L. Ronzoni
发表
A. Pantaleo,
F. Turrini,
M. Cappellini,
2014,
Haematologica.
G. Rembouskos,
R. Ficarella,
P. Volpe,
2020,
Prenatal diagnosis.
A. Iolascon,
S. Alper,
M. Cappellini,
2007,
Haematologica.
E. Monti,
M. Cappellini,
B. Venerando,
2006,
Glycoconjugate Journal.
D. Milani,
S. Esposito,
L. Ronzoni,
2015,
Journal of Pediatric Genetics.
M. Cappellini,
G. Fossati,
L. Porretti,
2014,
British journal of haematology.
M. Cappellini,
D. Rusconi,
L. Ronzoni,
2008,
Blood cells, molecules & diseases.
P. Chiurazzi,
D. Milani,
M. Viri,
2015
.
M. Cappellini,
A. Aghemo,
L. Porretti,
2014,
Journal of viral hepatitis.
D. Milani,
S. Esposito,
A. Tucci,
2016,
BMC Medical Genetics.
L. Valenti,
F. Peyvandi,
S. Pelusi,
2022,
JHEP Reports.
F. Peyvandi,
S. Pelusi,
A. Tripodi,
2022,
JHEP reports : innovation in hepatology.
S. Pelusi,
M. Maggioni,
Luca Valenti,
2022,
Liver international : official journal of the International Association for the Study of the Liver.
E. Agolini,
C. Cesaretti,
F. Natacci,
2022,
Prenatal diagnosis.
A. Novelli,
F. Triulzi,
M. Bedeschi,
2016,
Cytogenetic and Genome Research.
A. Barrett,
S. Morris,
S. Langlois,
2015,
European Journal of Human Genetics.
L. N. Valenti,
H. Reeves,
V. Vaira,
2022,
Journal of hepatology.
A. Iolascon,
M. Cappellini,
L. De Franceschi,
2011,
Haematologica.
D. Taramelli,
M. Cappellini,
S. Ward,
2010,
Toxicology.
G. Scuvera,
D. Milani,
S. Esposito,
2017,
American journal of medical genetics. Part A.
P. Vizziello,
F. Lalatta,
M. Bedeschi,
2020,
Prenatal diagnosis.
p57Kip2 is a downstream effector of BCR-ABL kinase inhibitors in chronic myelogenous leukemia cells.
S. Perrotta,
F. Della Ragione,
A. Borriello,
2011,
Carcinogenesis.
S. Perrotta,
F. Della Ragione,
A. Migliaccio,
2010,
PloS one.
S. Perrotta,
F. Della Ragione,
A. Migliaccio,
2010,
PloS one.
Claudio Cantú,
Vito Grande,
Ilaria Alborelli,
2010,
Nucleic Acids Res..
D. Milani,
S. Esposito,
A. Tucci,
2016,
American journal of medical genetics. Part A.
S. Perrotta,
B. Oostra,
F. Della Ragione,
2011,
Orphanet journal of rare diseases.
G. Melloni,
C. Cesaretti,
F. Natacci,
2013
.
Luca Valenti,
L. Ronzoni,
2022,
Liver international : official journal of the International Association for the Study of the Liver.
F. Lalatta,
M. Bedeschi,
S. Guerneri,
2015,
American journal of medical genetics. Part A.
M. Cappellini,
G. Graziadei,
E. Ferru,
2015,
Blood cells, molecules & diseases.
A. Lombardi,
F. Ceriotti,
L. Terranova,
2021,
Transfusion.
G. Targher,
A. Mantovani,
S. Pelusi,
2023,
Alimentary pharmacology & therapeutics.
F. Lalatta,
L. Ronzoni,
G. Silibello,
2018,
Prenatal Diagnosis.
L. Valenti,
S. Bosis,
C. Tagliabue,
2023,
Frontiers in Pediatrics.
L. N. Valenti,
E. Parks,
R. Rector,
2023,
JHEP reports : innovation in hepatology.
E. Ferrazzi,
C. Soldavini,
F. D’Ambrosi,
2020,
Journal of Ultrasound.
G. Scuvera,
V. Saletti,
D. Milani,
2015,
Congenital anomalies.
D. Milani,
S. Esposito,
L. Pezzani,
2017,
European journal of medical genetics.
D. Milani,
S. Esposito,
L. Ronzoni,
2015,
Journal of Pediatric Genetics.
A. Iolascon,
M. Cappellini,
L. De Franceschi,
2011,
Haematologica.
A. Pantaleo,
F. Turrini,
M. Cappellini,
2014,
Haematologica.
M. Cappellini,
G. Fossati,
L. Porretti,
2014,
British journal of haematology.
V. Hernández-Gea,
Luca Valenti,
L. Ronzoni,
2023,
Liver international : official journal of the International Association for the Study of the Liver.
S. Pelusi,
Luca Valenti,
C. Bianco,
2023,
Frontiers in Genetics.
A. Novelli,
F. Triulzi,
M. Bedeschi,
2016,
Cytogenetic and Genome Research.