Alessandro Ferretti | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
Expanding the Spectrum of Autosomal Dominant ATP6V1A-Related Disease: Case Report and Literature Review	GENES	2024
Probiotics and other adjuvants in allergen-specific immunotherapy for food allergy: a comprehensive review	FRONTIERS IN ALLERGY	2024
Effectiveness and safety of polyethylene‐glycol‐4000 versus sodium picosulphate plus magnesium oxide and citric acid for bowel cleansing before colonoscopy in children: a systematic review with meta‐analysis	JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION	2024
IL-17 in serum and cerebrospinal fluid of pediatric patients with acute neuropsychiatric disorders: Implications for PANDAS and PANS	EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY	2024
Migraine, Allergy, and Histamine: Is There a Link?	JOURNAL OF CLINICAL MEDICINE	2023
CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndrome	CEREBRAL CORTEX	2023
Pediatric hypnic headache: a systematic review	FRONTIERS IN NEUROLOGY	2023
Movement Disorders in Patients With Genetic Developmental and Epileptic Encephalopathies	NEUROLOGY	2023
Autonomic Involvement in Childhood Epilepsy	Autonomic Disorders in Clinical Practice	2023
A possible unexpected link: Could wheat elimination trigger food protein-induced enterocolitis syndrome in a celiac disease patient?	NUTRITION	2023
Neuroinflammation and status epilepticus: a narrative review unraveling a complex interplay	FRONTIERS IN PEDIATRICS	2023
Editorial: Stress neurobiology in COVID-19: diagnosis, neuroimaging and therapeutic tools	FRONTIERS IN NEUROLOGY	2023
Expanding Phenotype of Poirier-Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients	GENES	2022
The epilepsy-autism spectrum disorder phenotype in the era of molecular genetics and precision therapy	EPILEPSIA	2022
Neurophysiological Findings in Neuronal Ceroid Lipofuscinoses	FRONTIERS IN NEUROLOGY	2022
Risk of SUDEP during infancy	EPILEPSY & BEHAVIOR	2022
MED13 mutation: A novel cause of developmental and epileptic encephalopathy with infantile spasms	SEIZURE	2022
Therapeutic Drug Monitoring of Quinidine in Pediatric Patients with KCNT1 Genetic Variants	PHARMACEUTICS	2022
A Complex Genomic Rearrangement Resulting in Loss of Function of SCN1A and SCN2A in a Patient with Severe Developmental and Epileptic Encephalopathy	INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES	2022
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome	NEUROLOGY	2021