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There are 7663501 results for: content related to: Are substantia nigra neurons subject to mitochondrial dysfunction in early life more able to adapt?

  1. POLG, but not PEO1, is a frequent cause of cerebellar ataxia in Central Europe

    Movement Disorders

    Volume 25, Issue 15, 15 November 2010, Pages: 2678–2682, Julia Schicks, Matthis Synofzik, Claudia Schulte and Ludger Schöls

    Article first published online : 27 AUG 2010, DOI: 10.1002/mds.23286

  2. You have full text access to this OnlineOpen article
    Heterozygous Polg mutation causes motor dysfunction due to mtDNA deletions

    Annals of Clinical and Translational Neurology

    Volume 1, Issue 11, November 2014, Pages: 909–920, Satoshi Fuke, Mizue Kametani, Kazuyuki Yamada, Takaoki Kasahara, Mie Kubota-Sakashita, Gregory C. Kujoth, Tomas A. Prolla, Seiji Hitoshi and Tadafumi Kato

    Article first published online : 22 OCT 2014, DOI: 10.1002/acn3.133

  3. Myoclonus in mitochondrial disorders

    Movement Disorders

    Volume 29, Issue 6, May 2014, Pages: 722–728, Michelangelo Mancuso, Daniele Orsucci, Corrado Angelini, Enrico Bertini, Michela Catteruccia, Elena Pegoraro, Valerio Carelli, Maria L. Valentino, Giacomo P. Comi, Carlo Minetti, Claudio Bruno, Maurizio Moggio, Elena Caldarazzo Ienco, Tiziana Mongini, Liliana Vercelli, Guido Primiano, Serenella Servidei, Paola Tonin, Mauro Scarpelli, Antonio Toscano, Olimpia Musumeci, Isabella Moroni, Graziella Uziel, Filippo M. Santorelli, Claudia Nesti, Massimiliano Filosto, Costanza Lamperti, Massimo Zeviani and Gabriele Siciliano

    Article first published online : 7 FEB 2014, DOI: 10.1002/mds.25839

  4. “Atypical” atypical parkinsonism: New genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy—A diagnostic guide

    Movement Disorders

    Volume 28, Issue 9, August 2013, Pages: 1184–1199, Maria Stamelou, Niall P. Quinn and Kailash P. Bhatia

    Article first published online : 29 MAY 2013, DOI: 10.1002/mds.25509

  5. You have full text access to this OnlineOpen article
    Prospective study of POLG mutations presenting in children with intractable epilepsy: Prevalence and clinical features

    Epilepsia

    Volume 54, Issue 6, June 2013, Pages: 1002–1011, Johanna Uusimaa, Vasantha Gowda, Anthony McShane, Conrad Smith, Julie Evans, Annie Shrier, Manisha Narasimhan, Anthony O'Rourke, Yusuf Rajabally, Tammy Hedderly, Frances Cowan, Carl Fratter and Joanna Poulton

    Article first published online : 28 FEB 2013, DOI: 10.1111/epi.12115

  6. You have full text access to this Open Access content
    Age-dependent cardiomyopathy in mitochondrial mutator mice is attenuated by overexpression of catalase targeted to mitochondria

    Aging Cell

    Volume 9, Issue 4, August 2010, Pages: 536–544, Dao-Fu Dai, Tony Chen, Jonathan Wanagat, Michael Laflamme, David J. Marcinek, Mary J Emond, Calvin P. Ngo, Tomas A. Prolla and Peter S. Rabinovitch

    Article first published online : 29 APR 2010, DOI: 10.1111/j.1474-9726.2010.00581.x

  7. POLG mutations in Australian patients with mitochondrial disease

    Internal Medicine Journal

    Volume 43, Issue 2, February 2013, Pages: 150–156, P. Woodbridge, C. Liang, R. L. Davis, H. Vandebona and C. M. Sue

    Article first published online : 12 FEB 2013, DOI: 10.1111/j.1445-5994.2012.02847.x

  8. Mitochondrial DNA Polymerase γ Mutations and Their Implications in mtDNA Alterations in Colorectal Cancer

    Annals of Human Genetics

    Volume 79, Issue 5, September 2015, Pages: 320–328, Katarzyna Linkowska, Arkadiusz Jawień, Andrzej Marszałek, Boris A. Malyarchuk, Katarzyna Tońska, Ewa Bartnik, Katarzyna Skonieczna and Tomasz Grzybowski

    Article first published online : 7 APR 2015, DOI: 10.1111/ahg.12111

  9. Polymerase gamma disease through the ages

    Developmental Disabilities Research Reviews

    Volume 16, Issue 2, June 2010, Pages: 163–174, Russell P. Saneto and Robert K. Naviaux

    Article first published online : 27 AUG 2010, DOI: 10.1002/ddrr.105

  10. You have free access to this content
    Germline variants of base excision repair genes and breast cancer: A polymorphism in DNA polymerase gamma modifies gene expression and breast cancer risk

    International Journal of Cancer

    Volume 132, Issue 1, 1 January 2013, Pages: 55–62, Odilia Popanda, Petra Seibold, Ivaylo Nikolov, Christopher C. Oakes, Barbara Burwinkel, Sebastian Hausmann, Dieter Flesch-Janys, Christoph Plass, Jenny Chang-Claude and Peter Schmezer

    Article first published online : 26 JUN 2012, DOI: 10.1002/ijc.27665

  11. The syndrome of deafness-dystonia: Clinical and genetic heterogeneity

    Movement Disorders

    Volume 28, Issue 6, June 2013, Pages: 795–803, Maja Kojovic, Isabel Pareés, Tania Lampreia, Karolina Pienczk-Reclawowicz, Georgia Xiromerisiou, Ignacio Rubio-Agusti, Milica Kramberger, Miryam Carecchio, Anas M. Alazami, Francesco Brancati, Jaroslaw Slawek, Zvezdan Pirtosek, Enza Maria Valente, Fowzan S. Alkuraya, Mark J. Edwards and Kailash P. Bhatia

    Article first published online : 15 FEB 2013, DOI: 10.1002/mds.25394

  12. Structural studies of parkin and sacsin: Mitochondrial dynamics in neurodegenerative diseases

    Movement Disorders

    Volume 30, Issue 12, October 2015, Pages: 1610–1619, Xinlu Li and Kalle Gehring

    Article first published online : 11 SEP 2015, DOI: 10.1002/mds.26357

  13. Genetics of movement disorders in the next-generation sequencing era

    Movement Disorders

    Volume 31, Issue 4, April 2016, Pages: 458–470, Simone Olgiati, Marialuisa Quadri and Vincenzo Bonifati

    Article first published online : 22 FEB 2016, DOI: 10.1002/mds.26521

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    Poster Presentations

    Movement Disorders

    Volume 29, Issue S1, May 2014, Pages: S1–S571,

    Article first published online : 6 JUN 2014, DOI: 10.1002/mds.25914

  15. Screening for POLG W748S and A467T mutations in ataxia patients from Spain

    Movement Disorders

    Volume 27, Issue 10, 1 September 2012, Page: 1326, Ana L. Pelayo-Negro, Coro Sánchez-Quintana, Maria C. Rodríguez-Oroz, Victor Volpini, Massimo Zeviani, Miguel A. Tola-Arribas, José Berciano and Jon Infante

    Article first published online : 18 JUN 2012, DOI: 10.1002/mds.25085

  16. Treatable causes of cerebellar ataxia

    Movement Disorders

    Volume 30, Issue 5, 15 April 2015, Pages: 614–623, Adolfo Ramirez-Zamora, Warren Zeigler, Neeja Desai and José Biller

    Article first published online : 11 MAR 2015, DOI: 10.1002/mds.26158

  17. Valproic acid-induced hepatotoxicity in alpers syndrome is associated with mitochondrial permeability transition pore opening-dependent apoptotic sensitivity in an induced pluripotent stem cell model

    Hepatology

    Volume 61, Issue 5, May 2015, Pages: 1730–1739, Shengbiao Li, Jingyi Guo, Zhongfu Ying, Shen Chen, Liang Yang, Keshi Chen, Qi Long, Dajiang Qin, Duanqing Pei and Xingguo Liu

    Article first published online : 10 MAR 2015, DOI: 10.1002/hep.27712

  18. Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

    Movement Disorders

    Volume 31, Issue 4, April 2016, Pages: 436–457, Connie Marras, Anthony Lang, Bart P. van de Warrenburg, Carolyn M. Sue, Sarah J. Tabrizi, Lars Bertram, Saadet Mercimek-Mahmutoglu, Darius Ebrahimi-Fakhari, Thomas T. Warner, Alexandra Durr, Birgit Assmann, Katja Lohmann, Vladimir Kostic and Christine Klein

    Article first published online : 15 APR 2016, DOI: 10.1002/mds.26527

  19. You have full text access to this Open Access content
    Increase in mitochondrial DNA mutations impairs retinal function and renders the retina vulnerable to injury

    Aging Cell

    Volume 10, Issue 4, August 2011, Pages: 572–583, Yu X. G. Kong, Nicole Van Bergen, Ian A. Trounce, Bang V. Bui, Vicki Chrysostomou, Hayley Waugh, Algis Vingrys and Jonathan G. Crowston

    Article first published online : 7 APR 2011, DOI: 10.1111/j.1474-9726.2011.00690.x

  20. You have full text access to this OnlineOpen article
    Adult-onset myoclonus ataxia associated with the mitochondrial m.8993T>C “NARP” mutation

    Movement Disorders

    Volume 30, Issue 10, September 2015, Pages: 1432–1433, Mika H. Martikainen, Grainne S. Gorman, Paul Goldsmith, David J. Burn, Doug M. Turnbull and Andrew M. Schaefer

    Article first published online : 12 AUG 2015, DOI: 10.1002/mds.26358