F. Trucco
发表
C. Bruno,
V. Capra,
C. Minetti,
2016,
European journal of neurology.
G. Comi,
E. Bertini,
E. Hoffman,
2020,
Annals of clinical and translational neurology.
G. Novelli,
F. Sangiuolo,
G. Morcaldi,
2018,
DNA and cell biology.
Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 gene.
M. Valle,
C. Bruno,
F. Santorelli,
2013,
Biochemical and biophysical research communications.
A. Simonds,
A. Bush,
J. Davies,
2020,
Sleep medicine.
F. Muntoni,
A. Manzur,
F. Trucco,
2022,
Neurology.
V. Ricotti,
F. Muntoni,
L. Servais,
2021,
Muscle & nerve.
C. G. Tay,
F. Muntoni,
P. Munot,
2020,
Chest.
C. G. Tay,
F. Muntoni,
M. Burch,
2020,
Chest.
F. Muntoni,
A. Manzur,
G. Baranello,
2022,
Developmental medicine and child neurology.
R. Finkel,
E. Bertini,
M. Main,
2020,
Neurology.
C. Bruno,
C. Minetti,
C. Fiorillo,
2016,
Respiratory medicine.
G. Comi,
E. Bertini,
M. Pane,
2017,
Neuromuscular Disorders.
F. Zara,
C. Bruno,
C. Minetti,
2016,
Pediatric neurology.
S. Dimauro,
E. Bertini,
A. D’Amico,
2008,
Biochemical and biophysical research communications.
C. Bruno,
C. Minetti,
C. Fiorillo,
2017,
The Journal of international medical research.
M. Pane,
E. Mercuri,
L. Santoro,
2016,
Orphanet Journal of Rare Diseases.
R. Finkel,
E. Mercuri,
F. Muntoni,
2019,
Neuromuscular Disorders.
C. Bruno,
F. Santorelli,
G. Morcaldi,
2015,
Biochemical and biophysical research communications.
P. Lanteri,
C. Bruno,
F. Santorelli,
2018,
JIMD reports.
M. Rosenthal,
A. Bush,
F. Trucco,
2018,
Pediatric pulmonology.
C. Bruno,
F. Santorelli,
A. Romano,
2023,
Neuropediatrics.
M. Zeviani,
E. Lamantea,
C. Bruno,
2015,
JIMD reports.
C. Bruno,
C. Minetti,
A. Pistorio,
2018,
Journal of Telemedicine and Telecare.
M. Main,
F. Muntoni,
M. Scoto,
2020,
Neuromuscular Disorders.
R. Finkel,
M. Pane,
A. Mayhew,
2023,
Neurology and Therapy.
R. J. Ramamurthi,
S. Y. Kim,
H. Y. Wang,
2017,
The New England journal of medicine.
M. Rosenthal,
A. Bush,
F. Trucco,
2019,
Sleep medicine.
A. Covone,
R. Ravazzolo,
C. Minetti,
2016,
Clinical genetics.
M. Pane,
C. Heatwole,
N. Dilek,
2023,
Dysphagia.
Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 gene.
M. Valle,
C. Bruno,
F. Santorelli,
2013,
Biochemical and biophysical research communications.
A. Bush,
F. Trucco,
H. Tan,
2018,
European Respiratory Journal.
A. Bush,
F. Trucco,
2018
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