DOI: 10.1055/s-00000041

Neuropediatrics

Issue 05 · Volume 48 · October 2017 DOI: 10.1055/s-007-34783

Editorial

  • 323
    Wolf, Nicole I.; Plecko, Barbara; Neubauer, Bernd A.:

    Andrea Poretti–In Memoriam

  • In Memoriam

  • 325
    Boltshauser, Eugen; Huisman, Thierry A.G.M.:

    Prof. Andrea Poretti, MD (12.04.1977–22.03.2017)

  • Editorial Commentary

  • 327
  • Review Article

  • 329
  • 340
    Agarwal, Nivedita; Tekes, Aylin; Poretti, Andrea; Meoded, Avner; Huisman, Thierry A.G.M.:

    Pitfalls in Diffusion-Weighted and Diffusion Tensor Imaging of the Pediatric Brain

  • Original Article

  • 350
    Boltshauser, Eugen; Bauder, Florian; Giarrana, Miriam; Hackenberg, Anette; Lebon, Sébastien; Roulet-Perez, Eliane; Schmid, Regula; Schmitt-Mechelke, Thomas; Poretti, Andrea:

    Prenatal Brainstem Disruptions: Small Lesions–Big Problems

  • 356
    Darwish, Amira Hamed; Alshahawy, Azza Kamal; El-Shehaby, Walid Ahmed:

    Epileptiform Activity in Electroencephalogram of Normal Children

  • 363
    Şahin, Sevim; Özdoğan, Elif Bahat; Kaya, Gülay; Özgün, Nezir; Cansu, Ali; Kalyoncu, Mukaddes; Dilber, Embiya:

    Neurological Involvement in Pediatric Hemolytic Uremic Syndrome: A Symptom-Oriented Analysis

  • 371
    Schorling, David C.; Dietel, Tobias; Evers, Christina; Hinderhofer, Katrin; Korinthenberg, Rudolf; Ezzo, Daniel; Bönnemann, Carsten G.; Kirschner, Janbernd:

    Expanding Phenotype of De Novo Mutations in GNAO1: Four New Cases and Review of Literature

  • Short Communication

  • 378
    Haine, Elsa; Sevely, Annick; Boetto, Sergio; Delisle, Marie-Bernadette; Cances, Claude:

    Infantile Hemangioma of the Posterior Fossa in a Newborn: Early Management and Long-Term Follow-up

  • 382
    Sequeira, Sílvia; Rodrigues, Márcia; Jacinto, Sandra; Wevers, Ron A.; Wortmann, Saskia B.:

    MEGDEL Syndrome: Expanding the Phenotype and New Mutations

  • 385
    Sundaram, Senthil K.; Michelhaugh, Sharon K.; Klinger, Neil V.; Kupsky, William J.; Sood, Sandeep; Chugani, Harry T.; Mittal, Sandeep; Juhász, Csaba:

    GNAQ Mutation in the Venous Vascular Malformation and Underlying Brain Tissue in Sturge–Weber Syndrome

  • 390
  • Letter to the Editor

  • 394
  • Images in Neuropediatrics

  • 396
    Franco, Igor de Assis; Aragão, Marcelo de Melo; Poretti, Andrea; Silva, Mayara C. Vogel da; Diogo, Walter J. da Graça; Masruha, Marcelo Rodrigues:

    Middle Cerebellar Peduncles T2-Hyperintense Signal in Fazio–Londe Syndrome

  • 398
  • Book Review

  • 400
  • Erratum

  • 401
  • 402
    Canpolat, Mehmet; Gumus, Hakan; Gunduz, Zubeyde; Dusunsel, Ruhan; Kumandas, Sefer; Bayram, Ayşe Kaçar; Yel, Sibel; Poyrazoglu, Hatice Gamze; Yilmaz, Kenan; Doganay, Selim; Yikilmaz, Ali; Dundar, Munis; Per, Huseyin:

    Erratum: Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, Turkey

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