SPG11mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration

2009 ◽  
Vol 150B (7) ◽  
pp. 984-992 ◽  
Author(s):  
Hanna Örlén ◽  
Atle Melberg ◽  
Raili Raininko ◽  
Eva Kumlien ◽  
Miriam Entesarian ◽  
...  
Keyword(s):  
Corpus Callosum ◽  
Retinal Degeneration ◽  
Hereditary Spastic Paraplegia ◽  
Spastic Paraplegia ◽  
Thin Corpus Callosum

Neurological and neuroradiological progression in hereditary spastic paraplegia with a thin corpus callosum

2000 ◽  
Vol 102 (3) ◽  
pp. 196-199 ◽  
Author(s):  
S. Okubo ◽  
M. Ueda ◽  
T. Kamiya ◽  
S. Mizumura ◽  
A. Terashi ◽  
...  
Keyword(s):  
Corpus Callosum ◽  
Hereditary Spastic Paraplegia ◽  
Spastic Paraplegia ◽  
Thin Corpus Callosum

scholarly journals Hereditary Spastic Paraplegia With Mental Impairment and Thin Corpus Callosum in Tunisia

2008 ◽  
Vol 65 (3) ◽  
Author(s):  
Amir Boukhris ◽  
Giovanni Stevanin ◽  
Imed Feki ◽  
Elodie Denis ◽  
Nizar Elleuch ◽  
...  
Keyword(s):  
Corpus Callosum ◽  
Hereditary Spastic Paraplegia ◽  
Spastic Paraplegia ◽  
Thin Corpus Callosum ◽  
Mental Impairment
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