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There are 25983 results for: content related to: Enteric Fever Presenting as Acute Ataxia

  1. Plasmodium falciparum delayed cerebellar ataxia and late cerebral malaria

    Movement Disorders

    Volume 20, Issue 8, August 2005, Pages: 1087–1088, Mahavir D. Mohire

    Version of Record online : 2 JUN 2005, DOI: 10.1002/mds.20566

  2. Response to steroid treatment in anti–glutamic acid decarboxylase antibody-associated cerebellar ataxia, stiff person syndrome and polyendocrinopathy

    Movement Disorders

    Volume 21, Issue 12, December 2006, Pages: 2263–2264, Ji-Youn Kim, Eun Joo Chung, Jong-Hun Kim, Ki-Young Jung and Won Yong Lee

    Version of Record online : 29 SEP 2006, DOI: 10.1002/mds.21041

  3. Transient exacerbation of ataxia with smoking: A prevalence survey

    Movement Disorders

    Volume 24, Issue 6, 30 April 2009, Pages: 937–938, Raquel C. Gardner, Roy N. Alcalay and Jeremy D. Schmahmann

    Version of Record online : 19 FEB 2009, DOI: 10.1002/mds.22470

  4. You have full text access to this OnlineOpen article
    A de novo mutation in the NALCN gene in an adult patient with cerebellar ataxia associated with intellectual disability and arthrogryposis

    Clinical Genetics

    Volume 90, Issue 6, December 2016, Pages: 556–557, Y. Wang, K. Koh, Y. Ichinose, M. Yasumura, T. Ohtsuka and Y. Takiyama

    Version of Record online : 16 SEP 2016, DOI: 10.1111/cge.12851

  5. A case of neurosyphilis presenting with myoclonus, cerebellar ataxia, and speech disturbance

    Movement Disorders

    Volume 27, Issue 6, May 2012, Page: 794, Binit B. Shah and Anthony E. Lang

    Version of Record online : 7 MAR 2012, DOI: 10.1002/mds.24952

  6. Unilateral thalamic stimulation safely improved fragile X–associated tremor ataxia: A case report

    Movement Disorders

    Volume 27, Issue 6, May 2012, Pages: 797–799, Suhan Senova, Béchir Jarraya, Hiro Iwamuro, Naoki Tani, Naoufel Ouerchefani, Hélène Lepetit, Jean-Marc Gurruchaga, Pierre Brugières, Emmanuelle Apartis, Thomas de Broucker and Stéphane Palfi

    Version of Record online : 27 JAN 2012, DOI: 10.1002/mds.24923

  7. Diagnosis and management of early- and late-onset cerebellar ataxia

    Clinical Genetics

    Volume 71, Issue 1, January 2007, Pages: 12–24, E Brusse, JA Maat-Kievit and JC Van Swieten

    Version of Record online : 28 NOV 2006, DOI: 10.1111/j.1399-0004.2006.00722.x

  8. Opsoclonus myoclonus syndrome in the context of Salmonellosis

    Movement Disorders

    Volume 24, Issue 15, 15 November 2009, Pages: 2306–2308, Olivier Flabeau, Wassilios Meissner, Alexandra Foubert-Samier, Dominique Guehl, Patrice Desbordes and François Tison

    Version of Record online : 20 OCT 2009, DOI: 10.1002/mds.22832

  9. You have free access to this content
    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

  10. You have free access to this content
    Low-dose Methylphenidate Monotherapy for Features of Attention-Deficit/Hyperactivity Disorder Secondary to Hereditary Cerebellar Ataxia

    CNS Neuroscience & Therapeutics

    Volume 21, Issue 8, August 2015, Pages: 672–673, Li-Yu Hu, Yi-Liang Lin, Huei-Sing Chang, Ti Lu and Wan-Shan Lin

    Version of Record online : 15 MAY 2015, DOI: 10.1111/cns.12403

  11. C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia

    Movement Disorders

    Volume 27, Issue 14, December 2012, Pages: 1835–1836, Brent L. Fogel, Mochtar Pribadi, Sarah Pi, Susan L. Perlman, Daniel H. Geschwind and Giovanni Coppola

    Version of Record online : 18 OCT 2012, DOI: 10.1002/mds.25245

  12. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 30, Issue S1, June 2015, Pages: S1–S567,

    Version of Record online : 12 JUN 2015, DOI: 10.1002/mds.26295

  13. Exome sequencing reveals a novel ANO10 mutation in a Japanese patient with autosomal recessive spinocerebellar ataxia

    Clinical Genetics

    Volume 85, Issue 3, March 2014, Pages: 296–297, H. Maruyama, H. Morino, R. Miyamoto, N. Murakami, T. Hamano and H. Kawakami

    Version of Record online : 4 APR 2013, DOI: 10.1111/cge.12140

  14. Poster session 1, Abstracts 1–90

    Movement Disorders

    Volume 19, Issue S9, 2004, Pages: S19–S47,

    Version of Record online : 10 MAY 2004, DOI: 10.1002/mds.20168

  15. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I

    Annals of Neurology

    Volume 35, Issue 4, April 1994, Pages: 439–444, Dr. A. Benomar, E. Le Guern, A. Dürr, H. Ouhabi, G. Stevanin, M. Yahyaoui, T. Chkili, Y. Agid and A. Brice

    Version of Record online : 8 OCT 2004, DOI: 10.1002/ana.410350411

  16. Abstracts of The Movement Disorder Society's Twelfth International Congress of Parkinson's Disease and Movement Disorders

    Movement Disorders

    Volume 23, Issue S1, 15 May 2008, Pages: S1–S422,

    Version of Record online : 28 MAY 2008, DOI: 10.1002/mds.22133

  17. Ataxia and cerebellar atrophy—A novel manifestation of neuro-Behçet disease?

    Movement Disorders

    Volume 23, Issue 2, 30 January 2008, Pages: 307–308, Raquel C. Gardner and Jeremy D. Schmahmann

    Version of Record online : 28 NOV 2007, DOI: 10.1002/mds.21834

  18. Cerebellar ataxia and total albinism: A kindred suggesting pleiotropism or linkage

    Clinical Genetics

    Volume 5, Issue 3, March 1974, Pages: 196–204, H. Skre and K. Berg

    Version of Record online : 23 APR 2008, DOI: 10.1111/j.1399-0004.1974.tb01682.x

  19. You have full text access to this Open Access content
    Spongy Degeneration with Cerebellar Ataxia in Malinois Puppies: A Hereditary Autosomal Recessive Disorder?

    Journal of Veterinary Internal Medicine

    Volume 25, Issue 3, May/June 2011, Pages: 490–496, M. Kleiter, S. Högler, S. Kneissl, A. Url and M. Leschnik

    Version of Record online : 12 APR 2011, DOI: 10.1111/j.1939-1676.2011.0720.x


    Acta Paediatrica

    Volume 57, Issue 2, March 1968, Pages: 151–152, Georg Dano

    Version of Record online : 21 JAN 2008, DOI: 10.1111/j.1651-2227.1968.tb04668.x