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KCNT2-related disorders: phenotypes, functional and pharmacological properties.

Apr 17, 2023

ABOUT THE EXPERTS

  • Maria Cristina Cioclu

    Department of Epilepsy Genetics and Personalized Medicine (member of ERN EpiCARE), Danish Epilepsy Centre, Filadelfia, Dianalund, Denmark.

    Department of Biomedical, Metabolic, and Neural Science, University of Modena and Reggio Emilia, Modena, Italy.

    Ilaria Mosca

    Department of Medicine and Health Sciences “Vincenzo Tiberio”, University of Molise, Campobasso, Italy.

    Paolo Ambrosino

    Dept. of Science and Technology, University of Sannio, Benevento, Italy.

    Deborah Puzo

    Department of Medicine and Health Sciences “Vincenzo Tiberio”, University of Molise, Campobasso, Italy.

    Allan Bayat

    Department of Epilepsy Genetics and Personalized Medicine (member of ERN EpiCARE), Danish Epilepsy Centre, Filadelfia, Dianalund, Denmark.

    Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.

    Saskia B Wortmann

    University Children’s Hospital, Paracelsus Medical University, Salzburg, Austria.

    Amalia Children’s Hospital, Radboudumc, Nijmegen, The Netherlands.

    Johannes Koch

    University Children’s Hospital, Paracelsus Medical University, Salzburg, Austria.

    Vincent Strehlow

    Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.

    Kentaro Shirai

    Department of Pediatrics, Tsuchiura Kyodo General Hospital, Tsuchiura, Ibaraki, 300-0028, Japan.

    Naomichi Matsumoto

    Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Kanagawa, 236-0004, Japan.

    Stephan J Sanders

    Department of Psychiatry and Behavioral Sciences, UCSF Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, California, USA.

    Institute for Human Genetics, University of California, San Francisco, San Francisco, California, USA.

    Bakar Computational Health Sciences Institute, University of California, San Francisco, San Francisco, California, USA.

    Vincent Michaud

    Service de Génétique Médicale, Centre de Référence Anomalies du Développement et Syndrome Malformatifs, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France.

    Maladies rares: Génétique et Métabolisme (MRGM), INSERM U1211, Université de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France.

    Marine Legendre

    Service de Génétique Médicale, Centre de Référence Anomalies du Développement et Syndrome Malformatifs, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, Nouvelle-Aquitaine, France.

    Antonella Riva

    IRCCS Istituto Giannina Gaslini, Genoa, Italy.

    Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.

    Pasquale Striano

    IRCCS Istituto Giannina Gaslini, Genoa, Italy.

    Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.

    Hiltrud Muhle

    Department of Neuropediatrics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, Germany.

    Manuela Pendziwiat

    Department of Neuropediatrics, Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein, Campus Kiel, Germany.

    Gaetan Lesca

    Department of Medical Genetics, University Hospital of Lyon and Claude Bernard Lyon I University, Lyon, France.

    Pathophysiology and Genetics of Neuron and Muscle (PNMG), UCBL, CNRS UMR5261 – INSERM U1315, Lyon, France.

    Giuseppe Donato Mangano

    Department of Biomedicine, Neuroscience and Advanced Diagnostics, University of Palermo, Palermo, Italy.

    Rosaria Nardello

    Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties “G. D’Alessandro”, University of Palermo, Palermo, Italy.

    Johannes R Lemke

    Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.

    Center for Rare Diseases, University of Leipzig Medical Center, Leipzig, Germany.

    Rikke S Møller

    Department of Epilepsy Genetics and Personalized Medicine (member of ERN EpiCARE), Danish Epilepsy Centre, Filadelfia, Dianalund, Denmark.

    Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.

    Maria Virginia Soldovieri

    Department of Medicine and Health Sciences “Vincenzo Tiberio”, University of Molise, Campobasso, Italy.

    Guido Rubboli

    Department of Epilepsy Genetics and Personalized Medicine (member of ERN EpiCARE), Danish Epilepsy Centre, Filadelfia, Dianalund, Denmark.

    University of Copenhagen, Copenhagen, Denmark.

    Maurizio Taglialatela

    Department of Neuroscience, University of Naples “Federico II”, Naples, Italy.

REFERENCES & ADDITIONAL READING

PubMed

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