Luisa Antonini
A5032297548- Epilepsy research and treatment
- Pharmacological Effects and Toxicity Studies
- Olfactory and Sensory Function Studies
- Traumatic Brain Injury and Neurovascular Disturbances
- Cellular transport and secretion
- Kawasaki Disease and Coronary Complications
- Trypanosoma species research and implications
- Cerebrospinal fluid and hydrocephalus
- Lysosomal Storage Disorders Research
- Intraoperative Neuromonitoring and Anesthetic Effects
- Intensive Care Unit Cognitive Disorders
- Cerebrovascular and Carotid Artery Diseases
- Metabolism and Genetic Disorders
- Hemoglobinopathies and Related Disorders
- Musculoskeletal pain and rehabilitation
- Quality and Safety in Healthcare
- Dermatologic Treatments and Research
- Occupational Health and Safety Research
- Infrared Thermography in Medicine
- Intracranial Aneurysms: Treatment and Complications
- CNS Lymphoma Diagnosis and Treatment
- Anesthesia and Neurotoxicity Research
- Vascular Malformations and Hemangiomas
- Pregnancy and Medication Impact
- Celiac Disease Research and Management
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia
1991-2020
University of Brescia
1992-2000
Brescia University
1999
<h3>Objective</h3> Changes in prescribing patterns of antiepileptic drugs (AEDs) pregnant women with epilepsy would be expected to affect the risk major congenital malformations (MCMs). To test this hypothesis, we analyzed data from an international pregnancy registry (EURAP). <h3>Methods</h3> EURAP is observational prospective cohort study designed determine MCMs after prenatal exposure AEDs. The Cochrane-Armitage linear trend analysis was used assess changes AED treatment, prevalence MCMs,...
Neuroimaging has an important role in detecting CNS involvement children with systemic or isolated hemophagocytic lymphohistiocytosis. We characterized a cohort of pediatric patients lymphohistiocytosis focusing on neuroradiologic features and assessed whether distinct MR imaging patterns genotype correlations can be recognized.We retrospectively enrolled consecutive diagnosed treated at 2 neurology centers between 2010 2018. Clinical data were analyzed.Fifty-seven (40 primary, 70%) median...
Gaucher disease (GD) is an autosomal recessive lysosomal storage disorder caused by mutations in the acid β-glucosidase encoding gene (GBA1), resulting deficient activity of (GCase). To date, there no approved treatment for neurological manifestations disease. The role Ambroxol as a chaperone mutant GCase has been extensively demonstrated vitro. Furthermore, different authors have reported beneficial effects high doses on patients affected GD. In this report, we describe vitro and vivo two...
Summary: We report the electroclinical ictal findings of four epileptic patients with clinically asymptomatic celiac disease (CD). Celiac diagnosis was suspected by past history and/or computed tomography (CT) in all and confirmed laboratory tests jejunal biopsy. All had paroxysmal visual manifestations EEG discharges arising from occipital lobe. Epilepsy evolution favorable two severe 2, regardless CT evidence corticosubcortical calcifications 2 patients. Occipital lobe seizures may be...
La sindrome di Sturge-Weber è caratterizzata da un angioma cutaneo nel territorio innervazione una o più branche del nervo trigemino e un'angiomatosi meningo-corticale calcificante. Il reperto TC calcificazioni dall'aspetto tortuoso a prevalente localizzazione parieto-occipitale analoghe quello della riscontrabile tuttavia anche in pazienti che non presentano cutaneo. Più recentemente venuta delineandosi la possibilità dell'associazione quadro clinico epilessia gravità variabile, occipitali...