DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Issue 03 · Volume 07 · September 2009 DOI: 10.1055/s-005-29798

Original Article

  • 223
    Tomoum, Hoda Y.; El-Hadidi, Eman S.:

    Ghrelin and resistin levels in children with epilepsy on valproic acid

  • 231
    Kumar, Sameer; Sosinski, Kiera B.:

    Service delivery of care to children who have had strokes: Review of the initial diagnosis and ongoing treatments

  • 251
    Ünalp, Aycan; Bayram, Erhan; Ulusoy, Sadık; Uran, Nedret; Bayram, Meral; Öztürk, Aysel Aydoğan:

    Serum concentration of brain-derived neurotrophic factor in epileptic children

  • 257
    Awaad, Yasser; Michon, Anne Marie; Minarik, Sarah; Rizk, Tamer:

    Levetiracetam in Tourette syndrome: A randomized double blind, placebo controlled study

  • 265
    Khedr, Eman H.; Hamed, Sherifa A.; Mohammed, Gaafar A.; El Attar, Amal H.:

    A preliminary study of multimodal evoked potentials in relation to outcome in term infants with post-asphyxial hypoxic-ischemic encephalopathy

  • 275
    Bak, Mustafa; Gökgöz, Sevim Çakar; Ünalp, Aycan:

    Neurological manifestations of vitamin B12 deficiency in 15 infants

  • 279
    Shrimpton, Antony E.; Kessler, John A.; Shaffer, Lisa G.; Stack, Cindy; Jalali, Ali; Little, Robert; Goldstein, Joshua; Angle, Brad; Chary, Ajit; Coppinger, Justine; Mathison, David J.; Khan, Sophia; Poznanski, Andrew K.; Dobyns, William B.; Craig, David W.; Hoo, Joe J.; Sarco, Dean; Bassuk, Alexander G.:

    Variability of epilepsy, autism, brachydactyly, and other clinical features in familial and sporadic 2q37.3 deletion

    • Case Report

  • 285
    Olischar, Monika; Theda, Christiane; Lavery, Shelly; Coleman, Lee; Hunt, Rod W.:

    Amplitude-integrated EEG abnormalities in two neonates with encephalopathy due to mitochondrial dysfunction (respiratory chain complex I deficiency)

  • 293
    Cavanna, Andrea E.; Cavanna, Stefano; Bertero, Luca; Monaco, Francesco; Critchley, Hugo D.:

    Childhood-onset multiple self-injurious behaviors in Gilles de la Tourette syndrome

  • 297
    Bernhard, Matthias K.; Hugle, Boris; Merkenschlager, Andreas:

    Elevated liver enzymes under therapy with methylphenidate in a boy with T-cell leukemia

  • 301
    Sankhyan, Naveen; Kalra, Veena; Aksentijevich, Ivona; Kabra, Madhulika; Gulati, Sheffali; Sharma, Suvasini:

    Atypical late presentation in neonatal-onset multisystem inflammatory disease (NOMID)

  • 307
    Rohilla, Seema; Rawal, Manoj; Yadav, Rohtas K.; Ahuja, Amit; Nanda, Sanjiv; Dhaulakhandi, Dhara B.:

    Neurocysticercosis presenting as central diabetes insipidus in a boy

  • 311
    Melbourne Chambers, Roxanne H.; Johnson, Peter B.; Thame, Minerva M.:

    Fetal brain disruption sequence in surviving co-twins

  • 315
    Basu, Biswanath:

    Isoniazid toxicity: A treatable cause of status epilepticus

  • 317
    Rennert, Janine; Doelken, Regina; Doelken, Marc; Doerfler, Arnd:

    Menkes disease: MRI appearance of a rare neurodegenerative disorder

  • 321
    Kumar, Raj; Pande, Shilpi; Srivastava, Arun K.; Mahapatra, Ashok K.:

    Cervical myelocystocele: A case report

  • 325
    Kalane, Umesh; Kulkarni, Shilpa:

    A case of neurocutaneous syndrome associated with facial hemangioma: PHACE syndrome

  • 329
    Mandal, Subinay; Bid, Debashis:

    Vitiligo with spastic paraparesis: A rare neurocutaneous syndrome

    • Neuroimage of the Month

  • 333
    Arya, Ravindra; Sahu, Jitendra K.; Kabra, Madhulika:

    Neurofibromatosis type II (Wishart type)