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C. Sancricca · SciRah

Researcher profile · Semantic Scholar

C. Sancricca

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C. Sancricca — researcher profile on SciRah

h-index: 9
Works: 30
Citations: 228

Most-cited papers

Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional study.
Salvatore Rossi, G. Della Marca, M. Ricci, Alessia Perna +16 more
2019Journal of Neurological Sciences41 citations Open access
Semantic Scholar
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients
C. Piano, E. di Stasio, G. Primiano, D. Janiri +40 more
2020Frontiers in Neurology27 citations Open access
Semantic Scholar
Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review
Stefania Della Vecchia, A. Tessa, C. Dosi, J. Baldacci +35 more
2021Journal of Neurology26 citations Open access
Semantic Scholar
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity.
Domenico Gorgoglione, Daniele Sabbatini, Pietro Riguzzi, Giuliana Capece +59 more
2024Brain : a journal of neurology15 citations Open access
Semantic Scholar
Novel TNNT1 mutation and mild nemaline myopathy phenotype in an Italian patient.
A. Petrucci, G. Primiano, M. Savarese, C. Sancricca +2 more
2021Neuromuscular Disorders15 citations
Semantic Scholar
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report
C. Strafella, Giulia Campoli, Rosaria Maria Galota, V. Caputo +11 more
2019Frontiers in Neurology15 citations Open access
Semantic Scholar
Digital health and Clinical Patient Management System (CPMS) platform utility for data sharing of neuromuscular patients: the Italian EURO-NMD experience
F. Fortunato, Francesca Bianchi, G. Ricci, F. Torri +47 more
2023Orphanet Journal of Rare Diseases14 citations Open access
Semantic Scholar
Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study Group
M. Filosto, Stefano Cotti Piccinelli, S. Ravaglia, S. Servidei +26 more
2019Advances in Therapy13 citations
Semantic Scholar
Integrating D4Z4 methylation analysis into clinical practice: improvement of FSHD molecular diagnosis through distinct thresholds for 4qA/4qA and 4qA/4qB patients
C. Strafella, Domenica Megalizzi, Giulia Trastulli, Emma Proietti Piorgo +47 more
2024Clinical Epigenetics9 citations Open access
Semantic Scholar
Characterization of D4Z4 alleles and assessment of de novo cases in Facioscapulohumeral dystrophy (FSHD) in a cohort of Italian families
C. Strafella, L. Colantoni, Domenica Megalizzi, Giulia Trastulli +11 more
2023Clinical Genetics9 citations Open access
Semantic Scholar
Management of motor rehabilitation in individuals with muscular dystrophies. 1st Consensus Conference report from UILDM - Italian Muscular Dystrophy Association (Rome, January 25-26, 2019).
M. E. Lombardo, E. Carraro, C. Sancricca, M. Armando +6 more
2021Acta myologica7 citations
Semantic Scholar
Describing phenotypes in FSHD: an update of the comprehensive clinical evaluation form
Giulia Ricci, F. Torri, Lucia Ruggiero, L. Vercelli +56 more
2025Neurological Sciences6 citations Open access
Semantic Scholar
Deciphering the Complexity of FSHD: A Multimodal Approach as a Model for Rare Disorders
Domenica Megalizzi, Giulia Trastulli, L. Colantoni, Emma Proietti Piorgo +6 more
2024International Journal of Molecular Sciences5 citations
Semantic Scholar
Distribution of Exonic Variants in Glycogen Synthesis and Catabolism Genes in Late Onset Pompe Disease (LOPD)
P. de Filippi, E. Errichiello, A. Toscano, T. Mongini +28 more
2023Current Issues in Molecular Biology5 citations Open access
Semantic Scholar
Clinical, Histopathologic, and Genetic Features of Patients With Myofibrillar and Distal Myopathies
S. Bortolani, Marco Savarese, G. Vattemi, S. Bonanno +45 more
2024Neurology4 citations
Semantic Scholar
Inflammatory profile in mitochondrial diseases: A cohort study
G. Primiano, D. Plantone, G. Piro, C. Carbone +5 more
2023European Journal of Neurology3 citations
Semantic Scholar
Emergencies cards for neuromuscular disorders 1st Consensus Meeting from UILDM – Italian Muscular Dystrophy Association Workshop report
F. Racca, V. Sansone, F. Ricci, M. Filosto +46 more
2022Acta myologica3 citations
Semantic Scholar
Progressive axonal polyneuropathy in a mitochondrial disorder: an uncommon association with familial amyloid neuropathy
M. Luigetti, G. Primiano, G. Bisogni, C. Cuccagna +5 more
2018Amyloid: Journal of Protein Folding Disorders3 citations
Semantic Scholar
Analysis of the Italian cohort of late-onset Pompe disease (LOPD) patients after 10 and 15 years of therapy with alglucosidase alfa
T. Mongini, G. Gadaleta, P. Alonge, L. Vercelli +54 more
2025Journal of Neurology2 citations
Semantic Scholar
Correction to: Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review
Stefania Della Vecchia, A. Tessa, C. Dosi, J. Baldacci +35 more
2021Journal of Neurology2 citations Open access
Semantic Scholar
Genetic Counseling and NGS Screening for Recessive LGMD2A Families
C. Strafella, V. Caputo, Giulia Campoli, Rosaria Maria Galota +7 more
2020High-Throughput2 citations Open access
Semantic Scholar
P.179 - PLEC gene mutations cause familial disto-proximal myopathy and long QT syndrome mimicking mitochondrial disease
S. Servidei, G. Primiano, V. Muto, C. Cuccagna +6 more
20172 citations
Semantic Scholar
Spinal Cord Involvement in Adult Mitochondrial Diseases: A Cohort Study
G. Primiano, P. Mariotti, Ida Turrini, C. Sancricca +4 more
2021Life1 citations Open access
Semantic Scholar
3.01VP Late-onset Pompe disease adverse event management: a consensus for patient safety
O. Musumeci, Lucia Ruggiero, G. Primiano, M. Croce +8 more
2026Neuromuscular Disorders0 citations
Semantic Scholar
1.74eP Rehabilitation needs and care models in spinal muscular atrophy: a real-world analysis from an italian community rehabilitation center
A. Frongia, M. Briganti, Anna Lisa Branca, Valentina Saraceni +8 more
2026Neuromuscular Disorders0 citations
Semantic Scholar
Correction to: Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review
Stefania Della Vecchia, A. Tessa, C. Dosi, J. Baldacci +35 more
2023Journal of Neurology0 citations Open access
Semantic Scholar
Asymmetrical anterior thigh muscle atrophy as an atypical presentation of RYR1-core myopathy.
G. Primiano, F. Fattori, C. Sancricca, E. Bertini +1 more
2021Neuromuscular Disorders0 citations
Semantic Scholar
Reply to the letter entitled "Predictors of respiratory impairment in patients with myotonic dystrophy type 1".
Salvatore Rossi, G. Della Marca, M. Ricci, Alessia Perna +16 more
2019Journal of Neurological Sciences0 citations
Semantic Scholar
Afectación del Sistema Nervioso Central en las encefalomiopatías mitocondriales
S. Servidei, G. Primiano, Donato Sauchelli, C. Cuccagna +3 more
20160 citations
Semantic Scholar
Frequency of Cerebrovascular Abnormalities in Patients with Late-Onset Pompe Disease: Our Experience
C. Sancricca, G. Primiano, D. Bernardo, D. Sauchelli +2 more
2015Journal of Neuromuscular Diseases0 citations Open access
Semantic Scholar

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