DOI: 10.1055/s-00000041

Neuropediatrics

Issue 05 · Volume 51 · October 2020 DOI: 10.1055/s-010-49462

Editorial

313
Hartmann, Hans: Benign Convulsions with Mild Gastroenteritis—An Underestimated Phenomenon?

Review Article

315
Drechsler, Renate; Brem, Silvia; Brandeis, Daniel; Grünblatt, Edna; Berger, Gregor; Walitza, Susanne: ADHD: Current Concepts and Treatments in Children and Adolescents

Original Article

336
Hanci, Fatma; Türay, Sevim; Balci, Paşa; Kabakuş, Nimet: Reflex Epilepsy with Hot Water: Clinical and EEG Findings, Treatment, and Prognosis in Childhood
342
Blaschek, Astrid; Rodrigues, Martin; Ille, Lena; Idriess, Mohammed; Well, Therese; Warken, Birgit; Müller, Christine; Hannibal, Iris; Tacke, Moritz; Müller-Felber, Wolfgang; Vill, Katharina: Is Exercise-Induced Fatigue a Problem in Children with Duchenne Muscular Dystrophy?
349
Nasrallah, Fahmi; Hadj-Taieb, Sameh; Chehida, Amel Ben; Jelassi, Awatef; Ben Massoued, Sana; Charfi, Manel; Zidi, Wiem; Amri, Fethi; Helel, Khaled Ben; Mejaoual, Houssain; Seboui, Hassen; Mahdhaoui, Nabiha; Gargouri, Abdellatif; Monastiri, Kamel; Turki, Ilhem; Cheour, Myriam; Sanhaji, Haifa; Tebib, Neji; Feki, Moncef; Kaabachi, Naziha: Nonketotic Hyperglycinemia in Tunisia. Report upon a Series of 69 Patients
354
You, Su Jeong: Older Patients May Have More Frequent Seizures among Children Diagnosed as Benign Convulsions with Mild Gastroenteritis

Short Communication

359
Massimino, Carmela R.; Smilari, Pierluigi; Greco, Filippo; Marino, Silvia; Vecchio, Davide; Bartuli, Andrea; Parisi, Pasquale; Cho, Sung Y.; Pavone, Piero: Poland Syndrome with Atypical Malformations Associated to a de novo 1.5 Mb Xp22.31 Duplication
364
Gan, Siyi; Yang, Haiyan; Xiao, Ting; Pan, Zou; Wu, Liwen: AGRN Gene Mutation Leads to Congenital Myasthenia Syndromes: A Pediatric Case Report and Literature Review
368
Rademacher, Annika; Schwarz, Niklas; Seiffert, Simone; Pendziwiat, Manuela; Rohr, Axel; van Baalen, Andreas; Helbig, Ingo; Weber, Yvonne; Muhle, Hiltrud: Whole-Exome Sequencing in NF1-Related West Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for Epilepsy
Supplementary Material

Images in Neuropediatrics

373
Sharawat, Indar Kumar; Kasinathan, Ananthanarayanan; Dawman, Lesa: An Ominous Finding: Cerebellar Reversal Sign

Letter to Editor

375
von Stülpnagel, Celina; Hofmeister, Benedikt; Berweck, Steffen; Kluger, Gerhard; Weber, Peter: Response To: Overlapping Phenotype from Double Trouble SMARCA2 and POLG1 Variants c.2556A > C and c.3708G > T, Respectively