at now. If you click CrossRef Text and Data Mining Download icon, you will be able to get whole list of articles from literature included in CrossRef Text and Data Mining.

X-Linked Dystonia Parkinsonism: Clinical Phenotype, Genetics and Therapeutics

Raymond L. Rosales

JMD. 2010;3(2):32-38. DOI: https://doi.org/10.14802/jmd.10009

X-Linked Dystonia Parkinsonism: Clinical Phenotype, Genetics and Therapeutics

Raymond L. Rosales

Journal of Movement Disorders. 2010;3(2):32-38

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Clinicopathological Phenotype and Genetics of X-Linked Dystonia–Parkinsonism (XDP; DYT3; Lubag)

Toshitaka Kawarai, Ryoma Morigaki, Ryuji Kaji, Satoshi Goto

Brain Sciences. 2017;7(12):72

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An integrated OMICS approach unravels the elusive genetic cause of X-linked dystonia-parkinsonism

Charles Jourdan Reyes, Ana Westenberger

Movement Disorders. 2018;33(7):1095-1095

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X-linked dystonia (“Lubag”) presenting predominantly with parkinsonism: A more benign phenotype?

Virgilio Gerald H. Evidente, Katrina Gwinn-Hardy, John Hardy, Dena Hernandez, Andrew Singleton

Movement Disorders. 2001;17(1):200-202

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A specific subtype of Infantile Parkinsonism-dystonia identified

E Fisher

Clinical Genetics. 2011;79(4):332-334

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DYT3, X-linked Dystonia-parkinsonism (Lubag)

V.G.H. Evidente

Encyclopedia of Movement Disorders. 2010;408-412

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Eye movement deficits in X-linked dystonia-parkinsonism are related to striatal degeneration

Andreas Sprenger, Henrike Hanssen, Imke Hagedorn, Jannik Prasuhn, Raymond L. Rosales, Roland Dominic G. Jamora, Cid C. Diesta, Aloysius Domingo, Christine Klein, Norbert Brüggemann, Christoph Helmchen

Parkinsonism & Related Disorders. 2019;61:170-178

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Increased insula-putamen connectivity in X-linked dystonia-parkinsonism

Anne J. Blood, Jeff L. Waugh, Thomas F. Münte, Marcus Heldmann, Aloysius Domingo, Christine Klein, Hans C. Breiter, Lillian V. Lee, Raymond L. Rosales, Norbert Brüggemann

NeuroImage: Clinical. 2018;17:835-846

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Genetics in dystonia

Christine Klein

Parkinsonism & Related Disorders. 2014;20:S137-S142

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ATP1A3 mutation presenting as CAPOS syndrome + dystonia phenotype

Anjali Chouksey, Sanjay Pandey

Parkinsonism & Related Disorders. 2020;78:192-194

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