DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Issue 02 · Volume 07 · June 2009 DOI: 10.1055/s-005-29797

Review Article

  • 105
    Bennett, Emma; Thomas, Nick; Upadhyaya, Meena:

    Neurofibromatosis type 1: Its association with the Ras/MAPK pathway syndromes

    • Original Article

  • 117
    Kawakami, Yasuhiko; Matsumoto, Yoshiaki; Hashimoto, Kiyoshi; Kuwabara, Kentaro; Hirata, Kiyotaka; Suzuki, Takashi; Fujita, Takehisa; Fujino, Osamu:

    Clinical effectiveness of intravenous flunitrazepam administration for prolonged seizures

  • 123
    Castejón, Orlando J.:

    Ultrastructural pathology of human hydrocephalic cerebral cortex

  • 135
    Lagunju, IkeOluwa A.; Fatunde, Oluyemisi J.; Takon, Inyang:

    Profile of childhood epilepsy in Nigeria

  • 141
    Ong, Lai Choo; Wong, Sau Wei; Hamid, Hamzaini Abdul:

    Treatment of drooling in children with cerebral palsy using ultrasound guided intraglandular injections of botulinum toxin A

  • 147
    Muller, Carolyn W.; Jones, Harrison N.; O'Grady, Gwendolyn; Suárez, A. Habakkuk; Heller, James H.; Kishnani, Priya S.:

    Language and speech function in children with infantile Pompe disease

  • 157
    Karimzadeh, Parvaneh; Tonekaboni, Seyed H.; Shariatmadari, Fakhreddin:

    Benign external hydrocephalus and its relation to familial megalencephaly: An analysis of 20 cases

  • 165
    Ali, Mumtaz; Khan, Alamgir; Khan, Hamzullah; Khwanzada, Khalid:

    Short-term complications of ventriculoperitoeal shunt in children suffering from hydrocephalus

    • Case Report

  • 171
    Post, Bart; Ozelius, Laurie J.; Tijssen, Marina A.J.:

    Juvenile rapid-onset dystonia parkinsonism due to a ‘de novo’ mutation in the ATP1A3 gene

  • 175
    Sethi, Prahlad K.; Khandelwal, Dinesh; Sethi, Nitin K.; Torgovnick, Josh; Arsura, Edward:

    Hereditary infantile motor axonal neuropathy mimicking SMA: A case report

  • 181
    Currie, Stuart; Gains, Claire:

    A case of isolated sulfite oxidase deficiency and pyloric stenosis: Coincidence or common etiology?

  • 187
    Lagunju, IkeOluwa A.; Ogunbiyi, Adebola; Ogunseyinde, Ayotunde O.:

    Proteus syndrome, a rare cause of childhood epilepsy: A case report

  • 193
    Işık, Uğur; Dinçer, Alp; Sav, Aydın; Özek, Memet M.:

    Seizures as the sole manifestation of cerebellar lesions in three children

  • 199
    Mandal, Subinay; Hembram, Debasish:

    Interstitial deletion of chromosome 4

  • 203
    Singhi, Pratibha; Aulakh, Roosy; Singh, Paramjit:

    Infantile spasms, cerebral venous thrombosis and acute extrapyramidal symptoms in a child with methylmalonic acidemia

  • 209
    Akingbola, Olugbenga A.; Eduardo, Gonzalez-Toledo; Jeroudi, Majed A.:

    Oral cyclosporine, hypertension and hypomagnesemia are possible risk factors for posterior leukoencephalopathy syndrome in a boy with aplastic anemia

  • 215
    Farook, Shahme A.; Dherijha, Mohammed S.; Ismail, Azzam; Crimmins, Darach W.:

    Intraventricular abscess: A rare shunt related complication in a multiloculated ventricular system

    • Neuroimage of the Month

  • 219
    Kumar, Raj; Pandey, Shilpi; Mahapatra, Ashok Kumar:

    Neurocysticercosis