I. Bruno
发表
G. Gigli,
C. Cereda,
A. Federico,
2018,
Front. Neurol..
M. Pennesi,
F. Marchetti,
I. Bruno,
2003,
Pediatric Nephrology.
A. Tommasini,
I. Berti,
F. Faletra,
2012,
Acta paediatrica.
C. Stanley,
P. Gasparini,
S. Shyng,
2013,
Gene.
E. Barbi,
F. Sirchia,
I. Bruno,
2022,
Italian Journal of Pediatrics.
C. Mercer,
N. Brunetti‐Pierri,
M. Lindsay,
2022,
American journal of medical genetics. Part A.
A. Sarti,
A. Ventura,
E. Barbi,
2003,
Archives of pediatrics & adolescent medicine.
G. M. Severini,
S. Cappellani,
A. Fabretto,
2019,
Molecular genetics & genomic medicine.
N. Brunetti‐Pierri,
F. Santorelli,
T. Reimand,
2022,
Human molecular genetics.
A. d'Adamo,
E. Barbi,
A. Bianco,
2020,
American journal of medical genetics. Part A.
M. Bobbo,
G. Sinagra,
E. Barbi,
2022,
Pediatric Drugs.
P. Gasparini,
A. Tommasini,
I. Berti,
2012,
Dermatology.
E. Barbi,
F. Baldo,
I. Bruno,
2021,
BMC Pediatrics.
E. Barbi,
I. Berti,
Emma Sartor,
2021,
American journal of medical genetics. Part A.
A. Ventura,
I. Berti,
C. Belcaro,
2015,
Italian Journal of Pediatrics.
P. Gasparini,
A. d'Adamo,
S. Biskup,
2014,
American journal of medical genetics. Part A.
J. Hoenicka,
J. Baptista,
A. Fry,
2021,
American journal of medical genetics. Part A.
L. Basso,
E. Barbi,
M. Trojniak,
2020,
Pediatric Drugs.
A. Sarti,
A. Ventura,
E. Barbi,
2003
.
G. Cozzi,
E. Barbi,
S. Romano,
2019,
Italian Journal of Pediatrics.
A. Sarti,
E. Barbi,
G. Zanazzo,
2005,
Journal of pediatric hematology/oncology.
A. Tommasini,
I. Bruno,
A. Magnolato,
2018,
World journal of clinical pediatrics.
A. Occhipinti,
E. Favaretto,
I. Bruno,
2021,
The Journal of pediatrics.
P. Gasparini,
F. Faletra,
V. Pecile,
2012,
European journal of medical genetics.
F. Magni,
C. Chinello,
Andrew Smith,
2017,
Skin Pharmacology and Physiology.
P. Mazzanti,
C. Mussi,
D. Cucinotta,
2020,
Journal of the American Medical Directors Association.
A. Selicorni,
I. Bruno,
2021,
Medico e Bambino.
C. Palermo,
M. Pane,
A. D’Amico,
2023,
European journal of neurology.
P. Striano,
F. Zara,
M. Severino,
2023,
Frontiers in Pediatrics.
A Novel CRYBB2 Missense Mutation Causing Congenital Autosomal Dominant Cataract in an Italian Family
P. Gasparini,
A. d'Adamo,
S. Pensiero,
2013,
Ophthalmic genetics.
A. Ventura,
F. Faletra,
S. Naviglio,
2015,
Jornal de Pediatria.
I. Bruno,
2011
.
A. Ballabeni,
A. Lund,
N. Guffon,
2023,
Journal of inherited metabolic disease.
A. Ventura,
I. Bruno,
I. Rabach,
2016,
Archives of Disease in Childhood.
E. Barbi,
F. Sirchia,
I. Bruno,
2020,
American journal of medical genetics. Part A.
E. Barbi,
L. Calligaris,
I. Bruno,
2013,
Paediatric anaesthesia.
A. Ventura,
E. Barbi,
I. Bruno,
2005,
The Journal of pediatrics.
P. Mazzanti,
C. Mussi,
D. Cucinotta,
2020,
Journal of the American Medical Directors Association.