Marina Nikanorova

Marina Nikanorova

UNVERIFIED PROFILE

Are you Marina Nikanorova?   Register this Author

Register author
Marina Nikanorova

Marina Nikanorova

Publications by authors named "Marina Nikanorova"

Are you Marina Nikanorova?   Register this Author

28Publications

1170Reads

7Profile Views

Idiopathic encephalopathy related to status epilepticus during slow sleep (ESES) as a "pure" model of epileptic encephalopathy. An electroclinical, genetic, and follow-up study.

Epilepsy Behav 2019 Aug 26;97:244-252. Epub 2019 Jun 26.

Danish Epilepsy Centre - Filadelfia, Dianalund, Denmark; Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.yebeh.2019.05.030DOI Listing
August 2019

Current treatment options for Encephalopathy related to Status Epilepticus during slow Sleep.

Epileptic Disord 2019 Jun;21(S1):76-81

HUS Medical Imaging Center, Clinical Neurophysiology, University of Helsinki, Helsinki University Hospital and University of Helsinki, Finland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1684/epd.2019.1061DOI Listing
June 2019

Encephalopathy with continuous spike-waves during slow-wave sleep: evolution and prognosis.

Epileptic Disord 2019 Jun;21(S1):15-21

Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Harvard Medical School, Boston Children's Hospital, Boston, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1684/epd.2019.1052DOI Listing
June 2019

Rare coding variants in genes encoding GABA receptors in genetic generalised epilepsies: an exome-based case-control study.

Authors:
Patrick May Simon Girard Merle Harrer Dheeraj R Bobbili Julian Schubert Stefan Wolking Felicitas Becker Pamela Lachance-Touchette Caroline Meloche Micheline Gravel Cristina E Niturad Julia Knaus Carolien De Kovel Mohamad Toliat Anne Polvi Michele Iacomino Rosa Guerrero-López Stéphanie Baulac Carla Marini Holger Thiele Janine Altmüller Kamel Jabbari Ann-Kathrin Ruppert Wiktor Jurkowski Dennis Lal Raffaella Rusconi Sandrine Cestèle Benedetta Terragni Ian D Coombs Christopher A Reid Pasquale Striano Hande Caglayan Auli Siren Kate Everett Rikke S Møller Helle Hjalgrim Hiltrud Muhle Ingo Helbig Wolfram S Kunz Yvonne G Weber Sarah Weckhuysen Peter De Jonghe Sanjay M Sisodiya Rima Nabbout Silvana Franceschetti Antonietta Coppola Maria S Vari Dorothée Kasteleijn-Nolst Trenité Betul Baykan Ugur Ozbek Nerses Bebek Karl M Klein Felix Rosenow Dang K Nguyen François Dubeau Lionel Carmant Anne Lortie Richard Desbiens Jean-François Clément Cécile Cieuta-Walti Graeme J Sills Pauls Auce Ben Francis Michael R Johnson Anthony G Marson Bianca Berghuis Josemir W Sander Andreja Avbersek Mark McCormack Gianpiero L Cavalleri Norman Delanty Chantal Depondt Martin Krenn Fritz Zimprich Sarah Peter Marina Nikanorova Robert Kraaij Jeroen van Rooij Rudi Balling M Arfan Ikram André G Uitterlinden Giuliano Avanzini Stephanie Schorge Steven Petrou Massimo Mantegazza Thomas Sander Eric LeGuern Jose M Serratosa Bobby P C Koeleman Aarno Palotie Anna-Elina Lehesjoki Michael Nothnagel Peter Nürnberg Snezana Maljevic Federico Zara Patrick Cossette Roland Krause Holger Lerche

Lancet Neurol 2018 08 17;17(8):699-708. Epub 2018 Jul 17.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/S1474-4422(18)30215-1DOI Listing
August 2018

Real-world data on rufinamide treatment in patients with Lennox-Gastaut syndrome: Results from a European noninterventional registry study.

Epilepsy Behav 2017 11 15;76:63-70. Epub 2017 Sep 15.

Eisai Europe Ltd, European Knowledge Centre, Mosquito Way, Hatfield, Hertfordshire AL10 9SN, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.yebeh.2017.08.026DOI Listing
November 2017

Alternating hemiplegia of childhood and a pathogenic variant of ATP1A3: a case report and pathophysiological considerations.

Epileptic Disord 2017 Jun;19(2):226-230

Danish Epilepsy Centre - Epilepsihospitalet Filadelfia / University of Copenhagen, Dianalund, Denmark, IRCCS Institute of Neurological Sciences, Bellaria Hospital, Bologna, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1684/epd.2017.0913DOI Listing
June 2017

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

Brain 2017 May;140(5):1316-1336

The Danish Epilepsy Centre, Dianalund, Denmark.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/brain/awx054DOI Listing
May 2017

Mutations in GABRB3: From febrile seizures to epileptic encephalopathies.

Neurology 2017 01 4;88(5):483-492. Epub 2017 Jan 4.

From the Danish Epilepsy Centre (R.S.M., K.M.J., M.N.), Dianalund; Institute for Regional Health Services (R.S.M., K.M.J., M.N.), University of Southern Denmark, Odense; Department of Neurology and Epileptology (T.V.W., S.V., H.L., S.M.), Hertie Institute for Clinical Brain Research, and Department of Neurosurgery (T.V.W.), University of Tübingen; Department of Neuropediatrics (I.H., M.P., S.v.S., H.M.), University Medical Center Schleswig-Holstein, Kiel, Germany; Division of Neurology (I.H., S.H., H.D.), The Children's Hospital of Philadelphia, PA; Neuroscience Department (C.M., R.G.), Children's Hospital Anna Meyer-University of Florence, Italy; Department of Genetics (E.H.B., M.S., K.L.v.G.), University Medical Center Utrecht, the Netherlands; Department of Neurology and Neurorehabilitation (U.V., I.T., T.T.), Children's Clinic of Tartu University Hospital, Estonia; Department of Pediatric Neurology and Epilepsy Center (I.B.), LMU Munich, Germany; Department of Pediatrics (I.T., T.T.), University of Tartu; Tallinn Children's Hospital (I.T.), Tallinn, Estonia; Clinic for Neuropediatrics and Neurorehabilitation (G.K., C.B., H.H.), Epilepsy Center for Children and Adolescents, Schön Klinik Vogtareuth, Germany; Paracelsus Medical Private University (G.K.), Salzburg, Austria; Neuropeadiatric Department (L.L.F.), Hospices Civils de Lyon; Department of Genetics (G.L., N.C.), Lyon University Hospitals; Claude Bernard Lyon I University (G.L., N.C.); Lyon Neuroscience Research Centre (G.L., N.C.), CNRS UMR5292, INSERM U1028; Epilepsy, Sleep and Pediatric Neurophysiology Department (J.d.B.), Lyon University Hospitals, France; Clinic for Pediatric Neurology (S.B.), Pediatric Department, University Hospital, Herlev, Denmark; Kleinwachau (N.H.), Sächsisches Epilepsiezentrum Radeberg, Dresden; Department of Neuropediatrics/Epilepsy Center (J.J.), University Medical Center Freiburg; Department of General Paediatrics (S.S.), Division of Child Neurology and Inherited Metabolic Diseases, Centre for Paediatrics and Adolescent Medicine, University Hospital Heidelberg; Department of Women and Child Health (S.S.), Hospital for Children and Adolescents, University of Leipzig Hospitals and Clinics, Germany; Department of Pediatrics (C.T.M., H.C.M.), Division of Genetic Medicine, University of Washington, Seattle; Amplexa Genetics (L.H.G.L., H.A.D.), Odense, Denmark; Northern German Epilepsy Center for Children and Adolescents (S.v.S.), Schwentinental-Raisdorf, Germany; Wilhelm Johannsen Centre for Functional Genome Research (Y.M., N.T.), Department of Cellular and Molecular Medicine, University of Copenhagen; Danish Epilepsy Center (G.R.), Filadelfia/University of Copenhagen, Denmark; Department of Diagnostics (J.R.L.), Institute of Human Genetics, University of Leipzig; and Svt. Luka's Institute of Child Neurology and Epilepsy (K.M.), Moscow, Russia. Dr Maljevic is currently at the Florey Institute of Neuroscience and Mental Health, Melbourne, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1212/WNL.0000000000003565DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278942PMC
January 2017

Current role of rufinamide in the treatment of childhood epilepsy: literature review and treatment guidelines.

Eur J Paediatr Neurol 2014 Nov 28;18(6):685-90. Epub 2014 May 28.

Department of Systems Medicine, Child Neurology and Psychiatry Unit, Tor Vergata University Hospital of Rome, Italy. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejpn.2014.05.008DOI Listing
November 2014

GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.

Neurology 2014 Apr 12;82(14):1245-53. Epub 2014 Mar 12.

From the Division of Genetic Medicine, Department of Pediatrics (G.L.C., C.H., J.C., E.G., H.C.M.), and the Department of Genome Sciences (J.S.), University of Washington, Seattle; Neurogenetics Group (S.W.), Department of Molecular Genetics, VIB, Antwerp; Laboratory of Neurogenetics (S.W., A.S., P.D.J.), Institute Born-Bunge, University of Antwerp, Belgium; Epilepsy Centre Kempenhaeghe (S.W.), Oosterhout, the Netherlands; Epilepsy Research Centre (J.M.M., S.F.B., I.E.S.), Department of Medicine, University of Melbourne, Austin Health, Australia; Department of Neuropediatrics (C.H., H.M., S.v.S., I.H.), University Medical Center, Schleswig-Holstein, Christian-Albrechts University, Kiel, Germany; Danish Epilepsy Centre (R.S.M., H.H., M.N.), Dianalund; Institute for Regional Health Services (H.H., M.N.), University of Southern Denmark, Odense, Denmark; Department of Molecular and Medical Genetics (B.J.O.), Oregon Health and Science University, Portland; Florey Institute (S.P., A.C., E.V.G., I.E.S.), Victoria; TY Nelson Department of Neurology (D.G.), The Children's Hospital at Westmead, Sydney, NSW, Australia; Department of Paediatrics (L.G.S.), School of Medicine and Health Sciences, University of Otago, Wellington, New Zealand; Epilepsy Research Program (B.L.H., L.M.D.), School of Pharmacy and Medical Sciences, University of South Australia, Adelaide; Division of Neurology (P.D.J.), Antwerp University Hospital, Belgium; and the Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Australia.

View Article

Download full-text PDF

Source
http://www.washington.edu/medicine/pediatrics/meflab/doc/201
Web Search
http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000029
Publisher Site
http://dx.doi.org/10.1212/WNL.0000000000000291DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4001207PMC
April 2014

Efficacy of verapamil as an adjunctive treatment in children with drug-resistant epilepsy: a pilot study.

Seizure 2014 Jan 23;23(1):36-40. Epub 2013 Sep 23.

NESMOS Department, Chair of Pediatrics, Child Neurology, Faculty of Medicine and Psychology, "Sapienza" University of Rome, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.seizure.2013.09.009DOI Listing
January 2014

Transcranial direct current stimulation in refractory continuous spikes and waves during slow sleep: a controlled study.

Epilepsy Res 2011 Nov 31;97(1-2):142-5. Epub 2011 Aug 31.

Department of Neurophysiology, Danish Epilepsy Centre, Dianalund, Denmark.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.eplepsyres.2011.07.016DOI Listing
November 2011

A prospective study of levetiracetam efficacy in epileptic syndromes with continuous spikes-waves during slow sleep.

Seizure 2011 Oct 12;20(8):635-9. Epub 2011 Jul 12.

Danish Epilepsy Centre, Department of Neurophysiology, Kolonivej 1, 4293 Dianalund, Denmark.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.seizure.2011.06.007DOI Listing
October 2011

Lennox-Gastaut syndrome in adulthood: clinical and EEG features.

Epilepsy Res 2010 May 10;89(2-3):271-7. Epub 2010 Feb 10.

IRCCS Centro Neurolesi Bonino-Pulejo, Via Palermo, SS 113, C.da Casazza, 98124 Messina, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.eplepsyres.2010.01.012DOI Listing
May 2010

Ketogenic diet in the treatment of refractory continuous spikes and waves during slow sleep.

Epilepsia 2009 May 12;50(5):1127-31. Epub 2009 Feb 12.

Childrens Department, Danish Epilepsy Centre, Dianalund, Denmark.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1528-1167.2008.01958.xDOI Listing
May 2009