DOI: 10.1055/s-00000041

Neuropediatrics

eFirst

Publication Date: 11 August 2017

Short Communication

Ardicli, Didem; Taskiran, Ekim Z.; Kosukcu, Can; Temucin, Cagri; Oguz, Kader K.; Haliloglu, Goknur; Alikasifoglu, Mehmet; Topaloglu, Haluk: Neonatal-Onset Recurrent Guillain–Barré Syndrome-Like Disease: Clues for Inherited CD59 Deficiency

Publication Date: 09 August 2017

Erratum

Original Article

Wilbrand, Jan-Falco; Kaps, Kerstin; Tabak, Darko; Bierther, Uta; Wilbrand, Martina; Neubauer, Bernd Axel; Pons-Kuehnemann, Joern; Howaldt, Hans-Peter; Hahn, Andreas: Normal Head Shape Parameters in the First 2 Years of Life and Effect of Helmet Therapy

Review Article

Magalhães, Luiza Vieira da Silva; Winckler, Maria Isabel Bragatti; Bragatti, José Augusto; Procianoy, Renato; Silveira, Rita de Cássia Santos: The Role of Amplitude Integrated Electroencephalogram in Very Low-Birth-Weight Preterm Infants: A Literature Review

Publication Date: 04 August 2017

Erratum

Short Communication

Tard, Céline; Tiffreau, Vincent; Jaillette, Emmanuelle; Jouen, Fabienne; Nelson, Isabelle; Bonne, Gisèle; Yaou, Rabah Ben; Romero, Norma; Vallée, Louis; Vermersch, Patrick; Nguyen, Sylvie; Maurage, Claude-Alain; Cuisset, Jean-Marie: Anti-HMGCR Antibody–Related Necrotizing Autoimmune Myopathy Mimicking Muscular Dystrophy

Publication Date: 16 July 2017

Publication Date: 06 July 2017

Review Article

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

Publication Date: 30 June 2017

Letter to the Editor

Short Communication

Komulainen-Ebrahim, Jonna; Saastamoinen, Eemeli; Rahikkala, Elisa; Helander, Heli; Hinttala, Reetta; Risteli, Leila; Rantala, Heikki; Uusimaa, Johanna: Intractable Epilepsy due to MTR Deficiency: Importance of Homocysteine Analysis

Publication Date: 22 June 2017

Original Article

Vill, Katharina; Ille, Lena; Blaschek, Astrid; Rawer, Rainer; Landgraf, Mirjam N.; Gerstl, Lucia; Schroeder, Sebastian A.; Müller-Felber, Wolfgang: Jumping Mechanography as a Complementary Testing Tool for Motor Function in Children with Hereditary Motor and Sensory Neuropathy

Publication Date: 19 June 2017

Book Review

Original Article

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

Publication Date: 09 June 2017

Short Communication

Doneda, Chiara; Pinelli, Lorenzo; Scaramuzzi, Matteo; Galli, Jessica; Fazzi, Elisa; Parazzini, Cecilia; Righini, Andrea; Nucci, Paolo: Morning Glory Disc Anomaly Associated with Ipsilateral Optic Nerve and Chiasm Thickening: Three Cases and Review of the Literature

Publication Date: 05 June 2017

Publication Date: 01 June 2017

Book Review

Original Article

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

Original Article

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

Short Communication

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

Publication Date: 15 May 2017

Short Communication

Sequeira, Sílvia; Rodrigues, Márcia; Jacinto, Sandra; Wevers, Ron A.; Wortmann, Saskia B.: MEGDEL Syndrome: Expanding the Phenotype and New Mutations

Publication Date: 08 May 2017

Short Communication

Kropach, Nesia; Shkalim-Zemer, Vered; Orenstein, Naama; Scheuerman, Oded; Straussberg, Rachel: Novel RRM2B Mutation and Severe Mitochondrial DNA Depletion: Report of 2 Cases and Review of the Literature

Publication Date: 15 April 2017

Short Communication

Grzybowski, Michelle; Schänzer, Anne; Pepler, Alexander; Heller, Corina; Neubauer, Bernd A.; Hahn, Andreas: Novel STAC3 Mutations in the First Non-Amerindian Patient with Native American Myopathy

Publication Date: 11 April 2017

Review Article

Anestis, Dimitrios M.; Tsitsopoulos, Parmenion P.; Ble, Christina A.; Tsitouras, Vassilios; Tsonidis, Christos A.: Congenital Glioblastoma Multiforme: An Unusual and Challenging Tumor

Publication Date: 23 March 2017

Publication Date: 16 March 2017

Short Communication

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

Publication Date: 02 March 2017

Images in Neuropediatrics

Publication Date: 26 December 2016

Images in Neuropediatrics

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