Yin, Yingying;

Ren, Wei;

Wang, Xiuhai;

Liu, Shiguo:


Transmission disequilibrium test and haplotype analysis of the MCP-1 –2518G/A polymorphism with Tourette syndrome in Chinese Han trios

Sundaram, Venkataseshan;

Kumar, Praveen;

Saxena, Akshay;

Narang, Anil:


Trans-cranial Doppler in prediction of adverse outcome in asphyxiated neonates

García, Ana María Gómez;

Concepción, Otman Fernández;

Camfield, Carol S.;

Camfield, Peter R.:


Prevalence, syndromes and severity of childhood epilepsy in Cuba

Zerafati, Gazelle;

Dham, Bhavpreet S.;

Contreras, Liz;

Akbar, Umer;

Zayas, Luis;

Leone, Paola:


The prevalence, burden and cognizance of migraine in adolescent girls

Friedman, Brooke E.;

Gandrud, Laura M.;

Westphal, Lynn M.:


Primary amenorrhea in a 17-year-old patient with chronic hydrocephalus from an ependymoma

Papachristou, Fotios;

Ververi, Athina;

Printza, Nikoleta;

Mavridou, Irini;

Vargiami, Euthymia;

Giza, Styliani;

Michelakakis, Helen:


A case of galactosialidosis with renal failure and hippocampal sclerosis

Veeravigrom, Montida;

Serajee, Fatima:


A case of isolated oculomotor nerve palsy in a girl

Rogers, Karen;

Hurst, Daniel;

Nugent, Kenneth;

Raj, Rishi:


Vagus nerve stimulator-induced apneas and hypopneas in a child with refractory seizures

Hussain, Nahin;

Gosalakkal, Jayaprakash:


Post-pump chorea: Choreoathetosis after cardiac surgery with hypothermia and extracorporeal circulation

Ates, Omer;

Kurt, Semiha;

Firat, M. Murat;

Silan, Fatma:


A case of congenital muscular dystrophy similar to Fukuyama-type with a missense mutation in the fukutin gene

Suan, Lim Kia;

Mohd Jamil, Fadhilah;

Abdullah, Noor Kamila;

Desa, Norsiah Mohd:


Isolated sulfite oxidase deficiency, a rare neurodegenerative disorder which mimics hypoxic-ischemic encephalopathy

Verrips, Aad:


Linear scleroderma “en coup de sabre”

Mandelstam, Simone Alyson:


Retinal astrocytic hamartomas in tuberous sclerosis complex

Nizami, Furqan A.;

Ramzan, Altaf U.;

Malik, Nayil K.;

Shaheen, Feroz:


Sturge-Weber syndrome: A rare entity