Immacolata Andolfo - Search Results

Year	Number of Results
2009	2
2010	1
2011	4
2012	5
2013	5
2014	2
2015	4
2016	6
2017	7
2018	7
2019	12
2020	14
2021	24
2022	20
2023	8
2024	4

1

Nrf2 Plays a Key Role in Erythropoiesis during Aging.

Mbiandjeu SCT, Siciliano A, Mattè A, Federti E, Perduca M, Melisi D, Andolfo I, Amoresano A, Iolascon A, Valenti MT, Turrini F, Bovi M, Pisani A, Recchiuti A, Mattoscio D, Riccardi V, Dalle Carbonare L, Brugnara C, Mohandas N, De Franceschi L. Mbiandjeu SCT, et al. Among authors: andolfo i. Antioxidants (Basel). 2024 Apr 12;13(4):454. doi: 10.3390/antiox13040454. Antioxidants (Basel). 2024. PMID: 38671902 Free PMC article.

2

Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patients.

Marra R, Nostroso A, Rosato BE, Esposito FM, D'Onofrio V, Iscaro A, Gambale A, Bruschi B, Coccia P, Poloni A, Unal S, Romano A, Iolascon A, Andolfo I, Russo R. Marra R, et al. Among authors: andolfo i. Am J Hematol. 2024 Apr 26. doi: 10.1002/ajh.27350. Online ahead of print. Am J Hematol. 2024. PMID: 38666530

3

A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death.

Minnai F, Biscarini F, Esposito M, Dragani TA, Bujanda L, Rahmouni S, Alarcón-Riquelme ME, Bernardo D, Carnero-Montoro E, Buti M, Zeberg H, Asselta R, Romero-Gómez M; GEN-COVID Multicenter Study; Fernandez-Cadenas I, Fallerini C, Zguro K, Croci S, Baldassarri M, Bruttini M, Furini S, Renieri A, Colombo F. Minnai F, et al. Sci Rep. 2024 Feb 6;14(1):3000. doi: 10.1038/s41598-024-53310-x. Sci Rep. 2024. PMID: 38321133 Free PMC article.

4

First Case of a Dominant De Novo SEC23A Mutation with Neurological and Psychiatric Features: New Insights into Cranio-Lenticulo-Sutural Dysplasia with Literature Review.

Minale EMP, De Falco A, Agolini E, Novelli A, Russo R, Andolfo I, Iolascon A, Piscopo C. Minale EMP, et al. Among authors: andolfo i. Genes (Basel). 2024 Jan 20;15(1):130. doi: 10.3390/genes15010130. Genes (Basel). 2024. PMID: 38275611 Free PMC article. Review.

5

A stepwise diagnostic approach for undiagnosed Anemia in children: A model for low-middle income country.

Aly NH, Elalfy MS, Elhabashy SA, Mowafy NM, Russo R, Andolfo I, Iolascon A, Ragab IA. Aly NH, et al. Among authors: andolfo i. Blood Cells Mol Dis. 2023 Nov;103:102779. doi: 10.1016/j.bcmd.2023.102779. Epub 2023 Jul 16. Blood Cells Mol Dis. 2023. PMID: 37558589

6

Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder.

Bergantini L, Baldassarri M, d'Alessandro M, Brunelli G, Fabbri G, Zguro K, Degl'Innocenti A; GEN-COVID Multicenter study; Fallerini C, Bargagli E, Renieri A. Bergantini L, et al. Respir Res. 2023 Jun 16;24(1):158. doi: 10.1186/s12931-023-02458-7. Respir Res. 2023. PMID: 37328761 Free PMC article.

7

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: andolfo i. Haematologica. 2023 Oct 1;108(10):2872-2876. doi: 10.3324/haematol.2022.282457. Haematologica. 2023. PMID: 37102609 Free PMC article. No abstract available.

8

Evaluation of the main regulators of systemic iron homeostasis in pyruvate kinase deficiency.

Zaninoni A, Marra R, Fermo E, Consonni D, Andolfo I, Marcello AP, Rosato BE, Vercellati C, Barcellini W, Iolascon A, Bianchi P, Russo R. Zaninoni A, et al. Among authors: andolfo i. Sci Rep. 2023 Mar 16;13(1):4395. doi: 10.1038/s41598-023-31571-2. Sci Rep. 2023. PMID: 36927785 Free PMC article.

9

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: andolfo i. Am J Hematol. 2023 Jun;98(6):E130-E133. doi: 10.1002/ajh.26901. Epub 2023 Mar 17. Am J Hematol. 2023. PMID: 36882369

10

Duality of Nrf2 in iron-overload cardiomyopathy.

Federti E, Vinchi F, Iatcenko I, Ghigo A, Matte A, Toya SCM, Siciliano A, Chiabrando D, Tolosano E, Vance SZ, Riccardi V, Andolfo I, Iezzi M, Lamolinara A, Iolascon A, De Franceschi L. Federti E, et al. Among authors: andolfo i. Haematologica. 2023 May 1;108(5):1335-1348. doi: 10.3324/haematol.2022.281995. Haematologica. 2023. PMID: 36700398 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

114 results

Results by year

Search Page

Filters

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

Search Results

114 results

Results by year