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Items: 1 to 50 of 113

1.

Meloidae of Namibia (Coleoptera): taxonomy and faunistics with biogeographic and ecological notes.

Bologna MA, Amore V, Pitzalis M.

Zootaxa. 2018 Jan 15;4373(1):1-141. doi: 10.11646/zootaxa.4373.1.1.

PMID:
29689829
2.

Overexpression of the Cytokine BAFF and Autoimmunity Risk.

Steri M, Orrù V, Idda ML, Pitzalis M, Pala M, Zara I, Sidore C, Faà V, Floris M, Deiana M, Asunis I, Porcu E, Mulas A, Piras MG, Lobina M, Lai S, Marongiu M, Serra V, Marongiu M, Sole G, Busonero F, Maschio A, Cusano R, Cuccuru G, Deidda F, Poddie F, Farina G, Dei M, Virdis F, Olla S, Satta MA, Pani M, Delitala A, Cocco E, Frau J, Coghe G, Lorefice L, Fenu G, Ferrigno P, Ban M, Barizzone N, Leone M, Guerini FR, Piga M, Firinu D, Kockum I, Lima Bomfim I, Olsson T, Alfredsson L, Suarez A, Carreira PE, Castillo-Palma MJ, Marcus JH, Congia M, Angius A, Melis M, Gonzalez A, Alarcón Riquelme ME, da Silva BM, Marchini M, Danieli MG, Del Giacco S, Mathieu A, Pani A, Montgomery SB, Rosati G, Hillert J, Sawcer S, D'Alfonso S, Todd JA, Novembre J, Abecasis GR, Whalen MB, Marrosu MG, Meloni A, Sanna S, Gorospe M, Schlessinger D, Fiorillo E, Zoledziewska M, Cucca F.

N Engl J Med. 2017 Apr 27;376(17):1615-1626. doi: 10.1056/NEJMoa1610528.

3.

Mitogenome Diversity in Sardinians: A Genetic Window onto an Island's Past.

Olivieri A, Sidore C, Achilli A, Angius A, Posth C, Furtwängler A, Brandini S, Capodiferro MR, Gandini F, Zoledziewska M, Pitzalis M, Maschio A, Busonero F, Lai L, Skeates R, Gradoli MG, Beckett J, Marongiu M, Mazzarello V, Marongiu P, Rubino S, Rito T, Macaulay V, Semino O, Pala M, Abecasis GR, Schlessinger D, Conde-Sousa E, Soares P, Richards MB, Cucca F, Torroni A.

Mol Biol Evol. 2017 May 1;34(5):1230-1239. doi: 10.1093/molbev/msx082.

4.

Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation.

Andlauer TF, Buck D, Antony G, Bayas A, Bechmann L, Berthele A, Chan A, Gasperi C, Gold R, Graetz C, Haas J, Hecker M, Infante-Duarte C, Knop M, Kümpfel T, Limmroth V, Linker RA, Loleit V, Luessi F, Meuth SG, Mühlau M, Nischwitz S, Paul F, Pütz M, Ruck T, Salmen A, Stangel M, Stellmann JP, Stürner KH, Tackenberg B, Then Bergh F, Tumani H, Warnke C, Weber F, Wiendl H, Wildemann B, Zettl UK, Ziemann U, Zipp F, Arloth J, Weber P, Radivojkov-Blagojevic M, Scheinhardt MO, Dankowski T, Bettecken T, Lichtner P, Czamara D, Carrillo-Roa T, Binder EB, Berger K, Bertram L, Franke A, Gieger C, Herms S, Homuth G, Ising M, Jöckel KH, Kacprowski T, Kloiber S, Laudes M, Lieb W, Lill CM, Lucae S, Meitinger T, Moebus S, Müller-Nurasyid M, Nöthen MM, Petersmann A, Rawal R, Schminke U, Strauch K, Völzke H, Waldenberger M, Wellmann J, Porcu E, Mulas A, Pitzalis M, Sidore C, Zara I, Cucca F, Zoledziewska M, Ziegler A, Hemmer B, Müller-Myhsok B.

Sci Adv. 2016 Jun 17;2(6):e1501678. doi: 10.1126/sciadv.1501678. eCollection 2016 Jun.

5.

The burden of multiple sclerosis variants in continental Italians and Sardinians.

Barizzone N, Zara I, Sorosina M, Lupoli S, Porcu E, Pitzalis M, Zoledziewska M, Esposito F, Leone M, Mulas A, Cocco E, Ferrigno P, Guerini FR, Brambilla P, Farina G, Murru R, Deidda F, Sanna S, Loi A, Barlassina C, Vecchio D, Zauli A, Clarelli F, Braga D, Poddie F, Cantello R, Martinelli V, Comi G, Frau J, Lorefice L, Pugliatti M, Rosati G; PROGEMUS (PROgnostic GEnetic factors in MUltiple Sclerosis) Consortium PROGRESSO (Italian network of Primary Progressive Multiple Sclerosis) Consortium, Melis M, Marrosu MG, Cusi D, Cucca F, Martinelli Boneschi F, Sanna S, D'Alfonso S.

Mult Scler. 2015 Oct;21(11):1385-95. doi: 10.1177/1352458515596599.

PMID:
26438306
6.

Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers.

Sidore C, Busonero F, Maschio A, Porcu E, Naitza S, Zoledziewska M, Mulas A, Pistis G, Steri M, Danjou F, Kwong A, Ortega Del Vecchyo VD, Chiang CWK, Bragg-Gresham J, Pitzalis M, Nagaraja R, Tarrier B, Brennan C, Uzzau S, Fuchsberger C, Atzeni R, Reinier F, Berutti R, Huang J, Timpson NJ, Toniolo D, Gasparini P, Malerba G, Dedoussis G, Zeggini E, Soranzo N, Jones C, Lyons R, Angius A, Kang HM, Novembre J, Sanna S, Schlessinger D, Cucca F, Abecasis GR.

Nat Genet. 2015 Nov;47(11):1272-1281. doi: 10.1038/ng.3368. Epub 2015 Sep 14.

7.

Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.

Danjou F, Zoledziewska M, Sidore C, Steri M, Busonero F, Maschio A, Mulas A, Perseu L, Barella S, Porcu E, Pistis G, Pitzalis M, Pala M, Menzel S, Metrustry S, Spector TD, Leoni L, Angius A, Uda M, Moi P, Thein SL, Galanello R, Abecasis GR, Schlessinger D, Sanna S, Cucca F.

Nat Genet. 2015 Nov;47(11):1264-71. doi: 10.1038/ng.3307. Epub 2015 Sep 14.

8.

Genome-wide association study of susceptibility loci for breast cancer in Sardinian population.

Palomba G, Loi A, Porcu E, Cossu A, Zara I, Budroni M, Dei M, Lai S, Mulas A, Olmeo N, Ionta MT, Atzori F, Cuccuru G, Pitzalis M, Zoledziewska M, Olla N, Lovicu M, Pisano M, Abecasis GR, Uda M, Tanda F, Michailidou K, Easton DF, Chanock SJ, Hoover RN, Hunter DJ, Schlessinger D, Sanna S, Crisponi L, Palmieri G.

BMC Cancer. 2015 May 10;15:383. doi: 10.1186/s12885-015-1392-9.

9.

Allelic variant in CTLA4 is associated with thyroid failure and faster β-cell exhaustion in latent autoimmune diabetes in adults.

Delitala AP, Fanciulli G, Zoledziewska M, Pitzalis M, Pusceddu P, Frongia P, Puddu L, Errigo A, Maioli M, Delitala G, Pes GM.

J Diabetes. 2015 Jan;7(1):68-73.

PMID:
25695113
10.

Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs.

Pistis G, Porcu E, Vrieze SI, Sidore C, Steri M, Danjou F, Busonero F, Mulas A, Zoledziewska M, Maschio A, Brennan C, Lai S, Miller MB, Marcelli M, Urru MF, Pitzalis M, Lyons RH, Kang HM, Jones CM, Angius A, Iacono WG, Schlessinger D, McGue M, Cucca F, Abecasis GR, Sanna S.

Eur J Hum Genet. 2015 Jul;23(7):975-83. doi: 10.1038/ejhg.2014.216. Epub 2014 Oct 8.

11.

Population genomic analysis of ancient and modern genomes yields new insights into the genetic ancestry of the Tyrolean Iceman and the genetic structure of Europe.

Sikora M, Carpenter ML, Moreno-Estrada A, Henn BM, Underhill PA, Sánchez-Quinto F, Zara I, Pitzalis M, Sidore C, Busonero F, Maschio A, Angius A, Jones C, Mendoza-Revilla J, Nekhrizov G, Dimitrova D, Theodossiev N, Harkins TT, Keller A, Maixner F, Zink A, Abecasis G, Sanna S, Cucca F, Bustamante CD.

PLoS Genet. 2014 May 8;10(5):e1004353. doi: 10.1371/journal.pgen.1004353. eCollection 2014 May.

12.

Genetic variants regulating immune cell levels in health and disease.

Orrù V, Steri M, Sole G, Sidore C, Virdis F, Dei M, Lai S, Zoledziewska M, Busonero F, Mulas A, Floris M, Mentzen WI, Urru SA, Olla S, Marongiu M, Piras MG, Lobina M, Maschio A, Pitzalis M, Urru MF, Marcelli M, Cusano R, Deidda F, Serra V, Oppo M, Pilu R, Reinier F, Berutti R, Pireddu L, Zara I, Porcu E, Kwong A, Brennan C, Tarrier B, Lyons R, Kang HM, Uzzau S, Atzeni R, Valentini M, Firinu D, Leoni L, Rotta G, Naitza S, Angius A, Congia M, Whalen MB, Jones CM, Schlessinger D, Abecasis GR, Fiorillo E, Sanna S, Cucca F.

Cell. 2013 Sep 26;155(1):242-56. doi: 10.1016/j.cell.2013.08.041.

13.

Low-pass DNA sequencing of 1200 Sardinians reconstructs European Y-chromosome phylogeny.

Francalacci P, Morelli L, Angius A, Berutti R, Reinier F, Atzeni R, Pilu R, Busonero F, Maschio A, Zara I, Sanna D, Useli A, Urru MF, Marcelli M, Cusano R, Oppo M, Zoledziewska M, Pitzalis M, Deidda F, Porcu E, Poddie F, Kang HM, Lyons R, Tarrier B, Gresham JB, Li B, Tofanelli S, Alonso S, Dei M, Lai S, Mulas A, Whalen MB, Uzzau S, Jones C, Schlessinger D, Abecasis GR, Sanna S, Sidore C, Cucca F.

Science. 2013 Aug 2;341(6145):565-9. doi: 10.1126/science.1237947.

14.

Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1.

Matesanz F, González-Pérez A, Lucas M, Sanna S, Gayán J, Urcelay E, Zara I, Pitzalis M, Cavanillas ML, Arroyo R, Zoledziewska M, Marrosu M, Fernández O, Leyva L, Alcina A, Fedetz M, Moreno-Rey C, Velasco J, Real LM, Ruiz-Peña JL, Cucca F, Ruiz A, Izquierdo G.

PLoS One. 2012;7(5):e36140. doi: 10.1371/journal.pone.0036140. Epub 2012 May 3.

15.

T-cell receptor repertoire analysis in monozygotic twins concordant and discordant for type 1 diabetes.

Fozza C, Contini S, Corda G, Virdis P, Galleu A, Bonfigli S, Pacifico A, Maioli M, Mastinu F, Pitzalis M, Cucca F, Longinotti M.

Immunobiology. 2012 Sep;217(9):920-5. doi: 10.1016/j.imbio.2012.01.002. Epub 2012 Jan 4.

PMID:
22341303
16.

A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis.

Cagliani R, Guerini FR, Fumagalli M, Riva S, Agliardi C, Galimberti D, Pozzoli U, Goris A, Dubois B, Fenoglio C, Forni D, Sanna S, Zara I, Pitzalis M, Zoledziewska M, Cucca F, Marini F, Comi GP, Scarpini E, Bresolin N, Clerici M, Sironi M.

Mol Biol Evol. 2012 Jun;29(6):1599-613. doi: 10.1093/molbev/mss002. Epub 2012 Jan 6.

PMID:
22319148
17.

A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.

Naitza S, Porcu E, Steri M, Taub DD, Mulas A, Xiao X, Strait J, Dei M, Lai S, Busonero F, Maschio A, Usala G, Zoledziewska M, Sidore C, Zara I, Pitzalis M, Loi A, Virdis F, Piras R, Deidda F, Whalen MB, Crisponi L, Concas A, Podda C, Uzzau S, Scheet P, Longo DL, Lakatta E, Abecasis GR, Cao A, Schlessinger D, Uda M, Sanna S, Cucca F.

PLoS Genet. 2012 Jan;8(1):e1002480. doi: 10.1371/journal.pgen.1002480. Epub 2012 Jan 26.

18.

TCRBV20S1 polymorphism does not influence the susceptibility to type 1 diabetes and multiple sclerosis in the Sardinian population.

Fozza C, Zoledzieska M, Pitzalis M, Simula MP, Galleu A, Contini S, Bonfigli S, Cucca F, Longinotti M.

Immunogenetics. 2012 Feb;64(2):153-4. doi: 10.1007/s00251-011-0575-z. Epub 2011 Sep 17.

PMID:
21927869
19.

Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis.

Sanna S, Pitzalis M, Zoledziewska M, Zara I, Sidore C, Murru R, Whalen MB, Busonero F, Maschio A, Costa G, Melis MC, Deidda F, Poddie F, Morelli L, Farina G, Li Y, Dei M, Lai S, Mulas A, Cuccuru G, Porcu E, Liang L, Zavattari P, Moi L, Deriu E, Urru MF, Bajorek M, Satta MA, Cocco E, Ferrigno P, Sotgiu S, Pugliatti M, Traccis S, Angius A, Melis M, Rosati G, Abecasis GR, Uda M, Marrosu MG, Schlessinger D, Cucca F.

Nat Genet. 2010 Jun;42(6):495-7. doi: 10.1038/ng.584. Epub 2010 May 9.

20.

Variation within the CLEC16A gene shows consistent disease association with both multiple sclerosis and type 1 diabetes in Sardinia.

Zoledziewska M, Costa G, Pitzalis M, Cocco E, Melis C, Moi L, Zavattari P, Murru R, Lampis R, Morelli L, Poddie F, Frongia P, Pusceddu P, Bajorek M, Marras A, Satta AM, Chessa A, Pugliatti M, Sotgiu S, Whalen MB, Rosati G, Cucca F, Marrosu MG.

Genes Immun. 2009 Jan;10(1):15-7. doi: 10.1038/gene.2008.84. Epub 2008 Oct 23.

PMID:
18946483
21.

[Stapled transanal rectal resection (STARR) in the treatment of rectocele: personal experience].

Guarnieri A, Cesaretti M, Tirone A, Vuolo G, Verre L, Savelli V, Piccolomini A, Di Cosmo L, Carli AF, Burroni M, Pitzalis M.

Chir Ital. 2008 Mar-Apr;60(2):243-8. Italian.

PMID:
18689173
22.

Phylogeny and evolutionary history of the blister beetles (Coleoptera, Meloidae).

Bologna MA, Oliverio M, Pitzalis M, Mariottini P.

Mol Phylogenet Evol. 2008 Aug;48(2):679-93. doi: 10.1016/j.ympev.2008.04.019. Epub 2008 Apr 22.

PMID:
18514547
23.

Genetic loci linked to type 1 diabetes and multiple sclerosis families in Sardinia.

Pitzalis M, Zavattari P, Murru R, Deidda E, Zoledziewska M, Murru D, Moi L, Motzo C, Orrù V, Costa G, Solla E, Fadda E, Schirru L, Melis MC, Lai M, Mancosu C, Tranquilli S, Cuccu S, Rolesu M, Secci MA, Corongiu D, Contu D, Lampis R, Nucaro A, Pala G, Pacifico A, Maioli M, Frongia P, Chessa M, Ricciardi R, Lostia S, Marinaro AM, Milia AF, Landis N, Zedda MA, Whalen MB, Santoni F, Marrosu MG, Devoto M, Cucca F.

BMC Med Genet. 2008 Jan 20;9:3. doi: 10.1186/1471-2350-9-3.

24.

The 212A variant of the APJ receptor gene for the endogenous inotrope apelin is associated with slower heart failure progression in idiopathic dilated cardiomyopathy.

Sarzani R, Forleo C, Pietrucci F, Capestro A, Soura E, Guida P, Sorrentino S, Iacoviello M, Romito R, Dessì-Fulgheri P, Pitzalis M, Rappelli A.

J Card Fail. 2007 Sep;13(7):521-9.

PMID:
17826642
25.

Beta1- and beta2-adrenergic receptor polymorphisms affect susceptibility to idiopathic dilated cardiomyopathy.

Forleo C, Sorrentino S, Guida P, Romito R, De Tommasi E, Iacoviello M, Pitzalis M.

J Cardiovasc Med (Hagerstown). 2007 Aug;8(8):589-95.

PMID:
17667029
26.

Ventricular repolarization dynamicity provides independent prognostic information toward major arrhythmic events in patients with idiopathic dilated cardiomyopathy.

Iacoviello M, Forleo C, Guida P, Romito R, Sorgente A, Sorrentino S, Catucci S, Mastropasqua F, Pitzalis M.

J Am Coll Cardiol. 2007 Jul 17;50(3):225-31. Epub 2007 Jun 29.

27.

Role of septal to posterior wall motion delay in cardiac resynchronization therapy.

Pitzalis MV, Iacoviello M, Romito R, Luzzi G, Anaclerio M, Forleo C.

J Am Coll Cardiol. 2006 Aug 1;48(3):596-7. Epub 2006 Jul 12. No abstract available.

28.

SCN5A polymorphism restores trafficking of a Brugada syndrome mutation on a separate gene.

Poelzing S, Forleo C, Samodell M, Dudash L, Sorrentino S, Anaclerio M, Troccoli R, Iacoviello M, Romito R, Guida P, Chahine M, Pitzalis M, Deschênes I.

Circulation. 2006 Aug 1;114(5):368-76. Epub 2006 Jul 24.

29.

Alpha- and beta-adrenergic receptor polymorphisms in hypertensive and normotensive offspring.

Iacoviello M, Forleo C, Sorrentino S, Romito R, De Tommasi E, Lucarelli K, Guida P, Pitzalis MV.

J Cardiovasc Med (Hagerstown). 2006 May;7(5):316-21.

PMID:
16645408
30.

Prognostic value of brain natriuretic peptide in the management of patients receiving cardiac resynchronization therapy.

Pitzalis MV, Iacoviello M, Di Serio F, Romito R, Guida P, De Tommasi E, Luzzi G, Anaclerio M, Varraso L, Forleo C, Pansini N.

Eur J Heart Fail. 2006 Aug;8(5):509-14. Epub 2006 Feb 28.

31.

Independent and incremental prognostic value of endogenous ouabain in idiopathic dilated cardiomyopathy.

Pitzalis MV, Hamlyn JM, Messaggio E, Iacoviello M, Forleo C, Romito R, de Tommasi E, Rizzon P, Bianchi G, Manunta P.

Eur J Heart Fail. 2006 Mar;8(2):179-86. Epub 2005 Sep 26.

32.

High circulating levels of endogenous ouabain in the offspring of hypertensive and normotensive individuals.

Manunta P, Iacoviello M, Forleo C, Messaggio E, Hamlyn JM, Lucarelli K, Guida P, Romito R, De Tommasi E, Bianchi G, Rizzon P, Pitzalis MV.

J Hypertens. 2005 Sep;23(9):1677-81.

PMID:
16093912
33.

Dynamics of ventricular repolarization in patients with dilated cardiomyopathy versus healthy subjects.

Alonso JL, Martínez P, Vallverdú M, Cygankiewicz I, Pitzalis MV, Bayés Genís A, Cinca J, Rizzon P, Caminal P, Zareba W, Bayés de Luna A.

Ann Noninvasive Electrocardiol. 2005 Apr;10(2):121-8.

PMID:
15842422
34.

[Yentl syndrome. The underestimate of cardiovascular risk in women].

Pitzalis M.

Ital Heart J Suppl. 2005 Feb;6(2):72-6. Review. Italian.

PMID:
15822730
35.

Ventricular asynchrony predicts a better outcome in patients with chronic heart failure receiving cardiac resynchronization therapy.

Pitzalis MV, Iacoviello M, Romito R, Guida P, De Tommasi E, Luzzi G, Anaclerio M, Forleo C, Rizzon P.

J Am Coll Cardiol. 2005 Jan 4;45(1):65-9.

36.

Association of beta-adrenergic receptor polymorphisms and progression to heart failure in patients with idiopathic dilated cardiomyopathy.

Forleo C, Resta N, Sorrentino S, Guida P, Manghisi A, De Luca V, Romito R, Iacoviello M, De Tommasi E, Troisi F, Rizzon B, Guanti G, Rizzon P, Pitzalis MV.

Am J Med. 2004 Oct 1;117(7):451-8.

PMID:
15464701
37.

No association between variation of the FOXP3 gene and common type 1 diabetes in the Sardinian population.

Zavattari P, Deidda E, Pitzalis M, Zoa B, Moi L, Lampis R, Contu D, Motzo C, Frongia P, Angius E, Maioli M, Todd JA, Cucca F.

Diabetes. 2004 Jul;53(7):1911-4.

38.

QT-interval prolongation in right precordial leads: an additional electrocardiographic hallmark of Brugada syndrome.

Pitzalis MV, Anaclerio M, Iacoviello M, Forleo C, Guida P, Troccoli R, Massari F, Mastropasqua F, Sorrentino S, Manghisi A, Rizzon P.

J Am Coll Cardiol. 2003 Nov 5;42(9):1632-7.

39.

Comparison of the effect of valsartan and lisinopril on autonomic nervous system activity in chronic heart failure.

De Tommasi E, Iacoviello M, Romito R, Ceconi C, Guida P, Massari F, Francolini G, Bertocchi F, Ferrari R, Rizzon P, Pitzalis MV.

Am Heart J. 2003 Nov;146(5):E17.

PMID:
14597946
40.
41.

Allelic variants of natriuretic peptide receptor genes are associated with family history of hypertension and cardiovascular phenotype.

Pitzalis MV, Sarzani R, Dessì-Fulgheri P, Iacoviello M, Forleo C, Lucarelli K, Pietrucci F, Salvi F, Sorrentino S, Romito R, Guida P, Rappelli A, Rizzon P.

J Hypertens. 2003 Aug;21(8):1491-6.

PMID:
12872042
42.

Management of syncope referred urgently to general hospitals with and without syncope units.

Brignole M, Disertori M, Menozzi C, Raviele A, Alboni P, Pitzalis MV, Delise P, Puggioni E, Del Greco M, Malavasi V, Lunati M, Pepe M, Fabrizi D; Evaluation of Guidelines in Syncope Study group.

Europace. 2003 Jul;5(3):293-8.

PMID:
12842646
43.

Oral beclometasone dipropionate in the treatment of extensive and left-sided active ulcerative colitis: a multicentre randomised study.

Campieri M, Adamo S, Valpiani D, D'Arienzo A, D'Albasio G, Pitzalis M, Cesari P, Casetti T, Castiglione GN, Rizzello F, Manguso F, Varoli G, Gionchetti P.

Aliment Pharmacol Ther. 2003 Jun 15;17(12):1471-80.

44.

[Diagnosis of neurogenic syncope--current views].

Pitzalis M, Iacoviello M, Rizzon P.

Recenti Prog Med. 2003 Jun;94(6):271-7. Review. Italian.

PMID:
12793100
45.

Enhanced reflex response to baroreceptor deactivation in subjects with tilt-induced syncope.

Pitzalis M, Parati G, Massari F, Guida P, Di Rienzo M, Rizzon B, Castiglioni P, Iacoviello M, Mastropasqua F, Rizzon P.

J Am Coll Cardiol. 2003 Apr 2;41(7):1167-73.

46.

[Natriuretic peptides and essential arterial hypertension].

Lucarelli K, Iacoviello M, Dessì-Fulgheri P, Sarzani R, Romito R, Sorrentino S, Forleo C, Rizzon B, De Tommasi E, Rappelli A, Rizzon P, Pitzalis MV.

Ital Heart J Suppl. 2002 Nov;3(11):1085-91. Review. Italian.

PMID:
12506509
47.

[Mahaim fiber tachycardia and re-entry tachycardia through decremental atrioventricular accessory pathways with anterograde unidirectional block].

Pitzalis MV, Anaclerio M, Luzzi G, Rizzon P.

Cardiologia. 1999 Dec;44 Suppl 1(Pt 1):453-5. Review. Italian. No abstract available.

PMID:
12497951
48.

[Heart failure: a neurohormonal disorder?].

Forleo C, De Tommasi E, Pitzalis MV, Rizzon P.

Cardiologia. 1999 Dec;44 Suppl 1(Pt 1):291-4. Review. Italian. No abstract available.

PMID:
12497923
49.

[Significance of reliable data: informatics in the collection of data and centralized reading].

Mastropasqua F, Guida P, Massari F, Pitzalis MV, Rizzon P.

Cardiologia. 1999 Dec;44 Suppl 1(Pt 2):977-9. Italian. No abstract available.

PMID:
12497861
50.

[Persistent atrial fibrillation: electric cardioversion].

Di Biase M, Grimaldi M, Luzzi G, Anaclerio M, Pitzalis MV.

Cardiologia. 1999 Dec;44 Suppl 1(Pt 2):907-9. Review. Italian. No abstract available.

PMID:
12497845

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