I. Moroni
发表
M. Mancuso,
C. La Morgia,
G. Siciliano,
2020,
neurogenetics.
S. Franceschetti,
N. Nardocci,
E. Lamantea,
2019,
Acta neurologica Scandinavica.
M. Mancuso,
C. La Morgia,
G. Siciliano,
2021,
Journal of clinical medicine.
N. Romero,
E. Ricci,
L. Morandi,
2014,
Journal of Medical Genetics.
E. Bertini,
M. Pane,
E. Mercuri,
2015,
Journal of Neurology.
N. Nardocci,
L. Chiapparini,
B. Garavaglia,
2016,
Current Neurology and Neuroscience Reports.
M. Zeviani,
E. Lamantea,
G. Uziel,
2004,
Biochimica et biophysica acta.
A. Bizzi,
U. Danesi,
G. Uziel,
2002,
Annals of neurology.
Matthew J. Daniels,
N. Ashley,
M. Zeviani,
2017,
Neurology.
L. Lagae,
A. Vanderver,
K. Devriendt,
2015,
American journal of medical genetics. Part A.
A. Bizzi,
U. Danesi,
P. Barker,
2008,
American Journal of Neuroradiology.
E. Bertini,
G. Comi,
R. Caldara,
2007,
Neurology.
Robert W. Taylor,
T. Strom,
H. Prokisch,
2018,
JAMA neurology.
F. Morelli,
I. Ceccherini,
T. Bachetti,
2021,
Frontiers in Genetics.
N. Nardocci,
B. Garavaglia,
G. Zorzi,
2021,
Frontiers in Neurology.
G. Finocchiaro,
B. Pollo,
G. Uziel,
2004,
Neurology.
M. Ferrarin,
M. Rabuffetti,
D. Pareyson,
2015
.
S. Esposito,
L. Chiapparini,
C. Pantaleoni,
2019,
European journal of medical genetics.
R. Finkel,
F. Muntoni,
D. Herrmann,
2017,
Annals of neurology.
Refining clinical trial inclusion criteria to optimize the standardized response mean of the CMTPedS
R. Finkel,
F. Muntoni,
D. Herrmann,
2020,
Annals of clinical and translational neurology.
R. Finkel,
S. Züchner,
F. Muntoni,
2020,
Neurology.
G. Comi,
G. Vasco,
M. Pane,
2009,
Neurology.
C. Gellera,
A. Erbetta,
D. Pareyson,
2013,
Orphanet Journal of Rare Diseases.
R. Finkel,
F. Muntoni,
D. Herrmann,
2015,
Brain : a journal of neurology.
M. Zeviani,
M. Mancuso,
C. Angelini,
2014,
Movement disorders : official journal of the Movement Disorder Society.
G. Comi,
M. Zeviani,
E. Lamantea,
2003,
Neurology.
M. de Curtis,
A. Silvani,
P. Tiraboschi,
2021,
Neurological Sciences.
A. Pichiecchio,
N. Nardocci,
L. Chiapparini,
2018,
Orphanet Journal of Rare Diseases.
E. Lamantea,
D. Pareyson,
D. Ghezzi,
2015,
Neurology.
G. Comi,
E. Zanoteli,
N. Goemans,
2022,
Orphanet Journal of Rare Diseases.
Robert W. Taylor,
E. Bertini,
T. Meitinger,
2017
.
Robert W. Taylor,
E. Bertini,
T. Meitinger,
2014,
American journal of human genetics.
N. Bresolin,
G. Comi,
S. Corti,
2016,
Journal of Molecular Neuroscience.
B. Castellotti,
C. Gellera,
N. Nardocci,
2011,
neurogenetics.
A. Franke,
R. Płoski,
Michael A. Gonzalez,
2014,
American journal of human genetics.
D. Pareyson,
A. Ardissone,
E. Pagliano,
2022,
Journal of the peripheral nervous system : JPNS.
D. Pareyson,
A. Schenone,
R. Zuccarino,
2020,
Journal of the peripheral nervous system : JPNS.
R. Bellazzi,
S. Comincini,
F. Novara,
2020,
Cancer Genomics & Proteomics.
S. Salani,
N. Bresolin,
L. Morandi,
2008,
Human mutation.
M. Zeviani,
D. Pareyson,
E. Salsano,
2013,
The Lancet Neurology.
D. Pareyson,
F. Taroni,
M. Bugiani,
2009,
Neuromuscular Disorders.
D. Pareyson,
M. Bugiani,
I. Moroni,
2006,
Neurology.
L. Morandi,
F. Blàsevich,
M. Mora,
2014,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
Jun Yu Li,
R. Finkel,
S. Züchner,
2014,
Journal of Neurology, Neurosurgery & Psychiatry.
M. Baumgartner,
T. Wieland,
T. Meitinger,
2012,
American journal of human genetics.
Y. Crow,
G. Uziel,
C. Graziano,
2012,
Developmental medicine and child neurology.
A. Pichiecchio,
E. Lamantea,
L. Chiapparini,
2018,
Orphanet Journal of Rare Diseases.
J. Louwerens,
D. Pareyson,
M. Shy,
2017,
Neuromuscular Disorders.
R. Finkel,
F. Muntoni,
D. Herrmann,
2016,
JAMA neurology.
D. Ghezzi,
P. Goffrini,
A. Ardissone,
2016,
Human mutation.
D. Ghezzi,
A. Ardissone,
L. Farina,
2015,
Molecular genetics and metabolism reports.
E. Bertini,
R. Carrozzo,
A. D’Amico,
2019,
Human mutation.
R. Finkel,
F. Muntoni,
S. Garnett,
2021,
Neurology.
A. Bizzi,
N. Nardocci,
G. Uziel,
2003,
Neuropediatrics.
A. Bizzi,
E. Lamantea,
G. Uziel,
2002,
Neuropediatrics.
G. Uziel,
L. D'Incerti,
L. Farina,
1998,
Neuroradiology.
E. Bertini,
A. Bizzi,
A. D’Amico,
2012,
Neuromuscular Disorders.
E. Bertini,
R. Carrozzo,
E. Lamantea,
2016,
Journal of Neurology.
T. Wieland,
A. Munnich,
H. Smeets,
2018
.
M. Mora,
L. Matalonga,
A. Ardissone,
2019,
Neuromuscular Disorders.
E. Bertini,
G. Uziel,
M. Rimoldi,
1998,
The Italian Journal of Neurological Sciences.
L. Morandi,
G. Baranello,
I. Moroni,
2015,
Bone.
L. Morandi,
G. Baranello,
I. Moroni,
2015
.
M. Ferrarin,
D. Pareyson,
G. Baranello,
2011,
Journal of the peripheral nervous system.
G. Comi,
M. Zeviani,
M. Mancuso,
2014,
Journal of Neurology.
G. Uziel,
L. D'Incerti,
M. Rimoldi,
2000,
Neurological Sciences.
E. Bertini,
R. Carrozzo,
M. Zeviani,
2018,
Journal of Human Genetics.
Magnetic resonance imaging spectrum of succinate dehydrogenase–related infantile leukoencephalopathy
A. Vanderver,
R. Taft,
M. S. van der Knaap,
2016,
Annals of neurology.
G. Comi,
M. Zeviani,
M. Mancuso,
2017,
Journal of Neurology.
M. Zeviani,
E. Lamantea,
D. Ghezzi,
2014,
Front. Genet..
A. Albanese,
C. Gellera,
F. Panzica,
2012,
Parkinsonism & related disorders.
G. Uziel,
F. Santorelli,
E. Leão,
2008,
Molecular genetics and metabolism.
N. Nardocci,
L. Chiapparini,
E. Fazzi,
2017,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
C. Romano,
A. Coppola,
N. Brunetti‐Pierri,
2020,
European journal of medical genetics.
N. Bresolin,
G. Comi,
S. Corti,
2017,
Muscle & nerve.
V. Tiranti,
M. Zeviani,
A. Reyes,
2016,
Biochimica et biophysica acta.
E. Bertini,
A. Vanderver,
R. Carrozzo,
2016,
Brain : a journal of neurology.
G. Uziel,
M. Mora,
R. Barresi,
1996,
Neuromuscular Disorders.
N. Bresolin,
G. Scarlato,
A. Prelle,
1995,
Journal of Neurology.
Robert W. Taylor,
H. Prokisch,
H. Mandel,
2018,
Human mutation.
A. Vignoli,
E. Veneselli,
S. Maitz,
2019,
International journal of molecular sciences.
M. Zeviani,
Jianguo Zhang,
D. Ghezzi,
2012,
Molecular genetics and metabolism.
G. Comi,
M. Zeviani,
M. Mancuso,
2013,
Neurology.
M. Esposito,
G. Siciliano,
P. Tonin,
2020,
Neuromuscular Disorders.
L. Morandi,
M. Mora,
S. Zanotti,
2009,
Muscle & nerve.
N. Bresolin,
G. Comi,
S. Corti,
2020,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
E. Mazzone,
M. Pane,
A. Trabacca,
2022,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
S. Gabriel,
K. Shianna,
C. Walsh,
2012,
American journal of human genetics.
E. Bertini,
M. Pane,
E. Mercuri,
2020,
Frontiers in Genetics.
B. Castellotti,
C. Gellera,
D. Pareyson,
2014,
Brain : a journal of neurology.
R. Badolato,
A. Biondi,
C. Mazza,
2020,
British journal of haematology.
N. Bresolin,
C. Angelini,
G. Scarlato,
1990,
Journal of the Neurological Sciences.
G. Comi,
G. Vasco,
F. Bianco,
2012,
Neuromuscular Disorders.
E. Bertini,
A. Vanderver,
N. Brunetti‐Pierri,
2019,
Annals of clinical and translational neurology.
M. Pillon,
A. Di Cataldo,
C. Dufour,
2016,
JIMD reports.
N. Nardocci,
M. Eoli,
S. Esposito,
2018,
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
A. Bizzi,
M. Zeviani,
E. Lamantea,
2006,
Neurology.
F. Blàsevich,
M. Mora,
C. Gelfi,
2022,
International journal of molecular sciences.
E. Haan,
M. Mora,
P. Blumbergs,
2015,
Neuromuscular Disorders.
E. Hoffman,
R. Boostani,
A. Pittman,
2020,
Molecular genetics & genomic medicine.
M. Ferrarin,
M. Rabuffetti,
L. Padua,
2018,
Gait & posture.
Maurizio Ferrarin,
Davide Pareyson,
Isabella Moroni,
2017,
Neuromuscular Disorders.
Isabella Moroni,
Thomas Voit,
Hamid Galehdari,
2017,
American journal of human genetics.
G. Comi,
E. Bertini,
F. Bianco,
2015,
Neurology.
M. Pane,
E. Mercuri,
A. D’Amico,
2008,
Neuromuscular Disorders.
G. Uziel,
L. D'Incerti,
A. Selicorni,
2000,
Clinical dysmorphology.
R. Finkel,
F. Muntoni,
D. Herrmann,
2019,
Muscle & nerve.
Colin A. Johnson,
S. Gabriel,
T. Ideker,
2015,
eLife.
G. Comi,
M. Zeviani,
M. Mancuso,
2015,
Journal of Neurology.
Isabella Moroni,
Alberto Bizzi,
Massimo Zeviani,
2006,
Brain and Development.
G. Comi,
M. Zeviani,
M. Mancuso,
2016,
Neuromuscular Disorders.
N. Bresolin,
G. Comi,
R. Cagliani,
2006,
Journal of the Neurological Sciences.
P. Brioschi,
G. Uziel,
L. Morandi,
2005,
Archives of neurology.
C. Pantaleoni,
L. Morandi,
M. Mora,
1998,
Neuroradiology.
V. Sansone,
P. Bernasconi,
A. Ardissone,
2017,
Neuromuscular Disorders.
Isabella Moroni,
John H Livingston,
Odile Boespflug-Tanguy,
2016,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
E. Maccagnano,
L. Morandi,
F. Blàsevich,
2016,
European Journal of Pediatrics.
R. Finkel,
S. Züchner,
F. Muntoni,
2020,
Brain : a journal of neurology.
F. Taroni,
S. Baratta,
S. Magri,
2020,
Journal of the peripheral nervous system : JPNS.
M. Mancuso,
E. Lamantea,
C. Bruno,
2021,
Orphanet Journal of Rare Diseases.
Silvio C. E. Tosatto,
E. Bertini,
M. Pane,
2022,
Acta neuropathologica communications.
N. Nardocci,
L. Chiapparini,
B. Garavaglia,
2021,
Movement disorders : official journal of the Movement Disorder Society.
M. Zeviani,
E. Lamantea,
G. Uziel,
2015,
JIMD reports.
N. Bresolin,
G. Comi,
C. Angelini,
1991,
Revue neurologique.
R. Finkel,
M. Shy,
C. Siskind,
2022,
Journal of Neurology, Neurosurgery, and Psychiatry.
M. Zeviani,
A. Reyes,
A. Robinson,
2016,
Journal of Medical Genetics.
E. Lamantea,
D. Ghezzi,
D. Diodato,
2015,
JIMD reports.
E. Lamantea,
K. Gibson,
U. Caruso,
1999,
Journal of Inherited Metabolic Disease.
M. Zeviani,
E. Lamantea,
G. Uziel,
1997,
Journal of neurology, neurosurgery, and psychiatry.
Robert W. Taylor,
T. Wieland,
A. Munnich,
2018,
Orphanet Journal of Rare Diseases.
E. Bertini,
A. Pichiecchio,
N. Nardocci,
2019,
Journal of clinical medicine.
T. Mazza,
E. Valente,
T. Biagini,
2016,
neurogenetics.
D. Riva,
A. Pichiecchio,
L. Chiapparini,
2019,
Molecular genetics and metabolism.
E. Bertini,
R. Carrozzo,
E. Lamantea,
2017,
Orphanet Journal of Rare Diseases.
S. Maestrini,
L. Morandi,
F. Blàsevich,
2013,
BMC Medical Genetics.
N. Nardocci,
L. Chiapparini,
B. Garavaglia,
2017,
Neurology.
Maurizio Ferrarin,
Davide Pareyson,
Isabella Moroni,
2013,
Journal of NeuroEngineering and Rehabilitation.
Sita D Gupta,
K. Gable,
T. Dunn,
2022,
Neuropathology and applied neurobiology.
G. Vasco,
M. Pane,
E. Mercuri,
2010,
Neurology.
T. Foiadelli,
C. Pantaleoni,
R. Battini,
2021,
Molecular genetics and metabolism.
I. Ceccherini,
A. Ardissone,
L. Farina,
2016,
Neurological Sciences.
N. Bresolin,
G. Comi,
S. Corti,
2016,
Journal of Molecular Neuroscience.
Davide Pareyson,
Isabella Moroni,
Franco Taroni,
2016,
Journal of the peripheral nervous system : JPNS.
V. Tiranti,
E. Lamantea,
D. Ghezzi,
2023,
European journal of neurology.
Jun Yu Li,
R. Finkel,
F. Muntoni,
2022,
Annals of neurology.
Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease
C. Pantaleoni,
L. Morandi,
M. Mora,
2012,
Journal of the Neurological Sciences.
E. Bertini,
L. Di Marcotullio,
M. Pane,
2021,
eLife.
G. Zorzi,
A. Ardissone,
I. Moroni,
2015,
Muscle & nerve.
Tiziana,
N. Bresolin,
G. Comi,
2016
.
E. Bertini,
M. Sormani,
E. Mazzone,
2013,
Neuromuscular Disorders.
M Rabuffetti,
M Ferrarin,
I Moroni,
2012,
Gait & posture.
K. Refshauge,
D. Herrmann,
D. Pareyson,
2018,
Brain : a journal of neurology.
R. Finkel,
F. Muntoni,
D. Herrmann,
2013,
Journal of the peripheral nervous system : JPNS.
M. Mancuso,
C. La Morgia,
G. Siciliano,
2020,
neurogenetics.
G. Uziel,
A. Ardissone,
I. Moroni,
2014,
Muscle & nerve.
L. Santoro,
A. Quattrone,
L. Padua,
2023,
European journal of neurology.
D. Timmann,
A. Durr,
L. Schöls,
2023,
American journal of human genetics.
E. Bertini,
R. Borgatti,
L. Provenzi,
2021,
Disability and rehabilitation.
Association of Body Mass Index With Disease Progression in Children With Charcot-Marie-Tooth Disease
R. Finkel,
S. Garnett,
D. Herrmann,
2023,
Neurology.
L. Morandi,
F. Blàsevich,
M. Mora,
2012
.
E. Lamantea,
D. Pareyson,
D. Ghezzi,
2015,
Neurology.
E. Bertini,
C. Compagnucci,
M. Tartaglia,
2021,
Brain : a journal of neurology.
G. Uziel,
B. Garavaglia,
M. Rimoldi,
1995,
Pediatric neurology.
E. Lamantea,
L. Maggi,
D. Ghezzi,
2023,
Genes.
D. Riva,
C. Pantaleoni,
R. Mantegazza,
2010,
Journal of Neurology.
E. Bertini,
R. Carrozzo,
A. D’Amico,
2019,
Human mutation.
M. Baumgartner,
T. Wieland,
T. Meitinger,
2012,
American journal of human genetics.
T. Mazza,
E. Valente,
T. Biagini,
2016,
Neurogenetics.
G. Comi,
E. Bertini,
F. Bianco,
2015,
Neurology.
S. Gabriel,
K. Shianna,
C. Walsh,
2012,
American journal of human genetics.
I. Ceccherini,
T. Bachetti,
F. Caroli,
2022,
Frontiers in Genetics.
M. Ferrarin,
M. Rabuffetti,
P. Mazzoleni,
2011,
Gait & posture.
G. Comi,
M. Zeviani,
M. Mancuso,
2016,
Neuromuscular Disorders.
G. Uziel,
C. Rosano,
B. Bembi,
2012,
PloS one.