Nardo Nardocci

Nardo Nardocci

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Nardo Nardocci

Publications by authors named "Nardo Nardocci"

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Epileptic phenotypes in children with early-onset mitochondrial diseases.

Acta Neurol Scand 2019 Sep 6;140(3):184-193. Epub 2019 Jun 6.

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

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http://dx.doi.org/10.1111/ane.13130DOI Listing
September 2019

A causality algorithm to guide diagnosis and treatment of catatonia due to autoimmune conditions in children and adolescents.

Schizophr Res 2018 10 26;200:68-76. Epub 2017 Jun 26.

Department of Child and Adolescent Psychiatry, Université Pierre et Marie Curie, Hôpital Pitié-Salpêtrière, AP-HP, 47-83 Boulevard de l'Hôpital, 75013 Paris, France; Groupe de Recherche Clinique, Abord dimensionnel des épisodes psychotiques de l'enfant et de l'adolescent: implications génétiques, métaboliques et auto-immunes, Université Pierre et Marie Curie, Hôpital Pitié-Salpêtrière, AP-HP, 47-83 Boulevard de l'Hôpital, 75013 Paris, France.

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http://dx.doi.org/10.1016/j.schres.2017.06.036DOI Listing
October 2018

Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?

Eur J Med Genet 2018 Oct 3;61(10):581-584. Epub 2018 Apr 3.

Molecular Neurogenetics, Foundation IRCCS Neurological Institute Besta, Milan, Italy; Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2018.03.011DOI Listing
October 2018

SLC19A3 related disorder: Treatment implication and clinical outcome of 2 new patients.

Eur J Paediatr Neurol 2018 Mar 16;22(2):332-335. Epub 2017 Dec 16.

Child Neurology Unit, IRCCS-Fondazione Istituto Neurologico Carlo Besta, Milan, Italy.

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http://dx.doi.org/10.1016/j.ejpn.2017.11.012DOI Listing
March 2018

ATP1A3-related disorders: An update.

Eur J Paediatr Neurol 2018 Mar 21;22(2):257-263. Epub 2017 Dec 21.

Department of Pediatric Neurology, IRCCS Foundation Carlo Besta Neurological Institute, Via Celoria 11, 20131 Milan, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2017.12.009DOI Listing
March 2018

Pediatric NMDAR encephalitis: A single center observation study with a closer look at movement disorders.

Eur J Paediatr Neurol 2018 Mar 1;22(2):301-307. Epub 2018 Feb 1.

Department of Pediatric Neuroscience, Foundation IRCCS Neurological Institute "C. Besta", Milan, Italy.

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http://dx.doi.org/10.1016/j.ejpn.2018.01.012DOI Listing
March 2018

Diagnosis and treatment of pediatric onset isolated dystonia.

Eur J Paediatr Neurol 2018 Mar 17;22(2):238-244. Epub 2018 Jan 17.

Department of Paediatric Neurology, IRCCS Fondazione C. Besta, Milan, Italy.

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https://linkinghub.elsevier.com/retrieve/pii/S10903798173191
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http://dx.doi.org/10.1016/j.ejpn.2018.01.006DOI Listing
March 2018

CANS: Childhood acute neuropsychiatric syndromes.

Eur J Paediatr Neurol 2018 03;22(2):316-320

Fondazione IRCSS Istituto Neurologico Carlo Besta, Milan, Italy. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S10903798173191
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http://dx.doi.org/10.1016/j.ejpn.2018.01.011DOI Listing
March 2018

A PDE10A de novo mutation causes childhood-onset chorea with diurnal fluctuations.

Mov Disord 2017 11 26;32(11):1646-1647. Epub 2017 Sep 26.

Department of Neurology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.

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http://dx.doi.org/10.1002/mds.27175DOI Listing
November 2017

Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5.

Dev Med Child Neurol 2017 08 25;59(8):815-821. Epub 2017 May 25.

Molecular Medicine Unit and Child Neurology, IRCCS Fondazione Stella Maris, Pisa, Italy.

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http://doi.wiley.com/10.1111/dmcn.13473
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http://dx.doi.org/10.1111/dmcn.13473DOI Listing
August 2017

Thiamine-responsive disease due to mutation of : Importance of avoiding misdiagnosis.

Neurology 2017 08 26;89(8):870-871. Epub 2017 Jul 26.

From the Neurological Institute C. Besta Foundation IRCCS, Milan, Italy.

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http://www.neurology.org/lookup/doi/10.1212/WNL.000000000000
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http://dx.doi.org/10.1212/WNL.0000000000004270DOI Listing
August 2017

Alternating Hemiplegia and Epilepsia Partialis Continua: A new phenotype for a novel compound TBC1D24 mutation.

Seizure 2017 Apr 6;47:71-73. Epub 2017 Mar 6.

Department of Pediatric Neuroscience, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.seizure.2017.03.003DOI Listing
April 2017

DYT2 screening in early-onset isolated dystonia.

Eur J Paediatr Neurol 2017 Mar 13;21(2):269-271. Epub 2016 Oct 13.

Molecular Neurogenetics Unit, IRCCS Foundation C. Besta Neurological Institute, Milan, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2016.10.001DOI Listing
March 2017

Consensus clinical management guideline for pantothenate kinase-associated neurodegeneration (PKAN).

Mol Genet Metab 2017 03 27;120(3):278-287. Epub 2016 Dec 27.

Department of Molecular & Medical Genetics, Oregon Health & Science University, Portland, USA; Department of Neurology, Oregon Health & Science University, Portland, USA.

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http://dx.doi.org/10.1016/j.ymgme.2016.11.004DOI Listing
March 2017

Recognizing the Common Origins of Dystonia and the Development of Human Movement: A Manifesto of Unmet Needs in Isolated Childhood Dystonias.

Front Neurol 2016 19;7:226. Epub 2016 Dec 19.

Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta , Milano , Italy.

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http://dx.doi.org/10.3389/fneur.2016.00226DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5165260PMC
December 2016

Posteroventrolateral pallidotomy through implanted DBS electrodes monitored by recording local field potentials.

Br J Neurosurg 2015 17;29(6):888-90. Epub 2015 Jun 17.

c Clinical Center for Neurostimulation, Neurotechnologies and Movement Disorders, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico , Milan , Italy.

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http://www.angelofranzini.com/pvp.pdf
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http://www.tandfonline.com/doi/full/10.3109/02688697.2015.10
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http://dx.doi.org/10.3109/02688697.2015.1054363DOI Listing
October 2016

Vasculogenic and Angiogenic Pathways in Moyamoya Disease.

Curr Med Chem 2016 ;23(4):315-45

Laboratory of Cellular Neurobiology, Neurology Unit, UCV, Neurological Institute "C. Besta" IRCCS Foundation, Via Celoria 11, Milan 20133, Italy.

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http://dx.doi.org/10.2174/092986732304160204181543DOI Listing
October 2016

Childhood-onset ATP1A3-related conditions: Report of two new cases of phenotypic spectrum.

Parkinsonism Relat Disord 2016 09 1;30:81-2. Epub 2016 Jun 1.

Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Piazza Sant'Onofrio, 4, 00165, Rome, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2016.05.029DOI Listing
September 2016

Neurological Disorders Associated with Striatal Lesions: Classification and Diagnostic Approach.

Curr Neurol Neurosci Rep 2016 Jun;16(6):54

Child Neurology Department, Neurological Institute C. Besta Foundation IRCCS, Via Celoria 11, 20133, Milan, Italy.

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http://dx.doi.org/10.1007/s11910-016-0656-3DOI Listing
June 2016

Cognitive and neuropsychological evolution in children with anti-NMDAR encephalitis.

J Neurol 2016 Apr 17;263(4):765-71. Epub 2016 Feb 17.

Department of Pediatric Neuroscience, Foundation IRCCS Neurological Institute "C. Besta", Via Celoria 11, 20133, Milan, Italy.

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http://dx.doi.org/10.1007/s00415-016-8056-9DOI Listing
April 2016

Clinical and genetic features of paroxysmal kinesigenic dyskinesia in Italian patients.

Eur J Paediatr Neurol 2016 Jan 3;20(1):152-7. Epub 2015 Sep 3.

Unit of Neuropediatry, The Foundation "Carlo Besta" Institute of Neurology IRCCS, Milan, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2015.08.006DOI Listing
January 2016

Cerebrospinal Fluid Monoamine Metabolite Analysis in Pediatric Movement Disorders.

J Child Neurol 2015 Nov 23;30(13):1800-5. Epub 2015 Apr 23.

Department of Child Neurology, Neurological Institute C. Besta Foundation IRCCS, Milan, Italy

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http://dx.doi.org/10.1177/0883073815581608DOI Listing
November 2015

Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutations.

Neurology 2015 Jul 26;85(4):316-24. Epub 2015 Jun 26.

From the Neurophysiopathology and Epilepsy Centre (L. Canafoglia, I.G., S.B., V. Scaioli, S.F.), Neuropathology-Neurology 5 (V.F., M.M.), Neuroradiology (L. Chiapparini), and Child Neurology and Psychiatry (T.G., N.N.), IRCCS Foundation C. Besta Neurological Institute, Milan; Molecular Neurogenetics (F.I., B.G.), IRCCS Foundation C. Besta Neurological Institute-Bicocca, Milan; G.F. Ingrassia Department (V. Sofia), University of Catania, Italy; and Epilepsy Research Center (S.F.B.), Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Australia.

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http://dx.doi.org/10.1212/WNL.0000000000001784DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4520821PMC
July 2015

Focal seizure, focal dyskinesia, or both? A complex motor phenomenon reveals anti-NMDAR encephalitis.

Seizure 2015 Apr 14;27:16-8. Epub 2015 Feb 14.

Department of Pediatric Neuroscience, Foundation I.R.C.C.S. Neurological Institute C. Besta, Milan, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.seizure.2015.02.005DOI Listing
April 2015

Mitochondrial dysfunction in Parkinson disease: evidence in mutant PARK2 fibroblasts.

Front Genet 2015 11;6:78. Epub 2015 Mar 11.

Unit of Molecular Neurogenetics - Pierfranco and Luisa Mariani Center for the Study of Mitochondrial Disorders in Children, Foundation of the Carlo Besta Neurological Institute IRCCS, Milan, Italy.

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http://dx.doi.org/10.3389/fgene.2015.00078DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4356157PMC
March 2015

Downbeat nystagmus as the presenting symptom of infantile neuroaxonal dystrophy: a case report.

Brain Dev 2015 Feb 5;37(2):270-2. Epub 2014 May 5.

Pediatric Neurology Unit, Azienda Ospedaliera ASMN, Istituto e Cura a Carattere Scientifico, 42123 Reggio Emilia, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.braindev.2014.04.010DOI Listing
February 2015

A family with paroxysmal nonkinesigenic dyskinesias (PNKD): evidence of mitochondrial dysfunction.

Eur J Paediatr Neurol 2015 Jan 18;19(1):64-8. Epub 2014 Oct 18.

Neuropediatrics Unit, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Milan, Italy. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S10903798140017
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http://dx.doi.org/10.1016/j.ejpn.2014.10.003DOI 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

Therapeutic advances in neurodegeneration with brain iron accumulation.

Int Rev Neurobiol 2013 ;110:153-64

Department of Child Neurology, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Milan, Italy.

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http://dx.doi.org/10.1016/B978-0-12-410502-7.00008-9DOI Listing
July 2014

Axonal dystrophies.

Handb Clin Neurol 2013 ;113:1919-24

Department of Child Neurology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy. Electronic address:

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http://dx.doi.org/10.1016/B978-0-444-59565-2.00062-9DOI Listing
March 2014

Running apraxia as a presenting symptom of neuronal ceroid lipofuscinosis 6.

Mov Disord 2014 Feb 22;29(2):277-8. Epub 2013 Oct 22.

Department of Paediatrics, Child Neurology and Psychiatry, Sapienza Universitá di Roma, Rome, Italy.

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http://dx.doi.org/10.1002/mds.25725DOI Listing
February 2014

Pathophysiology and treatment of neurodegeneration with brain iron accumulation in the pediatric population.

Curr Treat Options Neurol 2013 Oct;15(5):652-67

Department of Neurology, University of Kiel, Arnold Heller Str 3, 24105, Kiel, Germany,

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http://dx.doi.org/10.1007/s11940-013-0254-5DOI Listing
October 2013

Phenomenology of psychogenic movement disorders in children.

Mov Disord 2012 Aug 7;27(9):1153-7. Epub 2012 Mar 7.

U.O. Neuropsichiatria Infantile Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italia.

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http://dx.doi.org/10.1002/mds.24947DOI Listing
August 2012

Cortical myoclonus in childhood and juvenile onset Huntington's disease.

Parkinsonism Relat Disord 2012 Jul 10;18(6):794-7. Epub 2012 Apr 10.

Dept. of Neurophysiopathology and Epilepsy Centre, IRCCS Foundation Carlo Besta Neurological Institute, Milan, Italy.

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http://dx.doi.org/10.1016/j.parkreldis.2012.03.011DOI Listing
July 2012

C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation.

Semin Pediatr Neurol 2012 Jun;19(2):75-81

Unit of Molecular Neurogenetics, Pierfranco and Luisa Mariani Center for the study of Mitochondrial Disorders in Children, IRCCS, Foundation Neurological Institute C. Besta, Milan, Italy.

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http://linkinghub.elsevier.com/retrieve/pii/S107190911200022
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http://dx.doi.org/10.1016/j.spen.2012.03.006DOI Listing
June 2012

Therapeutic advances in neurodegeneration with brain iron accumulation.

Semin Pediatr Neurol 2012 Jun;19(2):82-6

Department of Child Neurology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.

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http://dx.doi.org/10.1016/j.spen.2012.03.007DOI Listing
June 2012

Paroxysmal non-epileptic motor events in childhood: a clinical and video-EEG-polymyographic study.

Dev Med Child Neurol 2012 Apr 28;54(4):334-8. Epub 2012 Jan 28.

UO Neuropsichiatria Infantile Fondazione, IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.

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http://doi.wiley.com/10.1111/j.1469-8749.2011.04217.x
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http://dx.doi.org/10.1111/j.1469-8749.2011.04217.xDOI Listing
April 2012

Update on pediatric dystonias: etiology, epidemiology, and management.

Degener Neurol Neuromuscul Dis 2012 11;2:29-41. Epub 2012 Apr 11.

Child Neurology Department, Fondazione IRCCS Istituto Neurologico "C. Besta", Milano, Italy.

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http://dx.doi.org/10.2147/DNND.S16082DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065605PMC
April 2012

Diagnostic issues in childhood and adult dystonia.

Expert Opin Med Diagn 2011 Nov;5(6):483-500

Neurologia I, Fondazione Istituto Neurologico Carlo Besta , Via Celoria, 11, 20133 Milano , Italy +02 2394 2552 ; +02 2394 2539 ;

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http://dx.doi.org/10.1517/17530059.2011.615831DOI Listing
November 2011

Deep brain stimulation for movement disorders. Considerations on 276 consecutive patients.

J Neural Transm (Vienna) 2011 Oct 20;118(10):1497-510. Epub 2011 May 20.

Department of Neurosurgery, Fondazione IRCCS Istituto Neurologico C. Besta, Via Celoria 11, 20133, Milan, Italy.

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http://dx.doi.org/10.1007/s00702-011-0656-zDOI Listing
October 2011

The relationship between group A streptococcal infections and Tourette syndrome: a study on a large service-based cohort.

Dev Med Child Neurol 2011 Oct 17;53(10):951-7. Epub 2011 Jun 17.

Department of Neurological and Psychiatric Sciences, University of Bari, Bari, Italy.

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http://dx.doi.org/10.1111/j.1469-8749.2011.04018.xDOI Listing
October 2011

Reaching and writing movements: sensitive and reliable tools to measure genetic dystonia in children.

J Child Neurol 2011 Jul 18;26(7):822-9. Epub 2011 Mar 18.

Politecnico di Milano, Bioengineering Department, NearLab, Milan, Italy.

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http://dx.doi.org/10.1177/0883073810392997DOI Listing
July 2011

Myoclonus-dystonia syndrome.

Authors:
Nardo Nardocci

Handb Clin Neurol 2011 ;100:563-75

Department of Child Neurology, Fondazione IRCCS Istituto Neurologico "C. Besta", Milan, Italy.

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https://linkinghub.elsevier.com/retrieve/pii/B97804445201420
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http://dx.doi.org/10.1016/B978-0-444-52014-2.00041-0DOI Listing
July 2011

Sequence variations in mitochondrial ferritin: distribution in healthy controls and different types of patients.

Genet Test Mol Biomarkers 2010 Dec 12;14(6):793-6. Epub 2010 Oct 12.

Genomic Unit for the Diagnosis of Human Pathologies, Center for Genomics, Bioinformatics, and Biostatistics, San Raffaele Scientific Institute, Milan, Italy.

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http://dx.doi.org/10.1089/gtmb.2010.0076DOI Listing
December 2010

Measuring participation in children with Gilles de la Tourette syndrome: a pilot study with ICF-CY.

Disabil Rehabil 2009 ;31 Suppl 1:S116-20

Neurological Institute C. Besta IRCCS Foundation, Neurology, Public Health and Disability Unit - Scientific Directorate, Via Celoria 11, Milan, Italy.

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http://dx.doi.org/10.3109/09638280903317773DOI Listing
May 2010

Glucose transporter type 1 deficiency: ketogenic diet in three patients with atypical phenotype.

Brain Dev 2010 May 9;32(5):404-8. Epub 2009 Jun 9.

Department of Child Neurology and Psychiatry, Fondazione IRCCS Istituto Neurologico C.Mondino, Pavia, Italy.

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http://dx.doi.org/10.1016/j.braindev.2009.04.013DOI Listing
May 2010

Childhood-onset HAM/TSP with progressive cognitive impairment.

Neurol Sci 2010 Apr;31(2):209-12

Department of Child Neurology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.

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http://dx.doi.org/10.1007/s10072-009-0204-xDOI Listing
April 2010

Deep brain stimulation electrode used for radiofrequency lesion of the globus pallidus internus in dystonia.

Stereotact Funct Neurosurg 2009 10;87(6):348-52. Epub 2009 Sep 10.

Department of Neurosurgery, Fondazione Istituto Neurologico Carlo Besta, Milan, Italy.

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http://dx.doi.org/10.1159/000236368DOI Listing
February 2010

Early onset primary dystonia.

Eur J Paediatr Neurol 2009 Nov 20;13(6):488-92. Epub 2009 Jan 20.

Department of Child Neurology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133 Milano, Italy.

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http://linkinghub.elsevier.com/retrieve/pii/S109037980800222
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http://dx.doi.org/10.1016/j.ejpn.2008.12.001DOI Listing
November 2009

Age-related iron deposition in the basal ganglia: quantitative analysis in healthy subjects.

Radiology 2009 Jul;252(1):165-72

Departments of Neuroradiology, Foundation IRCCS, C. Besta Neurological Institute, Via Celoria 11, 20133 Milan, Italy.

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http://dx.doi.org/10.1148/radiol.2522081399DOI Listing
July 2009

Myoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 families.

Mov Disord 2008 Jan;23(1):28-34

Department of Child Neurology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, Milano, Italy.

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http://dx.doi.org/10.1002/mds.21715DOI Listing
January 2008

Respiratory failure in infants due to spinal muscular atrophy with respiratory distress type 1.

Intensive Care Med 2006 Nov 9;32(11):1851-5. Epub 2006 Sep 9.

Pediatric Intensive Care Unit, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Via della Commenda 9, 20122, Milan, Italy.

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http://link.springer.com/10.1007/s00134-006-0346-8
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http://dx.doi.org/10.1007/s00134-006-0346-8DOI Listing
November 2006

Stimulation of the globus pallidus internus for childhood-onset dystonia.

Mov Disord 2005 Sep;20(9):1194-200

Department of Child Neurology, Istituto Nazionale Neurologico Carlo Besta, Milano, Italy.

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http://dx.doi.org/10.1002/mds.20510DOI Listing
September 2005

Paroxysmal dyskinesias in childhood.

Pediatr Neurol 2003 Mar;28(3):168-72

Department of Child Neurology, Istituto Nazionale Neurologico "C. Besta", Milano, Italy.

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http://dx.doi.org/10.1016/s0887-8994(02)00512-xDOI Listing
March 2003

Myoclonic dystonia as unique presentation of isolated vitamin E deficiency in a young patient.

Mov Disord 2002 May;17(3):612-4

Department of Neuropediatrics, National Neurological Institute C. Besta, Milan, Italy.

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http://dx.doi.org/10.1002/mds.10026DOI Listing
May 2002

Frequency of DYT1 mutation in early onset primary dystonia in Italian patients.

Mov Disord 2002 Mar;17(2):407-8

Department of Child Neurology, National Neurological Institute C. Besta, Milan, Italy.

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March 2002