Lucia Fusco

Dr. Lucia Fusco

orcid

Research Focus & Metrics

Academic Career Length

42Years (1985-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 1999 in Epileptic Disorders
Verified
Journal Article
Closed access
LFLucia Fusco
Lucia Fusco
CPChrista Pachatz
Christa Pachatz
RCRaffaella Cusmai
Raffaella Cusmai
FVFederico Vigevano
Federico Vigevano
Sleep starts, also called hypnagogic or hypnic jerks, are bilateral, sometimes asymmetric, usually single, brief body jerks that coincide with sleep onset. We describe sleep starts occurring repetitively in three epileptic children with spastic‐dystonic diplegia and mental retardation. Repetitive sleep starts began at age 18 months in two children and at 9 months in the third. All three children had had feto‐neonatal asphyxia; two presented with spastic and one with dystonic tetraparesis. One had West syndrome and two had partial motor seizures in the first year of life. Seizures were controlled in all three patients by antiepileptic drug therapy. Video/EEG recordings of all the children during the afternoon nap revealed clusters of sleep starts during the transition between wakefulness and sleep. Cluster lasted 4‐15 min and comprised from twenty to twenty‐nine contractions. The EEG counterpart of the event sometimes showed an arousal response, at times inducing complete awakening. Repetitive sleep starts should be recognized and clearly differentiated from epileptic seizures, especially if they appear in epileptic subjects. In neurologically compromised patients, they could represent an intensification of an otherwise normal event, due to the lack of strong inhibitory influence of the pyramidal tract resulting from the pyramidal lesion.

1 July 2019 in Neuropsychiatric Disease and Treatment
Verified
Journal Article
Open access
PDF file
DSDomenico Serino
Domenico Serino
MSMarta Elena Santarone
Marta Elena Santarone
DCDavide Caputo
Davide Caputo
LFLucia Fusco
Lucia Fusco
Febrile infection-related epilepsy syndrome (FIRES) is a rare catastrophic epileptic encephalopathy with a yet undefined etiology, affecting healthy children. It is characterized by acute manifestation of recurrent seizures or refractory status epilepticus preceded by febrile illness, but without evidence of infectious encephalitis. To date, the absence of specific biomarkers poses a significant diagnostic challenge; nonetheless, early diagnosis is very important for optimal management. FIRES is mostly irreversible and its sequelae include drug-resistant epilepsy and neuropsychological impairments. The treatment of FIRES represents a significant challenge for clinicians and is associated with low success rates. Early introduction of ketogenic diet seems to represent the most effective and promising treatment. This review aims to highlight the most recent insights on clinical features, terminology, epidemiology, pathogenesis, diagnostic challenges and therapeutic options.

1 November 2001 in Brain and Development
Verified
Journal Article
Closed access
LFLucia Fusco
Lucia Fusco
CPChrista Pachatz
Christa Pachatz
MCMatteo Di Capua
Matteo Di Capua
FVFederico Vigevano
Federico Vigevano

15 August 2016 in European Journal of Paediatric Neurology
Verified
Journal Article
Closed access
PDF file
FCFabrizio Chiusolo
Fabrizio Chiusolo
ADAntonella Diamanti
Antonella Diamanti
RBR. Bianchi
R. Bianchi
LFLucia Fusco
Lucia Fusco
MEM. Elia
M. Elia
SPS. Picardo
S. Picardo

1 August 2020 in Seizure: European Journal of Epilepsy
Verified
Journal Article
Closed access
MSMarta Elena Santarone
Marta Elena Santarone
NPNicola Pietrafusa
Nicola Pietrafusa
LFLucia Fusco
Lucia Fusco