DOI: 10.1055/s-00000041

Neuropediatrics

Issue 03 · Volume 39 · June 2008 DOI: 10.1055/s-002-13857

Original Article

  • 139
    Brandão-Almeida, I. L.; Hage, S. R. V.; Oliveira, E. P. M.; Guimarães, C. A.; Teixeira, K. C. S.; Abramides, D. V. M.; Montenegro, M. A.; Santos, N. F.; Cendes, F.; Lopes-Cendes, I.; Guerreiro, M. M.:

    Congenital Bilateral Perisylvian Syndrome: Familial Occurrence, Clinical and Psycholinguistic Aspects Correlated with MRI

  • 146
    Dalen, K.; Bruarøy, S.; Wentzel-Larsen, T.; Lægreid, L. M.:

    Intelligence in Children with Hydrocephalus, Aged 4–15 Years: A Population-based, Controlled Study

  • 151
    Peres, E.; Wood, G. W.; Poulik, J.; Baynes, R.; Sood, S.; Abidi, M. H.; Klein, J.; Bhambhani, K.; Dansey, R.; Abella, E.:

    High-dose Chemotherapy and Adoptive Immunotherapy in the Treatment of Recurrent Pediatric Brain Tumors

  • 157
    Guzzetta, A.; Pecini, C.; Biagi, L.; Tosetti, M.; Brizzolara, D.; Chilosi, A.; Cipriani, P.; Petacchi, E.; Cioni, G.:

    Language Organisation in Left Perinatal Stroke

  • 164
    Pranzatelli, M. R.; Tate, E. D.; Crowley, J. M.; Toennies, B.; Creer, M.:

    Neurometabolic Effects of ACTH on Free Amino Compounds in Opsoclonus-myoclonus Syndrome

  • 172
    Zafeiriou, D. I.; Rodenburg, R. J. T.; Scheffer, H.; Heuvel, L. P. van den; Pouwels, P. J. W.; Ververi, A.; Athanasiadou-Piperopoulou, F.; Knaap, M. S. van der:

    MR Spectroscopy and Serial Magnetic Resonance Imaging in a Patient with Mitochondrial Cystic Leukoencephalopathy due to Complex I Deficiency and NDUFV1 Mutations and Mild Clinical Course

    • Short Communication

  • 176
    Larnaout, A.; Ammar, N.; Mourad, Z.; Naji, S.; Hentati, F.:

    Wilson's Disease: Appreciable Improvement of Sub-cortical White Matter Abnormalities after Copper Chelating Treatment: Five Years Follow-up

  • 179
    Brunetti-Pierri, N.; Selby, K.; O'Sullivan, M.; Hendson, G.; Truong, C.; Waters, P. J.; Wong, L.-J.:

    Rapidly Progressive Neurological Deterioration in a Child with Alpers Syndrome Exhibiting a Previously Unremarkable Brain MRI

  • 184
    Rougeot, C.; Chabrier, S.; Camdessanche, J.-P.; Prieur, F.; d’Anjou, M.-C.; Latour, P.:

    Clinical, Electrophysiological and Genetic Studies of Two Families with Mutations in the GDAP1 Gene

  • 188
    Beslow, L. A.; Ichord, R. N.; Zimmerman, R. A.; Smith, S. E.; Licht, D. J.:

    Role of Diffusion MRI in Diagnosis of Spinal Cord Infarction in Children