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
Willemsen, Michèl A.: Anemia in Glucose Transporter Type 1 Deficiency Syndrome: Often Expected, Rarely Encountered, and with a Fascinating Explanation

Review Article

329
Catala, Martin: The Cerebellum and Its Wrapping Meninge: Developmental Interplay between Two Major Structures
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
Supplementary Figures

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
Supplementary Figures
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
Supplementary Data

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
Shibata, Takashi; Kobayashi, Katsuhiro; Yoshinaga, Harumi; Ono, Hiroaki; Shinpo, Michiko; Kagitani-Shimono, Kuriko: Another Case of Glucose Transporter 1 Deficiency Syndrome with Periventricular Calcification, Cataracts, Hemolysis, and Pseudohyperkalemia
Supplementary Figure

Letter to the Editor

394
Avan, Abolfazl; de Bie, Rob M. A.; Hoogenraad, Tjaard U.: Wilson's Disease Should Be Treated with Zinc rather than Trientine or Penicillamine

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
Soares, Bruno P.; Calloni, Sonia F.; Shrot, Shai; Poretti, Andrea: MR Imaging of Acute Cerebellar Involvement in Pediatric Anti-N-Methyl-D-Aspartate Receptor Encephalitis

Book Review

400
Boltshauser, Eugen: Pediatric Neuroradiology: Clinical Practice Essentials

Erratum

401
Bölsterli Heinzle, Bigna Katrin; Bast, Thomas; Critelli, Hanne; Huber, Reto; Schmitt, Bernhard: Erratum: Age-Dependency of Location of Epileptic Foci in “Continuous Spike-and-Waves during Sleep”: A Parallel to the Posterior-Anterior Trajectory of Slow Wave Activity
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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Boltshauser, Eugen: Erratum: Pediatric Neuroradiology: Clinical Practice Essentials