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                                                   Volume 8, Number 2, Year 2010
                                                                   Contents

 

REVIEW ARTICLES
N. Gordon
131.The Churg-Strauss syndrome
abstract 

M. Castro-Gago
135.Biochemical parameters predictive of neuronal damage in children with neonatal hypoxic ischemia
abstract 

ORIGINAL ARTICLES
A. Balcerzyk, I. Zak, B. Sarecka-Hujar, P. Niemiec, I. Kopyta and E. Emich-Widera
151. Polymorphisms of the ABCA1 and PON1 genes in determining the predisposition to ischemic stroke in children
abstract 

C.C. Schell-Apacik, B. Ertl-Wagner, U. Hehr and H. von Voss
157. ARX and SHH gene mutation analyses revealed no mutation in patients with agenesis/dysgenesis of the corpus callosum
abstract 

O.S.M. Suliman, M.A. Khedr and M.S. Al Ruthae
163. Carbonic anhydrase II deficiency syndrome: A report of 18 new Saudi Arabian cases
abstract 

H.A. Al khayat, M.M. Awadalla, A. Al Wakad and Z.A. Marzook
175. Polyunsaturated fatty acids in children with idiopathic intractable epilepsy: Serum levels and therapeutic response
abstract 

G.A. Shehata, K.I. Elsayh, A.O. Mohamed, T.A. Rageh and N.H. Rafet
187. Cognitive function and event related potentials in children with beta-thalassemia
abstract 

S.M. Hassanien, M.M. Awadalla, A.A. Saad and N.A.Abdel Aziz
193. Tissue plasminogen activator in children with idiopathic and intractable epilepsies
abstract 

I. Kraoua, I.B. Youssef-Turki, H.B. Rhouma, N. Fraj, S. Nagi, A. Rouissi, I. Chelly, S. Haouat, M.B. Hamouda and N. Gouider-Khouja
199. Joubert syndrome and related disorders: Report of five Tunisian cases
abstract 

CASE REPORTS
A. Drakaki, G. Vassiliou, E. Sekerli, D. Dimopoulou, A. Topalidis, A. Koutra, D. Iliopoulos and N. Voyiatzis
205. Inverted duplication of chromosome 15 (dic15q11) diagnosed by FISH in a patient with neurological problems
abstract 

P. Khairkar, G. Bang, A. Agarwal, B. Lakhkar and T. Jagzape
211. Depersonalization disorder in pre-adolescent child of acute disseminated encephalomyelitis
abstract 

P. Singh, S. Vyas, M. Singhal, M. Ray and N. Khandelwal
215. Deep cerebral venous thrombosis: Rare cause of stroke in children
abstract 

D.R. Gondaliya, S.K. Shrama, S. Kundu and S. Roy
219. Hallervorden spatz disease: A case report
abstract 

R. Koul, A. Al Futaisi, F. Alzri and R. Jain
223. Rasmussen’s encephalitis: A case report
abstract 

J.A. Gosalakkal and B.A. Prasad
227. Ptosis as unusual presentation of a cerebral arteriovenous malformation
abstract 

T. Rajapakse, V. Ramaswamy, J. Scozzafava and D.B. Sinclair
231. Failure of diffusion weighted MRI to detect severe hypoxic-ischemic encephalopathy in a child
abstract 

S. Mandal and D. Hembram
237. Caudal regression syndrome with vestigial tail and esophageal duplication cyst
abstract 

NEUROIMAGE OF THE MONTH
S. Sharma, I. Nathaniand C. Sahu
241. Hemimegalencephaly with microgyric - Agyric cortex