|
🐜
|
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis
22 auth.
L. Corrado,
R. del Bo,
B. Castellotti,
A. Ratti,
Cristina Cereda,
S. Penco,
G. Soraru',
Y. Carlomagno,
S. Ghezzi,
V. Pensato,
...
C. Colombrita,
S. Gagliardi,
L. Cozzi,
V. Orsetti,
M. Mancuso,
G. Siciliano,
L. Mazzini,
G. Comi,
C. Gellera,
M. Ceroni,
S. D'alfonso,
V. Silani
|
7 |
2009 |
7
🐜
|
|
🐜
|
Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients
28 auth.
M. Guglieri,
F. Magri,
M. D'Angelo,
A. Prelle,
L. Morandi,
C. Rodolico,
R. Cagliani,
M. Mora,
F. Fortunato,
A. Bordoni,
R. del Bo,
S. Ghezzi,
S. Pagliarani,
S. Lucchiari,
S. Salani,
...
C. Zecca,
C. Lamperti,
D. Ronchi,
M. Aguennouz,
P. Ciscato,
C. Di Blasi,
A. Ruggieri,
I. Moroni,
A. Turconi,
A. Toscano,
M. Moggio,
N. Bresolin,
G. Comi
|
7 |
2008 |
7
🐜
|
|
🐜
|
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up
21 auth.
F. Magri,
A. Govoni,
M. D'Angelo,
R. Bo,
S. Ghezzi,
Gandossini Sandra,
A. Turconi,
M. Sciacco,
P. Ciscato,
A. Bordoni,
...
S. Tedeschi,
F. Fortunato,
V. Lucchini,
S. Bonato,
C. Lamperti,
D. Coviello,
Y. Torrente,
S. Corti,
M. Moggio,
N. Bresolin,
G. Comi
|
7 |
2011 |
7
🐜
|
|
🐜
|
Isolation and characterization of murine neural stem/progenitor cells based on Prominin-1 expression
12 auth.
S. Corti,
M. Nizzardo,
M. Nardini,
C. Donadoni,
F. Locatelli,
D. Papadimitriou,
...
S. Salani,
R. Bo,
S. Ghezzi,
S. Strazzer,
N. Bresolin,
G. Comi
|
6 |
2007 |
6
🐜
|
|
🐜
|
Vascular endothelial growth factor gene variability is associated with increased risk for AD
14 auth.
R. del Bo,
M. Scarlato,
S. Ghezzi,
F. Martinelli Boneschi,
C. Fenoglio,
Sara Galbiati,
R. Virgilio,
D. Galimberti,
G. Galimberti,
M. Crimi,
...
C. Ferrarese,
E. Scarpini,
N. Bresolin,
G. Comi
|
6 |
2005 |
6
🐜
|
|
🐜
|
Inhibiting angiotensin-converting enzyme promotes renal repair by limiting progenitor cell proliferation and restoring the glomerular architecture.
9 auth.
A. Benigni,
M. Morigi,
P. Rizzo,
E. Gagliardini,
Cinzia Rota,
M. Abbate,
...
S. Ghezzi,
A. Remuzzi,
G. Remuzzi
|
6 |
2011 |
6
🐜
|
|
🐜
|
TARDBP (TDP‐43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations
16 auth.
R. Bo,
S. Ghezzi,
S. Corti,
Massimo Pandolfo,
M. Ranieri,
D. Santoro,
Isabella Ghione,
A. Prelle,
V. Orsetti,
M. Mancuso,
...
G. Soraru',
Chiara Briani,
Corrado Angelini,
Gabriele Siciliano,
N. Bresolin,
Giacomo P. Comi
|
6 |
2009 |
6
🐜
|
|
🐜
|
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction
15 auth.
R. Bo,
M. Moggio,
M. Rango,
S. Bonato,
Mg D'Angelo,
S. Ghezzi,
G. Airoldi,
M. Bassi,
M. Guglieri,
L. Napoli,
...
C. Lamperti,
S. Corti,
Antonio Federico,
N. Bresolin,
G. Comi
|
6 |
2008 |
6
🐜
|
|
🐜
|
Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation
17 auth.
A. Bersano,
R. Bo,
C. Lamperti,
S. Ghezzi,
G. Fagiolari,
F. Fortunato,
E. Ballabio,
M. Moggio,
L. Candelise,
D. Galimberti,
...
R. Virgilio,
S. Lanfranconi,
Y. Torrente,
M. Carpo,
N. Bresolin,
G. Comi,
S. Corti
|
6 |
2009 |
6
🐜
|
|
🐜
|
Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutation
11 auth.
R. Bo,
Franco Locatelli,
S. Corti,
M. Scarlato,
S. Ghezzi,
A. Prelle,
...
G. Fagiolari,
M. Moggio,
M. Carpo,
N. Bresolin,
G. Comi
|
6 |
2006 |
6
🐜
|
