M. Neri
发表
G. Remuzzi,
D. Taruscio,
F. Brancati,
2020,
Italian Journal of Pediatrics.
G. Scarano,
A. Ferlini,
B. Mandriani,
2014,
Human mutation.
P. Tonin,
A. Ferlini,
M. Neri,
2010,
Journal of neuropathology and experimental neurology.
F. Muntoni,
A. Ferlini,
P. Spitali,
2007,
Neuromuscular Disorders.
E. Bertini,
M. Pane,
E. Mercuri,
2009,
Human mutation.
M. Uhlén,
C. Szigyarto,
R. Weiss,
2014,
Nature Medicine.
A. Ferlini,
M. Neri,
D. Vlodavets,
2020,
Neurology Genetics.
M. Fichera,
L. Caniatti,
M. Neri,
2004,
Neuromuscular Disorders.
M. Fichera,
M. Lo Giudice,
E. Calzolari,
2004,
Neurology.
M. Neri,
M. Sensi,
2022,
Parkinsonism & Related Disorders.
F. Muntoni,
E. Calzolari,
A. Ferlini,
2005,
American journal of medical genetics. Part A.
K. Bushby,
Hanns Lochmüller,
A. Ferlini,
2017,
Neuromuscular Disorders.
E. Bertini,
M. Tosetti,
A. Durr,
2006,
Neurogenetics.
F. Muntoni,
M. Falzarano,
A. Ferlini,
2008,
BMC Genomics.
E. Bertini,
Hui Jiang,
E. Arbustini,
2016,
The Journal of clinical investigation.
F. Muntoni,
C. Rapezzi,
A. Ferlini,
2012,
BMC Medical Genetics.
M. Falzarano,
H. Osman,
A. Ferlini,
2017,
Biochimica et biophysica acta. Gene regulatory mechanisms.
L. Caniatti,
G. Grieco,
E. Groppo,
2017,
The Journal of Headache and Pain.
A. Ferlini,
M. Neri,
F. Gualandi,
2013,
Neuromuscular Disorders.
D. De Grandis,
E. Valente,
B. Dallapiccola,
2013,
Molecular genetics and metabolism.
E. Bertini,
E. Mercuri,
A. Ferlini,
2010,
BMC Medical Genetics.
D. Taruscio,
P. Perri,
F. Brancati,
2019,
Front. Genet..
M. Falzarano,
A. Ferlini,
G. Perini,
2012,
PloS one.
Luciano Merlini,
Paola Braghetta,
Alessandra Ferlini,
2009,
Molecular therapy : the journal of the American Society of Gene Therapy.
P. Tonin,
A. Ferlini,
M. Neri,
2011,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
A. Ferlini,
B. Mandriani,
G. Merla,
2019,
Science Advances.
F. Muntoni,
E. Calzolari,
C. Angelini,
2006,
Gene.
F. Salvi,
A. Yuryev,
A. Ferlini,
2010,
BMC Medical Genetics.
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia
M. Zeviani,
M. Pane,
E. Mercuri,
2017,
Human mutation.
M. Uhlén,
C. Szigyarto,
R. Weiss,
2015
.
E. Bertini,
M. Pane,
E. Mercuri,
2009,
Human mutation.
Pieter B. T. Neerincx,
Spencer J. Gibson,
Farid Yavari Dizjikan,
2021,
European Journal of Human Genetics.
Pieter B. T. Neerincx,
Spencer J. Gibson,
Farid Yavari Dizjikan,
2021,
European Journal of Human Genetics.
Alessandra Ferlini,
Marcella Neri,
A. Ferlini,
2014,
Experimental cell research.
P. Tonin,
A. Ferlini,
G. Novelli,
2012,
The neurologist.
E. Bertini,
M. Pane,
E. Mercuri,
2020,
Frontiers in Genetics.
A. Ferlini,
M. Neri,
2014
.
A. Ferlini,
M. Neri,
F. Gualandi,
2013,
Neuromuscular Disorders.
A. Ferlini,
M. Neri,
L. Melchiorri,
2014,
Genetics in Medicine.
Francesco Muntoni,
Luciano Merlini,
Alessandra Ferlini,
2007
.
G. Comi,
E. Bertini,
M. Pane,
2021,
Neuromuscular Disorders.
P. Tonin,
A. Ferlini,
M. Neri,
2009,
Neuropathology and Applied Neurobiology.
A. Ferlini,
M. Neri,
P. Trevisi,
2011,
American journal of medical genetics. Part A.
Pieter B. T. Neerincx,
Spencer J. Gibson,
Farid Yavari Dizjikan,
2021,
European Journal of Human Genetics.
R. Carrozzo,
E. Lamantea,
A. Ferlini,
2022,
Cerebellum.
M. Fichera,
M. Lo Giudice,
E. Calzolari,
2006,
Archives of neurology.
A. Padovani,
A. Ferlini,
M. Neri,
2017,
Molecular and Cellular Neuroscience.
M. Bertini,
S. Straudi,
V. Tugnoli,
2023,
European journal of medical genetics.
G. Pesole,
E. Bertini,
K. Bushby,
2016,
Journal of Cell Science.
B. Wirth,
D. De Grandis,
V. Tugnoli,
2019,
Neuromuscular Disorders.
A. Ferlini,
M. Neri,
M. Cavallo,
2021,
Parkinsonism & related disorders.
R. Płoski,
P. Tonin,
M. Neri,
2020,
Neurological Sciences.
O. Pansarasa,
G. Grieco,
A. Ferlini,
2018,
The Journal of Headache and Pain.
Pieter B. T. Neerincx,
Spencer J. Gibson,
Farid Yavari Dizjikan,
2023,
Human Genomics.
F. Salvi,
A. Yuryev,
A. Ferlini,
2010,
BMC Medical Genetics.
A. Yuryev,
A. Ferlini,
M. Neri,
2009
.
D. Taruscio,
F. Brancati,
A. Ferlini,
2018,
European Journal of Human Genetics.