CITTADELLA, RITA
 Distribuzione geografica
Continente #
AS - Asia 20
EU - Europa 3
NA - Nord America 1
Totale 24
Nazione #
CN - Cina 9
KR - Corea 6
SG - Singapore 5
GB - Regno Unito 2
IT - Italia 1
US - Stati Uniti d'America 1
Totale 24
Città #
Seoul 6
Singapore 5
Guangzhou 3
London 2
Boardman 1
Bovalino 1
Totale 18
Nome #
CASP-9 exon 1 polymorphism in patients with Multiple Sclerosis. 2
Polymorphisms of the F8C-G6PD-R/G VC gene cluster in the ethnic minority of Albanian origin living in the Cosenza province 2
Apolipoprotein E genotype does not influence the progression of multiple sclerosis. 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
AK, ADA and 6-PGD polymorphisms in Cosenza province (Calabria, Italy) 1
A novel mutation in FKRP gene in Italian patient with LGMD. 1
A social-demographic, isonymyc and genetic investigation on an isolated Calabrian village 1
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis 1
A novel CAPN3 gene mutation in a LGMD patient from Southern Italy 1
Analisi mutazionale del gene OPA1 in una famiglia affetta da atrofia ottica autosomica dominante. 1
Lack of association between nonlesional temporal lobe epilepsy and the Apolipoprotein E epsilon 4 allele. 1
Alzheimer s Disease and the Cystatin C gene polymorphism: an association study. 1
Association between Synapsin III gene promoter polymorphisms and multiple sclerosis. 1
A WHOLE mtDNA NGS APPROACH TO IDENTIFY NOVEL VARIANTS IN PATIENTS AFFECTED BY MITOCHONDRIAL DISEASES 1
Identificazione di una nuova mutazione nel gene OPA1 in una famiglia affetta da atrofia ottica e sordità. 1
Alzheimer's Disease and the Cystatin C gene polymorphism: an association study 1
Huntington's disease-like syndrome: a case report 1
A new intronic deletion of presenilin 1 gene in a patient with early onset Alzheimer Disease 1
DRD2 gene polymorphism and the risk of peak-dose dyskinesias in Parkinson's disease. 1
Totale 24
Categoria #
all - tutte 1.544
article - articoli 825
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.369


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202419 0 0 0 0 0 0 0 0 3 0 15 1
2024/20255 5 0 0 0 0 0 0 0 0 0 0 0
Totale 24