Steffen Syrbe

Delineating the <i>GRIN1</i> phenotypic spectrum

Johannes R. Lemke, Kirsten Geider, Katherine L. Helbig et al. · Neurology · 2016 · 202 citations · Full text

Benign infantile seizures and paroxysmal dyskinesia caused by an <i>SCN8A</i> mutation

Elena Gardella, Felicitas Becker, Rikke S. Møller et al. · Annals of Neurology · 2015 · 187 citations

Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies

Silvia Masnada, Ulrike B. S. Hedrich, Elena Gardella et al. · Brain · 2017 · 158 citations · Full text

Children with multiphasic disseminated encephalomyelitis and antibodies to the myelin oligodendrocyte glycoprotein (MOG): Extending the spectrum of MOG antibody positive diseases

Matthias Baumann, Eva-Maria Hennes, Kathrin Schanda et al. · Multiple Sclerosis Journal · 2016 · 157 citations

The gain of function <i>SCN1A</i> disorder spectrum: novel epilepsy phenotypes and therapeutic implications

Andreas Brunklaus, Tobias Brünger, Tony Feng et al. · Brain · 2022 · 137 citations · Full text

Neurological Disorder, Scn1a Variants Cluster, Therapeutic Implications +18