Publications by authors named "Tiziana Pisano"

39Publications

Peer victimization and developmental psychopathology in childhood and adolescence Italian psychiatric emergency unit. A single center retrospective observational study.

Psychol Health Med 2020 Aug 20:1-9. Epub 2020 Aug 20.

Department of Education, Languages, Intercultures, Literatures and Psychology, University of Florence , Florence, Italy.

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http://dx.doi.org/10.1080/13548506.2020.1810721DOI Listing
August 2020

Early infantile epileptic-dyskinetic encephalopathy due to biallelic mutations.

Neurol Genet 2020 Feb 2;6(1):e387. Epub 2020 Jan 2.

Pediatric Neurology (A.V., T.P., S.C., E. Parrini, D.M., S.V., R.G.), Neurogenetics and Neurobiology Unit and Laboratories, Meyer Children's Hospital, University of Florence; Metabolic and Muscular Unit (E. Procopio), Meyer Children's Hospital, University of Florence; Department of Medical and Surgical Science (A.G.), University of Modena and Reggio Emilia; Pediatric Immunology (G.M., C.A.), Department of Health Sciences, Meyer Children's Hospital, University of Florence; and IRCCS Stella Maris (R.G.), Pisa, Italy.

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http://dx.doi.org/10.1212/NXG.0000000000000387DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6984131PMC
February 2020

Long-term efficacy of add-on stiripentol treatment in children, adolescents, and young adults with refractory epilepsies: A single center prospective observational study.

Epilepsia 2019 11 20;60(11):2255-2262. Epub 2019 Oct 20.

Neuroscience Center of Excellence, Meyer Children's Hospital, University of Florence, Florence, Italy.

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http://dx.doi.org/10.1111/epi.16363DOI Listing
November 2019

Response to the letter to the Editor regarding "Leigh-like neuroimaging features associated with new bi-allelic mutations in OPA1".

Eur J Paediatr Neurol 2017 11 8;21(6):923. Epub 2017 Aug 8.

Molecular Medicine, IRCCS Stella Maris, Italy.

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http://dx.doi.org/10.1016/j.ejpn.2017.06.005DOI Listing
November 2017

Leigh-like neuroimaging features associated with new biallelic mutations in OPA1.

Eur J Paediatr Neurol 2017 Jul 15;21(4):671-677. Epub 2017 Apr 15.

Molecular Medicine, IRCCS Stella Maris, Pisa, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2017.04.004DOI Listing
July 2017

Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes.

Hum Mutat 2017 02 9;38(2):216-225. Epub 2016 Dec 9.

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

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http://dx.doi.org/10.1002/humu.23149DOI Listing
February 2017

The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy.

Dev Med Child Neurol 2016 Jan 6;58(1):93-7. Epub 2015 Sep 6.

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

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http://dx.doi.org/10.1111/dmcn.12894DOI Listing
January 2016

Vertical extraventricular functional hemispherotomy: a new variant for hemispheric disconnection. Technical notes and results in three patients.

Childs Nerv Syst 2015 Nov 23;31(11):2151-60. Epub 2015 Jun 23.

Neurosurgery - Department of Neurosciences, Anna Meyer Pediatric Hospital, Viale Pieraccini 24, 50139, Florence, Italy.

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http://link.springer.com/content/pdf/10.1007%2Fs00381-015-27
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http://link.springer.com/10.1007/s00381-015-2788-1
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http://dx.doi.org/10.1007/s00381-015-2788-1DOI Listing
November 2015

Early and effective treatment of KCNQ2 encephalopathy.

Epilepsia 2015 May 16;56(5):685-91. Epub 2015 Apr 16.

Department of Neurology, University of California, San Francisco, San Francisco, California, U.S.A.

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http://dx.doi.org/10.1111/epi.12984DOI Listing
May 2015

Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients.

Neurology 2013 Nov 9;81(19):1697-703. Epub 2013 Oct 9.

From the Neurogenetics Group (S.W., R.H., A.S., P.D.J.), Department of Molecular Genetics, VIB, Antwerp; Laboratory of Neurogenetics (S.W., R.H., A.S., P.D.J.), Institute Born-Bunge, University of Antwerp, Belgium; Epilepsy Centre Kempenhaeghe (S.W.), Oosterhout, the Netherlands; Department of Paediatrics (V.I.), University Hospital Centre Zagreb, Croatia; Division of Pediatric Neurology and Metabolism (R.V.C.), Department of Pediatrics, University Hospital Ghent, Belgium; Danish Epilepsy Centre (H.H., R.S.M.), Dianalund; Institute for Regional Health Research (H.H.), University of Southern Denmark, Odense; Department of Child Neurology (S.G.), Juliane Marie Center, Rigshospital, Copenhagen, Denmark; Pediatric Neurology (A.-S.S., B.C.), Department of Neurology (A.-S.S., B.C., P.D.J.), Antwerp University Hospital, Antwerp University, Antwerp, Belgium; Epilepsy Research Centre (S.B.H., S.M., I.S.), Department of Medicine, University of Melbourne, Austin Health, Australia; Great Ormond Street Hospital (C.E.), London; Institute of Genetic Medicine (R.H.), Newcastle University, UK; Child Neurology and Neurorehabilitation Unit (G.C., M.A.), Department of Pediatrics, Central Hospital of Bolzano; Neurology Unit and laboratories (T.P., R.G., C.M.), A. Meyer Children's Hospital, Florence; Child Neuropsychiatry Unit (L.G.), Spedali Civili, Brescia, Italy; Pädiatrie I (K.R., E.H.), Division of Pediatric Neurology, University Hospital Innsbruck, Austria; University Hospital Essen (B.A.), University Duisburg-Essen; Department of Paediatric Neurology and Developmental Medicine (A.B.), University Children's Hospital Tübingen, Eberhard Karls University of Tübingen; Center for Child Neurology (I.B.), Sana Krankenhaus Gerresheim, Düsseldorf; Department of Neuropediatrics (S.S.), Hospital for Children and Adolescents, University of Leipzig, Germany; Department of Neurology (B.S., A.P.), Boston Children's Hospital, Harvard School of Medicine; Department of Biology (B.S.), Brandeis U

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http://dx.doi.org/10.1212/01.wnl.0000435296.72400.a1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812107PMC
November 2013

Functional characterization of a novel C-terminal ATP1A2 mutation causing hemiplegic migraine and epilepsy.

Cephalalgia 2013 Dec 9;33(16):1302-10. Epub 2013 Jul 9.

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

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http://dx.doi.org/10.1177/0333102413495116DOI Listing
December 2013

Efficacy and safety of ketamine in refractory status epilepticus in children.

Neurology 2012 Dec 28;79(24):2355-8. Epub 2012 Nov 28.

Pediatric Neurology Unit, Children's Hospital A. Meyer, University of Firenze, Florence, Italy.

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http://dx.doi.org/10.1212/WNL.0b013e318278b685DOI Listing
December 2012

Interictal autonomic abnormalities in idiopathic Rolandic epilepsy.

Epilepsy Behav 2012 Jun 3;24(2):241-5. Epub 2012 May 3.

Aston Brain Centre, School of Life and Health Sciences, Aston University, Birmingham, UK.

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http://dx.doi.org/10.1016/j.yebeh.2012.03.017DOI Listing
June 2012

Hypothermia for neonatal hypoxic-ischemic encephalopathy: may an early amplitude-integrated EEG improve the selection of candidates for cooling?

J Matern Fetal Neonatal Med 2012 Nov 4;25(11):2171-6. Epub 2012 May 4.

Neonatal Intensive Care Unit, Medical Surgical Feto-Neonatal Department, Florence, Italy.

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http://dx.doi.org/10.3109/14767058.2012.683896DOI Listing
November 2012

CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of life.

Dev Med Child Neurol 2011 Apr 11;53(4):354-60. Epub 2011 Feb 11.

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

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http://dx.doi.org/10.1111/j.1469-8749.2010.03889.xDOI Listing
April 2011

Progressive spastic paraplegia as a feature of tetrasomy 18p.

Am J Med Genet A 2010 Sep;152A(9):2173-5

Istituto di Neurogenetica e Neurofarmacologia, CNR Cittadella Universitaria, Monserrato, Cagliari, Italy.

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http://dx.doi.org/10.1002/ajmg.a.33576DOI Listing
September 2010

Compression of superficial temporal arteries by a handmade device: a simple way to block or attenuate migraine attacks in children and adolescents.

J Child Neurol 2010 Jan 12;25(1):67-70. Epub 2009 Jun 12.

Department of Neurosciences, Clinical Section of Neuropsichiatria Infantile, Azienda Ospedaliero-Universitaria, Cagliari, Italy.

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http://dx.doi.org/10.1177/0883073809333534DOI Listing
January 2010

Treatment of migraine attacks by compression of temporal superficial arteries using a device.

Med Sci Monit 2009 Apr;15(4):CR185-8

University Department of Neurosciences, Clinical Section of Neuropsichiatria Infantile, Azienda Ospedaliero-Universitaria, Cagliari, Italy.

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April 2009

Incidence of epilepsy in extremely low-birthweight infants (<1,000 g): a population study of central and southern Sardinia.

Epilepsia 2009 Jan;50 Suppl 1:37-40

Epilepsy Unit, Division of Child Neurology and Psychiatry, Azienda Ospedaliero-Universitaria, Cagliari, Italy.

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http://dx.doi.org/10.1111/j.1528-1167.2008.01968.xDOI Listing
January 2009

Progressive hemispheric shrinking in hemimegalencephaly: a possible role for seizure-related neuronal loss.

Dev Med Child Neurol 2008 Jul;50(7):553-7

Pathological Anatomy Section, Surgery Department, Azienda Ospedaliera Universitaria Pisana, University of Pisa, Italy.

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http://dx.doi.org/10.1111/j.1469-8749.2008.03003.xDOI Listing
July 2008

Megalencephaly, polymicrogyria, and hydrocephalus (MPPH) syndrome: a new case with syndactyly.

J Child Neurol 2008 Aug 12;23(8):916-8. Epub 2008 May 12.

Division of Child Neurology and Psychiatry, Azienda Ospedaliero-Universitaria di Cagliari, Cagliari, Italy.

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http://dx.doi.org/10.1177/0883073808315623DOI Listing
August 2008

Abnormal phonologic processing in familial lateral temporal lobe epilepsy due to a new LGI1 mutation.

Epilepsia 2005 Jan;46(1):118-23

Department of Child Neurology and Psychiatry, University of Cagliari, Cagliari, Italy.

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http://dx.doi.org/10.1111/j.0013-9580.2005.26304.xDOI Listing
January 2005