Spinocerebellar Ataxia
Links shared publicly online about this topic
Fatigue in spinocerebellar ataxia
neurology.org — “Fatigue in spinocerebellar ataxia” View full resource at neurology.org
Most Recently Shared on March 21, 2011 at 12:50 pm By:
Fatigue in spinocerebellar ataxia: Patient self-assessment of an early and disabling symptom http://bit.ly/eWKXW3 #neurology
Neurology Article - Spinocerebellar Ataxias
mdlinx.com — “Mapping of Autosomal Dominant Cerebellar Ataxia Without the Pathogenic PPP2R2B Mutation to the Locus for Spinocerebellar Ataxia 12” View full resource at mdlinx.com
Most Recently Shared on October 30, 2010 at 1:33 am By:
Mapping of Autosomal Dominant Cerebellar Ataxia Without the Pathogenic PPP2R2B Mutation to the Locus for Spi... http://bit.ly/b2JOlu #neuro
Sleep Disorders in Spinocerebellar Ataxia Type 2 Patients
content.karger.com — “Sleep Disorders in Spinocerebellar Ataxia Type 2 Patients” View full resource at content.karger.com
Most Recently Shared on April 15, 2011 at 3:10 am By:
Sleep Disorders in Spinocerebellar Ataxia Type 2 Patients: Neurodegenerative Dis (DOI:10.1159/000324374) (Source... http://bit.ly/dXCpSR
A randomized trial of varenicline (Chantix) for the treatment of spinocerebellar ataxia type 3
neurology.org — “A randomized trial of varenicline (Chantix) for the treatment of spinocerebellar ataxia type 3” View full resource at neurology.org
Most Recently Shared on February 22, 2012 at 9:05 pm By:
A randomized trial of varenicline (Chantix) for the treatment of spinocerebellar ataxia type 3 http://t.co/jldDFc22 #neurology
Ataxia Spinocerebellar (SCA) - Facts and Information
disabled-world.com — “Spinocerebellar ataxia (SCA) is a genetically inherited disorder characterized by abnormalities in brain functioning” View full resource at disabled-world.com
Most Recently Shared on April 13, 2010 at 12:28 pm By:
Ataxia Spinocerebellar (SCA) - Facts and Information http://ff.im/-iXB2N
Ataxia on #MDlinx
mdlinx.com — “Ataxia on #MDlinx” View full resource at mdlinx.com
Most Recently Shared on October 22, 2010 at 2:09 am By:
Ophthalmologic features of the common spinocerebellar ataxias: Current Opinion in Ophthalmology http://bit.ly/b2TCyz #neuro
Defective Protein Is A Double Hit For Ataxia
medicalnewstoday.com — “The neurodegenerative disease spinocerebellar ataxia type 5 (SCA5) damages nerve cells in two ways. University of Minnesota researchers now report that the defective protein responsible for the di” View full resource at medicalnewstoday.com
Most Recently Shared on April 6, 2010 at 6:09 pm By:
Defective Protein Is A Double Hit For Ataxia http://mnt.to/3zSh #neurology
Psychiatry Medical News about Ataxia
mdlinx.com — “Neuropsychological Features of Patients with Spinocerebellar Ataxia (SCA) Types 1, 2, 3, and 6” View full resource at mdlinx.com
Most Recently Shared on June 7, 2010 at 7:55 pm By:
Neuropsychological Features of Patients with Spinocerebellar Ataxia (SCA) Types 1, 2, 3, and 6: The Cerebellum http://bit.ly/aAz2vz #PSY
Defective protein is a double hit for ataxia
physorg.com — “The neurodegenerative disease spinocerebellar ataxia type 5 (SCA5) damages nerve cells in two ways. University of Minnesota researchers now report that the defective protein responsible for the disease cuts the number of synaptic terminals and snarls traffic inside neurons. The study appears in the ...” View full resource at physorg.com
Most Recently Shared on April 5, 2010 at 1:42 pm By:
Defective protein is a double hit for ataxia: The neurodegenerative disease spinocerebellar ataxia type 5 (SCA5) d... http://bit.ly/blVDgc
Exercise provides clue to deadly ataxia
sciencedaily.com — “When researchers prescribed mild exercise for mice with a neurodegenerative disorder called spinocerebellar ataxia 1, they did not know what to expect. What they found was the mice that exercised lived longer than those that had not.” View full resource at sciencedaily.com
Most Recently Shared on November 4, 2011 at 10:39 am By:
Exercise provides clue to deadly ataxia: http://t.co/cOiTjnlW via @AddThis
Defective protein is a double hit for ataxia
physorg.com — “The neurodegenerative disease spinocerebellar ataxia type 5 (SCA5) damages nerve cells in two ways. University of Minnesota researchers now report that the defective protein responsible for the disease cuts the number of synaptic terminals and snarls traffic inside neurons. The study appears in the ...” View full resource at physorg.com
Most Recently Shared on April 5, 2010 at 1:00 pm By:
Defective protein is a double hit for ataxia http://tw.physorg.com/189600520
Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond : The Lancet Neurology
thelancet.com — “Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond. By - Dr Alexandra Durr MD” View full resource at thelancet.com
Most Recently Shared on August 16, 2010 at 3:48 pm By:
Spinocerebellar ataxias: clinical features and pathophysiological mechanisms of autosomal dominant forms http://bit.ly/afaWzT #neurology
Family Medicine News & Articles - MDLinx - Ataxia on #MDlinx
mdlinx.com — “Family Medicine News & Articles - MDLinx - Ataxia on #MDlinx” View full resource at mdlinx.com
Most Recently Shared on September 21, 2010 at 1:54 am By:
Difference in the Effects of Tandospirone on Ataxia in Various Types of Spinocerebellar Degeneration: A... http://bit.ly/8Xoh8z #GM #mdlinx
Abnormality Discovered In Patients With Specific Ataxia That Could Be Target For Treatment
medicalnewstoday.com — “An abnormality discovered by U-M researchers in mice with Spinocerebellar Ataxia type 3 could represent a target for therapy.In a paper published this week in the Journal of Neuroscience,” View full resource at medicalnewstoday.com
Most Recently Shared on September 10, 2011 at 8:05 am By:
Abnormality Discovered In Patients With Specific Ataxia That Could Be Target For Treatment http://mnt.to/3ZyN #neurology
Rare goals: a diagnostic tool for every orphan disease by 2020 - SmartPlanet
smartplanet.com — “Von Hippel-Lindau syndrome. Serpiginous choroiditis. Prader--Willi syndrome. Polycythemia vera. Leiomyosarcoma. Fabry disease. Spinocerebellar ataxia” View full resource at smartplanet.com
Most Recently Shared on April 7, 2011 at 5:20 am By:
Rare goals: a diagnostic tool for every orphan disease by 2020 http://smrt.io/fQk7kX
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Neurology Journal
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