Aiello F - Search Results

1

Epilepsy in Rett syndrome: clinical and genetic features.

Pintaudi M, Calevo MG, Vignoli A, Parodi E, Aiello F, Baglietto MG, Hayek Y, Buoni S, Renieri A, Russo S, Cogliati F, Giordano L, Canevini M, Veneselli E. Pintaudi M, et al. Among authors: aiello f. Epilepsy Behav. 2010 Nov;19(3):296-300. doi: 10.1016/j.yebeh.2010.06.051. Epub 2010 Aug 21. Epilepsy Behav. 2010. PMID: 20728410 Free article.

2

SHP2's gain-of-function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction.

Priolo M, Palermo V, Aiello F, Ciolfi A, Pannone L, Muto V, Motta M, Mancini C, Radio FC, Niceta M, Leoni C, Pintomalli L, Carrozzo R, Rajola G, Mammì C, Zampino G, Martinelli S, Dallapiccola B, Pichierri P, Tartaglia M. Priolo M, et al. Among authors: aiello f. Clin Genet. 2022 Jul;102(1):12-21. doi: 10.1111/cge.14140. Epub 2022 Apr 17. Clin Genet. 2022. PMID: 35396703

3

RAD51 and mitotic function of mus81 are essential for recovery from low-dose of camptothecin in the absence of the WRN exonuclease.

Aiello FA, Palma A, Malacaria E, Zheng L, Campbell JL, Shen B, Franchitto A, Pichierri P. Aiello FA, et al. Nucleic Acids Res. 2019 Jul 26;47(13):6796-6810. doi: 10.1093/nar/gkz431. Nucleic Acids Res. 2019. PMID: 31114910 Free PMC article.

4

Author Correction: Rad52 prevents excessive replication fork reversal and protects from nascent strand degradation.

Malacaria E, Pugliese GM, Honda M, Marabitti V, Aiello FA, Spies M, Franchitto A, Pichierri P. Malacaria E, et al. Nat Commun. 2019 May 1;10(1):2023. doi: 10.1038/s41467-019-10072-9. Nat Commun. 2019. PMID: 31043602 Free PMC article.

5

Rad52 prevents excessive replication fork reversal and protects from nascent strand degradation.

Malacaria E, Pugliese GM, Honda M, Marabitti V, Aiello FA, Spies M, Franchitto A, Pichierri P. Malacaria E, et al. Nat Commun. 2019 Mar 29;10(1):1412. doi: 10.1038/s41467-019-09196-9. Nat Commun. 2019. PMID: 30926821 Free PMC article.

6

Trimethylaminuria in a girl with Prader-Willi syndrome and del(15)(q11q13).

Chen H, Aiello F. Chen H, et al. Among authors: aiello f. Am J Med Genet. 1993 Feb 1;45(3):335-9. doi: 10.1002/ajmg.1320450310. Am J Med Genet. 1993. PMID: 8434620 Review.

7

The Appraisal of Adults with Congenital Heart Disease: Lesson from Comparison of Surgical Outcomes.

Giamberti A, Ferrero P, Caldaroni F, Varrica A, Pasqualin G, D'Aiello F, Bergonzoni E, Ranucci M, Chessa M. Giamberti A, et al. Among authors: d aiello f. Pediatr Cardiol. 2024 May 27. doi: 10.1007/s00246-024-03517-6. Online ahead of print. Pediatr Cardiol. 2024. PMID: 38802599

8

A Squaramide-Based Organocatalyst as a Novel Versatile Chiral Solvating Agent for Carboxylic Acids.

Spiaggia F, Uccello Barretta G, Iuliano A, Baldassari C, Aiello F, Balzano F. Spiaggia F, et al. Among authors: aiello f. Molecules. 2024 May 19;29(10):2389. doi: 10.3390/molecules29102389. Molecules. 2024. PMID: 38792248 Free PMC article.

9

Outcomes and clinical characteristics of the compassionate use of plitidepsin in COVID-19 patients with solid tumours, haematological malignancies or anti-CD20 antibody treatment.

Aguareles J, Villares Fernández P, Forné C, Martí-Ballesteros EM, Pradillo Fernández V, Sotres-Fernandez G, de la Fuente-Burguera A, Navarro-San Francisco C, Buzón-Martín LM, García-Delangue T, Aiello FT, Carnevali-Ruiz D, Lloris R, Luepke-Estefan XE, López-Martín JA, Jimeno JM, García-Casas A, Guisado-Vasco P. Aguareles J, et al. Among authors: aiello ft. Infect Dis (Lond). 2024 Jul;56(7):575-580. doi: 10.1080/23744235.2024.2351043. Epub 2024 May 14. Infect Dis (Lond). 2024. PMID: 38743059

10

Prior authorization must make patient care the priority!

Aiello F. Aiello F. J Vasc Surg. 2024 May;79(5):1204-1205. doi: 10.1016/j.jvs.2023.12.010. J Vasc Surg. 2024. PMID: 38642970 No abstract available.

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