Sfoglia per AUTORE
VAULA G
Collezione ASL Torino 4

  

Items : 5

EARLY ONSET CEREBRAL SMALL VESSEL DISEASE DUE TO HETEROZYGOUS HTRA1 MUTATION: A CASE REPORT in Neurological Sciences

2022
ASL Torino 3
ASL Torino 4
ASL Asti
AOU Città della Salute di Torino
AOU Alessandria
ASL Città di Torino

Vaula G; Leombruni S; Romanelli M; Rubino E; Dentelli P; Cerrato P; Della Sala E; Bosco G; Brusco A; Fiume G;

Megalencephalic leukoencephalopathy with subcortical cysts type 1 (MLC1) due to a homozygous deep intronic splicing mutation (c.895-226T>G) abrogated in vitro using an antisense morpholino oligonucleotide in Neurogenetics

2012
ASL Torino 4

Mancini C; Vaula G; Scalzitti L; Cavalieri S; Bertini E; Aiello C; Lucchini C; Gatti RA; Brussino A; Brusco A;

Two Italian families with ITPR1 gene deletion presenting a broader phenotype of sca15 in Cerebellum

2010
ASL Torino 4

Di Gregorio E; Orsi L; Godani M; Vaula G; Jensen S; Salmon E; Ferrari G; Squadrone S; Abete MC; Cagnoli C; Brussino A; Brusco A;

Association between the interleukin-1alpha gene and Alzheimer's disease: a meta-analysis. in Neurobiology of aging / Neurobiol Aging. 2004 Nov-Dec;25(10):1293-8. doi: 10.1016/j.neurobiolaging.2004.02.011.

2004
AOU Città della Salute di Torino
ASL Torino 4

Rainero I; Bo M; Ferrero M; Valfrè W; Vaula G; Pinessi L;

Association between the interleukin-1? gene and Alzheimer's disease: A meta-analysis in Neurobiology of Aging

2004
ASL Torino 4

Rainero I; Bo M; Ferrero M; Valfrè W; Vaula G; Pinessi L;