DOI: 10.1055/s-00000041

Neuropediatrics

eFirst

Publication Date: 15 May 2017

Review Article

McMacken, Grace; Abicht, Angela; Evangelista, Teresinha; Spendiff, Sally; Lochmüller, Hanns: The Increasing Genetic and Phenotypical Diversity of Congenital Myasthenic Syndromes

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

Original Article

Kress, Wolfram; Rost, Simone; Kolokotronis, Konstantin; Meng, Gerhard; Pluta, Natalie; Müller-Reible, Clemens: The Genetic Approach: Next-Generation Sequencing-Based Diagnosis of Congenital and Infantile Myopathies/Muscle Dystrophies

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: 20 April 2017

Review Article

Domingos, Joana; Sarkozy, Anna; Scoto, Mariacristina; Muntoni, Francesco: Dystrophinopathies and Limb-Girdle Muscular Dystrophies

Publication Date: 15 April 2017

Original Article

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