Raffaele Falsaperla

University of Ferrara — Italy

Medicine · Health Sciences

41h-index5.2kcitations396works1.92yr avg
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Research Topics

Epilepsy research and treatment(66), Neonatal and fetal brain pathology(43), Genetics and Neurodevelopmental Disorders(37), Metabolism and Genetic Disorders(35), Neonatal Respiratory Health Research(26)

Publications394 total

A Systematic Review of Cutaneous Hypopigmentation Disorder Associated with Neurologic Involvement
Children·2025Open Access
The First 30 Days Postnatal of the GABA Receptor: A Comprehensive Overview
Molecular Neurobiology·2025· 1 cited
Chromothriptic Translocation t(1;18): A Paradigm of Genomic Complexity in a Child with Normal Intellectual Development and Pyridoxine-Dependent Epilepsy
Genes·2025Open Access
Is Vitamin B6 a Precision Therapy for Neonatal Seizures?
Neurology International·2025Open Access
Toward a working definition of ketogenic diet resistance in <scp>GLUT1</scp> deficiency syndrome
Epileptic Disorders·2025Open Access
A mutational hotspot in TUBB2A associated with impaired heterodimer formation and severe brain developmental disorders
Frontiers in Cellular Neuroscience·2025Open Access
Unraveling the link: SARS‑CoV‑2 infections and seizures in pediatric patients (Review)
World Academy of Sciences Journal·2025Open Access
The role of microglia in sepsis-associated encephalopathy: a narrative review
Translational Pediatrics·2025Open Access
SLC2A1 and Its Related Epileptic Phenotypes
Journal of Pediatric Neurology·2025Open Access
ALDH7A1 Gene and Its Related Pyridoxine-Dependent Epilepsy
Journal of Pediatric Neurology·2025Open Access
Treatment of neonatal seizures: from guidelines to precision therapy
Molecular and Cellular Pediatrics·2025· 3 citedOpen Access
AMPA Receptor Modulation Through Medium-Chain Triglycerides and Decanoic Acid Supports Nutritional Intervention in Pediatric Epilepsy
Nutrients·2025· 1 citedOpen Access
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1
Clinical and Experimental Pediatrics·2025Open Access
Congenital Localized Hypopigmentation Disorders as a Clue of Severe Neurologic Involvement: An Update Review
Journal of Child Neurology·2025· 1 cited
From abnormal fetal movements to neonatal seizures: A literature review
Epilepsy Research·2025· 4 citedOpen Access
Molecular Dynamics as a Precision Therapy: A Perspective on Epileptic Encephalopathies
Molecular Diagnosis & Therapy·2025· 1 cited
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy?
Molecular and Cellular Pediatrics·2025Open Access
Amplitude-integrated Electroencephalography in a Neonate with Isovaleric Acidaemia: A Case Report
Journal of Neonatology·2025
Microbiome and Pregnancy Dysbiosis: A Narrative Review on Offspring Health
Nutrients·2025· 14 citedOpen Access
Is Precision Therapy in Infantile-Onset Epileptic Encephalopathies Still Too Far to Call Upon?
Applied Sciences·2025· 1 citedOpen Access
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Frequent Co-authors

Piero Pavone(43), Martino Ruggieri(26), Andrea D. Praticò(18), Giovanni Corsello(16), Giovanna Vitaliti(12), Riccardo Lubrano(7), Renata Rizzo(7), Eloisa Gitto(5), Silvia Marino(4), Enrico Parano(4), Nassim Matin(4), Paola Di Mauro(4), Salvatore Cocuzza(4), Gabriella D’Angelo(4), Agnese Suppiej(4), Alberto Verrotti(4), Pasquale Striano(3), Vito Pavone(3), Cátia Romano(3), Agostino Serra(3)