Epilepsy Syndromes in the First Year of Life and Usefulness of Genetic Testing for Precision Therapy

by Allan Bayat, Michael Bayat, Guido Rubboli, Rikke S. Møller
Published 2021-07-01

Deep-Phenotyping the Less Severe Spectrum of PIGT Deficiency and Linking the Gene to Myoclonic Atonic Seizures

by Allan Bayat, Allan Bayat, Manuela Pendziwiat, Manuela Pendziwiat, Ewa Obersztyn, Paula Goldenberg, Pia Zacher, Jan Henje Döring, Steffen Syrbe, Amber Begtrup, Artem Borovikov, Artem Sharkov, Aneta Karasińska, Maria Giżewska, Wendy Mitchell, Eva Morava, Rikke S. Møller, Rikke S. Møller, Guido Rubboli, Guido Rubboli
Published 2021-05-01

Identification of miRNAs differentially expressed in human epilepsy with or without granule cell pathology.

by Silvia Zucchini, Gianluca Marucci, Beatrice Paradiso, Giovanni Lanza, Paolo Roncon, Pierangelo Cifelli, Manuela Ferracin, Marco Giulioni, Roberto Michelucci, Guido Rubboli, Michele Simonato
Published 2014-01-01

Refining Genotypes and Phenotypes in <i>KCNA2</i>-Related Neurological Disorders

by Jan H. Döring, Julian Schröter, Jerome Jüngling, Saskia Biskup, Kerstin A. Klotz, Thomas Bast, Tobias Dietel, G. Christoph Korenke, Sophie Christoph, Heiko Brennenstuhl, Guido Rubboli, Rikke S. Møller, Gaetan Lesca, Yves Chaix, Stefan Kölker, Georg F. Hoffmann, Johannes R. Lemke, Steffen Syrbe
Published 2021-03-01