G. Astrea
发表
R. Vallee,
C. Bruno,
F. Santorelli,
2014,
Human mutation.
L. Servais,
I. Nelson,
N. Romero,
2016,
American journal of human genetics.
G. Comi,
E. Bertini,
E. Hoffman,
2012,
Neurology.
E. Bertini,
M. Pane,
E. Mercuri,
2015,
Journal of Neurology.
P. Striano,
A. Orsini,
R. Battini,
2022,
Epilepsy & Behavior.
G. Cioni,
C. Bruno,
F. Santorelli,
2015,
Research in developmental disabilities.
M. Tosetti,
C. Bruno,
R. Battini,
2012,
Neurology.
L. Magliano,
M. Pane,
A. D’Amico,
2015,
Muscle & nerve.
L. Magliano,
M. Pane,
A. D’Amico,
2014,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
G. Gigli,
C. Cereda,
A. Federico,
2018,
Front. Neurol..
G. Comi,
E. Bertini,
E. Hoffman,
2020,
Annals of clinical and translational neurology.
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.
K. Bushby,
F. Muntoni,
A. Manzur,
2017,
Neuromuscular Disorders.
L. Magliano,
M. Pane,
A. D’Amico,
2013,
Journal of Neurology.
G. Cioni,
A. Tessa,
F. Santorelli,
2021,
Journal of the Neurological Sciences.
L. Billeci,
A. Tonacci,
R. Battini,
2022,
2022 IEEE International Conference on Pervasive Computing and Communications Workshops and other Affiliated Events (PerCom Workshops).
F. Santorelli,
R. Massa,
A. Petrucci,
2016,
BMC Medical Genetics.
F. Santorelli,
R. Battini,
M. Donati,
2015,
Journal of neuromuscular diseases.
G. Comi,
C. Angelini,
C. Bruno,
2018,
Neuromuscular Disorders.
E. Bertini,
G. Cioni,
R. Battini,
2021,
Brain and Development.
L. Magliano,
M. Pane,
A. D’Amico,
2017,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
E. Hoffman,
M. Pane,
E. Mercuri,
2022,
Journal of Neurology.
G. Cioni,
E. Mercuri,
F. Muntoni,
2015,
Pediatric neurology.
G. Comi,
E. Bertini,
M. Pane,
2017,
Italian Journal of Pediatrics.
E. Bertini,
A. D’Amico,
C. Bruno,
2018,
Neurological Sciences.
G. Tedeschi,
G. De Michele,
A. Filla,
2021,
International journal of molecular sciences.
E. Mercuri,
A. Federico,
G. Siciliano,
2019,
Neurology: Genetics.
N. Bresolin,
G. Comi,
S. Corti,
2020,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
F. Santorelli,
R. Battini,
G. Astrea,
2016,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
Raffaele Conte,
Francesco Sansone,
Alessandro Tonacci,
2018,
Converging Clinical and Engineering Research on Neurorehabilitation III.
C. Bruno,
F. Santorelli,
R. Biancheri,
2012,
neurogenetics.
M. Pane,
E. Mercuri,
F. Muntoni,
2020,
Genetics in Medicine.
Raffaele Conte,
Alessandro Tonacci,
Ilaria Ceppa,
2019,
HEALTHINF.
G. Comi,
E. Bertini,
P. Striano,
2018,
Orphanet Journal of Rare Diseases.
G. Comi,
E. Bertini,
E. Mercuri,
2016,
Neurology.
G. Comi,
E. Bertini,
F. Bianco,
2015,
Neurology.
E. Mercuri,
F. Muntoni,
T. Yousry,
2021,
Neuromuscular Disorders.
Alessandra Toncelli,
Gianluigi Tiberi,
Maria Evelina Fantacci,
2015,
2015 IEEE International Symposium on Medical Measurements and Applications (MeMeA) Proceedings.
Maria Evelina Fantacci,
Alessandra Retico,
Chiara Sottocornola,
2015,
2015 IEEE International Symposium on Medical Measurements and Applications (MeMeA) Proceedings.
M. Tosetti,
M. Fantacci,
A. Retico,
2015
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M. Tosetti,
G. Cioni,
E. Mercuri,
2009,
Neuromuscular Disorders.
A. Filla,
A. Tessa,
F. Santorelli,
2021,
Journal of Neurology.
M. Pane,
E. Mercuri,
L. Santoro,
2016,
Orphanet Journal of Rare Diseases.
P. Lanteri,
C. Bruno,
F. Santorelli,
2018,
JIMD reports.
G. Cioni,
M. Pane,
E. Mercuri,
2018,
PloS one.
E. Bertini,
G. Cioni,
R. Battini,
2015,
BMC Medical Genetics.
Silvio C. E. Tosatto,
E. Bertini,
M. Pane,
2022,
Acta neuropathologica communications.
P. Striano,
A. Coppola,
G. Cantalupo,
2022,
Neurology: Genetics.
E. Bertini,
A. Jezela-Stanek,
R. Płoski,
2019,
Journal of Neurology.
A. D’Amico,
F. Santorelli,
L. Politano,
2016,
Neuromuscular Disorders.
A. Durr,
F. Rivier,
G. Stevanin,
2018,
Human mutation.
C. Bruno,
F. Santorelli,
R. Battini,
2013,
Neuromuscular Disorders.
S. Roccella,
A. Tonacci,
F. Santorelli,
2021,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
F. Santorelli,
A. Rubegni,
G. Astrea,
2019,
Neurology.
Maria Evelina Fantacci,
Alessandra Retico,
Chiara Sottocornola,
2015,
BIOIMAGING.
Stefano Roccella,
Francesco Sansone,
Alessandro Tonacci,
2019,
2019 IEEE 23rd International Symposium on Consumer Technologies (ISCT).
M. Grandis,
L. Politano,
G. Astrea,
2021,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
F. Coppedè,
L. Migliore,
G. Siciliano,
2007,
American journal of medical genetics. Part A.
G. Comi,
G. Gigli,
G. Siciliano,
2023,
Genes.
F. Santorelli,
R. Battini,
L. Bartalena,
2014,
Journal of child neurology.
F. Santorelli,
R. Battini,
L. Bartalena,
2013
.
S. Robertson,
K. Devriendt,
M. Digilio,
2023,
Journal of Medical Genetics.
G. Siciliano,
A. Malandrini,
F. Santorelli,
2022,
International journal of molecular sciences.
M. Main,
E. Mazzone,
G. Vasco,
2009,
Neuromuscular Disorders.
L. Wilkins,
G. Comi,
E. Bertini,
2016,
Neurology.
A. Orsini,
R. Battini,
A. Rubegni,
2023,
Genes.
F. Santorelli,
R. Battini,
M. Donati,
2015,
Journal of neuromuscular diseases.
G. Comi,
E. Bertini,
F. Bianco,
2015,
Neurology.
L. Magliano,
M. Pane,
A. D’Amico,
2017,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
C. Bruno,
F. Santorelli,
R. Biancheri,
2012,
neurogenetics.
D. De Grandis,
A. Filla,
A. Tessa,
2014,
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.
M. Pane,
L. Bello,
A. Berardinelli,
2024,
Journal of neuromuscular diseases.
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.
G. Comi,
C. Angelini,
C. Bruno,
2018,
Neuromuscular Disorders.