Journal of Pediatric Neurology

Issue 02 · June 2010

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Issue
131
Gordon, Neil: The Churg-Strauss syndrome

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135
Castro-Gago, Manuel: Biochemical parameters predictive of neuronal damage in children with neonatal hypoxic ischemia

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151
Balcerzyk, Anna; Zak, Iwona; Sarecka-Hujar, Beata; Niemiec, Pawel; Kopyta, Ilona; Emich-Widera, Ewa: Polymorphisms of the ABCA1 and PON1 genes in determining the predisposition to ischemic stroke in children

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157
Schell-Apacik, Chayim Can; Ertl-Wagner, Birgit; Hehr, Ute; von Voss, Hubertus: ARX and SHH gene mutation analyses revealed no mutation in patients with agenesis/dysgenesis of the corpus callosum

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163
Suliman, Omer S.M.; Khedr, Mohammed A.; Al Ruthae, Mohammed S.: Carbonic anhydrase II deficiency syndrome: A report of 18 new Saudi Arabian cases

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175
Khayat, Hamed A. Al; Awadalla, Maha M.; Wakad, Amany Al; Marzook, Zehan A.: Polyunsaturated fatty acids in children with idiopathic intractable epilepsy: Serum levels and therapeutic response

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187
Shehata, Ghaydaa A.; Elsayh, Khaled I.; Mohamed, Amany O.; Rageh, Tarek A.; Rafet, Nafisa H.: Cognitive function and event related potentials in children with beta-thalassemia

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193
Hassanien, Sahar Mohamed; Awadalla, Maha Mohamed; Saad, Abeer Attia; Abdel Aziz, Nesreen Adel: Tissue plasminogen activator in children with idiopathic and intractable epilepsies

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199
Kraoua, Ichraf; Youssef-Turki, Ilhem Ben; Rhouma, Hanen Ben; Fraj, Narjes; Nagi, Sonia; Rouissi, Aida; Chelly, Ines; Haouat, Slim; Hamouda, Mohamed Ben; Gouider-Khouja, Neziha: Joubert syndrome and related disorders: Report of five Tunisian cases

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205
Drakaki, Alexandra; Vassiliou, Georgia; Sekerli, Eleni; Dimopoulou, Despina; Topalidis, Augerinos; Koutra, Aikaterini; Iliopoulos, Dimitrios; Voyiatzis, Nikolaos: Inverted duplication of chromosome 15 (dic15q11) diagnosed by FISH in a patient with neurological problems

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211
Khairkar, Praveen; Bang, Govind; Agarwal, Amit; Lakhkar, Bhavna; Jagzape, Tushar: Depersonalization disorder in pre-adolescent child of acute disseminated encephalomyelitis

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215
Singh, Paramjeet; Vyas, Sameer; Singhal, Manphool; Ray, Munni; Khandelwal, Niranjan: Deep cerebral venous thrombosis: Rare cause of stroke in children

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219
Gondaliya, Dushyant R.; Shrama, Surendra K.; Kundu, Sumita; Roy, Supriya: Hallervorden Spatz disease: A case report

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223
Koul, Roshan; Al Futaisi, Amna; Alzri, Faisal; Jain, Rajeev: Rasmussen's encephalitis: A case report

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227
Gosalakkal, Jayaprakash A.; Prasad, Balky A.: Ptosis as unusual presentation of a cerebral arteriovenous malformation

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231
Rajapakse, Thilinie; Ramaswamy, Vijay; Scozzafava, James; Sinclair, D. Barry: Failure of diffusion weighted MRI to detect severe hypoxic-ischemic encephalopathy in a child

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237
Mandal, Subinay; Hembram, Debasish: Caudal regression syndrome with vestigial tail and esophageal duplication cyst

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241
Sharma, Sanjay; Nathani, Inder; Sahu, Chandradev: Hemimegalencephaly with microgyric – Agyric cortex

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