F. Fattori
发表
N. Romero,
E. Ricci,
L. Morandi,
2014,
Journal of Medical Genetics.
E. Bertini,
M. Pane,
E. Mercuri,
2015,
Journal of Neurology.
E. Bertini,
I. Yavuz,
F. Fattori,
2012,
BMJ Case Reports.
E. Bertini,
A. D’Amico,
N. Romero,
2014,
Muscle & nerve.
N. Romero,
E. Bertini,
S. Sacconi,
2017,
Clinical genetics.
E. Bertini,
R. Carrozzo,
F. Santorelli,
2011,
neurogenetics.
E. Bertini,
A. Bruselles,
M. Tartaglia,
2018,
Human molecular genetics.
E. Bertini,
A. D’Amico,
C. Bruno,
2019,
Neuromuscular Disorders.
A. D’Amico,
M. Tartaglia,
C. Bruno,
2018,
Clinical genetics.
N. Bresolin,
G. Comi,
S. Corti,
2016,
Journal of Molecular Neuroscience.
E. Bertini,
A. D’Amico,
E. Ricci,
2015,
Neuromuscular Disorders.
I. Nelson,
A. D’Amico,
R. Carlier,
2021,
Brain : a journal of neurology.
A. D’Amico,
A. Amodeo,
A. Novelli,
2022,
Journal of cardiovascular development and disease.
E. Bertini,
Hui Jiang,
E. Arbustini,
2016,
The Journal of clinical investigation.
E. Bertini,
A. D’Amico,
C. Bruno,
2016,
Neuromuscular Disorders.
E. Bertini,
A. Bizzi,
A. D’Amico,
2012,
Neuromuscular Disorders.
L. Minati,
E. Prodi,
G. Uziel,
2013,
European journal of neurology.
E. Bertini,
V. Petruzzella,
R. Carrozzo,
2013,
Journal of Inherited Metabolic Disease.
E. Bertini,
M. Pane,
E. Mercuri,
2013,
Neuromuscular Disorders.
E. Bertini,
F. Callea,
E. Bellacchio,
2016,
Leukemia & lymphoma.
G. Comi,
E. Bertini,
M. Pane,
2017,
Italian Journal of Pediatrics.
E. Bertini,
C. Ottenheijm,
M. Salvetti,
2020,
Neuromuscular Disorders.
E. Bertini,
A. D’Amico,
M. Tartaglia,
2014,
Journal of Neurology.
E. Bertini,
E. Mercuri,
F. Muntoni,
2017,
Journal of Neurology, Neurosurgery, and Psychiatry.
M. Pane,
E. Mercuri,
A. D’Amico,
2022,
International journal of molecular sciences.
E. Ricci,
G. Tasca,
M. Monforte,
2020,
Journal of the Neurological Sciences.
E. Bertini,
M. Di Stazio,
E. Bellacchio,
2014,
Oral health and dental management.
N. Drouot,
M. Koenig,
F. Santorelli,
2010,
Journal of Neurology.
E. Bertini,
M. Pane,
E. Mercuri,
2020,
Frontiers in Genetics.
E. Bertini,
N. Romero,
C. Paradas,
2018,
Acta Neuropathologica Communications.
R. Carrozzo,
F. Zara,
A. Tessa,
2006,
Biochemical and biophysical research communications.
Alessandro Bruselles,
Bjarne Udd,
Alessandra Ferlini,
2017,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
F. Rivier,
C. Béroud,
E. Malfatti,
2021,
Journal of Neurology.
G. Comi,
E. Bertini,
P. Striano,
2018,
Orphanet Journal of Rare Diseases.
G. Comi,
E. Bertini,
E. Mercuri,
2018,
Genes.
V. Petruzzella,
A. Federico,
A. Tessa,
2007,
Biochemical and biophysical research communications.
E. Bertini,
F. Callea,
E. Bellacchio,
2017,
Leukemia & lymphoma.
A. Tessa,
F. Santorelli,
A. Romano,
2012,
Human mutation.
Silvio C. E. Tosatto,
E. Bertini,
M. Pane,
2022,
Acta neuropathologica communications.
E. Bertini,
R. Carrozzo,
A. D’Amico,
2018,
European Journal of Human Genetics.
R. Carrozzo,
A. Tessa,
F. Santorelli,
2007,
Bioscience reports.
A. D’Amico,
S. Vicari,
F. De Crescenzo,
2016,
The Journal of adolescent health : official publication of the Society for Adolescent Medicine.
L. Mesrob,
A. D’Amico,
E. Malfatti,
2018,
Muscle & nerve.
P. Tonali,
F. Santorelli,
M. Masciullo,
2008,
Journal of Neurology.
S. Servidei,
E. Bertini,
G. Primiano,
2021,
Neuromuscular Disorders.
E. Bertini,
E. Mercuri,
E. Ricci,
2012,
Acta Neuropathologica.
N. Bresolin,
G. Comi,
S. Corti,
2016,
Journal of Molecular Neuroscience.
E. Bertini,
N. Romero,
C. Paradas,
2018,
Acta neuropathologica communications.
C. Bruno,
F. Santorelli,
C. Minetti,
2011,
Biochemical and biophysical research communications.
E. Bertini,
S. Züchner,
F. Santorelli,
2021,
Frontiers in Neurology.
A. D’Amico,
A. Longo,
M. Paglietti,
2021,
Orphanet Journal of Rare Diseases.
A. D’Amico,
E. Bertini,
E. Bellacchio,
2013,
Neuromuscular Disorders.
Insights from genotype–phenotype correlations by novel SPEG mutations causing centronuclear myopathy
E. Bertini,
H. Per,
J. Bevilacqua,
2017,
Neuromuscular Disorders.
R. Carrozzo,
F. Pierelli,
F. Santorelli,
2009,
Neuromuscular Disorders.
S. Pro,
D. Diodato,
Guglielmo Salvatori,
2023,
Journal of personalized medicine.
Identification of a new mtDNA mutation (14724G>A) associated with mitochondrial leukoencephalopathy.
A. Tessa,
F. Santorelli,
L. Vilarinho,
2007,
Biochemical and biophysical research communications.
E. Bertini,
N. Romero,
J. Böhm,
2016,
Journal of neuromuscular diseases.
S. Dimauro,
R. Carrozzo,
M. Zeviani,
2007,
Journal of Medical Genetics.
A. Amodeo,
A. Novelli,
A. Secinaro,
2023,
Frontiers in cardiovascular medicine.
A. D’Amico,
M. Tartaglia,
C. Bruno,
2017,
Neuromuscular Disorders.
R. Boldrini,
E. Bertini,
E. Ricci,
2016,
Journal of Neurology.
E. Bertini,
R. Carrozzo,
A. D’Amico,
2018,
European Journal of Human Genetics.
L. Guyant‐Maréchal,
G. Demidov,
B. Udd,
2023,
Journal of Medical Genetics.
A. D’Amico,
S. Vicari,
F. De Crescenzo,
2016,
The Journal of adolescent health : official publication of the Society for Adolescent Medicine.