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There are 3045438 results for: content related to: Leukodystrophies in idiopathic adult-onset ataxia: Frequency and phenotype in 105 patients

  1. Leukodystrophies and genetic leukoencephalopathies in childhood: a national epidemiological study

    Developmental Medicine & Child Neurology

    Volume 58, Issue 7, July 2016, Pages: 680–689, Lesley A Stellitano, Anne Marie Winstone, Marjo S van der Knaap and Christopher M Verity

    Version of Record online : 11 FEB 2016, DOI: 10.1111/dmcn.13027

  2. Leukodystrophies underlying cryptic spastic paraparesis: frequency and phenotype in 76 patients

    European Journal of Neurology

    Volume 21, Issue 7, July 2014, Pages: 983–988, J. Müller vom Hagen, K. N. Karle, R. Schüle, I. Krägeloh-Mann and L. Schöls

    Version of Record online : 2 APR 2014, DOI: 10.1111/ene.12423

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

    Movement Disorders

    Volume 27, Issue 14, December 2012, Pages: 1831–1832, Bradley Osterman, Michel Sylvain, Sylvain Chouinard and Geneviève Bernard

    Version of Record online : 3 DEC 2012, DOI: 10.1002/mds.25270

  4. Death rates in the U.S. due to Krabbe disease and related leukodystrophy and lysosomal storage diseases

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2835–2842, Amy L. Barczykowski, Alexander H. Foss, Patricia K. Duffner, Li Yan and Randy L. Carter

    Version of Record online : 18 SEP 2012, DOI: 10.1002/ajmg.a.35624

  5. You have free access to this content
    Hypomyelinating leukodystrophies — a molecular insight into the white matter pathology

    Clinical Genetics

    Volume 90, Issue 4, October 2016, Pages: 293–304, A. Charzewska, J. Wierzba, E. Iżycka-Świeszewska, M. Bekiesińska-Figatowska, M. Jurek, A. Gintowt, A. Kłosowska, J. Bal and D. Hoffman-Zacharska

    Version of Record online : 17 JUN 2016, DOI: 10.1111/cge.12811

  6. You have free access to this content
    Pten Loss in Olig2 Expressing Neural Progenitor Cells and Oligodendrocytes Leads to Interneuron Dysplasia and Leukodystrophy

    STEM CELLS

    Volume 32, Issue 1, January 2014, Pages: 313–326, Cécile L. Maire, Shakti Ramkissoon, Marika Hayashi, Sam Haidar, Lori Ramkissoon, Emmanuelle DiTomaso and Keith L. Ligon

    Version of Record online : 3 JAN 2014, DOI: 10.1002/stem.1590

  7. PLP1 gene analysis in 88 patients with leukodystrophy

    Clinical Genetics

    Volume 84, Issue 6, December 2013, Pages: 566–571, P Martínez-Montero, M Muñoz-Calero, E Vallespín, J Campistol, L Martorell, MJ Ruiz-Falcó, A Santana, R Pons, A Dinopoulos, C Sierra, J Nevado and J Molano

    Version of Record online : 11 MAR 2013, DOI: 10.1111/cge.12103

  8. Metachromatic Leukodystrophy

    Acta Radiologica

    Volume 44, Issue 4, July 2003, Pages: 440–443, R. N. Sener

    Version of Record online : 4 JUL 2003, DOI: 10.1034/j.1600-0455.2003.00094.x

  9. Leukodystrophy

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    Encyclopedia of Special Education

    Paula Kilpatrick and Robert T. Brown

    Published Online : 7 FEB 2014, DOI: 10.1002/9781118660584.ese1417

  10. Metachromatic leukodystrophy: genetics, pathogenesis and therapeutic options

    Acta Paediatrica

    Volume 97, Issue s457, April 2008, Pages: 15–21, Volkmar Gieselmann

    Version of Record online : 13 MAR 2008, DOI: 10.1111/j.1651-2227.2008.00648.x

  11. Bridging the gap between metabolic profile determination and visualization in neurometabolic disorders: a multivariate analysis of proton magnetic resonance in vivo spectra

    Journal of Chemometrics

    Volume 27, Issue 3-4, March-April 2013, Pages: 76–90, Agnieszka Skorupa, Ewa Jamroz, Justyna Paprocka, Maria Sokół, Magdalena Wicher and Aleksandra Kiełtyka

    Version of Record online : 21 MAR 2013, DOI: 10.1002/cem.2494

  12. What can cell biology tell us about heterogeneity in lysosomal storage diseases?

    Acta Paediatrica

    Volume 94, Issue s447, March 2005, Pages: 80–86, V Gieselmann

    Version of Record online : 2 JAN 2007, DOI: 10.1111/j.1651-2227.2005.tb02118.x

  13. Adult onset pigmentary orthochromatic leukodystrophy with ovarian dysgenesis

    European Journal of Neurology

    Volume 9, Issue 6, November 2002, Pages: 663–670, J. Verghese, K. Weidenheim, S. Malik and I. Rapin

    Version of Record online : 9 DEC 2002, DOI: 10.1046/j.1468-1331.2002.00469.x

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    Preventable infections in children with leukodystrophy

    Annals of Clinical and Translational Neurology

    Volume 1, Issue 5, May 2014, Pages: 370–374, Holly M. Anderson, Jacob Wilkes, Ernest Kent Korgenski, Michael A. Pulsipher, Anne J. Blaschke, Adam L. Hersh, Rajendu Srivastava and Joshua L. Bonkowsky

    Version of Record online : 14 APR 2014, DOI: 10.1002/acn3.61

  15. Targeted leukodystrophy diagnosis based on charges and yields for testing

    American Journal of Medical Genetics Part A

    Volume 167, Issue 11, November 2015, Pages: 2541–2543, Jackson Richards, E. Kent Korgenski, Ryan J. Taft, Adeline Vanderver and Joshua L. Bonkowsky

    Version of Record online : 16 JUL 2015, DOI: 10.1002/ajmg.a.37215

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    Adult Onset Leukodystrophy with Neuroaxonal Spheroids: Clinical, Neuroimaging and Neuropathologic Observations

    Brain Pathology

    Volume 19, Issue 1, January 2009, Pages: 39–47, Stefanie H. Freeman, Bradley T. Hyman, Katherine B. Sims, E. T. Hedley-Whyte, Arastoo Vossough, Matthew P. Frosch and Jeremy D. Schmahmann

    Version of Record online : 15 APR 2008, DOI: 10.1111/j.1750-3639.2008.00163.x

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    Annals of Neurology

    Volume 60, Issue 4, October 2006, Page: 486, Louis Ptacek, Arnulf H. Koeppen and Ying-Hui Fu

    Version of Record online : 26 OCT 2006, DOI: 10.1002/ana.21005

  18. Leukodystrophy, Metachromatic

    Standard Article

    Encyclopedia of Special Education

    Paula Kilpatrick and Robert T. Brown

    Published Online : 7 FEB 2014, DOI: 10.1002/9781118660584.ese1418

  19. You have full text access to this OnlineOpen article
    Analysis of LMNB1 Duplications in Autosomal Dominant Leukodystrophy Provides Insights into Duplication Mechanisms and Allele-Specific Expression

    Human Mutation

    Volume 34, Issue 8, August 2013, Pages: 1160–1171, Elisa Giorgio, Harshvardhan Rolyan, Laura Kropp, Anish Baswanth Chakka, Svetlana Yatsenko, Eleonora Di Gregorio, Daniela Lacerenza, Giovanna Vaula, Flavia Talarico, Paola Mandich, Camilo Toro, Eleonore Eymard Pierre, Pierre Labauge, Sabina Capellari, Pietro Cortelli, Filippo Pinto Vairo, Diego Miguel, Danielle Stubbolo, Lourenco Charles Marques, William Gahl, Odile Boespflug-Tanguy, Atle Melberg, Sharon Hassin-Baer, Oren S. Cohen, Rastislav Pjontek, Armin Grau, Thomas Klopstock, Brent Fogel, Inge Meijer, Guy Rouleau, Jean-Pierre L. Bouchard, Madhavi Ganapathiraju, Adeline Vanderver, Niklas Dahl, Grace Hobson, Alfredo Brusco, Alessandro Brussino and Quasar Saleem Padiath

    Version of Record online : 28 MAY 2013, DOI: 10.1002/humu.22348

  20. De Novo mutations in the β-tubulin gene TUBB4: From DYT4 to leukoencephalopathy with hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC syndrome)

    Movement Disorders

    Volume 28, Issue 10, September 2013, Page: 1343, Athanasia Alexoudi and Susanne A. Schneider

    Version of Record online : 6 SEP 2013, DOI: 10.1002/mds.25565