scholarly journals Movement Disorder Due to Involvement of Bilateral Basal Ganglia in Diabetic Uremic Patient

2020 ◽  
Vol 28 (3) ◽  
pp. 192-195
Author(s):  
Merve Melodi ÇAKAR ◽  
Hülya ÖZKAN
2012 ◽  
Vol 58 ◽  
pp. 203-228 ◽  
Author(s):  
Niall Quinn ◽  
John Rothwell ◽  
Peter Jenner

David Marsden was the most outstanding UK clinical neuroscientist of his generation, making key discoveries in the neurophysiology, neurochemistry and clinical aspects of diseases of the basal ganglia, and their normal function. His legacies are the establishment, with Stanley Fahn in the USA, of movement disorders as a subspecialty within neurology, of the international Movement Disorder Society, and of the journal Movement Disorders ; his ex-students and fellows around the globe; and his research and teaching output embodied in his extraordinarily prolific publication record of more than 1360 papers, books and chapters, culminating in the posthumous completion and publication in December 2011 of Marsden’s book of movement disorders , a project he had started in 1984. All of these were achieved through the combination of his intellect and drive, his communication skills, and his forceful and charismatic personality.


2011 ◽  
Vol 14 (3) ◽  
pp. 211 ◽  
Author(s):  
GurusidheshwarM Wali ◽  
RajendraV Mali ◽  
MallikarjunS Khanpet

2012 ◽  
Vol 27 (4) ◽  
pp. 591-593
Author(s):  
Christos Ganos ◽  
Simone Zittel ◽  
Christian Gerloff ◽  
Alexander Münchau ◽  
Tobias Bäumer

2012 ◽  
Vol 4 (3) ◽  
pp. 156-158 ◽  
Author(s):  
Hipólito Nzwalo ◽  
Francisca Sá ◽  
Carlos Capela ◽  
Fátima Ferreira ◽  
Carlos Basílio
Keyword(s):  

2010 ◽  
Vol 67 (2) ◽  
Author(s):  
Toby C. Yaltho ◽  
Mya C. Schiess ◽  
Erin Furr-Stimming
Keyword(s):  

2014 ◽  
Vol 2014 ◽  
pp. 1-3 ◽  
Author(s):  
Rocco Salvatore Calabrò ◽  
Letteria Spadaro ◽  
Angela Marra ◽  
Placido Bramanti

Fahr’s disease (FD) is characterized by sporadic or familiar idiopathic calcification of the basal ganglia, dentate nuclei of the cerebellum, and centrum semiovale, mainly presenting with movement disorder, dementia, and behavioral abnormalities. We described a rare case of Fahr’s disease presenting at onset only with behavioral and neuropsychological alterations, whose diagnosis was supposed only after a brain CT, which showed extensive bilateral calcifications in the dentate nuclei of the cerebellum and basal ganglia. Since the onset of Fahr’s disease may be a dysexecutive syndrome with behavioral abnormalities, the clinical and radiological features are really important to do the appropriate diagnosis.


Author(s):  
Jeffrey S Raskin ◽  
Mered Parnes ◽  
Sandi Lam

A 9-year-old male with intellectual disability and epilepsy presenting with a progressive movement disorder characterized by chorea and dystonia primarily affecting the left face, arm, and leg and attributed to an arteriovenous malformation centered within the right thalamus with bilateral extension into the basal ganglia, midbrain and pons is reported.


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