-E Scarpini Researcher Activity Profile

Research Author Detailed Information 

E Scarpini Publication Rate By Year

E Scarpini has published 2 paper(s) in 1992, 6 paper(s) in 2007, 4 paper(s) in 2008, for a total of 12 research publications in total.

E E Scarpini Author Information

LAST NAME: scarpini

FIRST NAME: E

INITIALS: e

AFFILIATION:

Papers

E Scarpini's Publication Record

1. +10 T/C polymorphisms in the gene of transforming growth factor-beta1 are associated with neurodegeneration and its clinical evolution. Year Published: 2007
Geriatric Unit, Ospedale Maggiore Policlinico, IRCCS, University of Milan, Italy. beatrice.arosio@unimi.it
2. Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis. Year Published: 2007
Department of Neurological Sciences, Dino Ferrari Center, University of Milan, IRCCS Ospedale Maggiore Policlinico, Milan, Italy.
3. +10 T/C polymorphisms in the gene of transforming growth factor-beta1 are associated with neurodegeneration and its clinical evolution. Year Published: 2007
Geriatric Unit, Ospedale Maggiore Policlinico, IRCCS, University of Milan, Italy. beatrice.arosio@unimi.it
4. Presenilin-1 mutation E318G and familial Alzheimer's disease in the Italian population. Year Published: 2007
Department of Neuroscience, Mario Negri Institute for Pharmacological Research, via Eritrea 62, 20157 Milan, Italy. albani@marionegri.it
5. Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis. Year Published: 2007
Department of Neurological Sciences, Dino Ferrari Center, University of Milan, IRCCS Ospedale Maggiore Policlinico, Milan, Italy.
6. +10 T/C polymorphisms in the gene of transforming growth factor-beta1 are associated with neurodegeneration and its clinical evolution. Year Published: 2007
Geriatric Unit, Ospedale Maggiore Policlinico, IRCCS, University of Milan, Italy. beatrice.arosio@unimi.it
7. Congenital myopathy with type 2A muscle fiber uniformity and smallness. Year Published: 1992
8. Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration. Year Published: 2008
Department of Neurological Sciences, Dino Ferrari Center, University of Milan, IRCCS Ospedale Maggiore Policlinico, Milan, Italy.
9. Congenital myopathy with type 2A muscle fiber uniformity and smallness. Year Published: 1992
10. Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration. Year Published: 2008
Department of Neurological Sciences, Dino Ferrari Center, University of Milan, IRCCS Ospedale Maggiore Policlinico, Milan, Italy.
11. Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple Sclerosis. Year Published: 2008
Department of Neurological Sciences, "Dino Ferrari" Center, University of Milan, IRCCS Ospedale Maggiore Policlinico, Via F. Sforza, 35, 20122, Milan, Italy.
12. Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple Sclerosis. Year Published: 2008
Department of Neurological Sciences, Dino Ferrari Center, University of Milan, IRCCS Ospedale Maggiore Policlinico, Via F. Sforza, 35, 20122, Milan, Italy. daniela.galimberti@unimi.it