Barbara Gnidovec Stražišar

European guideline for the diagnosis and treatment of insomnia

Dieter Riemann, Chiara Baglioni, Claudio L. Bassetti et al. · Journal of Sleep Research · 2017 · 2K citations · Full text

Clinical spectrum of <i>SCN2A</i> mutations expanding to Ohtahara syndrome

Kazuyuki Nakamura, Mitsuhiro Kato, Hitoshi Osaka et al. · Neurology · 2013 · 196 citations

<i>TBC1D24</i> genotype–phenotype correlation

Simona Balestrini, Mathieu Milh, Claudia Castiglioni et al. · Neurology · 2016 · 126 citations · Full text

Early onset West syndrome with severe hypomyelination and coloboma‐like optic discs in a girl with <i>SPTAN1</i> mutation

Karin Writzl, Zvonka Rener Primec, Barbara Gnidovec Stražišar et al. · Epilepsia · 2012 · 40 citations

Early-onset epileptic encephalopathy with hearing loss in two siblings with TBC1D24 recessive mutations

Barbara Gnidovec Stražišar, David Neubauer, Darja Paro Panjan et al. · European Journal of Paediatric Neurology · 2014 · 27 citations

Mendelian Disorder, Early-onset Epileptic Encephalopathy, Genetic Disorder +8