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There are 7582584 results for: content related to: Genetic heterogeneity in patients with pantothenate kinase–associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern

  1. Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration

    Movement Disorders

    Volume 20, Issue 7, July 2005, Pages: 819–821, Yu-hu Zhang, Bei-sha Tang, Ai-ling Zhao, Kun Xia, Zhi-gao Long, Ji-feng Guo, Shawn K. Westaway and Susan J. Hayflick

    Version of Record online : 3 MAR 2005, DOI: 10.1002/mds.20408

  2. You have full text access to this OnlineOpen article
    Eye-of-the-Tiger sign is not Pathognomonic of Pantothenate Kinase-Associated Neurodegeneration in Adult Cases

    Brain and Behavior

    Volume 1, Issue 1, September 2011, Pages: 55–56, Chaw-Liang Chang and Chih-Ming Lin

    Version of Record online : 30 MAY 2011, DOI: 10.1002/brb3.8

  3. Indian-subcontinent NBIA: Unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms

    Movement Disorders

    Volume 25, Issue 10, 30 July 2010, Pages: 1424–1431, Annu Aggarwal, Susanne A. Schneider, Henry Houlden, Monty Silverdale, Reema Paudel, Coro Paisan-Ruiz, Shrinivas Desai, Mihir Munshi, Darshana Sanghvi, John Hardy, Kailash P. Bhatia and Mohit Bhatt

    Version of Record online : 1 APR 2010, DOI: 10.1002/mds.23095

  4. Clinical, imaging, and molecular findings in a sample of Mexican families with pantothenate kinase-associated neurodegeneration

    Clinical Genetics

    Volume 87, Issue 3, March 2015, Pages: 259–265, H. Morales-Briceño, O.F. Chacón-Camacho, E.A. Pérez-González, J. Arteaga-Vázquez, M. Rodríguez-Violante, A. Cervantes-Arriaga, L. Pérez-Rodríguez, J.C. Zenteno and O.M. Mutchinick

    Version of Record online : 6 JUN 2014, DOI: 10.1111/cge.12400

  5. Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation

    Annals of Neurology

    Volume 59, Issue 2, February 2006, Pages: 248–256, Monika B. Hartig, Konstanze Hörtnagel, Barbara Garavaglia, Giovanna Zorzi, Tomasz Kmiec, Thomas Klopstock, Kevin Rostasy, Marina Svetel, Vladimir S. Kostic, Markus Schuelke, Evelyn Botz, Adolf Weindl, Ivana Novakovic, Nardo Nardocci, Holger Prokisch and Thomas Meitinger

    Version of Record online : 25 JAN 2006, DOI: 10.1002/ana.20771

  6. Partial deficit of pantothenate kinase 2 catalytic activity in a case of tremor-predominant neurodegeneration with brain iron accumulation

    Movement Disorders

    Volume 21, Issue 5, May 2006, Pages: 718–722, Tsao-Wei Liang, Adam C. Truax, John Q. Trojanowski, Virginia M.-Y. Lee, Matthew B. Stern and Paul T. Kotzbauer

    Version of Record online : 31 JAN 2006, DOI: 10.1002/mds.20797

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    Missense PANK2 mutation without “Eye of the tiger” sign: MR findings in a large group of patients with pantothenate kinase-associated neurodegeneration (PKAN)

    Journal of Magnetic Resonance Imaging

    Volume 35, Issue 4, April 2012, Pages: 788–794, Rafael Fermin Delgado, Pedro Roa Sanchez, Herwin Speckter, Eddy Perez Then, Ramney Jimenez, Jairo Oviedo, Paulo R. Dellani, Bernd Foerster and Peter Stoeter

    Version of Record online : 29 NOV 2011, DOI: 10.1002/jmri.22884

  8. Pantothenate kinase-associated neurodegeneration in Korea: recurrent R440P mutation in PANK2 and outcome of deep brain stimulation

    European Journal of Neurology

    Volume 19, Issue 4, April 2012, Pages: 556–561, B. C. Lim, C.-S. Ki, A. Cho, H. Hwang, K. J. Kim, Y. S. Hwang, Y. E. Kim, J. Y. Yun, B. S. Jeon, Y. H. Lim, S. H. Paek and J. H. Chae

    Version of Record online : 22 NOV 2011, DOI: 10.1111/j.1468-1331.2011.03589.x

  9. Clinical heterogeneity of neurodegeneration with brain iron accumulation (Hallervorden-Spatz syndrome) and pantothenate kinase-associated neurodegeneration

    Movement Disorders

    Volume 19, Issue 1, January 2004, Pages: 36–42, Madhavi Thomas, Susan J. Hayflick and Joseph Jankovic

    Version of Record online : 28 OCT 2003, DOI: 10.1002/mds.10650

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    7-Tesla Magnetic Resonance Imaging for Brain Iron Quantification in Homozygous and Heterozygous PANK2 Mutation Carriers

    Movement Disorders Clinical Practice

    Volume 1, Issue 4, December 2014, Pages: 329–335, Petr Dusek, Elena Maria Tovar Martinez, Vince Istvan Madai, Robert Jech, Jan Sobesky, Friedemann Paul, Thoralf Niendorf, Jens Wuerfel and Susanne A. Schneider

    Version of Record online : 23 OCT 2014, DOI: 10.1002/mdc3.12080

  11. Tremor-Dominant Pantothenate Kinase-associated Neurodegeneration

    Movement Disorders Clinical Practice

    Mohammad Rohani, Gholamali Shahidi, Afagh Alavi, Anthony E. Lang, Niloufar Yousefi, Said Razme and Alfonso Fasano

    Version of Record online : 30 JUN 2017, DOI: 10.1002/mdc3.12512

  12. Syndromes of neurodegeneration with brain iron accumulation (NBIA): An update on clinical presentations, histological and genetic underpinnings, and treatment considerations

    Movement Disorders

    Volume 27, Issue 1, January 2012, Pages: 42–53, Susanne A. Schneider, John Hardy and Kailash P. Bhatia

    Version of Record online : 26 OCT 2011, DOI: 10.1002/mds.23971

  13. Neurodegeneration with Brain Iron Accumulation: Clinicoradiological Approach to Diagnosis

    Journal of Neuroimaging

    Volume 25, Issue 4, July/August 2015, Pages: 539–551, Lázaro L. F. Amaral, Santhosh Gaddikeri, Philip R. Chapman, Rasmoni Roy, Ramya S. Gaddikeri, Victor Hugo Marussi and Asim K. Bag

    Version of Record online : 24 DEC 2014, DOI: 10.1111/jon.12195

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    Childhood disorders of neurodegeneration with brain iron accumulation (NBIA)

    Developmental Medicine & Child Neurology

    Volume 53, Issue 5, May 2011, Pages: 394–404, MANJU A KURIAN, ALASDAIR MCNEILL, JEAN-PIERRE LIN and EAMONN R MAHER

    Version of Record online : 12 APR 2011, DOI: 10.1111/j.1469-8749.2011.03955.x

  15. Genetic, clinical, and imaging characterization of one patient with late-onset, slowly progressive, pantothenate kinase-associated neurodegeneration

    Movement Disorders

    Volume 21, Issue 3, March 2006, Pages: 417–418, Angelo Antonini, Stefano Goldwurm, Riccardo Benti, Holger Prokisch, Monika Ebhardt, Roberto Cilia, Michela Zini, Andrea Righini, Giovanni Cossu and Gianni Pezzoli

    Version of Record online : 2 NOV 2005, DOI: 10.1002/mds.20774

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    Panthotenate Kinase-Associated Neurodegeneration Has a Founder Mutation (c.215_216insa) in Indian Agrawal Patients

    Movement Disorders Clinical Practice

    Volume 4, Issue 1, January/February 2017, Pages: 96–99, Vrajesh Udani, Soma Das and Rahul Chhabria

    Version of Record online : 5 APR 2016, DOI: 10.1002/mdc3.12341

  17. PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation

    Movement Disorders

    Volume 28, Issue 2, February 2013, Pages: 228–231, Mitra Ansari Dezfouli, Afagh Alavi, Mohammad Rohani, Mohamad Rezvani, Tayebeh Nekuie, Brandy Klotzle, Seyed Hasan Tonekaboni, Gholam Ali Shahidi and Elahe Elahi

    Version of Record online : 19 NOV 2012, DOI: 10.1002/mds.25271

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    Poster Presentations

    Movement Disorders

    Volume 27, Issue S1, June 2012, Pages: S1–S523,

    Version of Record online : 19 JUN 2012, DOI: 10.1002/mds.25051

  19. Mitochondrial Localization of Human PANK2 and Hypotheses of Secondary Iron Accumulation in Pantothenate Kinase-Associated Neurodegeneration

    Annals of the New York Academy of Sciences

    Volume 1012, Issue 1, March 2004, Pages: 282–298, MONIQUE A. JOHNSON, YIEN MING KUO, SHAWN K. WESTAWAY, SUSAN M. PARKER, KATHERINE H. L. CHING, JANE GITSCHIER and SUSAN J. HAYFLICK

    Version of Record online : 12 JAN 2006, DOI: 10.1196/annals.1306.023

  20. You have full text access to this OnlineOpen article
    Pantothenate kinase-associated neurodegeneration is not a synucleinopathy

    Neuropathology and Applied Neurobiology

    Volume 39, Issue 2, February 2013, Pages: 121–131, A. Li, R. Paudel, R. Johnson, R. Courtney, A. J. Lees, J. L. Holton, J. Hardy, T. Revesz and H. Houlden

    Version of Record online : 25 JAN 2013, DOI: 10.1111/j.1365-2990.2012.01269.x