N. Nardocci

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

A. Priori, G. Messina, A. Franzini, 2015, British journal of neurosurgery.

Targeting the brain: considerations in 332 consecutive patients treated by deep brain stimulation (DBS) for severe neurological diseases

C. Marras, G. Broggi, A. Albanese, 2012, Neurological Sciences.

Focal lesion of the right cingulum: a case report in a child.

G Broggi, G. Broggi, N. Nardocci, 1981, Journal of neurology, neurosurgery, and psychiatry.

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

David B. Goldstein, Bertrand Fontaine, Stephany C. Koelewijn, 2012, Nature Genetics.

Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA.

T. Wieland, J. Hardy, T. Meitinger, 2012, American journal of human genetics.

Exome sequence reveals mutations in CoA synthase as a cause of neurodegeneration with brain iron accumulation.

T. Wieland, T. Strom, V. Tiranti, 2014, American journal of human genetics.

A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia.

Deborah Hughes, Christine Klein, Thomas Foltynie, 2015, American journal of human genetics.

Impaired body movement representation in DYT1 mutation carriers

A. Albanese, G. Moretto, A. Fiaschi, 2008, Clinical Neurophysiology.

Maria Grazia Bruzzone, Alberto Bizzi, Marina Grisoli, 2009, Radiology.

Alessandra Solari, Barbara Garavaglia, N. Nardocci, 2011, Movement disorders : official journal of the Movement Disorder Society.

Epileptic phenotypes in children with early‐onset mitochondrial diseases

S. Franceschetti, N. Nardocci, E. Lamantea, 2019, Acta neurologica Scandinavica.

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

N. Nardocci, T. Granata, S. Binelli, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

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

Sylvie Viaux, D. Cohen, N. Nardocci, 2017, Schizophrenia Research.

Paroxysmal movement disorders in GLUT1 deficiency syndrome

B. Castellotti, C. Gellera, N. Nardocci, 2008, Neurology.

EMG-Based Visual-Haptic Biofeedback: A Tool to Improve Motor Control in Children With Primary Dystonia

G. Zorzi, G. Ferrigno, A. Pedrocchi, 2013, IEEE Transactions on Neural Systems and Rehabilitation Engineering.

EFNS guidelines on diagnosis and treatment of primary dystonias

A. Albanese, J. Krauss, K. Bhatia, 2011, European journal of neurology.

Cardiac phenotype in ATP1A3-related syndromes

I. Scheffer, S. Sisodiya, M. Thom, 2020, Neurology.

ATP1A3-related disorders: An update.

N. Nardocci, G. Zorzi, M. Carecchio, 2017, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Reaching and Writing Movements: Sensitive and Reliable Tools to Measure Genetic Dystonia in Children

Giancarlo Ferrigno, Alessandra Pedrocchi, Claudia Casellato, 2011, Journal of child neurology.

Neurological Disorders Associated with Striatal Lesions: Classification and Diagnostic Approach

N. Nardocci, L. Chiapparini, B. Garavaglia, 2016, Current Neurology and Neuroscience Reports.

Axonal dystrophies.

N. Nardocci, G. Zorzi, 2013, Handbook of clinical neurology.

Neuronal ceroid lipofuscinoses: a review

N. Nardocci, F. Cardona, Francesco Cardona, 1998, The Italian Journal of Neurological Sciences.

SUSCEPTIBILITY TO DYT1 DYSTONIA IN EUROPEAN PATIENTS IS MODIFIED BY THE D216H POLYMORPHISM

A. Kupsch, I. Borggraefe, T. Gasser, 2008, Neurology.

Degenerative Neurological and Neuromuscular Disease Update on pediatric dystonias : etiology , epidemiology , and management

N. Nardocci, E. Fernández-Álvarez, 2012 .

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

N. Nardocci, E. Fernández-Álvarez, E. Fernández‐Álvarez, 2012, Degenerative neurological and neuromuscular disease.

Vascular Remodeling in Moyamoya Angiopathy: From Peripheral Blood Mononuclear Cells to Endothelial Cells

M. L. Dell'Acqua, P. Ferroli, E. Parati, 2020, International journal of molecular sciences.

Substantia Nigra Swelling and Dentate Nucleus T2 Hyperintensity May Be Early Magnetic Resonance Imaging Signs of β‐Propeller Protein‐Associated Neurodegeneration

B. Castellotti, N. Nardocci, L. Chiapparini, 2018, Movement disorders clinical practice.

GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease—study protocol and preliminary results

P. Ferroli, E. Parati, L. Pantoni, 2019, Neurological Sciences.

Pediatric Paroxysmal Exercise-Induced Neurological Symptoms: Clinical Spectrum and Diagnostic Algorithm

N. Nardocci, B. Garavaglia, G. Zorzi, 2021, Frontiers in Neurology.

Diagnosis and Treatment of Primary (Idiopathic) Dystonia

M. Vidailhet, A. Berardelli, A. Albanese, 2010 .

Infantile neuroaxonal dystrophy: neuroradiological studies in 11 patients

N. Nardocci, L. D'Incerti, M. Bruzzone, 1999, Neuroradiology.

Pathophysiology and Treatment of Neurodegeneration With Brain Iron Accumulation in the Pediatric Population

S. Schneider, N. Nardocci, G. Zorzi, 2013, Current Treatment Options in Neurology.

High prevalence of antiphospholipid antibodies in children with idiopathic cerebral ischemia.

N. Nardocci, R. Caporali, A. Martini, 1994, Pediatrics.

Psychiatric autoimmune conditions in children and adolescents: Is catatonia a severity marker?

P. Duverger, R. Jardri, D. Cohen, 2020, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

Progressive myoclonus epilepsies: an electroclinical, biochemical, morphological and molecular genetic study of 17 cases

M. Zeviani, G. Avanzini, S. Franceschetti, 1993, Acta neurologica Scandinavica.

White matter and cerebellar involvement in alternating hemiplegia of childhood

A. Capuano, N. Nardocci, G. Neri, 2020, Journal of Neurology.

Myoclonus–dystonia syndrome: Clinical presentation, disease course, and genetic features in 11 families

N. Nardocci, D. Ghezzi, B. Garavaglia, 2008, Movement disorders : official journal of the Movement Disorder Society.

Idiopathic dystonia with onset in childhood

N. Nardocci, E. Lamperti, L. Angelini, 1989, Journal of Neurology.

Acquired hemidystonia in childhood: a clinical and neuroradiological study of thirteen patients.

G. Broggi, N. Nardocci, M. Grisoli, 1996, Pediatric neurology.

Paroxysmal dyskinesias in childhood.

N. Nardocci, T. Granata, G. Zorzi, 2003, Pediatric neurology.

Status dystonicus induced by deep brain stimulation surgery

Suneil K. Kalia, A. Fasano, S. Kalia, 2019, Neurological Sciences.

Deep brain stimulation versus pallidotomy for status dystonicus: a single-center case series.

L. Romito, G. Messina, A. Franzini, 2019, Journal of neurosurgery.

Cerebrospinal Fluid Monoamine Metabolite Analysis in Pediatric Movement Disorders

N. Nardocci, D. Ghezzi, B. Garavaglia, 2015, Journal of child neurology.

Mitochondrial dysfunction in Parkinson disease: evidence in mutant PARK2 fibroblasts

Daniele Ghezzi, Barbara Garavaglia, A. Albanese, 2015, Front. Genet..

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

C. Gellera, N. Nardocci, C. Mariotti, 2002, Movement disorders : official journal of the Movement Disorder Society.

GTP-cyclohydrolase I gene mutations in patients with autosomal dominant and recessive GTP-CH1 deficiency: Identification and functional characterization of four novel mutations

M. Zeviani, N. Nardocci, D. Ghezzi, 2004, Journal of Inherited Metabolic Disease.

Typical and Atypical Forms of Paroxysmal Choreoathetosis

N. Nardocci, E. Lamperti, L. Angelini, 1989, Developmental medicine and child neurology.

Analysis of the ϵ‐sarcoglycan gene in familial and sporadic myoclonus‐dystonia: Evidence for genetic heterogeneity

A. Berardelli, A. Bentivoglio, C. Shaw-Smith, 2003, Movement disorders : official journal of the Movement Disorder Society.

The Movement disorder associated with NMDAR antibody-encephalitis is complex and characteristic: an expert video-rating study

V. Fung, A. Lang, K. Bhatia, 2018, Journal of Neurology, Neurosurgery, and Psychiatry.

Classification of dystonia

N. Nardocci, G. Zorzi, 2014 .

Response to letter by Dr Neil Murray

A. Albanese, J. Krauss, K. Bhatia, 2011 .

Phenomenology of psychogenic movement disorders in children

N. Nardocci, G. Zorzi, F. Zibordi, 2012, Movement disorders : official journal of the Movement Disorder Society.

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

M. Zeviani, N. Nardocci, C. Lamperti, 2016, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Neuro-telehealth for fragile patients in a tertiary referral neurological institute during the COVID-19 pandemic in Milan, Lombardy

M. de Curtis, A. Silvani, P. Tiraboschi, 2021, Neurological Sciences.

Encephalopathies with intracranial calcification in children: clinical and genetic characterization

A. Pichiecchio, N. Nardocci, L. Chiapparini, 2018, Orphanet Journal of Rare Diseases.

CANS: Childhood acute neuropsychiatric syndromes.

N. Nardocci, G. Zorzi, M. Carecchio, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Sporadic and familial glut1ds Italian patients: A wide clinical variability

C. Cereda, N. Nardocci, A. Tagliabue, 2015, Seizure.

Vasculogenic and Angiogenic Pathways in Moyamoya Disease.

P. Ferroli, E. Parati, D. Riva, 2016, Current medicinal chemistry.

Phenotype and natural history of variant late infantile ceroid‐lipofuscinosis 5

N. Nardocci, F. Santorelli, R. Battini, 2017, Developmental medicine and child neurology.

Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients

B. Castellotti, C. Gellera, N. Nardocci, 2011, neurogenetics.

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

M. Zeviani, N. Nardocci, P. Pinton, 2015, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Paroxysmal non‐epileptic motor events in childhood: a clinical and video‐EEG–polymyographic study

S. Franceschetti, N. Nardocci, L. Canafoglia, 2012, Developmental medicine and child neurology.

Progressive dystonia symptomatic of juvenile GM2 gangliosidosis

N. Nardocci, L. Angelini, B. Bertagnolio, 1992, Movement disorders : official journal of the Movement Disorder Society.

Screening of SLC2A1 in a large cohort of patients suspected for Glut1 deficiency syndrome: identification of novel variants and associated phenotypes

F. Villani, B. Castellotti, C. Gellera, 2019, Journal of Neurology.

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

N. Nardocci, A. Tagliabue, P. Veggiotti, 2010, Brain and Development.

Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutations

S. Berkovic, S. Franceschetti, N. Nardocci, 2015, Neurology.

N. NardocciM. MorbinM. BugianiE. LamanteaO. Bugiani Neuronal ceroid lipofuscinosis: detection of atypical forms

C. Besta, N. Nardocci, E. Lamantea, 2000 .

Neuronal ceroid lipofuscinoses: detection of atypical forms

N. Nardocci, E. Lamantea, O. Bugiani, 2000, Neurological Sciences.

Neuronal ceroid-lipofuscinosis: a clinical and morphological study of 19 patients.

N. Nardocci, O. Bugiani, S. Binelli, 1995, American journal of medical genetics.

Safety and efficacy of deferiprone for pantothenate kinase-associated neurodegeneration: a randomised, double-blind, controlled trial and an open-label extension study

A. Blamire, A. Basu, P. Hogarth, 2019, The Lancet Neurology.

Neurodegeneration associated with genetic defects in phospholipase A2

E. Bertini, P. Hogarth, N. Nardocci, 2008, Neurology.

Therapeutic advances in neurodegeneration with brain iron accumulation.

N. Nardocci, G. Zorzi, 2013, International review of neurobiology.

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

V. Tiranti, N. Nardocci, L. Chiapparini, 2012, Seminars in pediatric neurology.

Are Rare in Italian Patients With Neurodegeneration With Brain Iron Accumulation

V. Tiranti, N. Nardocci, L. Chiapparini, 2012 .

Extragenetic factors and clinical penetrance of DYT1 dystonia: an exploratory study

M. Edwards, S. Schneider, K. Bhatia, 2013, Journal of Neurology.

Consciousness disturbances in megalencephalic leukoencephalopathy with subcortical cysts.

A. Bizzi, N. Nardocci, G. Uziel, 2003, Neuropediatrics.

The calcium-independent phospholipase A2 gene, PLA2G6, is mutated in a spectrum of childhood neurodegenerative disorders with high brain iron

Colin A. Johnson, N. Nardocci, R. Trembath, 2006 .

DYT2 screening in early-onset isolated dystonia.

A. Bentivoglio, E. Valente, F. Morgante, 2017, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Hemidystonia symptomatic of primary antiphospholipid syndrome in childhood

N. Nardocci, M. Bruzzone, L. Angelini, 1993, Movement disorders : official journal of the Movement Disorder Society.

Cognitive and neuropsychological evolution in children with anti-NMDAR encephalitis

N. Nardocci, T. Granata, F. Zibordi, 2016, Journal of Neurology.

Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGAD

G. Cantalupo, Massimiliano Valeriani, N. Nardocci, 2022, Neurology: Neuroimmunology & Neuroinflammation.

Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6.

R. Boldrini, R. Carrozzo, N. Nardocci, 2009, Biochemical and biophysical research communications.

Corrigendum: Homozygosity mapping of the gene for Hallervoden-Spatz syndrome to chromosome 20p12.3-p13

T. Taylor, M. Pandolfo, N. Nardocci, 1997, Nature Genetics.

Error-enhancing robot therapy to induce motor control improvement in childhood onset primary dystonia

G. Ferrigno, A. Pedrocchi, N. Nardocci, 2012, Journal of NeuroEngineering and Rehabilitation.

PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron

Colin A. Johnson, N. Nardocci, R. Trembath, 2006, Nature Genetics.

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

A. Albanese, C. Gellera, F. Panzica, 2012, Parkinsonism & related disorders.

N. Nardocci, L. Chiapparini, E. Fazzi, 2017, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Metabolic consequences of mitochondrial coenzyme A deficiency in patients with PANK2 mutations.

V. Mootha, V. Tiranti, C. Clish, 2012, Molecular genetics and metabolism.

Neonatal dopa-responsive extrapyramidal syndrome in twins with recessive GTPCH deficiency

N. Nardocci, N. Blau, B. Garavaglia, 2003, Neurology.

Neglect after right unilateral thalamotomy. A case report

D. Perani, G. Broggi, N. Nardocci, 1982, The Italian Journal of Neurological Sciences.

Infantile neuroaxonal dystrophy

N. Nardocci, O. Bugiani, S. Binelli, 1999, Neurology.

Infantile Neuroaxonal Dystrophy Author : Doctor

A. Brice, N. Nardocci, 2004 .

Loss‐of‐Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal Abnormalities

K. Bötzel, R. Jech, B. Haslinger, 2020, Annals of neurology.

Autosomal recessive Rolandic epilepsy with paroxysmal exercise‐induced dystonia and writer's cramp: Delineation of the syndrome and gene mapping to chromosome 16p12‐11.2

A. Ballabio, P. Aridon, N. Nardocci, 1999, Annals of neurology.

Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy

E. Bertini, N. Nardocci, F. Santorelli, 2013, Orphanet Journal of Rare Diseases.

A pathophysiological study of neuronal ceroid lipofuscinoses in 17 patients: critical review and methodological proposal

N. Nardocci, V. Scaioli, 2000, Neurological Sciences.

Diagnostic issues in childhood and adult dystonia.

A. Albanese, N. Nardocci, G. Zorzi, 2011, Expert opinion on medical diagnostics.

Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single‐center cohort study

A. Bentivoglio, L. Romito, M. Topf, 2019, Movement disorders : official journal of the Movement Disorder Society.

The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort

J. Hardy, A. Batla, K. Bhatia, 2015, Human molecular genetics.

Corrigendum: PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron

Colin A. Johnson, N. Nardocci, R. Trembath, 2006, Nature Genetics.

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

B. Castellotti, C. Gellera, S. Franceschetti, 2017, Seizure.

Movement disorders in patients with Rett syndrome: A systematic review of evidence and associated clinical considerations

N. Nardocci, P. Santosh, J. Singh, 2021, Psychiatry and clinical neurosciences.

Role of UBE3A and ATP10A genes in autism susceptibility region 15q11-q13 in an Italian population: A positive replication for UBE3A

F. Macciardi, G. Guffanti, N. Nardocci, 2011, Psychiatry Research.

β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation.

J. Hardy, T. Meitinger, H. Prokisch, 2013, Brain : a journal of neurology.

De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions

L. Vissers, J. Hardy, C. Davies, 2016, American journal of human genetics.

Hemophagocytic lymphohistiocytosis with neurological presentation: MRI findings and a nearly miss diagnosis

A. Bizzi, N. Nardocci, G. Uziel, 2011, Neurological Sciences.

The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders

N. Nardocci, M. Eoli, S. Esposito, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

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

N. Nardocci, C. Brahe, A. Pinto, 2006, Intensive Care Medicine.

Recurrent, founder and hypomorphic variants contribute to the genetic landscape of Joubert syndrome

R. Borgatti, T. Mazza, E. Valente, 2023, Journal of Medical Genetics.

Refining the mutational spectrum and gene–phenotype correlates in pontocerebellar hypoplasia: results of a multicentric study

E. Bertini, R. Borgatti, T. Mazza, 2021, Journal of Medical Genetics.

Transient Paroxysmal Dystonia in Infancy

N. Nardocci, E. Lamperti, L. Angelini, 1988, Neuropediatrics.

Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosis.

P. Striano, F. Zara, N. Nardocci, 2007, Neuropediatrics.

Concomitant deficiency of β- and γ-sarcoglycans in 20 α-sarcoglycan (adhalin)-deficient patients: immunohistochemical analysis and clinical aspects

N. Nardocci, P. Boffi, L. Morandi, 1997, Acta Neuropathologica.

Concomitant deficiency of beta- and gamma-sarcoglycans in 20 alpha-sarcoglycan (adhalin)-deficient patients: immunohistochemical analysis and clinical aspects.

N. Nardocci, P. Boffi, L. Morandi, 1997, Acta neuropathologica.

Myoclonus-dystonia syndrome.

N. Nardocci, 2011, Handbook of clinical neurology.

R106C TFG variant causes infantile neuroaxonal dystrophy “plus” syndrome

V. Tiranti, T. Pippucci, N. Nardocci, 2018, neurogenetics.

Tourettism as clinical presentation of Huntington's disease with onset in childhood

N. Nardocci, G. Lanzi, L. Angelini, 1998, The Italian Journal of Neurological Sciences.

Complex tics, stereotypies, and compulsive behavior as clinical presentation of a juvenile progressive dystonia suggestive of hallervorden‐spatz disease

N. Nardocci, M. Bruzzone, L. Angelini, 1994, Movement Disorders.

Neurological disorders, other than stroke, associated with antiphospholipid antibodies in childhood.

N. Nardocci, R. Caporali, A. Martini, 1996, Neuropediatrics.

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

P. Hogarth, N. Nardocci, M. Kurian, 2017, Molecular genetics and metabolism.

Therapeutic advances in neurodegeneration with brain iron accumulation.

N. Nardocci, L. Chiapparini, G. Zorzi, 2012, Seminars in pediatric neurology.

Hallervorden-Spatz disease: MR and pathologic findings.

W. Halliday, N. Nardocci, L. D'Incerti, 1993, AJNR. American journal of neuroradiology.

Idiopathic dystonia: Neuropharmacological study

G. Broggi, N. Nardocci, F. Girotti, 2004, Journal of Neurology.

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

D. Martino, N. Nardocci, F. Cardona, 2011, Developmental medicine and child neurology.

Automatic imitation in youngsters with Gilles de la Tourette syndrome: A behavioral study

N. Bolognini, A. Cavanna, C. Turati, 2021, Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence.

Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation

T. Meitinger, A. Weindl, H. Prokisch, 2006, Annals of neurology.

Early onset primary dystonia.

Barbara Garavaglia, N. Nardocci, B. Garavaglia, 2009, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

A neurophysiological study of myoclonus in patients with DYT11 myoclonus‐dystonia syndrome

A. Albanese, F. Panzica, S. Franceschetti, 2008, Movement disorders : official journal of the Movement Disorder Society.

Childhood-onset HAM/TSP with progressive cognitive impairment

F. Guerini, N. Nardocci, P. Ferrante, 2010, Neurological Sciences.

CT and MRI in maple syrup urine disease

N. Nardocci, Graziella Uziel, Mario Savoiardo, 1988, Neurology.

Non‐DYT1 early‐onset primary torsion dystonia: Comparison with DYT1 phenotype and review of the literature

A. Bentivoglio, A. Albanese, A. Fasano, 2006, Movement disorders : official journal of the Movement Disorder Society.

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

M. Leonardi, N. Nardocci, F. Zibordi, 2009, Disability and rehabilitation.

J. Jankovic, M. Stamelou, K. Bhatia, 2017, Parkinsonism & related disorders.

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

D. Girelli, N. Nardocci, M. Ferrari, 2010, Genetic testing and molecular biomarkers.

THAP1 Dystonia with Globus Pallidus T2 Hypointensity: A Report of Two Cases

N. Nardocci, L. Chiapparini, B. Garavaglia, 2021, Movement disorders : official journal of the Movement Disorder Society.

Pallidal Deep Brain Stimulation in DYT6 Dystonia: Clinical Outcome and Predictive Factors for Motor Improvement

L. Romito, K. Lohmann, L. Cif, 2019, Journal of clinical medicine.

Diagnosis and treatment of pediatric onset isolated dystonia.

N. Nardocci, B. Garavaglia, G. Zorzi, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Inherited Isolated Dystonia in Children

N. Nardocci, G. Zorzi, M. Carecchio, 2015, Journal of Pediatric Neurology.

Mutation screening of the DYT6/THAP1 gene in Italy

A. Bentivoglio, A. Albanese, F. Brancati, 2009, Movement disorders : official journal of the Movement Disorder Society.

Socio-demographic characteristics and psychopathological assessment in a sample of 13 paediatric patients with functional neurological disorders: A preliminary report.

A. Priori, N. Nardocci, G. Zorzi, 2021, Clinical child psychology and psychiatry.

GLUT1-DS Italian registry: past, present, and future: a useful tool for rare disorders

R. Borgatti, P. Striano, N. Nardocci, 2023, Orphanet Journal of Rare Diseases.

Subacute cervical myelopathy in a child with cerebral palsy. Secondary to torsion dystonia?

G. Broggi, N. Nardocci, L. Angelini, 1982, Child's brain.

Infantile neuroaxonal dystrophy and pantothenate kinase-associated neurodegeneration

T. Meitinger, N. Nardocci, T. Klopstock, 2004, Neurology.

European multicentric cohort

J. Hardy, A. Batla, C. Besta, 2015 .

Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review

E. Bertini, A. Pichiecchio, N. Nardocci, 2019, Journal of clinical medicine.

Pallidal stimulation for acquired dystonia due to cerebral palsy: beyond 5 years

C. Marras, A. Albanese, L. Romito, 2015, European journal of neurology.

Clinical rating scale for pantothenate kinase‐associated neurodegeneration: A pilot study

M. Stamelou, P. Martínez-Martín, N. Nardocci, 2017, Movement disorders : official journal of the Movement Disorder Society.

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

N. Nardocci, Jean-Pierre Lin, 2016, Front. Neurol..

Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype

Pier D Lambiase, Henry Houlden, Josemir W Sander, 2015, Brain : a journal of neurology.

Hallervorden-Spatz disease: clinical and MRI study of 11 cases diagnosed in life

N. Nardocci, L. Angelini, M. Savoiardo, 1992, Journal of Neurology.

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

N. Nardocci, R. Pascarella, B. Garavaglia, 2015, Brain and Development.

Case report Downbeat nystagmus as the presenting symptom of infantile neuroaxonal dystrophy: A case report

N. Nardocci, R. Pascarella, B. Garavaglia, 2015 .

N. Nardocci, L. Chiapparini, S. Lubbe, 2021, Movement disorders : official journal of the Movement Disorder Society.

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

C. Marras, G. Broggi, A. Albanese, 2011, Journal of Neural Transmission.

Homozygosity mapping of Hallervorden–Spatz syndrome to chromosome 20p12.3–p13

T. Taylor, M. Pandolfo, N. Nardocci, 1996, Nature Genetics.

Thiamine-responsive disease due to mutation of tpk1: Importance of avoiding misdiagnosis

N. Nardocci, L. Chiapparini, B. Garavaglia, 2017, Neurology.

Long term perceptions of illness and self after Deep Brain Stimulation in pediatric dystonia: A narrative research.

M. Leonardi, N. Nardocci, G. Zorzi, 2020, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Deep Brain Stimulation Electrode Used for Radiofrequency Lesion of the Globus Pallidus Internus in Dystonia

C. Marras, C. Lenardi, G. Messina, 2009, Stereotactic and Functional Neurosurgery.

Stimulation of the globus pallidus internus for childhood‐onset dystonia

C. Marras, D. Caldiroli, G. Broggi, 2005, Movement disorders : official journal of the Movement Disorder Society.

Paroxysmal dystonia and paroxysmal tremor in a young patient with multiple sclerosis

N. Nardocci, G. Zorzi, M. Savoldelli, 1995, The Italian Journal of Neurological Sciences.

Status dystonicus: Predictors of outcome and progression patterns of underlying disease

A. Bentivoglio, A. Fasano, N. Nardocci, 2012, Movement disorders : official journal of the Movement Disorder Society.

Rhythmic cortical myoclonus in patients with 6Q22.1 deletion.

F. Panzica, S. Franceschetti, N. Nardocci, 2023, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

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

M. Zeviani, N. Nardocci, B. Garavaglia, 2002, Movement disorders : official journal of the Movement Disorder Society.

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

D. Krainc, N. Nardocci, S. Esposito, 2017, Movement disorders : official journal of the Movement Disorder Society.

Chronic GM1 Gangliosidosis Presenting as Dystonia: Clinical and Biochemical Studies in a New Case

N. Nardocci, L. Angelini, B. Bertagnolio, 1993, Neuropediatrics.

Early-onset bradykinetic rigid syndrome and reflex seizures in a child with PURA syndrome.

G. Cantalupo, N. Nardocci, R. Guerrini, 2021, Epileptic disorders.

Linguistic Development in a Patient with Landau-Kleffner Syndrome: A Nine-Year Follow-Up

G. Avanzini, N. Nardocci, T. Granata, 1995, Neuropediatrics.

Running apraxia as a presenting symptom of neuronal ceroid lipofuscinosis 6

N. Nardocci, B. Garavaglia, V. Leuzzi, 2014, Movement disorders : official journal of the Movement Disorder Society.

Transient paroxysmal dystonia in an infant possibly induced by cisapride

N. Nardocci, G. Zorzi, L. Angelini, 1996, The Italian Journal of Neurological Sciences.

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

N. Nardocci, T. Granata, S. Binelli, 2015, Seizure.

The “Eye-of-the-Tiger” Sign may be Absent in the Early Stages of Classic Pantothenate Kinase Associated Neurodegeneration

N. Nardocci, L. Chiapparini, B. Garavaglia, 2011, Neuropediatrics.

Variants in ATP5F1B are associated with dominantly inherited dystonia

L. Romito, H. Prokisch, D. Krainc, 2023, Brain : a journal of neurology.

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

E. Bertini, Massimiliano Valeriani, A. Capuano, 2016, Parkinsonism & related disorders.

Life‐threatening dystonia–dyskinesias in a child: Successful treatment with bilateral pallidal stimulation

G. Broggi, N. Nardocci, I. Dones, 2000, Movement disorders : official journal of the Movement Disorder Society.

Depression after stereotactic thalamotomy in patients with abnormal movements

G. Broggi, N. Nardocci, L. Angelini, 1982, The Italian Journal of Neurological Sciences.

Neuronal ceroid lipofuscinoses: a review

N. Nardocci, F. Cardona, 1998, The Italian Journal of Neurological Sciences.

C. Marras, A. Capuano, N. Nardocci, 2023, Parkinsonism & related disorders.

A perplexing case of juvenile extrapyramidal disease

G. Broggi, N. Nardocci, G. Moretti, 1981, The Italian Journal of Neurological Sciences.

Long term results of stereotactic thalamotomy for cerebral palsy.

G. Broggi, C. Giorgi, A. Franzini, 1983, Neurosurgery.