Search
Now showing items 1-5 of 5
Proton spectroscopic findings in children with epilepsy owing to tuberous sclerosis complex.
(2005)
ABSTRACTTuberous sclerosis complex is an autosomal dominant disorder that often causes refractory seizures. The presence of multiplelesions makes it difficult to identify a single lesion responsible for the epilepsy. Our ...
Bilateral demyelinating tumefactive lesions in three children with hemiparesis
(2002)
We present the results from the evaluations of three children ages of 2, 7, and 11 years with hemiparesis and multiple white-matter lesions on magnetic resonance images (MRIs). The initial symptoms were mainly acute/subacute ...
A genome screen for linkage disequilibrium in Turkish multiple sclerosis
(2003)
A genome screen for linkage disequilibrium in Turkish multiple sclerosisM. Eraksoya,*,1, A. Hensiekb,1, M. Kurtuncua,b, G. Akman-Demira, M. Kılıncc,M. Gedizlioglud, B. Petek-Balcıe, O¨ . Anlarf, C. Kutlug, G. Saruhan-Dir ...
Non-pProgressive congenital ataxia with cerebellar hypoplasia in three families.
(2005)
AbstractAim: Non-progressive ataxias with cerebellar hypoplasia are a rarely seen heterogeneous group of hereditary cerebellar ataxias.Method: Three sib pairs from three different families with this entity have been reviewed, ...
A whole genome screen for linkage in Turkish multiple sclerosis
(2003)
A whole genome screen for linkage in Turkish multiple sclerosisM. Eraksoya,*,1, M. Kurtuncua,b,1, G. Akman-Demira, M. Kılıncc, M. Gedizlioglud, M. Mirzae,O¨. Anlarf, C. Kutlug, M. Demirkıranh, H.A. I˙drisoglua, A. Compstonb, ...