Nahla Nagah Eldin Ibrahim <br/><br/>
Physiological and molecular study of autosomal dominant neurodegenerative diseases :   Huntington's disease and spinocerebellar ataxias in Egyptian patients /  
 دراسة فسيولوجية وجزيئية لأمراض تحلل المخ ذات الصفة السائدة :   مرض هنتينجتون وأمراض الترنح الشوكى المخيخى فى المرضى المصريين 
Nahla Nagah Eldin Ibrahim ; Supervised Said M. Rawi , Alice K. Abdelaleem , Nermeen A. Kishk 
 - Cairo :   Nahla Nagah Eldin Ibrahim ,   2010 
 - 178P. :   charts, facsimiles ;   25cm 
<br/><br/>Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Zoology 
<br/><br/> Huntington's disease (HD) and spinocerebellar ataxias are autosomal dominant neurodegenerative diseases that elicit several pathological symptoms including movement abnormalities cognitive and behavioral impairments . It was revealed that all genes associated with these genetic disorders contain CAG repeats in their coding region whose expansions are the major cause of disease progression  
<br/><br/>
<br/><br/><label>Subjects--Index Terms: </label>Autosomal dominant dominant spinocerebella ataxia Huntington's disease  Polymerase chain reaction