Abstracts (HTML) List of Authors

Tafelski, S.

Rehabilitative Outcome after Selective Dorsal Rhizotomy (SDR)

Tan, I.

Health-Related Quality of Life in Children and Adolescents with Spinal Dysraphic Disorders

Tempes, J.

Lunch and Cognitive Performance in School Children: The Crossover Intervention Trial CogniDo

Thiels, Ch.

Plasmapheresis as at Treatment Option in Anti-MOG–Related Neurological Disorders with Fulminant Progress
Unexpected Cause of Progressive Decrease in Sensorimotor Function of the Left Leg
CAPOS-Syndrome: A Rare Differential Diagnosis to Friedreich’s Ataxia

Thyen, U.

A Five-Year-Old Boy Diagnosed with an Anti-mGluR1 Positive Post–Streptococcal-Associated Cerebellitis

Tilton, A.

Time to Retreatment after AbobotulinumtoxinA (Dysport) Injections in Children with Dynamic Equinus Foot Deformity
Abobotulinumtoxin-A (DYSPORT) Injection Doses per Muscle in Pediatric Patients with Lower Limb Spasticity
Phase 3 Trial to Evaluate AbobotulinumtoxinA (Dysport) Injections in Children with Upper Limb Spasticity Due to Cerebral Palsy: A Study Design

Topaloglu, H.

Interim Efficacy and Safety Results from the Phase 3 ENDEAR Study of Nusinersen in Infants Diagnosed with Spinal Muscular Atrophy (SMA)

Tountopoulou, M.

Lacosamide Lowers Valproate and Levetiracetam Levels

Trauzettel-Klosinski, S.

Explorative Saccade Training in Children with Homonymous Hemianopia

Trifillis, P.

Lung Function in Ataluren-Treated, Nonambulatory Patients with Nonsense Mutation Duchenne Muscular Dystrophy from a Long-Term Extension Trial

Trollmann, R.

Toxic Rapidly Progressive Myelopathy Induced by Nelarabine in an Adolescent with Relapsed Pre-T-ALL
Histopathological Proof of the Pathogenetic Role of a Rare GFAP Mutation in Alexander´s Disease with Isolated Flaccid Paraparesis
Compound Heterozygous RYR1 Mutation in a Preterm with Arthrogryposis and Core Myopathy with Prenatal CNS Bleedings
BNS Epilepsy, Global Developmental Delay, Optic Coloboma, and Vesicoureteral Reflux as Leading Symptoms of COL4A1 Mutation: A Case Report

Tsikas, D.

The L-Arginine/NO Pathway in Children with Attention-Deficit/Hyperactivity Disorder (ADHD)

Tüngler, V.

Effects of Janus Kinase Inhibition in Two Children with Aicardi-Goutières Syndrome

Türk, M.

Compound Heterozygous RYR1 Mutation in a Preterm with Arthrogryposis and Core Myopathy with Prenatal CNS Bleedings