D. Diodato
发表
Daniele Ghezzi,
Massimo Zeviani,
Cristina Smiderle,
2011,
Nature Genetics.
E. Bertini,
D. Diodato,
D. Martinelli,
2015,
Orphanet Journal of Rare Diseases.
V. Tiranti,
D. Diodato,
A. Ardissone,
2022,
Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases.
M. Mancuso,
C. La Morgia,
G. Siciliano,
2020,
neurogenetics.
E. Bertini,
G. Vasco,
M. Petrarca,
2020,
Journal of Neuroscience Methods.
M. Mancuso,
C. La Morgia,
G. Siciliano,
2021,
Journal of clinical medicine.
Robert W. Taylor,
R. Boostani,
T. Haaf,
2018,
BMC Medical Genetics.
Ich,
M. Baumgartner,
H. Blom,
2019
.
M. Baumgartner,
H. Blom,
L. Vilarinho,
2016,
Journal of Inherited Metabolic Disease.
E. Bertini,
A. Vanderver,
Q. Waisfisz,
2017,
Neurology.
S. Pro,
D. Diodato,
D. Martinelli,
2019,
Neuroradiology.
E. Mercuri,
R. Battini,
D. Diodato,
2020,
Journal of inherited metabolic disease.
M. Minczuk,
T. Meitinger,
T. Strom,
2014,
Human mutation.
E. Bertini,
R. Carrozzo,
A. D’Amico,
2015,
European Journal of Human Genetics.
V. Tiranti,
D. Ghezzi,
D. Diodato,
2014,
International journal of cell biology.
M. L. Ciofi Degli Atti,
D. Diodato,
M. Paglietti,
2022,
Italian Journal of Pediatrics.
Robert W. Taylor,
E. Bertini,
T. Meitinger,
2017
.
Robert W. Taylor,
E. Bertini,
T. Meitinger,
2014,
American journal of human genetics.
D. Diodato,
S. Boenzi,
2018,
Essays in biochemistry.
M. Baumgartner,
B. Seifert,
H. Blom,
2018,
Journal of Inherited Metabolic Disease.
A. Vanderver,
R. Schiffmann,
T. Meitinger,
2014,
Neurology.
D. Diodato,
M. Mario,
F. Filippo,
2016
.
S. Pro,
Massimiliano Valeriani,
A. D’Amico,
2021,
Clinical Neurophysiology.
E. Bertini,
R. Carrozzo,
A. D’Amico,
2019,
Human mutation.
A. Vanderver,
R. Taft,
C. V. van Karnebeek,
2017,
Pediatric neurology.
E. Bertini,
R. Carrozzo,
E. Lamantea,
2016,
Journal of Neurology.
A. D’Amico,
E. Bertini,
D. Diodato,
2022,
Neuromuscular Disorders.
J. Nauta,
P. Delrée,
D. Diodato,
2021,
Kidney international reports.
T. Wieland,
A. Munnich,
H. Smeets,
2018
.
D. Diodato,
F. Cipullo,
S. Sampaolo,
2011,
Acta Myologica.
E. Bertini,
R. Carrozzo,
M. Zeviani,
2018,
Journal of Human Genetics.
R. Carrozzo,
D. Diodato,
D. Martinelli,
2018,
Clinica chimica acta; international journal of clinical chemistry.
G. Comi,
M. Zeviani,
M. Mancuso,
2017,
Journal of Neurology.
E. Bertini,
R. Carrozzo,
Domenico de Rasmo,
2018,
Human molecular genetics.
E. Bertini,
R. Carrozzo,
Domenico de Rasmo,
2018,
Human molecular genetics.
M. Baumgartner,
B. Seifert,
H. Blom,
2019,
Journal of inherited metabolic disease.
Robert W. Taylor,
A. Ballabio,
E. Bertini,
2020,
Journal of inherited metabolic disease.
E. Bertini,
A. Vanderver,
R. Carrozzo,
2016,
Brain : a journal of neurology.
E. Bertini,
R. Carrozzo,
M. Zeviani,
2017,
Biochimica et biophysica acta. Molecular basis of disease.
M. Zeviani,
E. Lamantea,
D. Ghezzi,
2012,
Neuromuscular Disorders.
Robert W. Taylor,
H. Prokisch,
H. Mandel,
2018,
Human mutation.
V. Tiranti,
M. Zeviani,
D. Diodato,
2016,
Brain : a journal of neurology.
E. Bertini,
R. Carrozzo,
M. Tartaglia,
2017,
Clinical genetics.
Robert W. Taylor,
J. Casey,
A. Vanderver,
2016,
Journal of Medical Genetics.
E. Bertini,
R. Carrozzo,
A. D’Amico,
2017,
Clinical genetics.
F. Gianfrancesco,
T. Esposito,
G. Limongelli,
2013,
Orphanet Journal of Rare Diseases.
E. Bertini,
R. Carrozzo,
G. Parisi,
2014,
Mitochondrion.
G. Comi,
M. Zeviani,
M. Mancuso,
2016,
Neuromuscular Disorders.
E. Bertini,
C. Compagnucci,
A. Coppola,
2016,
American journal of human genetics.
F. Gianfrancesco,
T. Esposito,
L. del Viscovo,
2013,
Orphanet Journal of Rare Diseases.
E. Bertini,
S. Pro,
D. Diodato,
2019,
Orphanet Journal of Rare Diseases.
M. Mancuso,
E. Lamantea,
C. Bruno,
2021,
Orphanet Journal of Rare Diseases.
N. Lax,
D. Turnbull,
D. Diodato,
2010,
Biochimica et biophysica acta.
M. Zeviani,
H. Prokisch,
E. Lamantea,
2015,
JIMD reports.
E. Bertini,
R. Carrozzo,
H. Prokisch,
2021,
Human mutation.
E. Lamantea,
D. Ghezzi,
D. Diodato,
2015,
JIMD reports.
M. Zeviani,
E. Lamantea,
C. Bruno,
2015,
JIMD reports.
Robert W. Taylor,
T. Wieland,
A. Munnich,
2018,
Orphanet Journal of Rare Diseases.
F. Santorelli,
S. Sotgiu,
D. Diodato,
2019,
BMC Medical Genetics.
E. Bertini,
R. Carrozzo,
E. Lamantea,
2017,
Orphanet Journal of Rare Diseases.
M. Zeviani,
E. Lamantea,
L. Morandi,
2016,
Molecular genetics and metabolism reports.
F. Gianfrancesco,
T. Esposito,
L. Griffiths,
2010,
BMC Medical Genetics.
D. Diodato,
D. Martinelli,
C. Dionisi-Vici,
2018,
Neurology.
Robert W. Taylor,
R. Horvath,
E. Ostergaard,
2021,
Human molecular genetics.
S. Pro,
D. Diodato,
Guglielmo Salvatori,
2023,
Journal of personalized medicine.
E. Bertini,
Q. Waisfisz,
M. Knaap,
2018
.
V. Tiranti,
D. Diodato,
I. Di Meo,
2023,
International journal of molecular sciences.
M. Mancuso,
C. La Morgia,
G. Siciliano,
2020,
neurogenetics.
S. Pro,
D. Diodato,
D. Martinelli,
2019,
Neuroradiology.
M. Digilio,
M. Tartaglia,
G. Merla,
2023,
Clinical genetics.
M. Baumgartner,
H. Blom,
L. Vilarinho,
2016,
Journal of Inherited Metabolic Disease.
Marni J. Falk,
H. Prokisch,
A. Rötig,
2023,
Neuromuscular Disorders.
E. Bertini,
R. Carrozzo,
A. D’Amico,
2019,
Human mutation.
Marni J. Falk,
Lishuang Shen,
B. Harding,
2023,
Annals of neurology.
G. Comi,
M. Zeviani,
M. Mancuso,
2016,
Neuromuscular Disorders.
M. Digilio,
L. Sinibaldi,
D. Diodato,
2024,
Parkinsonism & related disorders.