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Corrigendum: The new Italian registry of infantile thrombosis (RITI): a reflection on its journey, challenges and pitfalls.
Front Pediatr. 2024 Jan 31;12:1372754. doi: 10.3389/fped.2024.1372754. eCollection 2024.
Front Pediatr. 2024.
PMID: 38357512
Free PMC article.
Generation of two iPSC lines from Mowat-Wilson syndrome patients carrying heterozygous ZEB2 mutations.
Gorrieri G, Tamburro S, Baldassari S, Guerrisi S, Zara F, Ricci E, Maria Cordelli D, Scudieri P, Musante I.
Gorrieri G, et al. Among authors: maria cordelli d.
Stem Cell Res. 2024 Apr;76:103333. doi: 10.1016/j.scr.2024.103333. Epub 2024 Feb 9.
Stem Cell Res. 2024.
PMID: 38350246
Free article.
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The new Italian registry of infantile thrombosis (RITI): A reflection on its journey, challenges and pitfalls.
Pelizza MF, Martinato M, Rosati A, Nosadini M, Saracco P, Giordano P, Luciani M, Ilardi L, Lasagni D, Molinari AC, Bagna R, Palmieri A, Ramenghi LA, Grassi M, Magarotto M, Magnetti F, Francavilla A, Indolfi G, Suppiej A, Gentilomo C, Restelli R, Tufano A, Tormene D, Pin JN, Tona C, Meneghesso D, Rota L, Conti M, Russo G, Lorenzoni G, Gregori D, Sartori S, Simioni P; Collaborators of the R.I.T.I. (Italian Registry of Infantile Thrombosis).
Pelizza MF, et al.
Front Pediatr. 2023 Apr 20;11:1094246. doi: 10.3389/fped.2023.1094246. eCollection 2023.
Front Pediatr. 2023.
PMID: 37152311
Free PMC article.
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