Andolfo I - Search Results

1

PIEZO1 mutations impact on early clinical manifestations of myelodysplastic syndromes.

Attardi E, Andolfo I, Russo R, Tiberi L, Raddi MG, Rosato BE, Marra R, Formicola D, Del Giudice F, Brogi A, Consagra A, Amato C, Sanna A, Artuso R, Iolascon A, Santini V. Attardi E, et al. Among authors: andolfo i. 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.

2

Identification of ALK germline mutation (3605delG) in pediatric anaplastic medulloblastoma.

Coco S, De Mariano M, Valdora F, Servidei T, Ridola V, Andolfo I, Oberthuer A, Tonini GP, Longo L. Coco S, et al. Among authors: andolfo i. J Hum Genet. 2012 Oct;57(10):682-4. doi: 10.1038/jhg.2012.87. Epub 2012 Jul 19. J Hum Genet. 2012. PMID: 22810114

3

Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells.

Andolfo I, De Falco L, Asci R, Russo R, Colucci S, Gorrese M, Zollo M, Iolascon A. Andolfo I, et al. Haematologica. 2010 Aug;95(8):1244-52. doi: 10.3324/haematol.2009.020685. Epub 2010 Apr 21. Haematologica. 2010. PMID: 20410187 Free PMC article.

4

Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia.

Andolfo I, Alper SL, Delaunay J, Auriemma C, Russo R, Asci R, Esposito MR, Sharma AK, Shmukler BE, Brugnara C, De Franceschi L, Iolascon A. Andolfo I, et al. Am J Hematol. 2013 Jan;88(1):66-72. doi: 10.1002/ajh.23357. Epub 2012 Nov 24. Am J Hematol. 2013. PMID: 23180570 Free article.

5

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.

Andolfo I, Alper SL, De Franceschi L, Auriemma C, Russo R, De Falco L, Vallefuoco F, Esposito MR, Vandorpe DH, Shmukler BE, Narayan R, Montanaro D, D'Armiento M, Vetro A, Limongelli I, Zuffardi O, Glader BE, Schrier SL, Brugnara C, Stewart GW, Delaunay J, Iolascon A. Andolfo I, et al. Blood. 2013 May 9;121(19):3925-35, S1-12. doi: 10.1182/blood-2013-02-482489. Epub 2013 Mar 11. Blood. 2013. PMID: 23479567 Free article.

6

Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP⁺ as Parkinson's disease cellular model.

Asci R, Vallefuoco F, Andolfo I, Bruno M, De Falco L, Iolascon A. Asci R, et al. Among authors: andolfo i. Neurosci Res. 2013 Nov;77(3):121-7. doi: 10.1016/j.neures.2013.09.003. Epub 2013 Sep 17. Neurosci Res. 2013. PMID: 24055409

7

Hereditary xerocytosis revisited.

Archer NM, Shmukler BE, Andolfo I, Vandorpe DH, Gnanasambandam R, Higgins JM, Rivera A, Fleming MD, Sachs F, Gottlieb PA, Iolascon A, Brugnara C, Alper SL, Nathan DG. Archer NM, et al. Among authors: andolfo i. Am J Hematol. 2014 Dec;89(12):1142-6. doi: 10.1002/ajh.23799. Epub 2014 Jul 21. Am J Hematol. 2014. PMID: 25044010 Free PMC article.

8

Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: definition of clinical and molecular spectrum and identification of new diagnostic scores.

Russo R, Gambale A, Langella C, Andolfo I, Unal S, Iolascon A. Russo R, et al. Among authors: andolfo i. Am J Hematol. 2014 Oct;89(10):E169-75. doi: 10.1002/ajh.23800. Epub 2014 Jul 22. Am J Hematol. 2014. PMID: 25044164 Free article.

9

Red cells in post-genomic era: impact of personalized medicine in the treatment of anemias.

Iolascon A, Andolfo I, Russo R. Iolascon A, et al. Among authors: andolfo i. Haematologica. 2015 Jan;100(1):3-6. doi: 10.3324/haematol.2014.120733. Haematologica. 2015. PMID: 25552677 Free PMC article. No abstract available.

10

Inhibition of hypoxia inducible factors combined with all-trans retinoic acid treatment enhances glial transdifferentiation of neuroblastoma cells.

Cimmino F, Pezone L, Avitabile M, Acierno G, Andolfo I, Capasso M, Iolascon A. Cimmino F, et al. Among authors: andolfo i. Sci Rep. 2015 Jun 9;5:11158. doi: 10.1038/srep11158. Sci Rep. 2015. PMID: 26057707 Free PMC article.

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