Lucio Giordano

Lucio Giordano

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Lucio Giordano

Lucio Giordano

Publications by authors named "Lucio Giordano"

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Sleep in Mowat-Wilson Syndrome: a clinical and video-polysomnographic study.

Sleep Med 2019 Sep 26;61:44-51. Epub 2019 Apr 26.

Child Neurology and Psychiatry Unit, Department of Medical and Surgical Sciences (DIMEC), S. Orsola Hospital, University of Bologna, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.sleep.2019.04.011DOI Listing
September 2019

Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literature.

Am J Med Genet B Neuropsychiatr Genet 2018 12 22;177(8):687-690. Epub 2018 Oct 22.

Pediatric Neurology and Psychiatric Department, Ospedale dei Bambini di Brescia, Brescia, Lombardia, Italy.

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http://doi.wiley.com/10.1002/ajmg.b.32677
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http://dx.doi.org/10.1002/ajmg.b.32677DOI Listing
December 2018

Childhood Absence Epilepsy evolving to Eyelid Myoclonia with Absence Epilepsy.

Seizure 2018 Oct 18;61:1-3. Epub 2018 Jul 18.

Child Neurology and Psychiatry Unit, ASST Civil Hospital -Brescia, Italy. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S10591311183024
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http://dx.doi.org/10.1016/j.seizure.2018.07.009DOI Listing
October 2018

Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.

Genet Med 2018 09 4;20(9):965-975. Epub 2018 Jan 4.

Clinical Genetics Unit, Department of Obstetrics and Pediatrics, AUSL-IRCCS of Reggio Emilia, Reggio Emilia, Italy.

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http://www.nature.com/articles/gim2017221
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http://dx.doi.org/10.1038/gim.2017.221DOI Listing
September 2018

Dramatic relapse of seizures after everolimus withdrawal.

Eur J Paediatr Neurol 2018 Jan 3;22(1):203-206. Epub 2017 Aug 3.

Child Neuropsychiatry Unit - Epilepsy Center, ASST Santi Paolo e Carlo Hospital, Department of Health Sciences, University of Milan, Italy.

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http://dx.doi.org/10.1016/j.ejpn.2017.07.018DOI Listing
January 2018

Pyridoxine responsiveness in pyridox(am)ine-5-phosphate oxidase deficiency: The importance of early treatment.

Clin Neurol Neurosurg 2017 12 23;163:90-93. Epub 2017 Oct 23.

Child Neurology and Psychiatry Unit, Spedali Civili, Brescia, Italy.

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http://dx.doi.org/10.1016/j.clineuro.2017.10.019DOI Listing
December 2017

Efficacy of a new technique - INtubate-RECruit-SURfactant-Extubate - "IN-REC-SUR-E" - in preterm neonates with respiratory distress syndrome: study protocol for a randomized controlled trial.

Trials 2016 08 18;17:414. Epub 2016 Aug 18.

Ospedale Santa Maria di Ca' Foncello di Treviso, Treviso, Italy.

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http://dx.doi.org/10.1186/s13063-016-1498-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991115PMC
August 2016

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

CHD2 mutations are a rare cause of generalized epilepsy with myoclonic-atonic seizures.

Epilepsy Behav 2015 Oct 7;51:53-6. Epub 2015 Aug 7.

Neurology Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.yebeh.2015.06.029DOI Listing
October 2015

Antiepileptic drugs in Rett Syndrome.

Eur J Paediatr Neurol 2015 Jul 5;19(4):446-52. Epub 2015 Mar 5.

University of Genoa, DINOGMI, Italy; Department of Child Neuropsychiatry, Epilepsy Centre, Giannina Gaslini Institute, Italy.

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http://dx.doi.org/10.1016/j.ejpn.2015.02.007DOI Listing
July 2015

Do pure absence seizures occur in myoclonic epilepsy of infancy? A case series.

Seizure 2015 Jan 15;24:8-11. Epub 2014 Nov 15.

Pediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation, Ophtalmology, Genetics, Maternal and Child Health, University of Genoa, "G. Gaslini" Institute, Genova, Italy.

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http://dx.doi.org/10.1016/j.seizure.2014.11.002DOI Listing
January 2015

Sporadic and familial glut1ds Italian patients: A wide clinical variability.

Seizure 2015 Jan 26;24:28-32. Epub 2014 Nov 26.

Brain and Behaviour Department, University of Pavia, Pavia, Italy; Department of Child Neurology and Psychiatry, "C. Mondino" National Neurological Institute, Pavia, Italy. Electronic address:

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http://www.glut1.it/wp-content/uploads/2014/12/familial-glut
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http://dx.doi.org/10.1016/j.seizure.2014.11.009DOI Listing
January 2015

Non-epileptic myoclonic attacks in infancy: three cases.

Epileptic Disord 2014 Dec;16(4):433-8

Epilepsy Center, San Paolo Hospital, Milan, Italy, Department of Health Sciences, University of Milan, Italy.

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http://dx.doi.org/10.1684/epd.2014.0713DOI Listing
December 2014

Setleis syndrome: genetic and clinical findings in a new case with epilepsy.

Pediatr Neurol 2014 Apr 14;50(4):389-91. Epub 2013 Dec 14.

Division of Medical Genetics, Galliera Hospital, Genova, Italy.

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http://dx.doi.org/10.1016/j.pediatrneurol.2013.12.009DOI Listing
April 2014

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

Clinical features of Sturge-Weber syndrome without facial nevus: five novel cases.

Eur J Paediatr Neurol 2013 Jan 18;17(1):91-6. Epub 2012 Jul 18.

Neuropsichiatria Infantile Pediatria Ospedale San Paolo, Savona, Italy.

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http://dx.doi.org/10.1016/j.ejpn.2012.06.011DOI Listing
January 2013

Congenital systematized basaloid follicular hamartoma with microphthalmia and hemimegalencephaly.

Pediatr Dermatol 2011 Sep-Oct;28(5):555-60. Epub 2010 Nov 9.

Section of Dermatology, Department of Surgical Sciences, University of Parma, Parma, Italy.

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http://dx.doi.org/10.1111/j.1525-1470.2010.01225.xDOI Listing
February 2012

Clinical and molecular description of a Wilms tumor in a patient with tuberous sclerosis complex.

Am J Med Genet A 2011 Jun 12;155A(6):1419-24. Epub 2011 May 12.

Pediatric Oncology Unit, Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.

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http://doi.wiley.com/10.1002/ajmg.a.34001
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http://dx.doi.org/10.1002/ajmg.a.34001DOI Listing
June 2011

Epilepsy in Rett syndrome: clinical and genetic features.

Epilepsy Behav 2010 Nov 21;19(3):296-300. Epub 2010 Aug 21.

Department of Child Neuropsychiatry, Epilepsy Centre, G. Gaslini Institute, University of Genoa, Genoa, Italy.

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https://linkinghub.elsevier.com/retrieve/pii/S15255050100047
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http://dx.doi.org/10.1016/j.yebeh.2010.06.051DOI Listing
November 2010

Extracorporeal shock-wave therapy compared with surgery for hypertrophic long-bone nonunions.

J Bone Joint Surg Am 2009 Nov;91(11):2589-97

Department of Physical Medicine and Rehabilitation, San Salvatore Hospital of L'Aquila, via L. Natali 1, 67100 L'Aquila, Italy.

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http://Insights.ovid.com/crossref?an=00004623-200911000-0000
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http://dx.doi.org/10.2106/JBJS.H.00841DOI Listing
November 2009

Celiac disease-related antibodies in Italian children with epilepsy.

Pediatr Neurol 2009 Jul;41(1):34-6

Pediatric Neuropsychiatric Division, City Hospital of Brescia, Brescia, Italy.

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http://dx.doi.org/10.1016/j.pediatrneurol.2009.02.009DOI Listing
July 2009

Two novel ALDH7A1 (antiquitin) splicing mutations associated with pyridoxine-dependent seizures.

Epilepsia 2009 Apr;50(4):933-6

Department of Neurological Sciences, Epilepsy Center, Federico II University, Napoli, Italy.

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http://dx.doi.org/10.1111/j.1528-1167.2008.01741.xDOI Listing
April 2009

Detection of herpesvirus-6A in a case of subacute cerebellitis and myoclonic dystonia.

J Med Virol 2005 Mar;75(3):427-9

Department of Biomedical Science and Technology, University of Milan, Milan, Italy.

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http://doi.wiley.com/10.1002/jmv.20285
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http://dx.doi.org/10.1002/jmv.20285DOI Listing
March 2005