A. Orsini

发表

Advanced pharmacological therapies for neurofibromatosis type 1-related tumors

T. Foiadelli, Matteo Naso, A. Licari, 2020, Acta bio-medica : Atenei Parmensis.

Distal motor neuropathy associated with novel EMILIN1 mutation

P. Lanteri, P. Striano, F. Zara, 2020, Neurobiology of Disease.

The role of inflammatory mediators in epilepsy: Focus on developmental and epileptic encephalopathies and therapeutic implications

P. Striano, R. Consolini, T. Foiadelli, 2021, Epilepsy Research.

Posterior Reversible Encephalopathy Syndrome in infants and young children.

T. Foiadelli, A. Orsini, R. Masetti, 2020, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study

P. Striano, A. Orsini, S. Savasta, 2020, Epilepsy & Behavior.

De novo GRIN2A variants associated with epilepsy and autism and literature review

P. Striano, A. Orsini, R. Battini, 2022, Epilepsy & Behavior.

Mothers and fathers of children with epilepsy: gender differences in post-traumatic stress symptoms and correlations with mood spectrum symptoms

A. Orsini, D. Peroni, L. Dell’Osso, 2018, Neuropsychiatric disease and treatment.

A nationwide study on Sydenham's chorea: Clinical features, treatment and prognostic factors.

P. Striano, R. Consolini, A. Capuano, 2021, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Toward the Knowledge of the Epidemiological Impact of Acute Rheumatic Fever in Italy

R. Consolini, A. Orsini, N. Assanta, 2021, Frontiers in Pediatrics.

Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients.

F. Benfenati, P. Striano, F. Zara, 2020, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

The Clinical Impact of Methotrexate-Induced Stroke-Like Neurotoxicity in Paediatric Departments: An Italian Multi-Centre Case-Series

P. Striano, T. Foiadelli, A. Orsini, 2022, Frontiers in Neurology.

Recent advances in epilepsy genetics

P. Striano, F. Zara, A. Orsini, 2017, Neuroscience Letters.

Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus

P. Striano, A. Orsini, A. Verrotti, 2022, Italian Journal of Pediatrics.

Aromatic L-amino Acid Decarboxylase (AADC) deficiency: results from an Italian modified Delphi consensus

P. Striano, A. Orsini, R. Battini, 2021, Italian Journal of Pediatrics.

Peripheral Arterial Tonometry (EndoPAT)-measured Endothelial Dysfunction in Migraine with Aura children

P. Striano, M. Miccoli, T. Foiadelli, 2021, Acta bio-medica : Atenei Parmensis.

Parental Practices and Environmental Differences among Infants Living in Upper-Middle and High-Income Countries: A Cross-Sectional Study

G. Cioni, A. Orsini, R. Battini, 2022, International Journal of Environmental Research and Public Health.

Therapeutic aspects of Sydenham’s Chorea: an update

P. Striano, R. Consolini, T. Foiadelli, 2021, Acta bio-medica : Atenei Parmensis.

An Overview of The Role of Tumor Necrosis Factor-Alpha in Epileptogenesis and Its Terapeutic Implications

T. Foiadelli, A. Orsini, S. Savasta, 2021, Acta bio-medica : Atenei Parmensis.

An Italian consensus on the management of Lennox-Gastaut syndrome

P. Striano, A. Coppola, M. Puligheddu, 2022, Seizure.

Human Herpes Virus 7-related encephalopathy in children

F. Rovida, F. Baldanti, T. Foiadelli, 2021, Acta bio-medica : Atenei Parmensis.

Headache in progressive facial hemiatrophy (Parry-Romberg syndrome): A paradigmatic case and systematic review of the literature

T. Foiadelli, A. Orsini, C. Trabatti, 2021, Cephalalgia : an international journal of headache.

Pitt-Hopkins syndrome: report of a case with a TCF4 gene mutation

A. Orsini, E. Tarantino, A. Bonuccelli, 2010, Italian journal of pediatrics.

A Case of 22q11 Deletion Syndrome (22q11DS) with a Panayiotopoulos Epileptic Pattern: Are Additional Copy-Number Variations a Possible Second Hit in Modulating the 22q11DS Phenotype?

R. Consolini, A. Orsini, G. Saggese, 2017, Front. Pediatr..

Perampanel and childhood absence epilepsy: A real life experience

A. Orsini, A. Labate, F. Operto, 2022, Frontiers in Neurology.

Cyclic vomiting syndrome in children: a nationwide survey of current practice on behalf of the Italian Society of Pediatric Gastroenterology, Hepatology and Nutrition (SIGENP) and Italian Society of Pediatric Neurology (SINP)

P. Striano, A. Orsini, S. Savasta, 2022, Italian Journal of Pediatrics.

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.

PRES-like leukoencephalopathy presenting with status epilepticus associated with Brentuximab Vedotin treatment

P. Striano, T. Foiadelli, A. Orsini, 2021, Acta bio-medica : Atenei Parmensis.

Challenges and management of neurological and psychiatric manifestations in SARS-CoV-2 (COVID-19) patients

P. Striano, T. Foiadelli, A. Orsini, 2020, Neurological Sciences.

Personalized medicine in epilepsy patients

P. Striano, A. Orsini, D. Peroni, 2018 .

The best evidence for progressive myoclonic epilepsy: A pathway to precision therapy

P. Striano, R. Michelucci, A. Orsini, 2019, Seizure.

Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the ‘beyond epilepsy’ project

P. Striano, A. Orsini, C. Minetti, 2020, Italian Journal of Pediatrics.

Generalized epilepsy and mild intellectual disability associated with 13q34 deletion: A potential role for SOX1 and ARHGEF7

P. Striano, R. Consolini, A. Orsini, 2018, Seizure.

Phenotypic Spectrum of NFIA Haploinsufficiency: Two Additional Cases and Review of the Literature

A. Orsini, M. Elia, D. Peroni, 2022, Genes.

A prenatal case with multiple supernumerary markers identified as derivatives of chromosomes 13, 15, and 20: molecular cytogenetic characterization and review of the literature

A. Orsini, D. Peroni, V. Bertini, 2019, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Targeting Inflammatory Mediators in Epilepsy: A Systematic Review of Its Molecular Basis and Clinical Applications

P. Striano, R. Consolini, T. Foiadelli, 2022, Frontiers in Neurology.

Full and Partial DSM-5 PTSD in Parents of Children with Epilepsy: Exploring Gender Differences

A. Orsini, D. Peroni, L. Dell’Osso, 2017, European Psychiatry.

Post-traumatic stress spectrum symptoms in parents of children affected by epilepsy: Gender differences

A. Orsini, D. Peroni, L. Dell’Osso, 2020, Seizure.

Acute Disseminated Encephal Omyelitis (ADEM) After Pneumococcal Meningitis In A Child

T. Foiadelli, A. Licari, A. Orsini, 2020 .

Unilateral Lisch nodules in a pediatric patient: a sign for genetic mosaicism?

P. Striano, T. Foiadelli, A. Orsini, 2020, Minerva pediatrica.

Expanding Phenotype of Poirier–Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients

P. Striano, V. Capra, T. Foiadelli, 2022, Genes.

Molecular cytogenetic characterization of an interstitial deletion of chromosome 21 (21q22.13q22.3) in a patient with dysmorphic features, intellectual disability and severe generalized epilepsy.

P. Simi, A. Orsini, G. Saggese, 2012, European journal of medical genetics.

M. Reijnders, D. Segal, E. Wirrell, 2021, Neurology. Genetics.

The spectrum of intermediate SCN8A‐related epilepsy

M. Hammer, P. Striano, A. Coppola, 2019, Epilepsia.

Novel AMPD2 mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalities

P. Striano, F. Zara, V. Capra, 2017, Neurology: Genetics.

Genomic sequencing in severe epilepsy: a step closer to precision medicine

P. Striano, A. Orsini, D. Peroni, 2020 .

A quantitative polymerase chain reaction (PCR) assay completely discriminates between Duchenne and Becker muscular dystrophy deletion carriers and normal females.

M. G. Caporaso, L. Santoro, A. Orsini, 1996, Molecular and cellular probes.

Rasmussen's encephalitis: From immune pathogenesis towards targeted-therapy

P. Striano, R. Consolini, T. Foiadelli, 2020, Seizure.

Psychopathological Impact in Patients with History of Rheumatic Fever with or without Sydenham’s Chorea: A Multicenter Prospective Study

R. Consolini, A. Vignoli, T. Foiadelli, 2022, International journal of environmental research and public health.

Pediatric traumatic brain injury: a new relation between outcome and neutrophil-to-lymphocite ratio

T. Foiadelli, A. Orsini, S. Luzzi, 2021, Acta bio-medica : Atenei Parmensis.

Trait impulsivity in Juvenile Myoclonic Epilepsy

P. Striano, M. Richardson, K. Hamandi, 2020, Annals of clinical and translational neurology.

Electroclinical features of MEF2C haploinsufficiency-related epilepsy: A multicenter European study

P. Striano, R. Møller, E. Gardella, 2021, Seizure.

SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy

P. Striano, S. Topp, K. Hamandi, 2022, medRxiv.

17q12 Microduplications: A challenge for clinicians

P. Simi, A. Orsini, G. Saggese, 2015, American journal of medical genetics. Part A.

Sex-specific disease modifiers in juvenile myoclonic epilepsy

P. Striano, M. Richardson, K. Hamandi, 2022, Scientific Reports.

Methylenetetrahydrofolate reductase polymorphism (MTHFR C677T) and headache in children: a retrospective study from a tertiary level outpatient service

A. Orsini, D. Peroni, I. Sammartino, 2018, Italian Journal of Pediatrics.

The brain–heart interaction in epilepsy: implications for diagnosis, therapy, and SUDEP prevention

P. Striano, R. Brugada, A. Orsini, 2021, Annals of clinical and translational neurology.

DSM-5 criteria for PTSD in parents of pediatric patients with epilepsy: What are the changes with respect to DSM-IV-TR?

A. Orsini, G. Saggese, L. Dell’Osso, 2017, Epilepsy & Behavior.

Maternally derived 15q11.2‐q13.1 duplication in a child with Lennox–Gastaut‐type epilepsy and dysmorphic features: Clinical‐genetic characterization of the family and review of the literature

A. Orsini, M. Elia, A. Ferrari, 2017, American journal of medical genetics. Part A.

Medical management for neurosurgical related seizures

P. Striano, A. Orsini, A. Verrotti, 2017, Expert opinion on pharmacotherapy.

Autosomal dominant SCN8A mutation with an unusually mild phenotype.

A. Orsini, Z. Zaiwalla, S. Jayawant, 2016, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

A 6.5 mb deletion at 3q24q25.2 narrows Wisconsin syndrome critical region to a 750 kb interval: A potential role for MBNLI

A. Orsini, G. Saggese, Roberta Mazza, 2017, American journal of medical genetics. Part A.

Neurovisual Manifestations in Children with Mild COVID-19: An Association to Remember

R. Consolini, T. Foiadelli, A. Orsini, 2023, Neuro-ophthalmology.

Adult Autism Subthreshold Spectrum (AdAS Spectrum) in parents of pediatric patients with epilepsy: Correlations with post-traumatic stress symptoms.

A. Orsini, D. Peroni, L. Dell’Osso, 2018, Comprehensive psychiatry.

Case of Myhre syndrome with autism and peculiar skin histological findings.

A. Orsini, M. D'armiento, L. Santoro, 2001, American journal of medical genetics.

Advantages of Array Comparative Genomic Hybridization Using Buccal Swab DNA for Detecting Pallister-Killian Syndrome

A. Orsini, D. Peroni, S. Gana, 2018, Annals of laboratory medicine.

Case report - Thoracic general Microscopic thymoma

A. Orsini, C. Vial, L. Chalabreysse, 2007 .