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A. Berardinelli · SciRah

Researcher profile · Semantic Scholar

A. Berardinelli

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A. Berardinelli — researcher profile on SciRah

h-index: 12
Works: 45
Citations: 1,030

Most-cited papers

Reliability of the North Star Ambulatory Assessment in a multicentric setting.
E. Mazzone, S. Messina, G. Vasco, M. Main +32 more
2009Neuromuscular Disorders222 citations Open access
Semantic Scholar
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy.
E. Mazzone, D. Martinelli, A. Berardinelli, S. Messina +29 more
2010Neuromuscular Disorders211 citations
Semantic Scholar
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy
L. Bello, L. Piva, A. Barp, A. Taglia +33 more
2012Neurology84 citations Open access
Semantic Scholar
Reliability of the Hammersmith functional motor scale for spinal muscular atrophy in a multicentric study.
E. Mercuri, S. Messina, R. Battini, A. Berardinelli +22 more
2006Neuromuscular Disorders81 citations
Semantic Scholar
Early neurodevelopmental assessment in Duchenne muscular dystrophy.
M. Pane, R. Scalise, A. Berardinelli, G. D'Angelo +23 more
2013Neuromuscular Disorders79 citations
Semantic Scholar
Muscle ultrasound elastography and MRI in preschool children with Duchenne muscular dystrophy.
A. Pichiecchio, F. Alessandrino, C. Bortolotto, A. Cerica +7 more
2018Neuromuscular Disorders61 citations
Semantic Scholar
The Hammersmith functional score correlates with the SMN2 copy number: a multicentric study.
F. Tiziano, E. Bertini, S. Messina, C. Angelozzi +20 more
2007Neuromuscular Disorders52 citations
Semantic Scholar
POMT2 mutation in a patient with 'MEB-like' phenotype.
E. Mercuri, A. D'Amico, A. Tessa, A. Berardinelli +6 more
2006Neuromuscular Disorders50 citations
Semantic Scholar
1st Italian SMA Family Association Consensus Meeting: Management and recommendations for respiratory involvement in spinal muscular atrophy (SMA) types I-III, Rome, Italy, 30-31 January 2015.
V. Sansone, F. Racca, G. Ottonello, A. Vianello +3 more
2015Neuromuscular Disorders40 citations Open access
Semantic Scholar
Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiency
M. Pane, S. Messina, G. Vasco, A. R. Foley +19 more
2012Neuromuscular Disorders40 citations Open access
Semantic Scholar
Health-related quality of life and functional changes in DMD: A 12-month longitudinal cohort study
S. Messina, G. Vita, M. Sframeli, S. Mondello +22 more
2016Neuromuscular Disorders38 citations Open access
Semantic Scholar
Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study
Aurora Fusto, D. Cassandrini, C. Fiorillo, Valentina Codemo +30 more
2022Acta Neuropathologica Communications19 citations Open access
Semantic Scholar
Alexander disease evolution over time: data from an Italian cohort of pediatric-onset patients.
Eleonora Mura, F. Nicita, S. Masnada, R. Battini +13 more
2021Molecular Genetics and Metabolism12 citations
Semantic Scholar
Data monitoring roadmap. The experience of the Italian Multiple Sclerosis and Related Disorders Register
P. Mosconi, T. Guerra, Pasquale Paletta, A. D'Ettorre +151 more
2023Neurological Sciences11 citations Open access
Semantic Scholar
Six‐minute walk test as outcome measure of fatigability in adults with spinal muscular atrophy treated with nusinersen
A. Govoni, G. Ricci, S. Bonanno, L. Bello +41 more
2024Muscle and Nerve9 citations Open access
Semantic Scholar
Genetic modifiers of upper limb function in Duchenne muscular dystrophy
Daniele Sabbatini, Aurora Fusto, S. Vianello, Matteo Villa +29 more
2022Journal of Neurology5 citations Open access
Semantic Scholar
Do patients’ and referral centers’ characteristics influence multiple sclerosis phenotypes? Results from the Italian multiple sclerosis and related disorders register
R. Bergamaschi, E. Beghi, C. Bosetti, M. Ponzio +148 more
2022Neurological Sciences4 citations Open access
Semantic Scholar
M.P.2.01 Reliability of the north star ambulatory assessment in a multicentric setting
E. Mazzone, S. Messina, G. Vasco, M. Main +15 more
20094 citations
Semantic Scholar
P.2.7 6 min walk test 12 month changes in DMD: Correlation with genotype
M. Pane, E. Mazzone, M. Sormani, R. Scalise +29 more
20133 citations
Semantic Scholar
The Schwartz-Jampel Syndrome. A Minireview
A. Berardinelli, G. Lanzi, BasicAppl Myol
19972 citations
Semantic Scholar
T.P.4: Long term natural history data in ambulant boys with Duchenne muscular dystrophy: 36 month changes
E. Mazzone, M. Pane, S. Sivo, C. Palermo +15 more
20141 citations
Semantic Scholar
S.P.4 Functional changes in Duchenne muscular dystrophy: A 24 month longitudinal cohort study
E. Mazzone, Marika Pane, R. Scalise, M. Sormani +25 more
20121 citations
Semantic Scholar
G.P.15.15 The SOLE questionnaire: Development and validation of a new instrument for measuring quality of life in children with neuromuscular disorders
S. Orcesi, K. Gorni, Marta Rossi, A. Berardinelli +12 more
20071 citations
Semantic Scholar
G.P.15.16 Importance of self-report in pediatric quality of life assessment: Experience with the SOLE questionnaire in children with neuromuscular disorders
G. Ariaudo, S. Orcesi, K. Gorni, A. Berardinelli +8 more
20071 citations
Semantic Scholar
554PUncovering social and pragmatic communication in Duchenne muscular dystrophy: a preliminary cohort study
M. Dainesi, C. Quaranta, M. Corradini, A. Gardani +5 more
2025Neuromuscular Disorders0 citations
Semantic Scholar
207PThe Italian cohort of facio-scapular-humeral dystrophy type 1: a long-term follow-up up to 20 years
L. Vercelli, G. Gadaleta, L. Ruggiero, G. Ricci +15 more
2025Neuromuscular Disorders0 citations
Semantic Scholar
250P Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey
G. Cicala, A. Capasso, M. Ricci, M. Pane +15 more
2024Neuromuscular Disorders0 citations
Semantic Scholar
6MWT as measure of motor function and endurance in SMA type 3 patients treated with nusinersen
A. Govoni, G. Ricci, L. Maggi, M. Meneri +39 more
2021Journal of Neurological Sciences0 citations
Semantic Scholar
Communicating What Liberal Arts Colleges Contribute to Computer Science (Abstract Only)
Janet Davis, A. Berardinelli, Amanda M. Holland-Minkley, E. Walker
2017Technical Symposium on Computer Science Education0 citations
Semantic Scholar
Muscle MRI in sarcoglycanopathies
G. Tasca, M. Monforte, G. Brisca, A. D'Amico +11 more
20150 citations
Semantic Scholar
miRNAs as serum biomarkers for Duchenne muscular dystrophy: Correlation analysis in a multicentre study between miRNA levels and clinical status of DMD patients
A. D'Amico, J. Martone, S. Previtali, G. Baranello +10 more
20150 citations
Semantic Scholar
T.P.11
M. Pane, E. Mazzone, L. Fanelli, R. de Sanctis +13 more
20140 citations
Semantic Scholar
P.1.11 Development of a registry and a database for a nation-wide Italian collaborative network on congenital muscular dystrophy
F. Bianco, A. D'Amico, S. Messina, L. Politano +11 more
20130 citations
Semantic Scholar
P.2.3 Assessment of Upper Limb function in DMD patients: Comparison with normative data
E. Mazzone, Marika Pane, L. Fanelli, R. de Sanctis +17 more
20130 citations
Semantic Scholar
Osteopontin in Duchenne Muscular Dystrophy (S15.002)
E. Pegoraro, L. Bello, L. Piva, A. Barp +22 more
20120 citations
Semantic Scholar
P3.5 Oxidative defect in a large cohort of genetically-determined SMA cases
A. Berardinelli, G. Fagiolari, Dionis Vallejo, V. Lucchini +9 more
20110 citations
Semantic Scholar
G.P.2.02 Genotype–phenotype correlations in congenital muscular dystrophies with defective glycosylation of dystroglycan: A multicentric Italian study
S. Messina, F. Santorelli, M. Mora, Claudio Bruno +19 more
20080 citations
Semantic Scholar
Peculiar ultrastructural findings in congenital myopathies due to selenoprotein N1 gene new mutations
M. E. Fruguglietti, Rachele Cagliani, L. Napoli, A. Berardinelli +10 more
20080 citations
Semantic Scholar
G.P.13.04 Genetic and ultrastructural findings in Selenoprotein N1-related congenital myopathies
Rachele Cagliani, E. Fruguglietti, A. Berardinelli, Maria Grazia D'Angelo +8 more
20080 citations
Semantic Scholar
New Molecular and Ultrastructural Findings in Congenital Myopathies Due to Selenoprotein N1 Gene Mutations
Rachele Cagliani, A. Berardinelli, M. D'Angelo, A. Prelle +9 more
20080 citations
Semantic Scholar
C.P.3.02 Expanding the clinical spectrum of POMT1 and POMT2 phenotype: A multicentric study in the Italian population
S. Messina, M. Mora, E. Pegoraro, A. Pini +17 more
20070 citations
Semantic Scholar
G.P.10 01 Quantitative ultrasound measurements of bone density DMD and SMA patients
A. Berardinelli, K. Gorni, L. Pedrotti, R. Mora +2 more
20060 citations
Semantic Scholar
N.P.2 01 Spinal muscular atrophy: correlation between the number of SMN2 genes and functional ability
F. Tiziano, E. Bertini, Carla Angelozzi, S. Messina +11 more
20060 citations
Semantic Scholar
Epileptic seizures, arthrogryposis, and migrational brain disorders: a syndrome?
P. Veggiotti, A. Berardinelli, E. Fazzi, G. Lanzi +1 more
1995Acta Neurologica Scandinavica0 citations
Semantic Scholar
[Ehlers-Danlos syndrome. Description of 2 clinical cases].
A. Ottolini, A. Berardinelli, D. Besana, G. Cetta +2 more
1992Minerva Pediatrica0 citations
Semantic Scholar

Frequent co-authors

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E. Mercuri×25
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E. Mercuri — researcher profile on SciRah
T. Mongini×14
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T. Mongini — researcher profile on SciRah
S. Messina×13
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S. Messina — researcher profile on SciRah
A. D'Amico×12
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A. D'Amico — researcher profile on SciRah

×12

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G. Vita — researcher profile on SciRah

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C. Bruno — researcher profile on SciRah

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E. Mazzone — researcher profile on SciRah

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L. Bello — researcher profile on SciRah

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A. Pini — researcher profile on SciRah

S. Previtali×9

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S. Previtali — researcher profile on SciRah

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R. Battini — researcher profile on SciRah

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M. Pane — researcher profile on SciRah