G. De Michele

Y. Agid, R. Marconi, M. Breteler, 2001, Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology.

New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism

A. Destée, M. Farrer, S. Lincoln, 2003, Neurology.

Screening for RFC-1 pathological expansion in late-onset ataxias: a contribution to the differential diagnosis

S. Pappatà, G. De Michele, A. Filla, 2022, Journal of Neurology.

The effect of parental gender on the GAA dynamic mutation in the FRDA gene.

L. Pianese, F. Cavalcanti, A. Monticelli, 1997, American journal of human genetics.

Broadened Friedreich's ataxia phenotype after gene cloning

G. Caruso, L. Santoro, L. Pianese, 1997, Neurology.

Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes.

L. Santoro, F. Cavalcanti, G. De Michele, 1990, Journal of neurology, neurosurgery, and psychiatry.

Predictors of survival in spinocerebellar ataxia type 2 population from Southern Italy

D. Bruzzese, G. De Michele, A. Filla, 2018, Neurological Sciences.

Other autosomal recessive and childhood ataxias.

G. De Michele, A. Filla, 2012, Handbook of clinical neurology.

The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease.

C. Marsden, Y. Agid, A. Durr, 1998, Annals of neurology.

Degenerative and acquired sporadic adult onset ataxia

G. De Michele, A. Filla, F. Santorelli, 2019, Neurological Sciences.

Benign hereditary chorea: Clinical and neuroimaging features in an Italian family

S. Pappatà, P. Macchia, G. De Michele, 2010, Movement disorders : official journal of the Movement Disorder Society.

A novel NKX2.1 mutation in a family with hypothyroidism and benign hereditary chorea.

P. Macchia, G. De Michele, A. Filla, 2008, Thyroid : official journal of the American Thyroid Association.

Cognitive profile and 18F-fluorodeoxyglucose PET study in LRRK2-related Parkinson's disease.

S. Pappatà, A. Brunetti, G. De Michele, 2017, Parkinsonism & Related Disorders.

Longitudinal study of a cohort of MSA-C patients in South Italy: survival and clinical features

D. Bruzzese, G. De Michele, A. Filla, 2017, Journal of the Neurological Sciences.

Ataxia with oculomotor apraxia type 2

F. Pierelli, G. De Michele, A. Filla, 2006, Neurology.

Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations

M. T. Pellecchia, P. Barone, G. De Michele, 2018, Cell Death & Disease.

Pathological laughter as onset symptom in atypical parkinsonisms

S. Pappatà, G. De Michele, A. Filla, 2016, Journal of Neurology.

Assessment of brain white matter fiber bundle atrophy in patients with Friedreich ataxia.

M. Filippi, M. Mascalchi, F. Agosta, 2010, Radiology.

Paradoxical response to apomorphine in a case of atypical parkinsonism

M. T. Pellecchia, P. Barone, G. De Michele, 2002, Movement disorders : official journal of the Movement Disorder Society.

Electrophysiologic characterization in spinocerebellar ataxia 17

L. Santoro, M. Nolano, G. De Michele, 2006, Neurology.

Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism

Y. Agid, P. Pollak, P. Heutink, 2003, Neurology.

Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement

A. Bentivoglio, G. De Michele, A. Tessa, 2021, Genes.

Chorea-acanthocytosis without chorea: Expanding the clinical phenotype.

S. Pappatà, G. De Michele, M. Esposito, 2017, Parkinsonism & Related Disorders.

Possible gluten sensitivity in multiple system atrophy

M. T. Pellecchia, P. Barone, G. De Michele, 2002, Neurology.

[Recent findings on the olfactory acuity in epileptic patients].

G. De Michele, A. Filla, G. Campanella, 1976, Acta neurologica.

Spinocerebellar ataxia type 48: last but not least

G. De Michele, A. Filla, A. Tessa, 2020, Neurological Sciences.

Ataxia with oculomotor apraxia type 1 in Southern Italy

L. Santoro, A. Monticelli, G. De Michele, 2004, Neurology.

Screening of ARHSP‐TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion

E. Bertini, M. Tosetti, G. Cioni, 2009, Human mutation.

A Double-Blind Cross-over Trial of Amantadine Hydrochloride in Friedreich's Ataxia

G. De Michele, A. Filla, G. Campanella, 1993, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Noninvasive assessment of systolic and diastolic function in 50 patients with Friedreich's ataxia.

G. De Michele, A. Filla, G. Campanella, 1988, Cardiology.

Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2.

Giovanni Coppola, Fuying Gao, Genevieve Konopka, 2014, Human molecular genetics.

Constructional Impairments and Their Neural Correlates in Nondemented Adults With Cerebral Autosomal-dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy

M. Caulo, G. De Michele, A. Caiazzo, 2022, Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology.

Screening for RFC-1 pathological expansion in late-onset ataxias: a contribution to the differential diagnosis

S. Pappatà, G. De Michele, A. Filla, 2022, Journal of Neurology.

Non-motor symptoms and cardiac innervation in SYNJ1-related parkinsonism.

S. Pappatà, L. Santoro, G. De Michele, 2016, Parkinsonism & related disorders.

ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.

R. Ravazzolo, C. Marco-Marín, V. Rubio, 2016, Brain : a journal of neurology.

Autonomic disorders and myocardial 123I-metaiodobenzylguanidine scintigraphy in Huntington’s disease

S. Pappatà, G. De Michele, E. Salvatore, 2020, Journal of Nuclear Cardiology.

DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington disease

A. Porcellini, G. De Michele, R. Mechelli, 2018, Annals of neurology.

Can telomere shortening in human peripheral blood leukocytes serve as a disease biomarker of Friedreich's ataxia?

A. Monticelli, G. De Michele, A. Filla, 2013, Antioxidants & redox signaling.

Prevalence and phenotype of the c.1529C>T SPG7 variant in adult‐onset cerebellar ataxia in Italy

G. De Michele, A. Filla, A. Tessa, 2018, European journal of neurology.

A novel mutation in SACS gene in a family from southern Italy

L. Santoro, P. Gasparini, A. Monticelli, 2004, Neurology.

Jaw‐Opening Oromandibular Dystonia Associated With Spinocerebellar Ataxia Type 2

G. De Michele, A. Filla, F. Saccà, 2014, Movement disorders clinical practice.

Effective treatment of orthostatic hypotension by propranolol in the Shy-Drager syndrome.

M. Chiariello, G. De Michele, G. Campanella, 1981, American heart journal.

Powerhouse failure and oxidative damage in autosomal recessive spastic ataxia of Charlevoix-Saguenay

C. Procaccini, G. Matarese, G. De Michele, 2015, Journal of Neurology.

Interferon-β treatment decreases cholesterol plasma levels in multiple sclerosis patients

G. Coppola, G. De Michele, A. Filla, 2004, Neurology.

Peripheral markers of autophagy in polyglutamine diseases

G. De Michele, A. Filla, A. De Rosa, 2017, Neurological Sciences.

Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa and cataracts (PHARC) screening in an Italian population

G. De Michele, A. Filla, E. Salsano, 2013, European journal of neurology.

PRICKLE1 progressive myoclonus epilepsy in Southern Italy

G. De Michele, A. Filla, P. Sorrentino, 2010, Movement disorders : official journal of the Movement Disorder Society.

Parkin mutations are frequent in patients with isolated early-onset parkinsonism.

Y. Agid, M. Vidailhet, V. Fraix, 2003, Brain : a journal of neurology.

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.

Y. Agid, R. Marconi, B. Oostra, 1999, Human molecular genetics.

Normalization of timed neuropsychological tests with the PATA rate and nine‐hole pegboard tests

G. De Michele, A. Filla, F. Manganelli, 2018, Journal of neuropsychology.

Association between early-onset Parkinson's disease and mutations in the parkin gene.

Bonifati, N W Wood, A Dürr, 2000, The New England journal of medicine.

PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family

S. Pappatà, P. Barone, G. De Michele, 2014, neurogenetics.

The copying of geometric drawings in dementia: an experimental study of 218 subjects.

D. Grossi, G. De Michele, A. Orsini, 1978, Acta neurologica.

Short‐term continuous infusion of apomorphine hydrochloride for treatment of Huntington's chorea: A double blind, randomized cross‐over trial

P. Barone, K. Longo, G. De Michele, 2007, Movement disorders : official journal of the Movement Disorder Society.

SPG5 and multiple sclerosis: clinical and genetic overlap?

G. De Michele, A. Filla, M. Quarantelli, 2016, Acta neurologica Scandinavica.

NGS in Hereditary Ataxia: When Rare Becomes Frequent

G. Tedeschi, G. De Michele, A. Filla, 2021, International journal of molecular sciences.

Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia.

Janel O. Johnson, K. Fischbeck, C. Blackstone, 2015, JAMA neurology.

PDCD10 Gene Mutations in Multiple Cerebral Cavernous Malformations

Andrea Mosca, Silvana Penco, Stefano Parmigiani, 2014, PloS one.

Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa.

Stéphane Thobois, Yves Agid, Pablo Ibáñez, 2006, Brain : a journal of neurology.

A new model to study neurodegeneration in ataxia oculomotor apraxia type 2.

G. Coppola, G. De Michele, M. Lavin, 2015, Human molecular genetics.

PERK-Mediated Unfolded Protein Response Activation and Oxidative Stress in PARK20 Fibroblasts

M. T. Pellecchia, M. Renna, P. Barone, 2019, Front. Neurosci..

Overview of autosomal recessive ataxias.

G. De Michele, A. Filla, 2012, Handbook of clinical neurology.

The α‐synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases

C. Marsden, Y. Agid, A. Durr, 1998 .

Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxia.

L. Pianese, F. Cavalcanti, A. Monticelli, 1998, Human molecular genetics.

Parkinsonism is a Late, Not Rare, Feature of CADASIL: A Study on Italian Patients Carrying the R1006C Mutation

L. Pianese, G. De Michele, G. Cacchiò, 2013, Stroke.

Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber’s hereditary optic neuropathy

A. Torroni, P. Barboni, M. Carbonelli, 2018, PLoS genetics.

Parkinsonism may be part of the symptom complex of DOOR syndrome.

S. Pappatà, G. De Michele, G. Auletta, 2014, Parkinsonism & related disorders.

DNA damage induced by polyglutamine-expanded proteins.

Alessandro Filla, G. De Michele, A. Filla, 2003, Human molecular genetics.

Growth hormone response to arginine test distinguishes multiple system atrophy from Parkinson's disease and idiopathic late‐onset cerebellar ataxia

M. T. Pellecchia, P. Barone, G. De Michele, 2005, Clinical endocrinology.

Long‐term clinical experience with weekly interferon beta‐1a in relapsing multiple sclerosis

G. Coppola, G. De Michele, G. Vacca, 2006, European journal of neurology.

Postganglionic sudomotor denervation in patients with multiple system atrophy

M. T. Pellecchia, L. Santoro, M. Nolano, 2014, Neurology.

Age of onset, sex, and cardiomyopathy as predictors of disability and survival in Friedreich's disease

G. De Michele, A. Filla, G. Campanella, 1996, Neurology.

The Friedreich ataxia GAA triplet repeat: premutation and normal alleles.

M. Pandolfo, L. Montermini, L. Pianese, 1997, Human molecular genetics.

Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum

A. Rossi, G. De Michele, A. Filla, 2004, Neurology.

The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia.

G Campanella, L. Pianese, F. Cavalcanti, 1996, American journal of human genetics.

A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3.

A. Ballabio, R. Marconi, F. Cavalcanti, 1998, American journal of human genetics.

Insulin sensitivity and early-phase insulin secretion in normoglycemic Huntington's disease patients.

G. De Michele, A. Filla, A. Colao, 2013, Journal of Huntington's disease.

Clinical use of frataxin measurement in a patient with a novel deletion in the FXN gene

G. De Michele, A. Filla, A. Tessa, 2013, Journal of Neurology.

A Combined Nucleic Acid and Protein Analysis in Friedreich Ataxia: Implications for Diagnosis, Pathogenesis and Clinical Trial Design

G. De Michele, A. Filla, S. Cocozza, 2011, PloS one.

Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23

A. Ballabio, R. Marconi, G. De Michele, 2003, Annals of neurology.

Antiphospholipid-Related Chorea

G. De Michele, V. Morra, A. Roca, 2012, Front. Neur..

Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry

M. C. Savanelli, M. T. Pellecchia, G. Argenziano, 2021, Journal of public health.

Cervico-Oculo-Acoustic Syndrome in a Male with Consanguineous Parents

G. De Michele, A. Filla, E. Marciano, 2006, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Cerebral blood flow in spinocerebellar degenerations: a single photon emission tomography study in 28 patients

F. Di Salle, A. Soricelli, M. Salvatore, 1998, Journal of Neurology.

Genome-wide scan linkage analysis for Parkinson’s disease: the European genetic study of Parkinson’s disease

Miguel Ángel Martínez, M. Farrer, M. Breteler, 2004, Journal of Medical Genetics.

Neuroimaging follow‐up in a case of Rasmussen's encephalitis with dyskinesias

S. Pappatà, A. Varrone, G. De Michele, 2007, Movement disorders : official journal of the Movement Disorder Society.

International Guidelines for the Treatment of Huntington's Disease

R. Reilmann, J. Burgunder, D. Craufurd, 2019, Front. Neurol..

Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations

G. De Michele, A. Filla, A. Tessa, 2021, Journal of Neurology.

Early‐onset ataxia with cardiomyopathy and retained tendon reflexes maps to the friedreich's ataxia locus on chromosome 9q

S. di Donato, M. Pandolfo, G. De Michele, 1995, Annals of neurology.

Screening for Fabry disease in a series of Parkinson’s disease patients and literature review

P. Bauer, G. De Michele, A. De Rosa, 2022, Neurological Sciences.

Perseverative Behavior on Verbal Fluency Task in Patients with Huntington's Disease: a Retrospective Study on a Large Patient Sample.

L. Trojano, G. De Michele, E. Salvatore, 2019, Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists.

Closing-in Phenomenon in Huntington’s Disease: A Neuropsychological Marker of Frontal/Executive Dysfunction

G. De Michele, E. Salvatore, C. Russo, 2019, Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists.

Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian family

G. Coppola, G. De Michele, E. Ramos, 2019, neurogenetics.

Behavioral disorder, dementia, ataxia, and rigidity in a large family with TATA box-binding protein mutation.

Charles Duyckaerts, Giorgio Casari, Pio D'Adamo, 2004, Archives of neurology.

Neurophysiological study in a Spanish family with recessive spastic ataxia of Charlevoix‐Saguenay

G. De Michele, J. Berciano, C. Criscuolo, 2008, Muscle & nerve.

Prevalence and features of non-motor symptoms in Wilson's disease.

G. De Michele, C. Russo, A. De Rosa, 2022, Parkinsonism & related disorders.

Long‐term effect of epoetin alfa on clinical and biochemical markers in friedreich ataxia

G. Defazio, G. De Michele, A. Filla, 2016, Movement disorders : official journal of the Movement Disorder Society.

The influence of gender on phenotype and disease progression in patients with Huntington's disease.

H. Putter, A. Bentivoglio, J. Marinus, 2013, Parkinsonism & related disorders.

Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17

S. Pappatà, A. Varrone, L. Santoro, 2006, Movement disorders : official journal of the Movement Disorder Society.

Efficacy of dopamine agonist treatment in delayed-onset parkinsonism due to midbrain hemorrhage.

S. Pappatà, G. De Michele, F. Barbieri, 2015, Parkinsonism & related disorders.

Cerebellar vermis hypoplasia in a case of cri-du-chat syndrome.

F. Di Salle, G. De Michele, A. Filla, 1993, Acta neurologica.

Autosomal dominant hereditary spastic paraplegia: DHPLC‐based mutation analysis of SPG4 reveals eleven novel mutations

L. Santoro, G. De Michele, A. Filla, 2005, Human mutation.

Searching for Potential Lipid Biomarkers of Parkinson’s Disease in Parkin-Mutant Human Skin Fibroblasts by HILIC-ESI-MS/MS: Preliminary Findings

I. Losito, F. Palmisano, G. De Michele, 2019, International journal of molecular sciences.

Brain structural damage in spinocerebellar ataxia type 2. A voxel‐based morphometry study

Mario Mascalchi, Elena Salvatore, Carlo Tessa, 2008, Movement disorders : official journal of the Movement Disorder Society.

Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease

A. Singleton, M. Farrer, J. Hardy, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The Heterogeneity of Early Parkinson’s Disease: A Cluster Analysis on Newly Diagnosed Untreated Patients

Giuseppe Orefice, Marianna Amboni, Paolo Barone, 2013, PloS one.

The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson’s disease in European populations

A. Durr, D. Berg, B. Müller-Myhsok, 2005, Journal of Medical Genetics.

Mitochondrial DNA haplogroups influence the Friedreich’s ataxia phenotype

L. Pianese, A. Monticelli, G. De Michele, 2004, Journal of Medical Genetics.

Intergenerational instability and marked anticipation in SCA-17

G. Coppola, G. De Michele, A. Filla, 2003, Neurology.

Growth hormone response to arginine test differentiates between two subgroups of Huntington's disease patients

G. De Michele, A. Filla, A. Colao, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

How much phenotypic variation can be attributed to parkin genotype?

Alexandra Durr, Valérie Fraix, Vincenzo Bonifati, 2003, Annals of neurology.

Emotion Recognition and Psychological Comorbidity in Friedreich’s Ataxia

G. De Michele, A. Filla, A. De Rosa, 2018, The Cerebellum.

Non-motor symptoms in early Parkinson's disease: a 2-year follow-up study on previously untreated patients

M. T. Pellecchia, P. Barone, K. Longo, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

Epidemiology of progressive supranuclear palsy

C. Colosimo, P. Vieregge, R. Marconi, 2001, Neurological Sciences.

Epidemiology of multiple system atrophy. ESGAP Consortium. European Study Group on Atypical Parkinsonisms.

R. Marconi, U. Bonuccelli, G. De Michele, 2001, Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology.

Epidemiology of progressive supranuclear palsy. ESGAP Consortium. European Study Group on Atypical Parkinsonisms.

R. Marconi, U. Bonuccelli, G. De Michele, 2001, Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology.

Screening for dopa-responsive dystonia in patients with scans without evidence of dopaminergic deficiency (SWEDD)

Sabina Pappatà, Francesco Saccà, S. Pappatà, 2014, Journal of Neurology.

Reversible Valproate-Induced Subacute Encephalopathy Associated With a MT-ATP8 Variant in the Mitochondrial Genome

G. De Michele, A. Filla, F. Santorelli, 2018, Front. Neurol..

The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from Southern Italy

B. Oostra, G. De Michele, A. Filla, 2011, Movement disorders : official journal of the Movement Disorder Society.

Alteration of endosomal trafficking is associated with early-onset parkinsonism caused by SYNJ1 mutations

M. T. Pellecchia, P. Barone, G. De Michele, 2018, Cell Death & Disease.

Co-existence of primary hyperparathyroidism and Parkinson's disease in three patients: an incidental finding?

S. Pappatà, G. De Michele, A. Faggiano, 2011, Parkinsonism & Related Disorders.

A case of restless leg syndrome in a family with LRRK2 gene mutation

G. De Michele, M. Massarelli, Luigi del Gaudio, 2013, The International journal of neuroscience.

Infusion treatments and deep brain stimulation in Parkinson's Disease: The role of nursing.

A. Tessitore, G. De Michele, A. De Rosa, 2016, Geriatric nursing.

The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families

G. De Michele, A. Filla, A. Tessa, 2020, European journal of neurology.

Overt Hypogonadism May Not Be a Sentinel Sign of RING Finger Protein 216: Two Novel Mutations Associated with Ataxia, Chorea, and Fertility

G. De Michele, A. Filla, F. Santorelli, 2019, Movement disorders clinical practice.

Spinocerebellar ataxia 48 presenting with ataxia associated with cognitive, psychiatric, and extrapyramidal features: A report of two Italian families.

S. Pappatà, G. De Michele, A. Filla, 2019, Parkinsonism & related disorders.

Ataxia and Hypogonadism: a Review of the Associated Genes and Syndromes.

G. De Michele, A. Filla, S. Cocozza, 2023, Cerebellum.

Mild cognitive impairment in drug-naive patients with PD is associated with cerebral hypometabolism

S. Pappatà, D. Aarsland, P. Barone, 2011, Neurology.

Novel mutation of SACS gene in a Spanish family with autosomal recessive spastic ataxia

O. Combarros, G. De Michele, A. Filla, 2005, Movement disorders : official journal of the Movement Disorder Society.

Suppression of myoclonus in SCA2 by piracetam

P. Striano, G. De Michele, A. Filla, 2006, Movement disorders : official journal of the Movement Disorder Society.

Reduced striatal [123I]FP‐CIT binding in SCA2 patients without parkinsonism

M. T. Pellecchia, S. Pappatà, P. Barone, 2004, Annals of neurology.

Introversion and Neuroticism in Akinetic-Rigid Parkinson's Disease: Association With Frontal-Executive Dysfunction.

G. De Michele, R. Sperandeo, N. Maldonato, 2023, The Journal of neuropsychiatry and clinical neurosciences.

Genetic screening for the LRRK2 R1441C and G2019S mutations in Parkinsonian patients from Campania.

M. T. Pellecchia, A. Tessitore, P. Barone, 2014, Journal of Parkinson's disease.

Does motor cortex plasticity depend on the type of mutation in the leucine‐rich repeat kinase 2 gene?

L. Santoro, G. De Michele, M. Esposito, 2017, Movement disorders : official journal of the Movement Disorder Society.

Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population.

L. Pianese, F. Cavalcanti, A. Monticelli, 1994, Journal of medical genetics.

Genetic screening for LRRK2 gene G2019S mutation in Parkinson's disease patients from Southern Italy.

S. Pappatà, G. De Michele, A. Filla, 2009, Parkinsonism & related disorders.

Environmental and genetic risk factors in Parkinson's disease: A case–control study in southern italy

R. Marconi, G. De Michele, A. Filla, 1996, Movement disorders : official journal of the Movement Disorder Society.

Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathy

M. T. Pellecchia, L. Santoro, G. De Michele, 2001, Neurology.

Friedreich's ataxia: from the patient to the gene

G. De Michele, A. Filla, S. Cocozza, 2001, Neurological Sciences.

Why do some Friedreich’s ataxia patients retain tendon reflexes?

G. Caruso, G. Coppola, L. Santoro, 1999, Journal of Neurology.

Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus.

L. Pianese, F. Cavalcanti, A. Monticelli, 1994, Journal of neurology, neurosurgery, and psychiatry.

Late onset recessive ataxia with Friedreich's disease phenotype.

L. Santoro, G. De Michele, A. Filla, 1989, Journal of neurology, neurosurgery, and psychiatry.

Imaging of dopaminergic dysfunction with [123I]FP-CIT SPECT in early-onset parkin disease

M. T. Pellecchia, S. Pappatà, P. Barone, 2004, Neurology.

Plasma lipoprotein concentration and erythrocyte membrane lipids in patients with Friedreich's ataxia.

G. De Michele, A. Filla, G. Campanella, 1980, Acta neurologica.

NMDA receptor gene variations as modifiers in Huntington disease: a replication study

J. Schiefer, R. Barker, R. Reilmann, 2011, PLoS currents.

Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort

D. Arkadir, M. Farrer, E. Tolosa, 2023, Movement disorders : official journal of the Movement Disorder Society.

Impulsive-compulsive behaviors in parkin-associated Parkinson disease

M. T. Pellecchia, A. Bentivoglio, A. Fasano, 2016, Neurology.

Smoking habits in multiple system atrophy and progressive supranuclear palsy

R. Marconi, U. Bonuccelli, G. De Michele, 2000, Neurology.

The Italian version of the quick mild cognitive impairment (Qmci-I) screen: normative study on 307 healthy subjects

M. Illario, P. Abete, G. De Michele, 2018, Aging Clinical and Experimental Research.

Why do some Friedreich's ataxia patients retain tendon reflexes? A clinical, neurophysiological and molecular study.

G. Caruso, G. Coppola, L. Santoro, 1999, Journal of neurology.

Stability of erythropoietin repackaging in polypropylene syringes for clinical use

G. Defazio, G. De Michele, A. Filla, 2016, Saudi Pharmaceutical Journal.

Epoetin alfa increases frataxin production in Friedreich's ataxia without affecting hematocrit

G. De Michele, A. Filla, S. Cocozza, 2011, Movement disorders : official journal of the Movement Disorder Society.

Interferon-beta treatment decreases cholesterol plasma levels in multiple sclerosis patients.

G. Coppola, G. De Michele, A. Filla, 2004, Neurology.

Application of the p9NORM correction method to timed neuropsychological tests in Parkinson’s disease and multiple system atrophy

G. De Michele, A. Filla, A. De Rosa, 2020, Neurological Sciences.

Othello syndrome in Parkinson’s disease: a systematic review and report of a case series

G. De Michele, A. De Rosa, F. Saccà, 2021, Neurological Sciences.

Is serum uric acid related to non-motor symptoms in de-novo Parkinson's disease patients?

M. T. Pellecchia, P. Barone, K. Longo, 2014, Parkinsonism & related disorders.

Stimulation of growth hormone release in multiple system atrophy, Parkinson's disease and idiopathic cerebellar ataxia

M. T. Pellecchia, P. Barone, G. De Michele, 2001, Neurological Sciences.

Cutaneous sensory and autonomic denervation in progressive supranuclear palsy

P. Barone, L. Santoro, M. Nolano, 2021, Neuropathology and applied neurobiology.

Relationship of neurological and psychological signs to physical and metabolic risk factors in elderly persons living in retirement facilities: a multidisciplinary approach.

G. De Michele, G. Campanella, L. Sinisi, 1989, Functional neurology.

Very late onset in ataxia oculomotor apraxia type I

G. De Michele, A. Filla, S. Banfi, 2005, Annals of neurology.

The flavor test is a sensitive tool in identifying the flavor sensorineural dysfunction in Parkinson’s disease

P. Macchia, I. C. Nettore, D. Bruzzese, 2019, Neurological Sciences.

POEMS syndrome: clinical, pathological and immunological study of a case.

R. Cerini, G. De Michele, G. Borgia, 1994, Neurological research.

A genetic study of Parkinson's disease.

R. Marconi, G. De Michele, A. Filla, 1995, Journal of neural transmission. Supplementum.

Accuracy of clinical diagnostic criteria for Friedreich's ataxia

G. Caruso, P. Barone, G. Coppola, 2000, Movement disorders : official journal of the Movement Disorder Society.

Regional distribution of glutamate dehydrogenase in rat brain.

G. De Michele, A. Filla, G. Campanella, 1984, Acta neurologica.

Serum vitamin E in inherited ataxias.

A. Federico, G. De Michele, A. Filla, 1990, Acta neurologica.

Relation between trinucleotide GAA repeat length and sensory neuropathy in Friedreich’s ataxia

G. Caruso, C. Crisci, L. Santoro, 1999, Journal of Neurology Neurosurgery & Psychiatry.

Electrophysiological and histological follow‐up study in 15 Friedreich's ataxia patients

G. Caruso, R. Massini, C. Crisci, 1990, Muscle & nerve.

A pathogenetic classification of hereditary ataxias: Is the time ripe?

G. Coppola, G. De Michele, A. Filla, 2004, Journal of Neurology.

A randomized trial of varenicline (Chantix) for the treatment of spinocerebellar ataxia type 3.

G. De Michele, A. Filla, F. Saccà, 2012, Neurology.

A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A

G. De Michele, A. Filla, F. Santorelli, 2023, Journal of Neurology.

Spinocerebellar ataxia type 48: last but not least

G. De Michele, F. Santorelli, 2020, Neurological Sciences.

G. De Michele, F. Santorelli, S. Cocozza, 2020, Movement disorders clinical practice.

Serum transferrin receptor levels in Friedreich’s and other degenerative ataxias

A. Monticelli, G. De Michele, A. Filla, 2001, Neurology.

Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity

E. Bertini, M. Tosetti, A. Durr, 2006, Neurogenetics.

Predictors of Survival in a Huntington's Disease Population from Southern Italy

G. De Michele, A. Filla, V. Morra, 2012, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Is serum uric acid related to non-motor symptoms in de-novo Parkinson's disease patients?

M. T. Pellecchia, P. Barone, K. Longo, 2014, Parkinsonism & related disorders.

False negative polymerase chain reaction on cerebrospinal fluid samples in tuberculous meningitis

M. T. Pellecchia, G. De Michele, C. Ciacci, 1999, Journal of neurology, neurosurgery, and psychiatry.

Epidemiology of multiple system atrophy

R. Marconi, U. Bonuccelli, G. De Michele, 2001, Neurological Sciences.

Neurophysiological evidence of corticospinal tract abnormality in patients with Parkin mutations

A. Brice, L. Santoro, G. De Michele, 2006, Journal of Neurology.

Extrapyramidal side-effects of flunarizine.

G. De Michele, A. Filla, G. Buscaino, 1987, Acta neurologica.

Nigrostriatal involvement in ataxia with oculomotor apraxia type 1

S. Pappatà, A. Varrone, M. Salvatore, 2007, Journal of Neurology.

Motor and non-motor features in Parkinson’s Disease patients carrying GBA gene mutations

G. De Michele, E. Valente, A. De Rosa, 2023, Acta Neurologica Belgica.

Measuring cognitive impairment and monitoring cognitive decline in Huntington’s disease: a comparison of assessment instruments

J. Kulisevsky, M. de Tommaso, J. López-Sendón, 2023, Journal of Neurology.