A. Botta
发表
G. Novelli,
U. Tarantino,
S. Fittipaldi,
2020,
Epigenomics.
C. Angelini,
G. Novelli,
A. Viola,
2010,
Journal of Translational Medicine.
R. Mango,
G. Novelli,
F. Sangiuolo,
2018,
Journal of molecular and cellular cardiology.
G. Novelli,
A. Botta,
A. Morrone,
2020,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
G. Novelli,
A. Orlandi,
S. Bernardini,
2017,
Neuromuscular Disorders.
F. Brancati,
G. Novelli,
F. Sangiuolo,
2017,
European Journal of Human Genetics.
G. Meola,
E. Bugiardini,
A. Botta,
2014,
Neuromuscular Disorders.
G. Novelli,
L. Vergani,
R. Massa,
2012,
Neurobiology of Disease.
C. Angelini,
G. Novelli,
A. Viola,
2008,
Journal of Medical Genetics.
G. Novelli,
P. Borgiani,
A. Botta,
2005,
Molecular and cellular probes.
A. Bradley,
A. Baldini,
S. Carattini-Rivera,
1999,
Nature.
R. Mango,
G. Novelli,
F. Sangiuolo,
2018,
Journal of molecular recognition : JMR.
D. Corrado,
S. Iliceto,
E. Pegoraro,
2020,
Heart rhythm.
N. Vanacore,
A. Botta,
M. Garibaldi,
2018,
Journal of Neurology.
G. Novelli,
M. Masciullo,
G. Silvestri,
2017,
Clinical genetics.
G. Meola,
S. Greco,
F. Martelli,
2016,
Scientific Reports.
F. Coppedè,
D. Furling,
M. Simili,
2018,
Cell Death & Disease.
U. Tarantino,
S. Fittipaldi,
Virginia Veronica Visconti,
2021,
International journal of molecular sciences.
C. Piantadosi,
G. Novelli,
C. Casali,
2016,
Neuroepidemiology.
G. Novelli,
U. Tarantino,
M. Scimeca,
2018,
Aging and disease.
G. Novelli,
G. Silvestri,
L. Politano,
2008,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
T. Meitinger,
T. Strom,
H. Prokisch,
2016,
American journal of human genetics.
M. Delledonne,
G. Novelli,
M. Rossato,
2022,
bioRxiv.
G. Novelli,
M. Clementi,
A. Tacconelli,
2005,
Neurology.
B. Dallapiccola,
G. Novelli,
F. Sangiuolo,
1995,
International journal of clinical & laboratory research.
G. Novelli,
G. Silvestri,
R. Massa,
2018,
Biochimica et biophysica acta. Molecular basis of disease.
L. Vergani,
G. Szabadkai,
E. Loro,
2013,
Genes.
G. Meola,
C. Angelini,
G. Novelli,
2022
.
G. Della Marca,
G. Silvestri,
E. Rastelli,
2019,
Journal of the Neurological Sciences.
G. Meola,
G. Novelli,
F. Sangiuolo,
2021,
Frontiers in Genetics.
G. Meola,
I. Rivolta,
A. Botta,
2018,
Scientific Reports.
G. Novelli,
R. Mingarelli,
S. Semprini,
2002,
Human Genetics.
U. Tarantino,
M. Scimeca,
A. Botta,
2021,
Frontiers in Immunology.
M. Mirabella,
V. Nociti,
A. Botta,
2020,
European review for medical and pharmacological sciences.
G. Novelli,
F. Sangiuolo,
A. Botta,
2009,
Genetic testing and molecular biomarkers.
G. D’Arcangelo,
V. Tancredi,
G. Novelli,
2020,
Biomedicines.
U. Tarantino,
S. Fittipaldi,
A. Botta,
2021,
Journal of Orthopaedic Surgery and Research.
B. Dallapiccola,
G. Novelli,
M. Clementi,
1999,
The Journal of investigative dermatology.
G. Meola,
A. Botta,
R. Cardani,
2014,
European journal of histochemistry : EJH.
G. Meola,
G. Novelli,
G. Colombo,
2013,
PloS one.
U. Tarantino,
A. Botta,
B. Gasperini,
2022,
Genes.
C. Angelini,
G. Novelli,
A. Viola,
2010
.
G. Novelli,
F. Sangiuolo,
M. Cassone,
2017,
Clinica chimica acta; international journal of clinical chemistry.
G. Novelli,
A. Botta,
F. Rinaldi,
2010,
The Journal of molecular diagnostics : JMD.
G. Novelli,
A. Botta,
E. Giardina,
2004,
Diagnostic molecular pathology : the American journal of surgical pathology, part B.
C. Marcocci,
M. Brandi,
F. Giusti,
2022,
The Journal of clinical endocrinology and metabolism.
G. Novelli,
F. Amati,
A. Botta,
2001,
Trends in genetics : TIG.
G. Novelli,
S. Fittipaldi,
A. Botta,
2021,
International journal of molecular sciences.
C. Angelini,
G. Novelli,
M. Sandri,
2010,
Cell Death and Differentiation.
G. Meola,
G. Novelli,
F. Sangiuolo,
2018,
Front. Physiol..
B. Dallapiccola,
G. Novelli,
F. Amati,
2002,
Cell biochemistry and function.
M. Delledonne,
G. Novelli,
A. Salviati,
2021,
Frontiers in Genetics.
A. Brunati,
G. Novelli,
H. Monaco,
2013,
Cell Death and Disease.
Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2
G. Meola,
G. Novelli,
B. Udd,
2012,
Journal of Neurology.
G. Novelli,
F. Amati,
A. Botta,
2001
.
G. Novelli,
F. Sangiuolo,
F. Amati,
2020,
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.
A. Baldini,
A. Botta,
V. Jurecic,
1997,
Mammalian Genome.
G. Meola,
I. Rivolta,
A. Botta,
2018,
Scientific Reports.
G. Meola,
I. Rivolta,
E. Bugiardini,
2015,
Neuromuscular Disorders.
T. Kiyono,
F. Sangiuolo,
E. Pegoraro,
2016,
Experimental cell research.
C. Marcocci,
M. Brandi,
G. Novelli,
2020,
International journal of molecular sciences.
F. Coppedè,
D. Furling,
M. Simili,
2018,
Cell Death & Disease.
A Mari,
J. Korenberg,
M. Digilio,
1999,
Journal of medical genetics.
B. Dallapiccola,
G. Novelli,
F. Sangiuolo,
2001,
American journal of medical genetics.
Alessandra Ferlini,
Paola Rimessi,
Marina Grasso,
2018,
PloS one.
T. Beccari,
C. Ciccacci,
M. Bertelli,
2022,
Frontiers in Nutrition.
G. Spalletta,
F. Macciardi,
J. Trakalo,
2001,
American journal of medical genetics.
B. Dallapiccola,
G. Novelli,
F. Sangiuolo,
1999,
Genomics.
P. Pandolfi,
G. Citro,
S. Sidhu,
2022,
Cells.
B. Dallapiccola,
G. Novelli,
A. Botta,
2001,
Gene.
B. Dallapiccola,
A. Pizzuti,
G. Novelli,
2001,
Cytogenetic and Genome Research.
A. Pizzuti,
G. Novelli,
F. Amati,
2001
.
G. Bernardi,
G. Novelli,
R. Massa,
2011,
European journal of neurology.
C. Angelini,
G. Novelli,
R. Massa,
2007,
Genetic testing.
G. Novelli,
F. Sangiuolo,
A. Botta,
2006
.
L. Mannucci,
G. Novelli,
F. Sangiuolo,
2020,
Annals of human genetics.
Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues.
Antonio Novelli,
Gennaro Citro,
Annalisa Botta,
2004,
Gene.
G. Meola,
A. Botta,
V. Milani,
2019,
Front. Neurol..
M. Brandi,
C. Ciccacci,
A. Botta,
2023,
Genes.
B. Dallapiccola,
G. Novelli,
S. Servidei,
1998,
Human mutation.
C. Semenza,
E. Pegoraro,
L. Bello,
2019,
Journal of the International Neuropsychological Society.
C. Semenza,
B. de Gelder,
E. Pegoraro,
2020,
Cortex.
B. Dallapiccola,
G. Novelli,
F. Sangiuolo,
1998,
Human Mutation.
L. Frati,
F. Belardelli,
E. Anastasiadou,
2015,
International journal of cancer.
F. Brancati,
G. Novelli,
F. Sangiuolo,
2015,
Cellular reprogramming.
F. Brancati,
G. Novelli,
F. Sangiuolo,
2016,
European Journal of Human Genetics.
G. Meola,
G. Novelli,
A. Botta,
2009,
Neuromuscular Disorders.
G. Della Marca,
G. Silvestri,
E. Rastelli,
2019,
Journal of the Neurological Sciences.
L. Palombi,
A. Botta,
R. Iundusi,
2023,
Scientific reports.
G. Novelli,
E. Leoncini,
M. Masciullo,
2015,
Biochimica et biophysica acta.
G. Novelli,
F. Loreni,
R. Massa,
2006,
Biochimica et biophysica acta.
E. Brunetti,
G. Novelli,
A. Botta,
2006,
Clinical chemistry.
E. Rastelli,
R. Massa,
A. Botta,
2018,
Neuromuscular Disorders.