Andolfo I - Search Results

1

Recommendations for diagnosis and treatment of methemoglobinemia.

Iolascon A, Bianchi P, Andolfo I, Russo R, Barcellini W, Fermo E, Toldi G, Ghirardello S, Rees D, Van Wijk R, Kattamis A, Gallagher PG, Roy N, Taher A, Mohty R, Kulozik A, De Franceschi L, Gambale A, De Montalembert M, Forni GL, Harteveld CL, Prchal J; SWG of red cell and iron of EHA and EuroBloodNet. Iolascon A, et al. Among authors: andolfo i. Am J Hematol. 2021 Dec 1;96(12):1666-1678. doi: 10.1002/ajh.26340. Epub 2021 Sep 23. Am J Hematol. 2021. PMID: 34467556 Free PMC article. Review.

2

SOCS3 and IRS-1 gene expression differs between genotype 1 and genotype 2 hepatitis C virus-infected HepG2 cells.

Persico M, Russo R, Persico E, Svelto M, Spano D, Andolfo I, La Mura V, Capasso M, Tiribelli C, Torella R, Iolascon A. Persico M, et al. Among authors: andolfo i. Clin Chem Lab Med. 2009;47(10):1217-25. doi: 10.1515/CCLM.2009.280. Clin Chem Lab Med. 2009. PMID: 19803812

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

Detection of erbB2 copy number variations in plasma of patients with esophageal carcinoma.

Andolfo I, Petrosino G, Vecchione L, De Antonellis P, Capasso M, Montanaro D, Gemei M, Troncone G, Iolascon A, Orditura M, Ciardiello F, De Vita F, Zollo M. Andolfo I, et al. BMC Cancer. 2011 Apr 11;11:126. doi: 10.1186/1471-2407-11-126. BMC Cancer. 2011. PMID: 21481261 Free PMC article.

5

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.

6

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.

7

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

8

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.

9

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.

10

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.

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