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Luca Pradotto

Observed names: L Pradotto, L. G. Pradotto, L. Pradotto, Luca G. Pradotto, Luca Guglielmo Pradotto, Luca Guglielmo Pradotto, PRADOTTO, Luca Guglielmo, Pradotto, Luca, Pradotto, Luca Guglielmo
Observed institutions: Università Cattolica del Sacro Cuore, Università degli Studi del Piemonte Orientale “Amedeo Avogadro”, University of Campania "Luigi Vanvitelli", Azienda Ospedaliera Citta' della Salute e della Scienza di Torino, Istituti Clinici Scientifici Maugeri, Fondazione Salvatore Maugeri, Ospedale Civile Di Ivrea, Azienda Ospedaliero Universitaria Maggiore della Carita, IRCCS Istituto Auxologico Italiano, Ospedale San Giuseppe, University of Turin, University of Genoa
ORCID: 0000-0003-1103-1964
Observed ORCID: 0000-0003-1103-1964
OpenAlex ID: A5060442771
Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area
2016 · A. Cortese, G. Vita, et al. · Journal of Neurology · 98
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ATTRv amyloidosis Italian Registry: clinical and epidemiological data
2020 · Massimo Russo, Laura Obici, et al. · Amyloid · 91
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ATXN2 polyQ intermediate repeats are a modifier of ALS survival
2014 · Adriano Chiò, Andrea Calvo, et al. · Neurology · 66
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Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus
2020 · M. Grandis, L. Obici, et al. · Orphanet Journal of Rare Diseases · 52
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Nerve Compression Injuries After Prolonged Prone Position Ventilation in Patients With SARS-CoV-2: A Case Series
2020 · Luigia Brugliera, Massimo Filippi, et al. · Archives of Physical Medicine and Rehabilitation · 51
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MDM2 overexpression is associated with short survival in adults with medulloblastoma
2002 · Maria Teresa Giordana, Debora Duó, et al. · Neuro-Oncology · 51
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A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy
2009 · A Brussino, G Vaula, et al. · Journal of Neurology Neurosurgery & Psychiatry · 38
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Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis
2017 · Andrea Iorio, Antonella De Lillo, et al. · European Journal of Human Genetics · 37
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Molecular Genetic Changes in a Series of Neuroepithelial Tumors of Childhood
2002 · Alessia Di Sapio, Isabella Morra, et al. · Journal of Neuro-Oncology · 28
Most recent common ancestor ofTTRVal30Met mutation in Italian population and its potential role in genotype-phenotype correlation
2014 · Andrea Iorio, Flavio De Angelis, et al. · Amyloid · 26
Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
2012 · S. Testi, G. Malerba, et al. · Journal of the Neurological Sciences · 26
Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis
2017 · Andrea Iorio, Flavio De Angelis, et al. · BMC Genomics · 24
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Episodic ataxia and SCA6 within the same family due to the D302N CACNA1A gene mutation
2016 · Luca Pradotto, Monica Mencarelli, et al. · Journal of the Neurological Sciences · 24
Psychosocial burden and professional and social support in patients with hereditary transthyretin amyloidosis (ATTRv) and their relatives in Italy
2021 · ATTRv Collaborators, Lorenza Magliano, et al. · Orphanet Journal of Rare Diseases · 21
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Prevalence and phenotype of the c.1529C>T SPG 7 variant in adult‐onset cerebellar ataxia in Italy
2018 · C. Mancini, E. Giorgio, et al. · European Journal of Neurology · 19
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Patisiran in ATTRv amyloidosis with polyneuropathy: “PatisiranItaly” multicenter observational study
2025 · Vincenzo Di Stefano, Pietro Guaraldi, et al. · Journal of Neurology · 17
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Utility of Boston Qualitative Scoring System for Rey-Osterrieth Complex Figure: evidence from a Parkinson’s Diseases sample
2016 · Federica Scarpina, Erika Ambiel, et al. · Neurological Sciences · 15
A new NOTCH3 mutation presenting as primary intracerebral haemorrhage
2011 · Luca Pradotto, Laura Orsi, et al. · Journal of the Neurological Sciences · 14
Amyloid polyneuropathy following domino liver transplantation
2011 · Luca Pradotto, Alessandro Franchello, et al. · Muscle & Nerve · 14
Recurrent transient global amnesia as presenting symptoms of CADASIL
2016 · Luca Pradotto, Laura Orsi, et al. · Clinical Case Reports · 13
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Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene
2008 · L. Pradotto, G. Azan, et al. · Journal of the Neurological Sciences · 13
Solid Lipid Nanoparticles Carrying Oligonucleotides Inhibit Vascular Endothelial Growth Factor Expression in Rat Glioma Models
2009 · Andrea M. Brioschi, Sara Calderoni, et al. · Journal of Nanoneuroscience · 11
Severe Postoperative Chronic Constipation Related to Anorectal Malformation Managed with Osteopathic Manipulative Treatment
2020 · Luca Vismara, Vincenzo Cozzolino, et al. · Case Reports in Gastroenterology · 7
An atypical case of sporadic fatal insomnia
2009 · L Priano, G Giaccone, et al. · Journal of Neurology Neurosurgery & Psychiatry · 7
Reliability and Validity of the Variability Model Testing Procedure for Somatic Dysfunction Assessment: A Comparison with Gait Analysis Parameters in Healthy Subjects
2024 · Luca Vismara, Andrea Bergna, et al. · Healthcare · 6
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Works count: 66
Citation count: 787
H-index: 16
I10-index: 22
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