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Items: 1 to 50 of 67

1.

Crosslinking Allosteric Sites on the Nucleosome.

Batchelor LK, De Falco L, von Erlach T, Sharma D, Adhireksan Z, Roethlisberger U, Davey CA, Dyson PJ.

Angew Chem Int Ed Engl. 2019 Sep 3. doi: 10.1002/anie.201906423. [Epub ahead of print]

PMID:
31478581
2.

Right ventricular dysfunction in right coronary artery infarction: A primary PCI registry analysis.

Santangelo S, Fabris E, Stolfo D, Merlo M, Vitrella G, Rakar S, Barbati G, Falco L, Lardieri G, Perkan A, Sinagra G.

Cardiovasc Revasc Med. 2019 Apr 25. pii: S1553-8389(19)30256-8. doi: 10.1016/j.carrev.2019.04.022. [Epub ahead of print] No abstract available.

PMID:
31189522
3.

Wearable Sensors Reveal Menses-Driven Changes in Physiology and Enable Prediction of the Fertile Window: Observational Study.

Goodale BM, Shilaih M, Falco L, Dammeier F, Hamvas G, Leeners B.

J Med Internet Res. 2019 Apr 18;21(4):e13404. doi: 10.2196/13404.

4.

[Tricuspid regurgitation and indications for treatment].

Vitrella G, Fabris E, Gatti G, Falco L, Rakar S, Perkan A, Sinagra G.

G Ital Cardiol (Rome). 2019 Apr;20(4):27-35. doi: 10.1714/3146.31276. Italian.

PMID:
30994631
5.

An LDI-MSI approach for targeted and untargeted differentiation and assessment of pharmaceutical formulations.

Falco LFG, Melo CFOR, de Oliveira DN, Guerreiro TM, Catharino RR.

Talanta. 2019 May 15;197:92-97. doi: 10.1016/j.talanta.2018.12.044. Epub 2018 Dec 20.

PMID:
30771993
6.

Fyn kinase is a novel modulator of erythropoietin signaling and stress erythropoiesis.

Beneduce E, Matte A, De Falco L, Mbiandjeu S, Chiabrando D, Tolosano E, Federti E, Petrillo S, Mohandas N, Siciliano A, Babu W, Menon V, Ghaffari S, Iolascon A, De Franceschi L.

Am J Hematol. 2019 Jan;94(1):10-20. doi: 10.1002/ajh.25295. Epub 2018 Oct 25.

PMID:
30252956
7.

Normalizing hepcidin predicts TMPRSS6 mutation status in patients with chronic iron deficiency.

Heeney MM, Guo D, De Falco L, Campagna DR, Olbina G, Kao PP, Schmitz-Abe K, Rahimov F, Gutschow P, Westerman K, Ostland V, Jackson T, Klaassen RJ, Markianos K, Finberg KE, Iolascon A, Westerman M, London WB, Fleming MD.

Blood. 2018 Jul 26;132(4):448-452. doi: 10.1182/blood-2017-03-773028. Epub 2018 Jun 12. No abstract available. Erratum in: Blood. 2018 Sep 20;132(12):1355.

8.

Role of cone-beam computed tomography with a large field of view in Goldenhar syndrome.

Nardi C, De Falco L, Selvi V, Lorini C, Calistri L, Colagrande S.

Am J Orthod Dentofacial Orthop. 2018 Feb;153(2):269-277. doi: 10.1016/j.ajodo.2017.06.024.

PMID:
29407505
9.

The role of TMPRSS6 and HFE variants in iron deficiency anemia in celiac disease.

De Falco L, Tortora R, Imperatore N, Bruno M, Capasso M, Girelli D, Castagna A, Caporaso N, Iolascon A, Rispo A.

Am J Hematol. 2018 Mar;93(3):383-393. doi: 10.1002/ajh.24991. Epub 2017 Dec 18.

10.

Modern fertility awareness methods: wrist wearables capture the changes in temperature associated with the menstrual cycle.

Shilaih M, Goodale BM, Falco L, Kübler F, De Clerck V, Leeners B.

Biosci Rep. 2018 Nov 30;38(6). pii: BSR20171279. doi: 10.1042/BSR20171279. Print 2018 Dec 21.

11.

Repetition of Examination Due to Motion Artifacts in Horizontal Cone Beam CT: Comparison among Three Different Kinds of Head Support.

Nardi C, Taliani GG, Castellani A, De Falco L, Selvi V, Calistri L.

J Int Soc Prev Community Dent. 2017 Jul-Aug;7(4):208-213. doi: 10.4103/jispcd.JISPCD_17_17. Epub 2017 Jul 31.

12.

Peroxiredoxin-2: A Novel Regulator of Iron Homeostasis in Ineffective Erythropoiesis.

Matte A, De Falco L, Federti E, Cozzi A, Iolascon A, Levi S, Mohandas N, Zamo A, Bruno M, Lebouef C, Janin A, Siciliano A, Ganz T, Federico G, Carlomagno F, Mueller S, Silva I, Carbone C, Melisi D, Kim DW, Choi SY, De Franceschi L.

Antioxid Redox Signal. 2018 Jan 1;28(1):1-14. doi: 10.1089/ars.2017.7051. Epub 2017 Sep 6.

PMID:
28793778
13.

Pulse Rate Measurement During Sleep Using Wearable Sensors, and its Correlation with the Menstrual Cycle Phases, A Prospective Observational Study.

Shilaih M, Clerck V, Falco L, Kübler F, Leeners B.

Sci Rep. 2017 May 2;7(1):1294. doi: 10.1038/s41598-017-01433-9.

14.

Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblings.

Falco M, Franzè A, Iossa S, De Falco L, Gambale A, Marciano E, Iolascon A.

Am J Med Genet A. 2017 May;173(5):1348-1352. doi: 10.1002/ajmg.a.38146. Epub 2017 Mar 21.

PMID:
28322498
15.

Increased levels of ERFE-encoding FAM132B in patients with congenital dyserythropoietic anemia type II.

Russo R, Andolfo I, Manna F, De Rosa G, De Falco L, Gambale A, Bruno M, Mattè A, Ricchi P, Girelli D, De Franceschi L, Iolascon A.

Blood. 2016 Oct 6;128(14):1899-1902. doi: 10.1182/blood-2016-06-724328. Epub 2016 Aug 18. No abstract available.

16.

Impact of Diabetes on Outcomes of Sorafenib Therapy for Hepatocellular Carcinoma.

Di Costanzo GG, Tortora R, Morisco F, Addario L, Guarino M, Cordone G, Falco L, Caporaso N.

Target Oncol. 2017 Feb;12(1):61-67. doi: 10.1007/s11523-016-0454-5.

PMID:
27503006
17.

Iron-refractory iron deficiency anemia (IRIDA) cases with 2 novel TMPRSS6 mutations.

Sal E, Keskin EY, Yenicesu I, Bruno M, De Falco L.

Pediatr Hematol Oncol. 2016 Apr;33(3):226-32. doi: 10.3109/08880018.2016.1157229. Epub 2016 Apr 27.

PMID:
27120435
18.

The role of Matriptase-2 during the early postnatal development in humans.

De Falco L, Bruno M, Yilmaz-Keskin E, Sal E, Büyükavci M, Kaya Z, Girelli D, Iolascon A.

Haematologica. 2016 Apr;101(4):e126-8. doi: 10.3324/haematol.2015.139808. Epub 2016 Jan 22. No abstract available.

19.

How I Diagnose Non-thalassemic Microcytic Anemias.

Bruno M, De Falco L, Iolascon A.

Semin Hematol. 2015 Oct;52(4):270-8. doi: 10.1053/j.seminhematol.2015.05.002. Epub 2015 Jun 3. Review.

PMID:
26404439
20.

The Interplay Between Peroxiredoxin-2 and Nuclear Factor-Erythroid 2 Is Important in Limiting Oxidative Mediated Dysfunction in β-Thalassemic Erythropoiesis.

Matte A, De Falco L, Iolascon A, Mohandas N, An X, Siciliano A, Leboeuf C, Janin A, Bruno M, Choi SY, Kim DW, De Franceschi L.

Antioxid Redox Signal. 2015 Dec 1;23(16):1284-97. doi: 10.1089/ars.2014.6237. Epub 2015 Jul 14.

21.

Earthworm assemblages in different intensity of agricultural uses and their relation to edaphic variables.

Falco LB, Sandler R, Momo F, Di Ciocco C, Saravia L, Coviella C.

PeerJ. 2015 May 26;3:e979. doi: 10.7717/peerj.979. eCollection 2015.

22.

Differential contribution of soil biota groups to plant litter decomposition as mediated by soil use.

Castro-Huerta RA, Falco LB, Sandler RV, Coviella CE.

PeerJ. 2015 Mar 5;3:e826. doi: 10.7717/peerj.826. eCollection 2015.

23.

Our experience in the management of obstructing colorectal cancer.

Formisano V, Di Muria A, Connola G, Cione G, Falco L, De Angelis CP, Angrisani L.

Ann Ital Chir. 2014 Nov-Dec;85(6):563-8.

PMID:
25711439
24.

Functional and clinical impact of novel TMPRSS6 variants in iron-refractory iron-deficiency anemia patients and genotype-phenotype studies.

De Falco L, Silvestri L, Kannengiesser C, Morán E, Oudin C, Rausa M, Bruno M, Aranda J, Argiles B, Yenicesu I, Falcon-Rodriguez M, Yilmaz-Keskin E, Kocak U, Beaumont C, Camaschella C, Iolascon A, Grandchamp B, Sanchez M.

Hum Mutat. 2014 Nov;35(11):1321-9. doi: 10.1002/humu.22632. Epub 2014 Sep 10.

PMID:
25156943
25.

Is the acronym IRIDA acceptable for slow responders to iron in the presence of TMPRSS6 mutations?

Yilmaz-Keskin E, Sal E, de Falco L, Bruno M, Iolascon A, Koçak U, Yenicesu I.

Turk J Pediatr. 2013 Sep-Oct;55(5):479-84.

PMID:
24382527
26.

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.

Neurosci Res. 2013 Nov;77(3):121-7. doi: 10.1016/j.neures.2013.09.003. Epub 2013 Sep 17.

PMID:
24055409
27.

Human skin-derived keratinocytes and fibroblasts co-cultured on 3D poly ε-caprolactone scaffold support in vitro HSC differentiation into T-lineage committed cells.

Palamaro L, Guarino V, Scalia G, Antonini D, De Falco L, Bianchino G, Fusco A, Romano R, Grieco V, Missero C, Del Vecchio L, Ambrosio L, Pignata C.

Int Immunol. 2013 Dec;25(12):703-14. doi: 10.1093/intimm/dxt035. Epub 2013 Sep 13.

PMID:
24038600
28.

Resveratrol accelerates erythroid maturation by activation of FoxO3 and ameliorates anemia in beta-thalassemic mice.

Franco SS, De Falco L, Ghaffari S, Brugnara C, Sinclair DA, Matte' A, Iolascon A, Mohandas N, Bertoldi M, An X, Siciliano A, Rimmelé P, Cappellini MD, Michan S, Zoratti E, Anne J, De Franceschi L.

Haematologica. 2014 Feb;99(2):267-75. doi: 10.3324/haematol.2013.090076. Epub 2013 Aug 23.

29.

Bradykinin and its role in osteoarthritis.

De Falco L, Fioravanti A, Galeazzi M, Tenti S.

Reumatismo. 2013 Jul 23;65(3):97-104. doi: 10.4081/reumatismo.2013.97. Review.

PMID:
23884024
30.

Iron refractory iron deficiency anemia.

De Falco L, Sanchez M, Silvestri L, Kannengiesser C, Muckenthaler MU, Iolascon A, Gouya L, Camaschella C, Beaumont C.

Haematologica. 2013 Jun;98(6):845-53. doi: 10.3324/haematol.2012.075515. Review.

31.

Recovery of manganese oxides from spent alkaline and zinc-carbon batteries. An application as catalysts for VOCs elimination.

Gallegos MV, Falco LR, Peluso MA, Sambeth JE, Thomas HJ.

Waste Manag. 2013 Jun;33(6):1483-90. doi: 10.1016/j.wasman.2013.03.006. Epub 2013 Apr 4.

PMID:
23562448
32.

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.

Blood. 2013 May 9;121(19):3925-35, S1-12. doi: 10.1182/blood-2013-02-482489. Epub 2013 Mar 11.

33.

Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC11A2 gene.

De Falco L, Bruno M, Andolfo I, David BP, Girelli D, Di Noce F, Camaschella C, Iolascon A.

Br J Haematol. 2012 Nov;159(4):492-5. doi: 10.1111/bjh.12062. Epub 2012 Sep 27. No abstract available.

PMID:
23016933
34.

Parvovirus b19 DNA CpG dinucleotide methylation and epigenetic regulation of viral expression.

Bonvicini F, Manaresi E, Di Furio F, De Falco L, Gallinella G.

PLoS One. 2012;7(3):e33316. doi: 10.1371/journal.pone.0033316. Epub 2012 Mar 7.

35.

Oxidative stress modulates heme synthesis and induces peroxiredoxin-2 as a novel cytoprotective response in β-thalassemic erythropoiesis.

De Franceschi L, Bertoldi M, De Falco L, Santos Franco S, Ronzoni L, Turrini F, Colancecco A, Camaschella C, Cappellini MD, Iolascon A.

Haematologica. 2011 Nov;96(11):1595-604. doi: 10.3324/haematol.2011.043612. Epub 2011 Jul 12.

36.

A dielectric inverse problem applied to human skin measurements during glucose excursions.

Dewarrat F, Falco L, Mueller M, Reinhard S, Caduff A, Talary MS.

Physiol Meas. 2011 Aug;32(8):1285-300. doi: 10.1088/0967-3334/32/8/018. Epub 2011 Jul 8.

PMID:
21743123
37.

Data processing for noninvasive continuous glucose monitoring with a multisensor device.

Mueller M, Talary MS, Falco L, De Feo O, Stahel WA, Caduff A.

J Diabetes Sci Technol. 2011 May 1;5(3):694-702.

38.

A novel microdeletion in the IGF2/H19 imprinting centre region defines a recurrent mutation mechanism in familial Beckwith-Wiedemann syndrome.

De Crescenzo A, Coppola F, Falco P, Bernardo I, Ausanio G, Cerrato F, Falco L, Riccio A.

Eur J Med Genet. 2011 Jul-Aug;54(4):e451-4. doi: 10.1016/j.ejmg.2011.04.009. Epub 2011 May 4.

39.

Congenital dyserythropoietic anaemias: new acquisitions.

Iolascon A, Russo R, Esposito MR, Piscopo C, Asci R, De Falco L, Di Noce F.

Blood Transfus. 2011 Jul;9(3):278-80. doi: 10.2450/2010.0085-10. Epub 2010 Dec 13. Review. No abstract available.

40.

Bicoherence analysis of model-scale jet noise.

Gee KL, Atchley AA, Falco LE, Shepherd MR, Ukeiley LS, Jansen BJ, Seiner JM.

J Acoust Soc Am. 2010 Nov;128(5):EL211-6. doi: 10.1121/1.3484492.

PMID:
21110528
41.

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.

Haematologica. 2010 Aug;95(8):1244-52. doi: 10.3324/haematol.2009.020685. Epub 2010 Apr 21.

42.

Novel TMPRSS6 mutations associated with iron-refractory iron deficiency anemia (IRIDA).

De Falco L, Totaro F, Nai A, Pagani A, Girelli D, Silvestri L, Piscopo C, Campostrini N, Dufour C, Al Manjomi F, Minkov M, Van Vuurden DG, Feliu A, Kattamis A, Camaschella C, Iolascon A.

Hum Mutat. 2010 May;31(5):E1390-405. doi: 10.1002/humu.21243.

PMID:
20232450
43.

Validation of human skin models in the MHz region.

Huclova S, Fröhlich J, Falco L, Dewarrat F, Talary MS, Vahldieck R.

Conf Proc IEEE Eng Med Biol Soc. 2009;2009:4461-4. doi: 10.1109/IEMBS.2009.5333820.

PMID:
19964633
44.

Mutations in the gene encoding DMT1: clinical presentation and treatment.

Iolascon A, De Falco L.

Semin Hematol. 2009 Oct;46(4):358-70. doi: 10.1053/j.seminhematol.2009.06.005. Review.

PMID:
19786204
45.

A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis.

Iolascon A, De Falco L, Borgese F, Esposito MR, Avvisati RA, Izzo P, Piscopo C, Guizouarn H, Biondani A, Pantaleo A, De Franceschi L.

Haematologica. 2009 Aug;94(8):1049-59. doi: 10.3324/haematol.2008.002873.

46.

Beta-spectrinBari: a truncated beta-chain responsible for dominant hereditary spherocytosis.

Perrotta S, Della Ragione F, Rossi F, Avvisati RA, Di Pinto D, De Mieri G, Scianguetta S, Mancusi S, De Falco L, Marano V, Iolascon A.

Haematologica. 2009 Dec;94(12):1753-7. doi: 10.3324/haematol.2009.010124. Epub 2009 Jul 16.

47.

Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.

Schwarz K, Iolascon A, Verissimo F, Trede NS, Horsley W, Chen W, Paw BH, Hopfner KP, Holzmann K, Russo R, Esposito MR, Spano D, De Falco L, Heinrich K, Joggerst B, Rojewski MT, Perrotta S, Denecke J, Pannicke U, Delaunay J, Pepperkok R, Heimpel H.

Nat Genet. 2009 Aug;41(8):936-40. doi: 10.1038/ng.405. Epub 2009 Jun 28.

PMID:
19561605
48.

Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis.

Iolascon A, De Falco L, Beaumont C.

Haematologica. 2009 Mar;94(3):395-408. doi: 10.3324/haematol.13619. Epub 2009 Jan 30. Review.

49.

Complex juxtapapillary capillary hemangioma: a case report.

Reynolds SA, Shechtman D, Falco L.

Optometry. 2008 Sep;79(9):512-7. doi: 10.1016/j.optm.2007.11.013.

PMID:
18722963
50.

[New types of microcytic anemia].

Iolascon A, De Falco L, Boschetto L, Piscopo C, Pirolo C, Di Noce F.

Minerva Pediatr. 2007 Oct;59(5):525-7. Italian. No abstract available.

PMID:
17947902

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