MANNA, IDA
 Distribuzione geografica
Continente #
AS - Asia 16
EU - Europa 9
NA - Nord America 3
Totale 28
Nazione #
CN - Cina 11
IT - Italia 9
KR - Corea 4
US - Stati Uniti d'America 3
SG - Singapore 1
Totale 28
Città #
Capua 5
Seoul 4
Boardman 2
Milan 2
Bovalino 1
Guangzhou 1
New York 1
Totale 16
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
ASSOCIATION OF A GABA(B) GENE HAPLOTYPE AND TEMPORAL LOBE EPILEPSY 3
Exosome-associated miRNA profile as a prognostic tool for therapy response monitoring in multiple sclerosis patients. 2
A Functional Genetic Variation of the 5-HTR2A Receptor Affects Age at Onset in Patients with Temporal Lobe Epilepsy. 2
Dropped head syndrome in a patient with FTD-ALS caused by abnormal expansion of C9orf72 gene. 1
A common SCN1A polymorphisms does not influence drug responsiveness in Italian epilepsy patients. 1
A family with dominant optic atrophy and deafness due to a novel Opa1 mutation. 1
Cognitive impairment and brain atrophy in patients with relapsing-remitting Multiple Sclerosis (RRMS): the role of brain derived neurotrophic factor (BDNF) gene. 1
BRAIN-DERIVED NEUROTROPHIC FACTOR (BDNF) GENE IN RELAPSING-REMITTING MULTIPLE SCLEROSIS (RRMS): LONGITUDINAL EVALUATION 1
Association study between synapsin III gene and Multiple Sclerosis (MS). 1
A novel mutation in FKRP gene in Italian patient with LGMD. 1
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis 1
Apolipoprotein E polymorphisms and Parkinson's disease. 1
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 1
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy. 1
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis. 1
Identificazione di una nuova mutazione nel gene OPA1 in una famiglia affetta da atrofia ottica e sordità. 1
A longitudinal observation of brain-derived neurotrophic factor mRNA levels in patients with relapsing-remitting multiple sclerosis. 1
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy 1
Totale 28
Categoria #
all - tutte 1.001
article - articoli 643
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 1.644


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202426 0 0 0 0 0 0 0 0 6 0 16 4
2024/20252 2 0 0 0 0 0 0 0 0 0 0 0
Totale 28