Francesca Darra

Francesca Darra

UNVERIFIED PROFILE

Are you Francesca Darra?   Register this Author

Register author
Francesca Darra

Francesca Darra

Publications by authors named "Francesca Darra"

Are you Francesca Darra?   Register this Author

47Publications

1082Reads

34Profile Views

Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults.

Epilepsia 2019 Dec;60 Suppl 3:S49-S58

Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, member of ERN EpiCare, Milan, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/epi.16297DOI Listing
December 2019

Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center study.

Eur J Paediatr Neurol 2019 Nov 21;23(6):808-818. Epub 2019 Sep 21.

Laboratory of Clinical Analysis and Biomechanics of Movement, University Hospital of Padova, Padova, Italy; NEUROMOVE-Rehab, Department of Neuroscience, University of Padova, Padova, Italy; PNC, Padova Neuroscience Center, Padova, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejpn.2019.09.010DOI Listing
November 2019

EEG features in Encephalopathy related to Status Epilepticus during slow Sleep.

Epileptic Disord 2019 Jun;21(S1):22-30

Department of Child Neuropsychiatry, Department of Life and Reproduction Sciences, University of Verona, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1684/epd.2019.1054DOI Listing
June 2019

Clinical spectrum of -related epileptic disorders.

Neurology 2019 03 8;92(11):e1238-e1249. Epub 2019 Feb 8.

From the University of Tübingen (S. Wolking, J.M., Y.G.W., H.L., J.S.), Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, Tübingen, Germany; Luxembourg Centre for Systems Biomedicine (P.M.), University of Luxembourg, Esch-sur-Alzette; Pediatric Neurology and Neurogenetics Unit and Laboratories (D.M., R.G., C.M.), Children's Hospital Anna Meyer, University of Florence, Italy; Danish Epilepsy Centre (R.S.M.), Dianalund; Institute for Regional Health Services (R.S.M.), University of Southern Denmark, Odense; Department of Clinical and Experimental Epilepsy (S.B.), UCL Institute of Neurology and Epilepsy Society, UK, London; Division of Neurology (K.L.H., I.H.), Children's Hospital of Philadelphia, PA; Department of Pediatric Neurology (C.D.A.), Centre de Compétences Maladies Rares, CHU Besançon; Service de Génétique (N.C.), Hospices Civils des Lyon, Bron; GENDEV Team (N.C.), Neurosciences Research Center of Lyon, Bron, France; Neuropediatric Clinic and Clinic for Neurorehabilitation (K.S.), Epilepsy Center for Children and Adolescents, Schoen Klinik Vogtareuth, Germany; Beaumont Hospital (P.W.-W.), Dublin, Ireland; Department of Pediatrics, Division of Medical Genetics, Institute of Human Genetics (B.A.M.), Departments of Neurology and Pediatrics (A.N.), and Departments of Neurology and Pediatrics, and Institute of Human Genetics (M.R.C.), University of California, San Francisco; Department of Neurology (W.V.P.), University Hospitals Leuven, Belgium; Department of Pediatrics (L.L.S.), Hvidovre Hospital, Denmark; King's College Hospital (S.O., E.H., S.G., D.K.P.), London; Evelina London Children's Hospital (S.O., E.H., S.G.), London, UK; Section of Genetics (K.B., M.S.S.), Department of Pediatrics, University of Colorado and Children's Hospital Colorado, Aurora; Clinique Bernoise Montana (T.D.), Crans-Montana, Switzerland; Department of Neuropediatrics (H.M.), University Medical Center Schleswig-Holstein, Christian-Albrechts University, Kiel, Germany; National Institute for Health Research Oxford Biomedical Research Centre, Wellcome Centre for Human Genetics (A.T.P., S.J.L.K., J.C.T.) and Department of Oncology (D.V.V.), University of Oxford, UK; Epilepsy Center (M.P.C.), Health Sciences Department, San Paolo Hospital, University of Milan; Child Neuropsychiatry (F.D.), Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Italy; Departments of Neurology and Clinical Genomics (R.H.G.) and Health Sciences Research and Clinical Genomics (E.W.K., C.K.), Mayo Clinic, Rochester, MN; Ambry Genetics (Z.P.), Aliso Viejo, CA; Department of Clinical Neuroscience (S.T.), King's College London; New Medicines (M.A., D.M.), UCB Pharma, Slough, UK; Neuropediatric Clinic and Clinic for Neurorehabilitation (G.J.K.), Epilepsy Center for Children and Adolescents, Schoen Klinik Vogtareuth, Germany; Research Institute for Rehabilitation, Transition and Palliation (G.J.K.), PMU Salzburg, Austria; Department of Neurology (D.H.L.), University of California, San Francisco; Neurogenetics Group (S. Weckhuysen), Center for Molecular Neurology, VIB, Antwerp; Laboratory of Neurogenetics (S. Weckhuysen), Institute Born-Bunge, University of Antwerp; Department of Neurology (S. Weckhuysen), Antwerp University Hospital, Antwerp, Belgium; Department of Basic & Clinical Neuroscience, Institute of Psychiatry, Psychology & Neuroscience (D.K.P.), MRC Centre for Neurodevelopmental Disorders (D.K.P.), King's College London, UK; Evelina London Children's Hospital (D.K.P.), London, UK; Department of Neuropediatrics (I.H.), University Medical Center Schleswig-Holstein, Christian-Albrechts University, Kiel, Germany; Institute of Neuroscience (R.H.T.), Henry Wellcome Building, Newcastle University; Neurology Research Group (M.I.R.), Institute of Life Science, Swansea University Medical School, Swansea, UK; Service de Génétique (G.L.), Hospices Civils des Lyon, Bron; GENDEV Team (G.L.), Neurosciences Research Center of Lyon, Bron, France; NIHR University College London Hospitals Biomedical Research Centre (S.M.S.), UCL Institute of Neurology, London, UK; Cologne Center for Genomics (D.L.), University of Cologne, Germany; Stanley Center for Psychiatric Research (D.L.) and Program in Medical and Population Genetics (D.L.), Broad Institute of MIT and Harvard, Cambridge; Psychiatric and Neurodevelopmental Genetics Unit (D.L.), Massachusetts General Hospital and Harvard Medical School, Boston.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1212/WNL.0000000000007089DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6511102PMC
March 2019

Diaper changing-induced reflex seizures in CDKL5-related epilepsy.

Epileptic Disord 2018 10;20(5):428-433

Child Neuropsychiatry, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona.

View Article

Download full-text PDF

Source
http://www.john-libbey-eurotext.fr/medline.md?doi=10.1684/ep
Publisher Site
http://dx.doi.org/10.1684/epd.2018.0999DOI Listing
October 2018

The phenotype of developmental and epileptic encephalopathy.

Neurology 2018 09 31;91(12):e1112-e1124. Epub 2018 Aug 31.

From the Department of Clinical Neurophysiology (E.G., S.B.), Danish Epilepsy Centre, Dianalund; Institute for Regional Health Services (E.G., K.M.J., R.S.M.), University of Southern Denmark, Odense, Denmark; Neuroscience Department (C.M., R.G., M.M.), Children's Hospital A. Meyer, University of Florence; Department of Neuroscience (M.T., N.S., F.V.), Bambino Gesù Children's Hospital, IRCCS, Rome, Italy; Division of Neurology (M.P.F., I.H.), The Children's Hospital of Philadelphia; Departments of Pediatrics and Neurology (M.P.F., I.H.), Perelman School of Medicine at the University of Pennsylvania, Philadelphia; Universitätskinderklinik Tübingen (M.A., M.W.), Germany; Department of Neurology (K.H.), Royal Children's Hospital Melbourne; Department of Paediatrics (K.H.), University of Melbourne; Australia Neurosciences Group (K.H.), Murdoch Children's Research Institute, Melbourne, Australia; Servizio di Neuropsichiatria Infantile (F.D., E.F.), Policlinico G.B. Rossi, Universita Degli Studi di Verona; Department of Child Neurology (S.S., G.A.), Ospedale Pediatrico G. Salesi-Ospedali Riuniti, Ancona, Italy; Division of Clinical Neurophysiology (B.B.), Children's Research Center, University Children's Hospital Zurich, Switzerland; Brain and Behaviour Department (S.M.), University of Pavia; Department of Pediatric Neuroradiology (A.P.), IRCCS "C. Mondino" National Neurological Institute, Pavia, Italy; Department of Epilepsy Genetics (K.J., R.S.M.), Danish Epilepsy Centre Dianalund; Department of Child Neurology (B.J.), Danish Epilepsy Centre, Dianalund, Denmark; Cytogenetic and Molecular Genetic Laboratory (S.R., F.C.), Istituto Auxologico Italiano, IRCCS, Milano, Italy; Department of Adult Neurology (G.R.), Danish Epilepsy Centre, Dianalund; University of Copenhagen (G.R.), Denmark; Struttura Complessa di Neurologia Pediatrica Ospedale Vittore Buzzi (P.V.), Milano; Dipartimento di Scienze Biomediche e Cliniche L. Sacco (P.V.), Università di Milano, Italy; Århus University (S.B.), Denmark; Department of Child Neurology (I.E.S.), University of Melbourne, Austin Health, Florey Institute; and Department of Child Neurology (I.E.S.), The Royal Children's Hospital, Melbourne, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1212/WNL.0000000000006199DOI Listing
September 2018

Chiari 1 Malformation in a Child with Febrile Seizures, Parasomnias, and Sleep Apnea Syndrome.

Case Rep Pediatr 2017 17;2017:8189790. Epub 2017 Dec 17.

Pediatric Division, Department of Surgical Sciences, Dentistry, Gynecology and Pediatrics, University of Verona, Verona, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1155/2017/8189790DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748138PMC
December 2017

The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy.

Seizure 2017 Oct 11;51:1-5. Epub 2017 Jul 11.

Servizio di Neuropsichiatria Infantile, Policlinico G.B. Rossi, Universita degli Studi di Verona, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.seizure.2017.07.002DOI Listing
October 2017

Progressive Myoclonus Epilepsy in Congenital Generalized Lipodystrophy type 2: Report of 3 cases and literature review.

Seizure 2016 Nov 5;42:1-6. Epub 2016 Sep 5.

University Hospital of Verona, Department of Surgical Sciences, Gynecology and Pediatrics, Section of Child Neuropsychiatry, piazzale L.A. Scuro 10, 37134 Verona, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.seizure.2016.08.008DOI Listing
November 2016

Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy.

Dev Med Child Neurol 2016 10 13;58(10):1085-91. Epub 2016 May 13.

Pediatric Neurology Unit and Laboratories, A. Meyer Children's Hospital - University of Florence, Florence, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/dmcn.13141DOI Listing
October 2016

Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boys.

Epilepsia 2014 Nov 29;55(11):1748-53. Epub 2014 Sep 29.

Pediatric Neurology and Neurogenetics Unit and Laboratories, A. Meyer Children's Hospital-University of Florence, Florence, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/epi.12803DOI Listing
November 2014

Epilepsy-related brain networks in ring chromosome 20 syndrome: an EEG-fMRI study.

Epilepsia 2014 Mar 31;55(3):403-13. Epub 2014 Jan 31.

Department of Biomedical Sciences, Metabolic, and Neuroscience, NOCSAE Hospital, University of Modena and Reggio Emilia, Modena, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/epi.12539DOI Listing
March 2014

Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20.

Clin Neurophysiol 2014 Feb 19;125(2):239-49. Epub 2013 Aug 19.

Department of Biomedical Sciences, Metabolism and Neuroscience, University of Modena and Reggio Emilia, NOCSE Hospital, Modena, Italy. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.clinph.2013.07.009DOI Listing
February 2014

Epilepsy with myoclonic atonic seizures: an electroclinical study of 69 patients.

Pediatr Neurol 2013 May;48(5):355-62

Servicio de Neurologia, Hospital de Pediatría Prof Dr Juan P Garrahan, Buenos Aires, Argentina.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.pediatrneurol.2012.12.022DOI Listing
May 2013

Individually tailored extratemporal epilepsy surgery in children: anatomo-electro-clinical features and outcome predictors in a population of 53 cases.

Epilepsy Behav 2012 Sep 17;25(1):68-80. Epub 2012 Aug 17.

Infantile Neurology Service, Complex Unit of Infantile Neuropsychiatry, Niguarda Ca'Granda Hospital, Milan, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.yebeh.2012.05.008DOI Listing
September 2012

Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations.

Epilepsia 2011 Jul 11;52(7):1251-7. Epub 2011 Apr 11.

Neurology Unit, Department of Neuroscience, Bambino Gesu' Children's Hospital-IRCCS, Piazza S. Onofrio 4, Rome, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1528-1167.2011.03063.xDOI Listing
July 2011

Electroclinical findings in four patients with karyotype 47,XYY.

Brain Dev 2011 May 16;33(5):384-9. Epub 2010 Sep 16.

Child Neuropsychiatry Unit, University of Verona, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.braindev.2010.07.010DOI Listing
May 2011

Absence seizures in the first 3 years of life: an electroclinical study of 46 cases.

Epilepsia 2011 Feb 26;52(2):393-400. Epub 2011 Jan 26.

Department of Neurology, Hospital Nacional de Pediatría Prof Dr Juan P Garrahan, Buenos Aires, Argentina.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1528-1167.2010.02926.xDOI Listing
February 2011

A study of 63 cases with eyelid myoclonia with or without absences: type of seizure or an epileptic syndrome?

Seizure 2009 Jul 5;18(6):440-5. Epub 2009 May 5.

Neurology Department, Hospital Nacional de Pediatría. Prof Dr Juan P Garrahan, Buenos Aires, Argentina.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.seizure.2009.04.004DOI Listing
July 2009

Childhood absence epilepsy and electroencephalographic focal abnormalities with or without clinical manifestations.

Seizure 2008 Oct;17(7):617-24

Neurology Department, National Pediatric Hospital Prof Dr Juan P. Garrahan, Combate de los Pozos 1881, 1245 Buenos Aires, Argentina.

View Article

Download full-text PDF

Source
http://linkinghub.elsevier.com/retrieve/pii/S105913110800069
Publisher Site
http://dx.doi.org/10.1016/j.seizure.2008.03.009DOI Listing
October 2008

Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients.

J Child Neurol 2008 May 29;23(5):497-506. Epub 2008 Jan 29.

Neurology Department, Hospital de Pediatría Prof Dr Juan P. Garrahan, Combate de los Pozos 1881, CP 1245, Buenos Aires, Argentina.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/0883073807309771DOI Listing
May 2008

Uncombable hair syndrome, mental retardation, single palmar crease and arched palate in a patient with neurofibromatosis type I.

Pediatr Dermatol 2007 Sep-Oct;24(5):E73-5

Department of Biomedical and Surgical Sciences, Section of Dermatology and Venereology, University of Verona, Verona, Italy.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1111/j.1525-1470.2007.00446.x
Publisher Site
http://dx.doi.org/10.1111/j.1525-1470.2007.00446.xDOI Listing
December 2007

Scotosensitive and photosensitive myoclonic seizures in an infant with trisomy 13.

Epilepsia 2007 Nov 28;48(11):2177-80. Epub 2007 Jul 28.

Child Neuropsychiatry Unit, University of Verona, Policlinico G.B. Rossi, Piazzale L.A. Scuro 10, Verona, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1528-1167.2007.01220.xDOI Listing
November 2007

Restless legs syndrome and attention-deficit/hyperactivity disorder: a review of the literature.

Sleep 2005 Aug;28(8):1007-13

Service de Psychopathologie de l'Enfant et de l'Adolescent, Hôpital Robert Debré, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/sleep/28.8.1007DOI Listing
August 2005

Myoclonic status in nonprogressive encephalopathies.

Adv Neurol 2005 ;95:59-70

Servizio Neuropsichiatria Infantile, Policlinico G.B. Rossi, Studi di Verona, Verona, Italy.

View Article

Download full-text PDF

Source
December 2004