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ORIGINAL ARTICLES
75. Duchenne muscular dystrophy: study of double deletions and familial cases
Satish V. Khadilkar, Shekhar G. Patil, Rashna S. Dastur, Pradnya S. Gaitonde,
Jayashree J. Nadkarni
83. HCN2, NRTN, CAPS and GPX4 gene are not associated with simple febrile seizures in Chinese Han population
MA Yinan, Ql Yu, Chen Zhiyue, Zou Liping, Fang Fang, Wang Liwen, Song Fuying,
Zhang Jianhui, Bu Dingfang, Wang Tianjun, Lin Qing, Wu Xiru
89. Neurophysiologic evaluation of peripheral nerve function in uremic Egyptian children
Mohammad Al-Haggar, Mostafa Al-Aiouty, Mohamed Ragab, Soheir Yehia
97. Levetiracetam in intractable childhood onset epilepsy
Elsayed A. Mohammed, Mohammed M. Jan
103. Clinical pleomorphism of neurocysticercosis in children: some unusual manifestations
Sanjeev Jha, Rajesh Kumar, Raj Kumar
CASE REPORTS
111. Isolated unilateral palatal palsy in an adolescent
Yuval Karmon, Natan Gadoth
115. Gigantic intracranial hydatid cysts: an unusual case report
Neeraj Awasthy, Karam Chand, Avninder P. Singh
121. Fulminant subacute sclerosing panencephalitis: report of a case and review of literature
Jayantee Kalita, Usha K. Misra, Vikas Bansal, Susarla K. Shankar, Anita Mahadevan
127. Biphasic botulism diagnosed by electromyogram
Tanıl Kendirli, Serap Tiras Teber, Tuba Pekacar, Mustafa Argun, Gulhis Deda
131. Increased carotid artery flow rate in patient with Parry-Romberg syndrome
Seref Olgar, Turkan Ertugrul, Memduh Dursun, Kemal Nisli, Meral Ozmen
135. Schwartz-Jampel syndrome: a case report
Natwar Sharma, Venkataraman Vishwanathan, Kalpana Gowrishankar
139. Behçet’s disease as cause of sinovenous thrombosis in a pediatric patient
Serap Teber, Ozlem unal, Gulhis Deda, Suat Fitoz, Zumrut Uysal, Nejat Akar
143. Canavan disease: the first case from Jordan
Amira Masri, Hanan Hamamy
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