scholarly journals A novel MT-CO2 variant causing cerebellar ataxia and neuropathy: the role of muscle biopsy in diagnosis and defining pathogenicity

Author(s):  
Karen Baty ◽  
Maria E. Farrugia ◽  
Sila Hopton ◽  
Gavin Falkous ◽  
Andrew M. Schaefer ◽  
...  
2004 ◽  
Vol 14 (10) ◽  
pp. 650-658 ◽  
Author(s):  
Sylvie Tuffery-Giraud ◽  
Céline Saquet ◽  
Sylvie Chambert ◽  
Bernard Echenne ◽  
Jean Marie Cuisset ◽  
...  

2013 ◽  
Vol 47 (6) ◽  
pp. 835-839 ◽  
Author(s):  
Stephen A. Goutman ◽  
Richard A. Prayson

2017 ◽  
Vol 6 (1) ◽  
pp. 30-41
Author(s):  
Yu-Ting Tseng ◽  
Sanaz Khosravani ◽  
Arash Mahnan ◽  
Jürgen Konczak

This review addresses the role of exercise as an intervention for treating neurological disease. It focuses on three major neurological diseases that either present in acute or neurodegenerative forms—Parkinson’s disease, cerebellar ataxia, and cortical stroke. Each of the diseases affects primarily different brain structures, namely the basal ganglia, the cerebellum, and the cerebrum. These structures are all known to be involved in motor control, and the dysfunction of each structure leads to distinct movement deficits. The review summarizes current knowledge on how exercise can aid rehabilitation or therapeutic efforts. In addition, it addresses the role of robotic devices in enhancing available therapies by reviewing how robot-aided therapies may promote the recovery for stroke survivors. It highlights recent scientific evidence in support of exercise as a treatment for brain dysfunction, but also outlines the still open challenges for unequivocally demonstrating the benefits of exercise.


PEDIATRICS ◽  
1983 ◽  
Vol 72 (6) ◽  
pp. 847-849
Author(s):  
Giovanni Nigro ◽  
Maddalena Castellani Pastoris ◽  
Mirella Mazzotti Fantasia ◽  
Mario Midulla

Acute-phase and convalescent-phase sera of 66 children, aged 3 months to 12 years, with neurologic disorders of unknown etiology were tested against Legioneila pneumophila polyvalent and monovalent antigens (groups 1 to 4). Three significant antibody titer increases were obtained, all in childlren with acute cerebellar ataxia. This neurologic syndrome was characterized by sudden onset of muscle hypotonia and inability to sit or walk, with no other specific neurologic or systemic symptoms. Persisting pharyngitis always preceded ataxia. Fever of short duration was still present. Gastrointestinal disturbance occurred in two of the three children. Abnormal laboratory findings were, not always simultaneously, high ESR and leukocytosis with lymphocytosis. CSF levels and electromyographic findings were normal in two of the children. Two children received oral betamethasone. Recovery was complete within seven to ten days without antibiotic treatment. These studies indicate the possible etiologic role of L pneumophila in acute cerebellar ataxia.


2013 ◽  
Vol 20 (7) ◽  
pp. 997-1005 ◽  
Author(s):  
T. Kyriakides ◽  
C. Angelini ◽  
J. Schaefer ◽  
T. Mongini ◽  
G. Siciliano ◽  
...  
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document