Search Results

Kempeneers, Marinus A; Buis, Dennis; Feller, Ricardo E.; Roosendaal, Stefan; Slot, K. Mariam; Wolf, Nicole; Vandertop, W. Peter: Torticollis with Atlantoaxial Rotatory Subluxation in Children: A clinical review Neuropediatrics; Accepted Manuscripts

Chadda, Aditya; Kumar, Pawan; Bhatia, Anmol; Vyas, Sameer; Sankhyan, Naveen: Redness in a Squinted Eye: Is that a Clue? Neuropediatrics; eFirst

Ohshiro, Ikko; Okanishi, Tohru; Ohta, Ryo; Ohta, Kento; Arai, Yuto; Kanai, Sotaro; Fujimoto, Ayataka; Maegaki, Yoshihiro: Three Patients of the Early Onset Epileptic Spasms without Hypsarrhythmia Neuropediatrics; eFirst

Prithviraj, Prithviraj R; Banerjee, Bidisha; Acharya, Ullas V; Hafis, Muhammed; Sasidharan, Sruthi K: Clinico-radiologic spectrum and outcome of paediatric acquired demyelinating disorders (ADS) of central nervous system: a retrospective Indian tertiary care hospital cohort. Neuropediatrics; Accepted Manuscripts

Nenadic-Baranasic, Natasa; Nemir, Jakob; Borovecki, Fran; Njiric, Niko; Lehman, Ivan: Deep Brain Stimulation in a 10-Year-Old Child with Pantothenate Kinase-associated Neurodegeneration Neuropediatrics; eFirst

Kutlutürk Yıkılmaz, Seval; Tanrıverdi, Müberra; Öktem, Sedat: Reliability and Validity of the Turkish Translation of the PedsQL™ 3.0 Neuromuscular Module for 2-to 4-Year-Olds in Spinal Muscular Atrophy Neuropediatrics; eFirst

Asakura, Mari; Ogasawara, Masashi; Igarashi, Mizuho; Takeshima, Keigo; Fukao, Eri; Ikuta, Yoji: Pediatric Tolosa–Hunt Syndrome with Ptosis and Transient Periorbital Headache Neuropediatrics; eFirst

Jacob, Maureen; Brugger, Melanie; Andres, Stephanie; Wagner, Matias; Graf, Elisabeth; Berutti, Riccardo; Tilch, Erik; Pavlov, Martin; Mayerhanser, Katharina; Hoefele, Julia; Meitinger, Thomas; Winkelmann, Juliane; Brunet, Theresa: Genome Sequencing for Cases Unsolved by Exome Sequencing: Identifying a Single-Exon Deletion in TBCK in a Case from 30 Years Ago Neuropediatrics; eFirst

Yıldırım, Miraç; Yarenci, Gülçin Bilicen; Genç, Mustafa Berk; Uçar, Çiğdem İlter; Bayav, Secahattin; Tekin, Merve Nur; Bektaş, Ömer; Teber, Serap: VAMP1-Related Congenital Myasthenic Syndrome: A Case Report and Literature Review Neuropediatrics; eFirst

Almomen, Momen; Burgon, Patrick G.: Why Craniofacial Surgeons/Researchers Need to be Aware of Native American Myopathy? Neuropediatrics; eFirst

Kalampokini, Stefania; Xiromerisiou, Georgia; Bargiotas, Panagiotis; Anastasiadou, Violetta Christophidou; Costeas, Paul; Hadjigeorgiou, Georgios M.: PDE10A Mutation as an Emerging Cause of Childhood-Onset Hyperkinetic Movement Disorders: A Review of All Published Cases Neuropediatrics; eFirst

Kahl, Niklas; Lüsebrink, Natalia; Schubert-Bast, Susanne; Freiman, Thomas M.; Kieslich, Matthias: Bilateral Foramina Parietalia Permagna – A Calvarial Defect Caused by Haploinsufficiency of the Msh Homeobox 2 Gene: A Case Report and Current Literature Review Neuropediatrics; eFirst

Gerstner, Thorsten; Henning, Oliver; Løhaugen, Gro; Skranes, Jon: Reduced Interhemispheric Coherence and Cognition in Children with Fetal Alcohol Spectrum Disorder (FASD)—A Quantitative EEG Study Neuropediatrics; eFirst

Almomen, Momen; Amer, Fawzia; Alfaraj, Fatima; Burgon, Patrick G.; Bashir, Shahid; Alghamdi, Fouad: STAC3-related myopathy: A Report of a Cohort of Seven Saudi Arabian Patients Neuropediatrics; eFirst

Öz Yıldız, Sibel; Yalnızoğlu, Dilek; Şimsek Kiper, Pelin Özlem; Göçmen, Rahşan; Soğukpınar, Merve; Utine, Gülen Eda; Haliloğlu, Göknur: Delineation of ADPRHL2 Variants: Report of Two New Patients with Review of the Literature Neuropediatrics; eFirst

Öz Yıldız, Sibel; Yalnızoğlu, Dilek; Şimsek Kiper, Pelin Özlem; Göçmen, Rahşan; Soğukpınar, Merve; Utine, Gülen Eda; Haliloğlu, Göknur: Delineation of ADPRHL2 Variants: Report of Two New Patients with Review of the Literature Neuropediatrics; Issue NPED Women, 2024

Gebert, Johannes; Brunet, Theresa; Wagner, Matias; Rath, Jakob; Aull-Watschinger, Susanne; Pataraia, Ekaterina; Krenn, Martin: A Homozygous PTRHD1 Missense Variant (p.Arg122Gln) in an Individual with Intellectual Disability, Generalized Epilepsy, and Juvenile Parkinsonism Neuropediatrics; eFirst

Zaddach, Malin; Wagner, Johanna; Kunz, Mathias; Paolini, Marco; Borggraefe, Ingo; Heinen, Florian: Colloid Cyst Causing Massive Headache Attacks Neuropediatrics; eFirst

Franquelim, Catarina; Romana, Andreia; Rachão, Augusto; Martins, Joana Sousa; Monteiro, José Paulo; Carvalho, João: Early-Onset Dystonia and Visual Impairment Preceding Epileptic Encephalopathy Associated with PIGA Gene Mutation Neuropediatrics; eFirst

Fearns, Nicholas; Wagner, Matias; Borggräfe, Ingo; Kunz, Mathias; Rémi, Jan; Vollmar, Christian: Good Outcome of Resective Epilepsy Surgery in a 1-Year-Old Child with Drug-Resistant Focal Epilepsy with a Novel Pathogenic COL4A1 Mutation Neuropediatrics; eFirst