VILLA, CHIARA

VILLA, CHIARA  

DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)  

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Risultati 1 - 20 di 77 (tempo di esecuzione: 0.01 secondi).
Titolo Data di pubblicazione Autori
Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis 1-gen-2007 Villa C. +
Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration 1-gen-2008 Villa C. +
Novel exon 1 progranulin gene variant in Alzheimer's disease 1-gen-2008 Villa C. +
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration 1-gen-2008 Villa C. +
MCP-1 A-2518G polymorphism: Effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels 1-gen-2009 Villa C. +
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration 1-gen-2009 Villa C. +
DCUN1D1 is a risk factor for frontotemporal lobar degeneration 1-gen-2009 Villa C. +
Candidate gene analysis of selectin cluster in patients with multiple sclerosis 1-gen-2009 Villa C. +
CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degeneration 1-gen-2009 Villa C. +
Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with alzheimer's disease 1-gen-2009 Villa C. +
Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration? 1-gen-2010 Villa C. +
GRN variability contributes to sporadic frontotemporal lobar degeneration 1-gen-2010 Villa C. +
FUS/TLS genetic variability in sporadic frontotemporal lobar degeneration 1-gen-2010 Villa C. +
Candidate gene analysis of semaphorins in patients with Alzheimer's disease 1-gen-2010 Villa C. +
BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease 1-gen-2011 VILLA, CHIARA +
From genotype to phenotype: two cases of genetic frontotemporal lobar degeneration with premorbid bipolar disorder 1-gen-2011 VILLA, CHIARA +
Causal Frontotemporal Lobar Degeneration mutations: a novel MAPT mutation associated with the clinical phenotype of Progressive nonfluent Aphasia 1-gen-2011 VILLA, CHIARA +
Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosis 1-gen-2011 VILLA, CHIARA +
Causal frontotemporal lobar degeneration mutations: a novel mutation in MAPT associated with non-fluent progressive aphasia phenotype 1-gen-2011 VILLA, CHIARA +
Genetics and expression analysis of Sp4 transcription factor in patients with Alzheimer’s disease and frontotemporal lobar degeneration. 1-gen-2011 VILLA, CHIARA +