World Society of Child Science

Volume 8, Number 2, Year 2010

Original Articles
Neil Gordon
The Churg-Strauss syndrome

• Abstract
• PDF 26 KB

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

• Abstract
• PDF 127 KB

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

• Abstract
• PDF 94 KB

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

• Abstract
• PDF 257 KB

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

• Abstract
• PDF 2503 KB

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

• Abstract
• PDF 120 KB

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

• Abstract
• PDF 48 KB

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

• Abstract
• PDF 417 KB

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

• Abstract
• PDF 551 KB

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

• Abstract
• PDF 243 KB

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

• Abstract
• PDF 220 KB

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

• Abstract
• PDF 1178 KB

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

• Abstract
• PDF 307 KB

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

• Abstract
• PDF 153 KB

Jayaprakash A. Gosalakkal and Balky A. Prasad
Ptosis as unusual presentation of a cerebral arteriovenous malformation

• Abstract
• PDF 2130 KB

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

• Abstract
• PDF 829 KB

Subinay Mandal and Debasish Hembram
Caudal regression syndrome with vestigial tail and esophageal duplication cyst

• Abstract
• PDF 1044 KB

Sanjay Sharma, Inder Nathani, and Chandradev Sahu
Hemimegalencephaly with microgyric – Agyric cortex

• Abstract
• PDF 538 KB