|
π
|
Emergence of KRAS mutations and acquired resistance to anti-EGFR therapy in colorectal cancer
26 auth.
S. Misale,
R. Yaeger,
S. Hobor,
E. Scala,
M. Janakiraman,
D. LΓΕ‘ka,
E. Valtorta,
R. Schiavo,
M. Buscarino,
G. Siravegna,
K. Bencardino,
A. Cercek,
Ching-Tung Chen,
S. Veronese,
C. Zanon,
...
A. Sartore-Bianchi,
M. Gambacorta,
M. Gallicchio,
E. Vakiani,
Valentina Boscaro,
E. Medico,
M. Weiser,
S. Siena,
F. Nicolantonio,
D. Solit,
A. Bardelli
|
10 |
2012 |
10
π
|
|
π
|
Amplification of the MET receptor drives resistance to anti-EGFR therapies in colorectal cancer.
28 auth.
A. Bardelli,
S. Corso,
A. Bertotti,
S. Hobor,
E. Valtorta,
G. Siravegna,
A. Sartore-Bianchi,
E. Scala,
A. Cassingena,
D. Zecchin,
M. Apicella,
Giorgia Migliardi,
F. Galimi,
C. Lauricella,
C. Zanon,
...
T. Perera,
S. Veronese,
G. Corti,
A. Amatu,
M. Gambacorta,
L. Diaz,
M. Sausen,
V. Velculescu,
P. Comoglio,
L. Trusolino,
F. Di Nicolantonio,
S. Giordano,
S. Siena
|
9 |
2013 |
9
π
|
|
π
|
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome.
20 auth.
F. Mari,
Sara Azimonti,
I. Bertani,
F. Bolognese,
E. Colombo,
R. Caselli,
E. Scala,
I. Longo,
S. Grosso,
C. Pescucci,
...
F. Ariani,
G. Hayek,
P. Balestri,
Anna Bergo,
G. Badaracco,
M. Zappella,
V. Broccoli,
A. Renieri,
C. Kilstrup-Nielsen,
N. Landsberger
|
8 |
2005 |
8
π
|
|
π¦
|
CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms
12 auth.
E. Scala,
F. Ariani,
F. Mari,
R. Caselli,
C. Pescucci,
I. Longo,
...
I. Meloni,
D. Giachino,
M. Bruttini,
G. Hayek,
M. Zappella,
A. Renieri
|
7 |
2005 |
7
π¦
|
|
π
|
KRAS gene amplification in colorectal cancer and impact on response to EGFRβtargeted therapy
21 auth.
E. Valtorta,
S. Misale,
A. Sartore-Bianchi,
I. Nagtegaal,
F. Paraf,
C. Lauricella,
V. Dimartino,
S. Hobor,
B. Jacobs,
Cristiana Ercolani,
...
S. Lamba,
E. Scala,
S. Veronese,
P. Laurent-Puig,
S. Siena,
S. Tejpar,
M. Mottolese,
C. Punt,
M. Gambacorta,
A. Bardelli,
F. Nicolantonio
|
7 |
2013 |
7
π
|
|
π
|
Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene.
12 auth.
C. Pescucci,
F. Mari,
I. Longo,
P. Vogiatzi,
R. Caselli,
E. Scala,
...
C. Abaterusso,
R. Gusmano,
M. Seri,
N. Miglietti,
E. Bresin,
A. Renieri
|
7 |
2004 |
7
π
|
|
π
|
Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)
11 auth.
A. Renieri,
F. Mari,
M. Mencarelli,
E. Scala,
F. Ariani,
I. Longo,
...
I. Meloni,
Gabriele Cevenini,
Giorgio Pini,
G. Hayek,
M. Zappella
|
6 |
2009 |
6
π
|
|
π¦
|
MECP2 deletions and genotypeβphenotype correlation in Rett syndrome
16 auth.
E. Scala,
I. Longo,
F. Ottimo,
C. Speciale,
K. Sampieri,
E. Katzaki,
R. Artuso,
M. Mencarelli,
T. D'Ambrogio,
Giuseppina Vonella,
...
M. Zappella,
G. Hayek,
A. Battaglia,
F. Mari,
A. Renieri,
F. Ariani
|
5 |
2007 |
5
π¦
|
|
π
|
Autosomal recessive Alport syndrome: an in-depth clinical and molecular analysis of five families.
15 auth.
I. Longo,
E. Scala,
F. Mari,
R. Caselli,
C. Pescucci,
M. Mencarelli,
C. Speciale,
M. Giani,
E. Bresin,
D. Caringella,
...
Z. Borochowitz,
K. Siriwardena,
I. Winship,
A. Renieri,
I. Meloni
|
5 |
2006 |
5
π
|
|
π
|
Italian Rett database and biobank
16 auth.
K. Sampieri,
I. Meloni,
E. Scala,
F. Ariani,
R. Caselli,
C. Pescucci,
I. Longo,
R. Artuso,
M. Bruttini,
M. Mencarelli,
...
C. Speciale,
V. Causarano,
G. Hayek,
M. Zappella,
A. Renieri,
F. Mari
|
5 |
2007 |
5
π
|
|
π
|
Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis--a collaborative study of the Italian Renal Immunopathology Group.
14 auth.
G. FrascΓ ,
A. OnettiβMuda,
F. Mari,
I. Longo,
E. Scala,
C. Pescucci,
D. Roccatello,
M. Alpa,
R. Coppo,
G. Li Volti,
...
S. Feriozzi,
F. Bergesio,
F. Schena,
A. Renieri
|
4 |
2005 |
4
π
|
