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federico del giudice
(289 results)?
PIEZO1 mutations impact on early clinical manifestations of myelodysplastic syndromes.
Am J Hematol. 2023 Apr;98(4):E72-E75. doi: 10.1002/ajh.26863. Epub 2023 Feb 14.
Am J Hematol. 2023.
PMID: 36695705
Free article.
No abstract available.
SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic Cells.
Rosato BE, Marra R, D'Onofrio V, Del Giudice F, Della Monica S, Iolascon A, Andolfo I, Russo R.
Rosato BE, et al. Among authors: del giudice f.
Int J Mol Sci. 2022 Jan 24;23(3):1304. doi: 10.3390/ijms23031304.
Int J Mol Sci. 2022.
PMID: 35163229
Free PMC article.
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Clinical exome-based panel testing for medically actionable secondary findings in a cohort of 383 Italian participants.
Martone S, Buonagura AT, Marra R, Rosato BE, Del Giudice F, Bonfiglio F, Capasso M, Iolascon A, Andolfo I, Russo R.
Martone S, et al. Among authors: del giudice f.
Front Genet. 2022 Nov 10;13:956723. doi: 10.3389/fgene.2022.956723. eCollection 2022.
Front Genet. 2022.
PMID: 36437915
Free PMC article.
Item in Clipboard
Coinheritance of PIEZO1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriers.
Pinto VM, Russo R, Quintino S, Rosato BE, Marra R, Del Giudice F, Mogni M, Maffei M, Iolascon A, Forni GL, Andolfo I.
Pinto VM, et al. Among authors: del giudice f.
Am J Hematol. 2023 Jun;98(6):E130-E133. doi: 10.1002/ajh.26901. Epub 2023 Mar 17.
Am J Hematol. 2023.
PMID: 36882369
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Rationale and design of the pragmatic clinical trial tREatment with Beta-blockers after myOcardial infarction withOut reduced ejection fracTion (REBOOT).
Rossello X, Raposeiras-Roubin S, Latini R, Dominguez-Rodriguez A, Barrabés JA, Sánchez PL, Anguita M, Fernández-Vázquez F, Pascual-Figal D, De la Torre Hernandez JM, Ferraro S, Vetrano A, Pérez-Rivera JA, Prada-Delgado O, Escalera N, Staszewsky L, Pizarro G, Agüero J, Pocock S, Ottani F, Fuster V, Ibáñez B; REBOOT-CNIC investigators.
Rossello X, et al.
Eur Heart J Cardiovasc Pharmacother. 2022 May 5;8(3):291-301. doi: 10.1093/ehjcvp/pvab060.
Eur Heart J Cardiovasc Pharmacother. 2022.
PMID: 34351426
Clinical Trial.
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Rapid and portable, lab-on-chip, point-of-care genotyping for evaluating clopidogrel metabolism.
Marziliano N, Notarangelo MF, Cereda M, Caporale V, Coppini L, Demola MA, Guidorossi A, Crocamo A, Pigazzani F, Boffetti F, del Giudice F, Orsini F, Pirola D, Cocci A, Manzalini C, Casu G, Bianchessi M, Ardissino D, Merlini PA.
Marziliano N, et al. Among authors: del giudice f.
Clin Chim Acta. 2015 Dec 7;451(Pt B):240-6. doi: 10.1016/j.cca.2015.10.003. Epub 2015 Oct 8.
Clin Chim Acta. 2015.
PMID: 26453416
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One gene, two opposite phenotypes: a case report of hereditary anemia due to a loss-of-function variant in the EPAS1 gene.
Rosato BE, Marra R, Del Giudice F, Nostroso A, Gobbi S, Bruschi B, Coccia P, Monaco V, Monti M, Iolascon A, Andolfo I, Russo R.
Rosato BE, et al. Among authors: del giudice f.
Haematologica. 2023 Oct 1;108(10):2872-2876. doi: 10.3324/haematol.2022.282457.
Haematologica. 2023.
PMID: 37102609
Free PMC article.
No abstract available.
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