Gulati, Sheffali;

Choudhary, Anita:


Treatment of mitochondrial disorders

Alderson, Lucy;

Barkey, Sinead;

Griggs, Heidi-Marie;

Edwards, Alexandra;

Phillips, Katy;

Doyle, Wendy;

Prabhakar, Prab:


Medically unexplained neurological symptoms in children and adolescents: A study within WHO’s international classification of functioning, disability and health framework

Reilly, David P.:


Reducing case fatality rate of acute encephalitis syndrome in developing countries

Shiva, Shadi;

Bonyadi, Mortaza Jabbarpour;

Toopchizadeh, Vahideh:


Correlation between deletion patterns of SMN1 and NAIP genes and clinical subtypes of spinal muscular atrophy in Iranian Azeri Turk ethnic patients

El-Serogy, Hesham:


Plasma carnitine levels in children with idiopathic epilepsy treated with old and new antiepileptic drugs

Kirchhoff, Maria;

Ronsbro, Lise;

Born, Alfred P.;

Kjaergaard, Susanne;

Uldall, Peter:


Report of two cases of infantile spasms caused by a de novo deletion in the STXBP1 gene

Rangaswamy, Pradeep M.:


Conversion disorder in childhood presenting as movement disorder with severe injuries

Nabizadeh, Sayyed;

Malek, Adel M.;

Tang, Ju;

Padulsky, Kristen;

Khazanie, Uma;

Helm, Patricia;

Wills, Kelly;

Tarui, Tomo:


Pediatric internal carotid aneurysm as a complication of sphenoid sinusitis

Velayuthan, Sujithra;

Riel-Romero, Rosario;

Kalra, Arun;

Gonzalez-Toledo, Eduardo:


Thalamic involvement in HSV type 1 encephalitis in children

Bozarth, Xiuhua L.;

Barboi, Alexandru C.:


Myopathy as the initial presentation of Addison’s disease

Shatila, Abdul-Rahman S.;

Yassin, Nabil A.;

Muwakkit, Samar A.;

Ibrahim, Ahmad O.:


Cyclosporine-induced PRES in a child recipient of allogeneic bone marrow transplantation

Bounta, Adriana;

Pardalos, Grigoris;

Gombakis, Nikos;

Zafeiriou, Dimitrios:


Cerebral embolism secondary to atrial myxoma in a child