Lucia Margari

ORCID: 0000-0002-9203-3373
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About
Contact & Profiles
Research Areas
  • Autism Spectrum Disorder Research
  • Genetics and Neurodevelopmental Disorders
  • Attention Deficit Hyperactivity Disorder
  • Epilepsy research and treatment
  • Child and Adolescent Psychosocial and Emotional Development
  • Child Development and Digital Technology
  • Multiple Sclerosis Research Studies
  • Family and Disability Support Research
  • Child Nutrition and Feeding Issues
  • Pharmacological Effects and Toxicity Studies
  • Neurological disorders and treatments
  • Schizophrenia research and treatment
  • Genomic variations and chromosomal abnormalities
  • Bipolar Disorder and Treatment
  • Fetal and Pediatric Neurological Disorders
  • Diet and metabolism studies
  • Neonatal and fetal brain pathology
  • Migraine and Headache Studies
  • Genetic Neurodegenerative Diseases
  • Obsessive-Compulsive Spectrum Disorders
  • Ophthalmology and Eye Disorders
  • COVID-19 and Mental Health
  • Maternal Mental Health During Pregnancy and Postpartum
  • Suicide and Self-Harm Studies
  • EEG and Brain-Computer Interfaces

University of Bari Aldo Moro
2016-2025

University of Siena
2023

Weatherford College
2021

Azienda Universitaria Ospedaliera Consorziale - Policlinico Bari
1999-2020

Moscow Research and Clinical Center for Neuropsychiatry
2011-2016

Fondazione Salvatore Maugeri
1999

University of Parma
1997

Paroxysmal dyskinesias are episodic movement disorders that can be inherited or sporadic in nature. The pathophysiology underlying these remains largely unknown but may involve disrupted ion homeostasis due to defects cell-surface channels nutrient transporters. In this study, we describe a family with paroxysmal exertion-induced dyskinesia (PED) over 3 generations. Their PED was accompanied by epilepsy, mild developmental delay, reduced CSF glucose levels, hemolytic anemia echinocytosis,...

10.1172/jci34438 article EN Journal of Clinical Investigation 2008-04-30

Recent studies support several overlapping traits between autism spectrum disorders (ASD) and attention-deficit/hyperactivity disorder (ADHD), assuming the existence of a combined phenotype. The aim our study was to evaluate common or distinctive clinical features ASD ADHD in order identify possible different phenotypes that could have value. We enrolled 181 subjects divided into four diagnostic groups: group, ASD+ADHD group (that met criteria for both ADHD), control group. Intelligent...

10.1002/aur.1449 article EN cc-by-nc-nd Autism Research 2015-01-20

Learning Disorders (LD) are complex diseases that affect about 2-10% of the school-age population. We performed neuropsychological and psychopathological evaluation, in order to investigate comorbidity children with LD. Our sample consisted 448 patients from 7 16 years age a diagnosis LD, divided two subgroups: Specific (SLD), including reading, writing, mathematics disorders, Not Otherwise Specified (LD NOS). Comorbidity neuropsychopathologies was found 62.2% total sample. In LSD subgroup,...

10.1186/1471-2377-13-198 article EN cc-by BMC Neurology 2013-12-01

Autism Spectrum Disorder (ASD) has historically been studied, known, and diagnosed in males. Females tend to remain unidentified, especially those with average intelligence abilities. This sex/gender difference might be partially explained by biological risk factors, but it is probably also bound methodological issues. The present study aims examine phenotypic characteristics (cognitive, emotive, socio-communicative, academic) of a group 54 females ASD matched 55 males (3–18 years), all...

10.3389/fpsyt.2021.539835 article EN cc-by Frontiers in Psychiatry 2021-07-09

Attention-deficit/hyperactivity disorder (ADHD) is one of the most common neurodevelopmental conditions and highly heterogeneous in terms symptom profile, associated cognitive deficits, comorbidities, outcomes. Heterogeneity may also affect ability to recognize diagnose this condition. The diagnosis ADHD primarily clinical but there are increasing research efforts aiming at identifying biomarkers that can aid diagnosis.

10.1080/14737159.2024.2333277 article EN Expert Review of Molecular Diagnostics 2024-03-20

Multiple sclerosis (MS) is a complex disease of the CNS that usually affects young adults, although 3–5% cases are diagnosed in childhood and adolescence (hence called pediatric MS, PedMS). Genetic predisposition, among other factors, seems to contribute risk onset, as adult ages, but few studies have investigated genetic 'environmentally naïve' load PedMS. The main goal this study was identify circulating markers (miRNAs), target genes (mRNAs) functional pathways associated with PedMS; we...

10.1093/hmg/ddx385 article EN Human Molecular Genetics 2017-10-25

Since Hans Asperger's first description (Arch Psych Nervenkrankh 117:76-136, 1944), through Lorna Wing's translation and definition (Psychol Med 11:115-129, 1981), to its introduction in the fourth edition of Diagnostic Statistical Manual Mental Disorders (DSM, 1994), Asperger Syndrome has always aroused huge interest debate, until vanishing DSM fifth (2013). The debate regarded diagnostic validity differentiation from high functioning autism (HFA). present study aimed examine whether AS...

10.1007/s10803-018-3689-4 article EN cc-by Journal of Autism and Developmental Disorders 2018-07-24
Damiano Baroncini Marta Simone Pietro Iaffaldano Vincenzo Brescia Morra Roberta Lanzillo and 86 more Massimo Filippi Marzia Romeo Francesco Patti Clara Grazia Chisari Eleonora Cocco Giuseppe Fenu Giuseppe Salemi Paolo Ragonese Matilde Inglese Maria Cellerino Lucia Margari Giancarlo Comi Mauro Zaffaroni Angelo Ghezzi Umberto Aguglia Maria Pia Amato Roberto Balgera Paola Banfi Valeria Barcella Paolo Bellantonio Roberto Bergamaschi Antonio Bertolotto Roberto Bombardi Ardito Bonaventura Placido Bramati Giampaolo Brichetto Lorenzo Capone Daniela Cargnelutti Elisabetta Cartechini Guido Cavaletti Paola Cavalla Luca Chiveri Raffaella Clerici Marinella Clerico Cristoforo Comi Francesco Corea Salvatore Cottone Paola Crociani Francesco D'Andrea Maura Danni Francesca De Robertis Mario Di Napoli Alessia Di Sapio Diana Ferraro Elisabetta Ferraro Maria Teresa Ferrò Antonio Gallo Claudio Gasperini Maurizia Gatto Paola Gazzola Franco Granella Maria Grazia Grasso Alessandra Lugaresi Giacomo Lus Davide Maimone Giorgia Teresa Maniscalco Girolama Alessandra Marfia Nerina Mascoli Luca Massacesi Massimiliano Mirabella Fiorella Mondino Sara Montepietra Davide Nauselli Marco Onofrj Sergio Parodi Ilaria Pesci Carlo Piantadosi Carlo Pozzilli Alessandra Protti R. Quatrale Augusto Rini Marco Rovaris Marco Salvetti Giuseppe Santuccio Elio Scarpini Leonardo Sinisi Patrizia Sola Daniele Spitaleri Silvia Strumia Tiziana Tassinari Simone Tonietti Valentina Torri Clerici Rocco Totaro Paola Valentino Simonetta Venturi Marika Vianello

Availability of new disease-modifying therapies (DMTs) and changes therapeutic paradigms have led to a general improvement multiple sclerosis (MS) prognosis in adults. It is still unclear whether this also involves patients with pediatric-onset MS (POMS), whose early management more challenging.To evaluate the POMS over time association managing standards.Retrospective, multicenter, observational study. Data were extracted collected May 2019 from Italian Registry, digital database including...

10.1001/jamaneurol.2021.1008 article EN JAMA Neurology 2021-05-03

Abstract Background Heterogeneous mental health outcomes during the COVID-19 pandemic are documented in general population. Such heterogeneity has not been systematically assessed youth with autism spectrum disorder (ASD) and related neurodevelopmental disorders (NDD). To identify distinct patterns of impact their predictors ASD/NDD youth, we focused on pandemic-related changes symptoms access to services. Methods Using a naturalistic observational design, parent responses Coronavirus Health...

10.1186/s13229-022-00536-z article EN cc-by Molecular Autism 2023-02-14

Sleep disorders represent an important comorbidity in individuals with ADHD. While the links between ADHD and sleep disturbances have been extensively investigated, research on management of is relatively limited, albeit expanding.

10.1080/14737175.2024.2353692 article EN cc-by-nc-nd Expert Review of Neurotherapeutics 2024-05-13

The treatment of cognitive deficits is challenging in pediatric onset multiple sclerosis (POMS) and patients with attention deficit hyperactivity disorder (ADHD). We performed a pilot double-blind RCT to evaluate the efficacy home-based computerized-program for retraining two cohorts POMS ADHD patients. failing at least 2/4 tests on neuropsychological battery were randomized specific or nonspecific computerized training (ST, nST), one-hour sessions, twice/week 3 months. primary outcome was...

10.1186/s12883-018-1087-3 article EN cc-by BMC Neurology 2018-06-08

Objective To assess prognostic factors for a second clinical attack and first disability‐worsening event in pediatric clinically isolated syndrome (pCIS) suggestive of multiple sclerosis (MS) patients. Methods A cohort 770 pCIS patients was followed up at least 10 years. Cox proportional hazard models Recursive Partitioning Amalgamation (RECPAM) tree‐regression were used to analyze data. Results In pCIS, female sex multifocal onset risk (hazard ratio [HR], 95% confidence interval [CI] =...

10.1002/ana.24938 article EN Annals of Neurology 2017-04-25

Over the last few years, new studies focused their attention on gender-related features in high-functioning autism spectrum disorder (HFA), often leading to controversial results. Another interesting aspect of these subtype patients is linked complexity clinical presentation, where besides core symptoms, other co-occurrence disorders may complicate diagnostic evaluation. Therefore, we retrospectively studied 159 HFA patients, male and female, investigating comorbidities find any gender...

10.3389/fpsyt.2019.00159 article EN cc-by Frontiers in Psychiatry 2019-03-26

Over the last decade, several studies investigated outcomes in children born very preterm. Only recently there has been an increasing interest late preterm infants (born between 34 + 0 and 36 6 weeks). This population is at high risk of morbidity mortality first years life. Other reported that they are also long-term developmental problem. Therefore, aim this study to describe neurodevelopmental emotional-behavioral outcome a sample patients.The included adolescents who had neuropsychiatric...

10.1186/s12887-018-1293-6 article EN cc-by BMC Pediatrics 2018-10-08

Vitamin D plays a role in central nervous system (CNS) development. Recent literature focused on vitamin status children and adolescents with autism spectrum disorder (ASD), but inconsistent results. Our case-control study is aimed at evaluating serum 25-hydroxyl-vitamin (25(OH)D) concentration ASD (ASD group, n = 54) compared to affected by other neurological psychiatric disorders (non-ASD 36). All patients were admitted the Complex Operative Unit of Child Neuropsychiatry, Polyclinic Bari,...

10.1155/2020/9292560 article EN Disease Markers 2020-09-19

The dopaminergic system (DS) is one of the most important neuromodulator systems involved in complex functions that are compromised both autism spectrum disorder (ASD) and attention deficit/hyperactivity (ADHD), conditions frequently occur overlap. This evidence suggests disorders might have common neurobiological pathways involving DS. Therefore, aim this study was to examine DRD1 DRD2 dopamine receptor single nucleotide polymorphisms (SNPs) as potential risk factors for ASD, ADHD, ASD/ADHD...

10.3389/fnins.2021.705890 article EN cc-by Frontiers in Neuroscience 2021-09-29
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