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Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.
22 auth.
P. Noris,
S. Perrotta,
M. Seri,
A. Pecci,
C. Gnan,
G. Loffredo,
N. Pujol-Moix,
M. Zecca,
F. Scognamiglio,
D. De Rocco,
...
F. Punzo,
Federica Melazzini,
S. Scianguetta,
M. Casale,
C. Marconi,
T. Pippucci,
G. Amendola,
L. Notarangelo,
C. Klersy,
E. Civaschi,
C. Balduini,
A. Savoia
|
8 |
2011 |
8
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ANKRD26-related thrombocytopenia and myeloid malignancies.
29 auth.
P. Noris,
R. Favier,
M. Alessi,
A. Geddis,
S. Kunishima,
P. Heller,
P. Giordano,
K. Niederhoffer,
J. Bussel,
G. Podda,
N. Vianelli,
R. Kersseboom,
A. Pecci,
C. Gnan,
C. Marconi,
...
A. Auvrignon,
W. Cohen,
Jennifer C. Yu,
A. Iguchi,
Allison Miller Imahiyerobo,
F. Boehlen,
Dorsaf Ghalloussi,
D. De Rocco,
P. Magini,
E. Civaschi,
G. Biino,
M. Seri,
A. Savoia,
C. Balduini
|
7 |
2013 |
7
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Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders.
23 auth.
P. Noris,
G. Biino,
A. Pecci,
E. Civaschi,
A. Savoia,
M. Seri,
Federica Melazzini,
G. Loffredo,
G. Russo,
V. Bozzi,
...
L. Notarangelo,
P. Gresele,
P. Heller,
N. Pujol-Moix,
S. Kunishima,
M. Cattaneo,
J. Bussel,
E. De Candia,
C. Cagioni,
U. Ramenghi,
S. Barozzi,
F. Fabris,
C. Balduini
|
7 |
2014 |
7
🐜
|
|
🐜
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Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations
12 auth.
A. Savoia,
A. Pastore,
D. De Rocco,
E. Civaschi,
M. Di Stazio,
R. Bottega,
...
Federica Melazzini,
V. Bozzi,
A. Pecci,
S. Magrin,
C. Balduini,
P. Noris
|
6 |
2011 |
6
🐜
|
|
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Platelet size for distinguishing between inherited thrombocytopenias and immune thrombocytopenia: a multicentric, real life study
17 auth.
P. Noris,
C. Klersy,
P. Gresele,
F. Giona,
P. Giordano,
P. Minuz,
G. Loffredo,
A. Pecci,
Federica Melazzini,
E. Civaschi,
...
A. Mezzasoma,
M. Piedimonte,
F. Semeraro,
D. Veneri,
F. Menna,
L. Ciardelli,
C. Balduini
|
6 |
2013 |
6
🐜
|
|
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Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation)
22 auth.
P. Noris,
S. Perrotta,
R. Bottega,
A. Pecci,
Federica Melazzini,
E. Civaschi,
S. Russo,
S. Magrin,
G. Loffredo,
V. Di Salvo,
...
G. Russo,
M. Casale,
D. De Rocco,
Claudio Grignani,
M. Cattaneo,
C. Baronci,
A. Dragani,
V. Albano,
M. Jankovic,
S. Scianguetta,
A. Savoia,
C. Balduini
|
6 |
2012 |
6
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|
|
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Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia
65 auth.
P. Noris,
N. Schlegel,
C. Klersy,
P. Heller,
E. Civaschi,
N. Pujol-Moix,
F. Fabris,
R. Favier,
P. Gresele,
V. Latger‐Cannard,
A. Cuker,
P. Nurden,
A. Greinacher,
M. Cattaneo,
E. De Candia,
...
A. Pecci,
M. Hurtaud-Roux,
Ana C Glembotsky,
E. Muñiz-Díaz,
M. Randi,
N. Trillot,
L. Bury,
T. Lecompte,
C. Marconi,
A. Savoia,
C. Balduini,
Sophie Bayart,
A. Bauters,
Schéhérazade Benabdallah-Guedira,
F. Boehlen,
J. Borg,
R. Bottega,
J. Bussel,
D. De Rocco,
E. de Maistre,
M. Faleschini,
E. Falcinelli,
S. Ferrari,
A. Ferster,
T. Fierro,
D. Fleury,
P. Fontana,
C. James,
F. Lanza,
V. Le Cam Duchez,
G. Loffredo,
P. Magini,
D. Martin‐Coignard,
F. Ménard,
S. Mercier,
A. Mezzasoma,
P. Minuz,
I. Nichele,
L. Notarangelo,
T. Pippucci,
G. Podda,
C. Pouymayou,
A. Rigouzzo,
B. Royer,
P. Sié,
V. Siguret,
Catherine Trichet,
A. Tucci,
B. Saposnik,
D. Veneri
|
6 |
2014 |
6
🐜
|
|
🦁
|
Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders
16 auth.
E. Civaschi,
C. Klersy,
Federica Melazzini,
N. Pujol-Moix,
C. Santoro,
M. Cattaneo,
C. Lavenu‐Bombled,
L. Bury,
P. Minuz,
P. Nurden,
...
A. Cid,
A. Cuker,
V. Latger‐Cannard,
R. Favier,
I. Nichele,
P. Noris
|
5 |
2015 |
5
🦁
|
|
🐬
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Personalized reference intervals for platelet count reduce the number of subjects with unexplained thrombocytopenia
Carlo Zaninetti,
G. Biino,
P. Noris,
Federica Melazzini,
E. Civaschi,
C. Balduini
|
4 |
2015 |
4
🐬
|
