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Year | Number of Results |
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2021 | 2 |
2022 | 3 |
2023 | 2 |
2024 | 2 |
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Page 1
Atypical, Composite, or Blended Phenotypes: How Different Molecular Mechanisms Could Associate in Double-Diagnosed Patients.
Genes (Basel). 2022 Jul 19;13(7):1275. doi: 10.3390/genes13071275.
Genes (Basel). 2022.
PMID: 35886058
Free PMC article.
Guidelines for Vascular Anomalies by the Italian Society for the study of Vascular Anomalies (SISAV).
Stillo F, Mattassi R, Diociaiuti A, Neri I, Baraldini V, Dalmonte P, Amato B, Ametrano O, Amico G, Bianchini G, Campisi C, Cattaneo E, Causin F, Cavalli R, Colletti G, Corbeddu M, Coppo P, DE Fiores A, DI Giuseppe P, El Hachem M, Esposito F, Fulcheri E, Gandolfo C, Grussu F, Guglielmo A, Leuzzi M, Manunza F, Moneghini L, Monzani N, Nicodemi E, Occella C, Orso M, Pagella F, Paolantonio G, Pasetti F, Rollo M, Ruggiero F, Santecchia L, Spaccini L, Taurino M, Vaghi M, Vercellio G, Zama M, Zocca A, Aguglia M, Castronovo EL, DE Lorenzi E, Fontana E, Gusson E, Lanza J, Lizzio R, Mancardi MM, Rosina E.
Stillo F, et al. Among authors: rosina e.
Int Angiol. 2022 Apr;41(2 Suppl 1):1-130. doi: 10.23736/S0392-9590.22.04902-1.
Int Angiol. 2022.
PMID: 35546136
Free article.
No abstract available.
Item in Clipboard
Comparison of first-tier whole-exome sequencing with a multi-step traditional approach for diagnosing paediatric outpatients: An Italian prospective study.
Rosina E, Pezzani L, Apuril E, Pezzoli L, Marchetti D, Bellini M, Lucca C, Meossi C, Massimello M, Mariani M, Scatigno A, Cattaneo E, Colombo L, Maitz S, Cereda A, Milani D, Spaccini L, Bedeschi MF, Selicorni A, Iascone M.
Rosina E, et al.
Mol Genet Genomic Med. 2024 Jan;12(1):e2316. doi: 10.1002/mgg3.2316. Epub 2023 Dec 2.
Mol Genet Genomic Med. 2024.
PMID: 38041506
Free PMC article.
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Double somatic mosaicism in Cornelia de Lange syndrome.
Pezzani L, Pezzoli L, Rosina E, Scatigno A, Cereda A, Lucca C, Bellini M, Marchetti D, Maino M, Mangili G, Selicorni A, Iascone M.
Pezzani L, et al. Among authors: rosina e.
Am J Med Genet A. 2024 May;194(5):e63512. doi: 10.1002/ajmg.a.63512. Epub 2023 Dec 22.
Am J Med Genet A. 2024.
PMID: 38135466
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Management of BRCA Tumour Testing in an Integrated Molecular Tumour Board Multidisciplinary Model.
Azzollini J, Vingiani A, Agnelli L, Tamborini E, Perrone F, Conca E, Capone I, Busico A, Peissel B, Rosina E, Ducceschi M, Mantiero M, Lopez S, Raspagliesi F, Niger M, Duca M, Damian S, Proto C, de Braud F, Pruneri G, Manoukian S.
Azzollini J, et al. Among authors: rosina e.
Front Oncol. 2022 Apr 8;12:857515. doi: 10.3389/fonc.2022.857515. eCollection 2022.
Front Oncol. 2022.
PMID: 35463374
Free PMC article.
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Correction to: Incidental finding of APC deletion in a child: double trouble or double chance? - a case report.
Rosina E, Rinaldi B, Silipigni R, Bergamaschi L, Gattuso G, Signoroni S, Guerneri S, Carnevali A, Marchisio PG, Milani D.
Rosina E, et al.
Ital J Pediatr. 2021 Sep 14;47(1):185. doi: 10.1186/s13052-021-01135-z.
Ital J Pediatr. 2021.
PMID: 34521463
Free PMC article.
No abstract available.
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Incidental finding of APC deletion in a child: double trouble or double chance? - a case report.
Rosina E, Rinaldi B, Silipigni R, Bergamaschi L, Gattuso G, Signoroni S, Guerneri S, Carnevali A, Marchisio PG, Milani D.
Rosina E, et al.
Ital J Pediatr. 2021 Feb 15;47(1):31. doi: 10.1186/s13052-021-00969-x.
Ital J Pediatr. 2021.
PMID: 33588901
Free PMC article.
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