DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Issue 01 · Volume 10 · March 2012 DOI: 10.1055/s-005-29788

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    Wazir, Sanjay; Sundaram, Venkataseshan; Kumar, Praveen; Saxena, Akshay; Narang, Anil:

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

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  • 023
    Gómez, Nicolás Garófalo; García, Ana María Gómez; Concepción, Otman Fernández; Camfield, Carol S.; Camfield, Peter R.:

    Prevalence, syndromes and severity of childhood epilepsy in Cuba

  • 029
    Assadi, Mitra; Zerafati, Gazelle; Dham, Bhavpreet S.; Contreras, Liz; Akbar, Umer; Zayas, Luis; Leone, Paola:

    The prevalence, burden and cognizance of migraine in adolescent girls

  • 035
  • 041
    Jun, Sunny H.; Friedman, Brooke E.; Gandrud, Laura M.; Westphal, Lynn M.:

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

  • 045
    Zafeiriou, Dimitrios I.; Papachristou, Fotios; Ververi, Athina; Printza, Nikoleta; Mavridou, Irini; Vargiami, Euthymia; Giza, Styliani; Michelakakis, Helen:

    A case of galactosialidosis with renal failure and hippocampal sclerosis

  • 049
    Khanal, Deependra R.; Veeravigrom, Montida; Serajee, Fatima:

    A case of isolated oculomotor nerve palsy in a girl

  • 053
    Parhizgar, Fuzhan; Rogers, Karen; Hurst, Daniel; Nugent, Kenneth; Raj, Rishi:

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

  • 057
  • 063
    Ozcetin, Mustafa; 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

  • 067
    Balasubramaniam, Shanti; 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

  • 073
    Berghuis, Johan; Verrips, Aad:

    Linear scleroderma “en coup de sabre”

  • 075
    Rashid, Muddassir; Mandelstam, Simone Alyson:

    Retinal astrocytic hamartomas in tuberous sclerosis complex

  • 077
    Wani, Abrar A.; Nizami, Furqan A.; Ramzan, Altaf U.; Malik, Nayil K.; Shaheen, Feroz:

    Sturge-Weber syndrome: A rare entity

  • 079