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P. Accorsi · SciRah

Researcher profile · Semantic Scholar

P. Accorsi

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P. Accorsi — researcher profile on SciRah

h-index: 31
Works: 168
Citations: 3,330

Most-cited papers

STXBP1 encephalopathy
H. Stamberger, M. Nikanorova, M. Willemsen, P. Accorsi +53 more
2016Neurology188 citations Open access
Semantic Scholar
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
K. Johannesen, Yuan-Yuan Liu, M. Koko, C. E. Gjerulfsen +124 more
2021medRxiv132 citations Open access
Semantic Scholar
Mutation Spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and Genotype–Phenotype Correlations in Warburg Micro Syndrome and Martsolf Syndrome
Mark T. Handley, D. Morris-Rosendahl, Stephen Brown, F. Macdonald +31 more
2013Human Mutation132 citations Open access
Semantic Scholar
Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care
Ivan Ivanovski, O. Djuric, S. Caraffi, Daniela Santodirocco +76 more
2018Genetics in Medicine88 citations Open access
Semantic Scholar
The spectrum of intermediate SCN8A‐related epilepsy
Kathrine M. Johannesen, E. Gardella, A. Encinas, A. Lehesjoki +41 more
2019Epilepsia83 citations Open access
Semantic Scholar
LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance.
C. Dallabona, T. Abbink, R. Carrozzo, A. Torraco +30 more
2016Brain : a journal of neurology65 citations Open access
Semantic Scholar
Neuroimaging Findings in Mowat-Wilson Syndrome: A Study of 54 Patients
L. Garavelli, Ivan Ivanovski, S. Caraffi, Daniela Santodirocco +54 more
2016Genetics in Medicine55 citations Open access
Semantic Scholar
Early visual training and environmental adaptation for infants with visual impairment
E. Fazzi, S. Micheletti, S. Calza, L. Merabet +17 more
2021Developmental Medicine & Child Neurology52 citations Open access
Semantic Scholar
Defining the electroclinical phenotype and outcome of PCDH19‐related epilepsy: A multicenter study
M. Trivisano, N. Pietrafusa, A. Terracciano, C. Marini +36 more
2018Epilepsia49 citations
Semantic Scholar
Depression and Anxiety in Mothers Who Were Pregnant During the COVID-19 Outbreak in Northern Italy: The Role of Pandemic-Related Emotional Stress and Perceived Social Support
Serena Grumi, L. Provenzi, P. Accorsi, Giacomo Biasucci +21 more
2021Frontiers in Psychiatry48 citations Open access
Semantic Scholar
Epilepsy in the setting of full trisomy 18: A multicenter study on 18 affected children with and without structural brain abnormalities
S. Matricardi, A. Spalice, V. Salpietro, G. Di Rosa +15 more
2016American Journal of Medical Genetics. Part C, Seminars in Medical Genetics48 citations Open access
Semantic Scholar
Evidence- and consensus-based recommendations for phlebotomy in polycythemia vera
T. Barbui, F. Passamonti, P. Accorsi, F. Pane +5 more
2018Leukemia44 citations
Semantic Scholar
Pediatric epilepsy following neonatal seizures symptomatic of stroke.
A. Suppiej, M. Mastrangelo, L. Mastella, P. Accorsi +7 more
2016Brain & development (Tokyo. 1979)43 citations
Semantic Scholar
Neurodevelopmental profile in Angelman syndrome: more than low intelligence quotient
S. Micheletti, Filippo Palestra, P. Martelli, P. Accorsi +4 more
2016Italian Journal of Pediatrics39 citations Open access
Semantic Scholar
The hyperkinetic movement disorder of FOXG1‐related epileptic–dyskinetic encephalopathy
E. Cellini, A. Vignoli, Tiziana Pisano, M. Falchi +6 more
2016Developmental Medicine & Child Neurology39 citations Open access
Semantic Scholar
Oral-facial-digital syndrome type VI: is C5orf42 really the major gene?
M. Romani, F. Mancini, A. Micalizzi, A. Poretti +29 more
2014Human Genetics37 citations Open access
Semantic Scholar
Refractory absence seizures: An Italian multicenter retrospective study.
E. Franzoni, S. Matricardi, V. Di Pisa, G. Capovilla +22 more
2015European journal of paediatric neurology36 citations Open access
Semantic Scholar
CHD2 mutations are a rare cause of generalized epilepsy with myoclonic-atonic seizures.
M. Trivisano, P. Striano, Jacopo Sartorelli, L. Giordano +7 more
2015Epilepsy & Behavior36 citations
Semantic Scholar
Thyroid hormones increase collagen I and cartilage oligomeric matrix protein (COMP) expression in vitro human tenocytes.
A. Berardi, F. Oliva, M. Berardocco, Marina la Rovere +2 more
2014Muscles Ligaments and Tendons Journal35 citations Open access
Semantic Scholar
Epilepsy Course and Developmental Trajectories in STXBP1-DEE
G. Balagura, J. Xian, A. Riva, Francesca Marchese +54 more
2022Neurology: Genetics34 citations Open access
Semantic Scholar
BORN study: a multicenter randomized trial investigating cord blood red blood cell transfusions to reduce the severity of retinopathy of prematurity in extremely low gestational age neonates
L. Teofili, P. Papacci, N. Orlando, M. Bianchi +23 more
2022Trials32 citations Open access
Semantic Scholar
Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants
Federica Malerba, Giulio Alberini, G. Balagura, Francesca Marchese +36 more
2020Neurology: Genetics30 citations Open access
Semantic Scholar
Apheresis treatment of cryoglobulinemic vasculitis: A multicentre cohort study of 159 patients.
P. Marson, G. Monti, F. Montani, A. Riva +15 more
2018Transfusion and Apheresis Science28 citations Open access
Semantic Scholar
Clinical features of Sturge-Weber syndrome without facial nevus: five novel cases.
L. Siri, L. Giordano, P. Accorsi, M. Cossu +3 more
2013European journal of paediatric neurology26 citations
Semantic Scholar
Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study
L. Giordano, A. Vignoli, R. Cusmai, P. Parisi +10 more
2013Epilepsia26 citations
Semantic Scholar
Severe Streptococcus equi Subspecies zooepidemicus Outbreak from Unpasteurized Dairy Product Consumption, Italy
Serena Bosica, A. Chiaverini, M. D. De Angelis, A. Petrini +21 more
2023Emerging Infectious Diseases25 citations Open access
Semantic Scholar
Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort
C. Po', M. Nosadini, M. Zedde, R. Pascarella +50 more
2022Frontiers in Pediatrics25 citations Open access
Semantic Scholar
Position paper on the preparation of immune plasma to be used in the treatment of patients with COVID-19
P. Accorsi, Pierluigi Berti, Vincenzo de Angelis, G. De Silvestro +2 more
2020Transfusion and Apheresis Science24 citations Open access
Semantic Scholar
Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients.
G. Balagura, A. Riva, Francesca Marchese, M. Iacomino +28 more
2020European journal of paediatric neurology24 citations
Semantic Scholar
NOTCH1 Is Aberrantly Activated in Chronic Lymphocytic Leukemia Hematopoietic Stem Cells
M. Di Ianni, S. Baldoni, B. Del Papa, Patrizia Aureli +16 more
2018Frontiers in Oncology22 citations Open access
Semantic Scholar
MR Imaging Diagnosis of Diencephalic-Mesencephalic Junction Dysplasia in Fetuses with Developmental Ventriculomegaly
M. Severino, A. Righini, D. Tortora, L. Pinelli +6 more
2017American Journal of Neuroradiology21 citations Open access
Semantic Scholar
CLINICAL-GRADE EXPANDED TREGS ARE ENRICHED WITH HIGHLY SUPPRESSIVE CELLS PRODUCING IL-10, GRANZYME B AND IL-35.
Francesca Ulbar, Ida Villanova, R. Giancola, S. Baldoni +24 more
2020Biology of Blood and Marrow Transplantation20 citations Open access
Semantic Scholar
Efficacy and safety of rufinamide in children under four years of age with drug-resistant epilepsies.
S. Grosso, G. Coppola, Serena Donetti Dontin, G. Gobbi +5 more
2014European journal of paediatric neurology20 citations
Semantic Scholar
A registry for Dravet syndrome: The Italian experience
S. Balestrini, Viola Doccini, S. Giometto, E. Lucenteforte +43 more
2023Epilepsia Open19 citations Open access
Semantic Scholar
Secondary solid cancer following hematopoietic cell transplantation in patients with thalassemia major
S. Santarone, A. Pepe, A. Meloni, A. Natale +13 more
2018Bone Marrow Transplantation18 citations Open access
Semantic Scholar
Electroclinical findings and long‐term outcomes in epileptic patients with inv dup (15)
S. Matricardi, F. Darra, A. Spalice, C. Basti +17 more
2018Acta Neurologica Scandinavica18 citations Open access
Semantic Scholar
Oral melatonin as a new tool for neuroprotection in preterm newborns: study protocol for a randomized controlled trial
F. Garofoli, S. Longo, Camilla Pisoni, P. Accorsi +10 more
2021Trials16 citations Open access
Semantic Scholar
Clinical dissection of early onset absence epilepsy in children and prognostic implications
S. Agostinelli, P. Accorsi, F. Beccaria, V. Belcastro +26 more
2013Epilepsia16 citations
Semantic Scholar
A policy for the disposal of autologous hematopoietic progenitor cells: report from an Italian consensus panel
P. Perseghin, M. Marchetti, L. Pierelli, A. Olivieri +6 more
2014Transfusion15 citations
Semantic Scholar
Higher cyclophosphamide dose grants optimal stem cell collection after daratumumab-based induction in multiple myeloma
C. Liberatore, T. Perini, C. Passeri, V. Ferla +17 more
2023Haematologica13 citations Open access
Semantic Scholar
NOTCH and Graft-Versus-Host Disease
M. Di Ianni, B. Del Papa, S. Baldoni, A. Di Tommaso +11 more
2018Frontiers in Immunology12 citations Open access
Semantic Scholar
Expanding the phenotype of MED 17 mutations: Description of two new cases and review of the literature
A. Agostini, D. Marchetti, C. Izzi, I. Cocco +4 more
2018American Journal of Medical Genetics Part B: Neuropsychiatric Genetics12 citations
Semantic Scholar
High seroprevalence of HCV in the Abruzzo Region, Italy: results on a large sample from opt-out pre-surgical screening
E. Polilli, M. Tontodonati, M. Flacco, T. Ursini +9 more
2016Infection12 citations
Semantic Scholar
Cerebral folate transporter deficiency syndrome in three siblings: Why genetic testing for developmental and epileptic encephalopathies should be performed early and include the FOLR1 gene
S. Brunetti, L. Malerba, L. Giordano, E. Parrini +5 more
2021American Journal of Medical Genetics. Part A11 citations
Semantic Scholar
Further delineation and long-term evolution of electroclinical phenotype in Mowat Wilson Syndrome. A longitudinal study in 40 individuals.
Emilia Ricci, A. Fetta, L. Garavelli, S. Caraffi +29 more
2021Epilepsy & Behavior11 citations
Semantic Scholar
Treg-protected donor lymphocyte infusions: a new tool to address the graft-versus-leukemia effect in the absence of graft-versus-host disease in patients relapsed after HSCT
M. Di Ianni, P. Olioso, R. Giancola, S. Santarone +8 more
2017International journal of hematology11 citations
Semantic Scholar
Identification of circulating CD31+CD45+ cell populations with the potential to differentiate into erythroid cells
M. C. Monaco, D. Maric, O. Salvucci, C. Passeri +3 more
2021Stem cell research & therapeutics10 citations Open access
Semantic Scholar
Sleep in Mowat-Wilson Syndrome: a clinical and video-polysomnographic study.
V. Di Pisa, F. Provini, S. Ubertiello, S. Bonetti +12 more
2019Sleep Medicine10 citations
Semantic Scholar
Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients.
A. Verrotti, R. Cusmai, F. Darra, P. Martelli +15 more
2014Epilepsy Research10 citations
Semantic Scholar
A PUS7 gene pathogenic variant causing self‐injurious behavior, sleep disturbances, and developmental delay: A case report
A. Muda, L. Malerba, L. Giordano, E. Fazzi +1 more
2023American Journal of Medical Genetics. Part A9 citations
Semantic Scholar

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P. Striano×15
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S. Savasta×8
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A. Spalice — researcher profile on SciRah

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F. Darra — researcher profile on SciRah

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L. Pinelli — researcher profile on SciRah

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N. Specchio — researcher profile on SciRah

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S. Matricardi — researcher profile on SciRah

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