CNR Institutional Research Information System

GAMBARDELLA, ANTONIO
 Distribuzione geografica
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Continente #
AS - Asia 16
EU - Europa 8
NA - Nord America 5
Totale 29
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Nazione #
CN - Cina 10
IT - Italia 5
KR - Corea 5
US - Stati Uniti d'America 5
FR - Francia 2
GB - Regno Unito 1
SG - Singapore 1
Totale 29
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Città #
Seoul 5
Boardman 4
Capua 2
Guangzhou 2
Paris 2
Genoa 1
London 1
New York 1
Rende 1
Totale 19
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Nome #
An SNP site in pri-miR-124, a brain expressed miRNA gene, no contribution to mesial temporal lobe epilepsy in an Italian sample 3
Circulating microRNAs as Potential Novel Diagnostic Biomarkers to Predict Drug Resistance in Temporal Lobe Epilepsy: A Pilot Study 3
A Functional Genetic Variation of the 5-HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy. 2
Value of Clinical Features to Differentiate Refractory Epilepsy from Mimics A prospective longitudinal cohort study. 2
Opicapone-induced reversible myopathy in a patient with advanced Parkinson's disease and familial hyperCKemia 2
A common SCN1A polymorphisms does not influence drug responsiveness in Italian epilepsy patients. 1
TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis. 1
Clinical and genetic study of an Italian family linked to SPG26 locus 1
"Schwann cells", a historical landmark in neurology 1
A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1. 1
Color vision inpatients with Parkinson disease. Usefulness of three pseudoisochromatic tests 1
A familial t(4;8) translocation segregates with epilepsy and migraine with aura. 1
A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit. 1
A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. 1
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. 1
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 1
Focal Neuromyotonia Associated With a C9ORF72 Expansion Mutation 1
Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 1
Diagnostic biomarkers of epilepsy 1
Hans Berger: father of electroencephalography 1
Mutational analysis of the CHRNA4 and CHRNB2 genes in a family with autosomal dominant nocturnal frontal lobe epilepsy 1
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy 1
Totale 29
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Categoria #
all - tutte 2.035
article - articoli 1.410
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 3.445
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202427 0 0 0 0 0 0 0 0 4 0 17 6
2024/20252 2 0 0 0 0 0 0 0 0 0 0 0
Totale 29