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27 results

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Page 1
Precursory worldwide signatures of earthquake occurrences on Swarm satellite data.
De Santis A, Marchetti D, Pavón-Carrasco FJ, Cianchini G, Perrone L, Abbattista C, Alfonsi L, Amoruso L, Campuzano SA, Carbone M, Cesaroni C, De Franceschi G, De Santis A, Di Giovambattista R, Ippolito A, Piscini A, Sabbagh D, Soldani M, Santoro F, Spogli L, Haagmans R. De Santis A, et al. Among authors: cesaroni c. Sci Rep. 2019 Dec 30;9(1):20287. doi: 10.1038/s41598-019-56599-1. Sci Rep. 2019. PMID: 31889060 Free PMC article.
Geosystemics View of Earthquakes.
De Santis A, Abbattista C, Alfonsi L, Amoruso L, Campuzano SA, Carbone M, Cesaroni C, Cianchini G, De Franceschi G, De Santis A, Di Giovambattista R, Marchetti D, Martino L, Perrone L, Piscini A, Rainone ML, Soldani M, Spogli L, Santoro F. De Santis A, et al. Among authors: cesaroni c. Entropy (Basel). 2019 Apr 18;21(4):412. doi: 10.3390/e21040412. Entropy (Basel). 2019. PMID: 33267126 Free PMC article.
Guillain-Barrè Syndrome-Retrospective Analysis of Data from a Cohort of Patients Referred to a Tertiary Care Pediatric Neuromuscular Center from 2000 to 2017: Electrophysiological Findings, Outcomes, and a Brief Literature Review.
Cavirani B, Baga M, Cesaroni CA, Rizzi S, Spagnoli C, Frattini D, Della Giustina E, Pisani F, Fusco C. Cavirani B, et al. Among authors: cesaroni ca. Medicina (Kaunas). 2024 Sep 12;60(9):1490. doi: 10.3390/medicina60091490. Medicina (Kaunas). 2024. PMID: 39336531 Free PMC article. Review.
Two novel compound heterozygous HOXB1 variants in congenital facial palsy: A case report and a brief review of the literature.
Brugnoli C, Rizzi S, Cesaroni CA, Spagnoli C, Pregnolato G, Caraffi SG, Napoli M, Pascarella R, Zuntini R, Peluso F, Garavelli L, Chiarotto E, Leon A, Frattini D, Fusco C. Brugnoli C, et al. Among authors: cesaroni ca. Am J Med Genet A. 2025 Jan;197(1):e63848. doi: 10.1002/ajmg.a.63848. Epub 2024 Sep 5. Am J Med Genet A. 2025. PMID: 39235314 Review.
Early-onset dysphagia and severe neurodevelopmental disorder as early signs in a patient with two novel variants in NARS1: a case report and brief review of the literature.
Cesaroni CA, Contrò G, Spagnoli C, Cancelliere F, Caraffi SG, Leon A, Stefanini C, Frattini D, Rizzi S, Cavalli A, Garavelli L, Fusco C. Cesaroni CA, et al. Neurogenetics. 2024 Jul;25(3):287-291. doi: 10.1007/s10048-024-00760-0. Epub 2024 Apr 23. Neurogenetics. 2024. PMID: 38652341 Review.
27 results