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Items: 1 to 50 of 93

1.

Benefits of Organized Mammographic Screening Programs in Women Aged 50 to 69 years: A Surgical Perspective.

Fancellu A, Sanna V, Sedda ML, Delrio D, Cottu P, Spanu A, Giuliani G, Conti M, Piras R, Crivelli P, Porcu A.

Clin Breast Cancer. 2019 May 2. pii: S1526-8209(19)30150-8. doi: 10.1016/j.clbc.2019.04.013. [Epub ahead of print]

PMID:
31130366
2.

Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUS.

Valoti E, Alberti M, Iatropoulos P, Piras R, Mele C, Breno M, Cremaschi A, Bresin E, Donadelli R, Alizzi S, Amoroso A, Benigni A, Remuzzi G, Noris M.

Front Immunol. 2019 May 1;10:853. doi: 10.3389/fimmu.2019.00853. eCollection 2019.

3.

Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study Group.

Filosto M, Cotti Piccinelli S, Ravaglia S, Servidei S, Moggio M, Musumeci O, Donati MA, Pegoraro E, Di Muzio A, Maggi L, Tonin P, Marrosu G, Sancricca C, Lerario A, Sacchini M, Semplicini C, Bozzoni V, Telese R, Bonanno S, Piras R, Maioli MA, Ricci G, Vercelli L, Galvagni A, Gallo Cassarino S, Caria F, Mongini T, Siciliano G, Padovani A, Toscano A.

Adv Ther. 2019 May;36(5):1177-1189. doi: 10.1007/s12325-019-00926-5. Epub 2019 Mar 16.

PMID:
30879255
4.

An Ex Vivo Test of Complement Activation on Endothelium for Individualized Eculizumab Therapy in Hemolytic Uremic Syndrome.

Galbusera M, Noris M, Gastoldi S, Bresin E, Mele C, Breno M, Cuccarolo P, Alberti M, Valoti E, Piras R, Donadelli R, Vivarelli M, Murer L, Pecoraro C, Ferrari E, Perna A, Benigni A, Portalupi V, Remuzzi G.

Am J Kidney Dis. 2019 Jul;74(1):56-72. doi: 10.1053/j.ajkd.2018.11.012. Epub 2019 Mar 7.

PMID:
30851964
5.

Unraveling the Molecular Mechanisms Underlying Complement Dysregulation by Nephritic Factors in C3G and IC-MPGN.

Donadelli R, Pulieri P, Piras R, Iatropoulos P, Valoti E, Benigni A, Remuzzi G, Noris M.

Front Immunol. 2018 Oct 15;9:2329. doi: 10.3389/fimmu.2018.02329. eCollection 2018.

6.

Fibronectin glomerulopathy - A sporadic case with unusual clinical manifestation.

Mandal SN, Shrivastava S, Piras R, Gowrishankar S.

Saudi J Kidney Dis Transpl. 2017 Nov-Dec;28(6):1416-1420. doi: 10.4103/1319-2442.220860.

7.

Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex-Mediated Membranoproliferative GN.

Iatropoulos P, Daina E, Curreri M, Piras R, Valoti E, Mele C, Bresin E, Gamba S, Alberti M, Breno M, Perna A, Bettoni S, Sabadini E, Murer L, Vivarelli M, Noris M, Remuzzi G; Registry of Membranoproliferative Glomerulonephritis/C3 Glomerulopathy; Nastasi.

J Am Soc Nephrol. 2018 Jan;29(1):283-294. doi: 10.1681/ASN.2017030258. Epub 2017 Oct 13.

8.

X-Linked Hypohidrotic Ectodermal Dysplasia: New Features and a Novel EDA Gene Mutation.

Savasta S, Carlone G, Castagnoli R, Chiappe F, Bassanese F, Piras R, Salpietro V, Brazzelli V, Verrotti A, Marseglia GL.

Cytogenet Genome Res. 2017;152(3):111-116. doi: 10.1159/000478922. Epub 2017 Sep 7.

PMID:
28877528
9.

Nephrotic-Range Proteinuria and Peripheral Edema in a Child: Not Only Idiopathic Nephrotic Syndrome.

Dolcemascolo V, Vivarelli M, Colucci M, Diomedi-Camassei F, Piras R, Alberti M, Emma F.

Case Rep Nephrol Dial. 2016 Nov 1;6(3):120-127. eCollection 2016 Sep-Dec.

10.

Preventing antiblastic drug-related cardiomyopathy: old and new therapeutic strategies.

Cadeddu C, Mercurio V, Spallarossa P, Nodari S, Triggiani M, Monte I, Piras R, Madonna R, Pagliaro P, Tocchetti CG, Mercuro G.

J Cardiovasc Med (Hagerstown). 2016 May;17 Suppl 1 Special issue on Cardiotoxicity from Antiblastic Drugs and Cardioprotection:e64-e75. Review.

PMID:
27755244
11.

Preventing antiblastic drug-related cardiomyopathy: old and new therapeutic strategies.

Cadeddu C, Mercurio V, Spallarossa P, Nodari S, Triggiani M, Monte I, Piras R, Madonna R, Pagliaro P, Tocchetti CG, Mercuro G.

J Cardiovasc Med (Hagerstown). 2016 May;17 Suppl 1:S64-75. doi: 10.2459/JCM.0000000000000382. Review.

PMID:
27183527
12.

Metabolomic patterns associated to QTc interval in shiftworkers: an explorative analysis.

Campagna M, Locci E, Piras R, Noto A, Lecca LI, Pilia I, Cocco P, d'Aloja E, Scano P.

Biomarkers. 2016 Nov;21(7):607-13. doi: 10.3109/1354750X.2016.1171900. Epub 2016 Apr 28.

13.

Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome.

Iatropoulos P, Noris M, Mele C, Piras R, Valoti E, Bresin E, Curreri M, Mondo E, Zito A, Gamba S, Bettoni S, Murer L, Fremeaux-Bacchi V, Vivarelli M, Emma F, Daina E, Remuzzi G.

Mol Immunol. 2016 Mar;71:131-142. doi: 10.1016/j.molimm.2016.01.010. Epub 2016 Feb 16.

PMID:
26895476
14.

Late-onset polyglucosan body myopathy in five patients with a homozygous mutation in GYG1.

Akman HO, Aykit Y, Amuk OC, Malfatti E, Romero NB, Maioli MA, Piras R, DiMauro S, Marrosu G.

Neuromuscul Disord. 2016 Jan;26(1):16-20. doi: 10.1016/j.nmd.2015.10.012. Epub 2015 Nov 10.

15.

Thrombotic microangiopathy without renal involvement: two novel mutations in complement-regulator genes.

Peyvandi F, Rossio R, Ferrari B, Lotta LA, Pontiggia S, Ghiringhelli Borsa N, Pizzuti M, Donadelli R, Piras R, Cugno M, Noris M.

J Thromb Haemost. 2016 Feb;14(2):340-5. doi: 10.1111/jth.13210. Epub 2016 Feb 1.

16.

Absorption F-sum rule for the exciton binding energy in methylammonium lead halide perovskites.

Sestu N, Cadelano M, Sarritzu V, Chen F, Marongiu D, Piras R, Mainas M, Quochi F, Saba M, Mura A, Bongiovanni G.

J Phys Chem Lett. 2015 Nov 19;6(22):4566-72. doi: 10.1021/acs.jpclett.5b02099. Epub 2015 Nov 5.

PMID:
26517760
17.

Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome.

Mele C, Lemaire M, Iatropoulos P, Piras R, Bresin E, Bettoni S, Bick D, Helbling D, Veith R, Valoti E, Donadelli R, Murer L, Neunhäuserer M, Breno M, Frémeaux-Bacchi V, Lifton R, Remuzzi G, Noris M.

Clin J Am Soc Nephrol. 2015 Jun 5;10(6):1011-9. doi: 10.2215/CJN.08520814. Epub 2015 Apr 8.

18.

Correlated electron-hole plasma in organometal perovskites.

Saba M, Cadelano M, Marongiu D, Chen F, Sarritzu V, Sestu N, Figus C, Aresti M, Piras R, Lehmann AG, Cannas C, Musinu A, Quochi F, Mura A, Bongiovanni G.

Nat Commun. 2014 Sep 30;5:5049. doi: 10.1038/ncomms6049.

PMID:
25266869
19.

Influence of treatments in multiple sclerosis disability: a cohort study.

Cocco E, Sardu C, Spinicci G, Musu L, Massa R, Frau J, Lorefice L, Fenu G, Coghe G, Massole S, Maioli MA, Piras R, Melis M, Porcu G, Mamusa E, Carboni N, Contu P, Marrosu MG.

Mult Scler. 2015 Apr;21(4):433-41. doi: 10.1177/1352458514546788. Epub 2014 Sep 25.

PMID:
25257611
20.

Kidney transplantation from a donor with acute kidney injury: an unexpected outcome.

Mescia F, Piras R, Noris M, Marchetti G, Rossini G, Remuzzi G, Ruggenenti P.

Am J Transplant. 2014 Apr;14(4):977-8. doi: 10.1111/ajt.12648. Epub 2014 Feb 6. No abstract available.

21.

Expanding the mutational spectrum of CRLF1 in Crisponi/CISS1 syndrome.

Piras R, Chiappe F, Torraca IL, Buers I, Usala G, Angius A, Akin MA, Basel-Vanagaite L, Benedicenti F, Chiodin E, El Assy O, Feingold-Zadok M, Guibert J, Kamien B, Kasapkara CS, Kiliç E, Boduroğlu K, Kurtoglu S, Manzur AY, Onal EE, Paderi E, Roche CH, Tümer L, Unal S, Utine GE, Zanda G, Zankl A, Zampino G, Crisponi G, Crisponi L, Rutsch F.

Hum Mutat. 2014 Apr;35(4):424-33. doi: 10.1002/humu.22522. Epub 2014 Mar 6.

PMID:
24488861
22.

Partial lipodystrophy associated with muscular dystrophy of unknown genetic origin.

Carboni N, Brancati F, Cocco E, Solla E, D'Apice MR, Mateddu A, McIntyre A, Fadda E, Mura M, Lattanzi G, Piras R, Maioli MA, Marrosu G, Novelli G, Marrosu MG, Hegele RA.

Muscle Nerve. 2014 Jun;49(6):928-30. doi: 10.1002/mus.24157. No abstract available.

PMID:
24375490
23.

Post-transplant recurrence of atypical hemolytic uremic syndrome in a patient with thrombomodulin mutation.

Sinibaldi S, Guzzo I, Piras R, Bresin E, Emma F, Dello Strologo L.

Pediatr Transplant. 2013 Dec;17(8):E177-81. doi: 10.1111/petr.12151. Epub 2013 Sep 30.

PMID:
24118826
24.

Crisponi syndrome: a new mutation in CRLF1 gene associated with moderate outcome.

Uzunalic N, Zenciroglu A, Beken S, Piras R, Dilli D, Aydin B, Chiappe F, Okumus N, Crisponi L.

Genet Couns. 2013;24(2):161-6.

PMID:
24032286
25.

Overlapping syndromes in laminopathies: a meta-analysis of the reported literature.

Carboni N, Politano L, Floris M, Mateddu A, Solla E, Olla S, Maggi L, Antonietta Maioli M, Piras R, Cocco E, Marrosu G, Giovanna Marrosu M.

Acta Myol. 2013 May;32(1):7-17. Review.

26.

Partial duplication of the PARK2 gene in a child with developmental delay and her normal mother: a second report.

Mariani M, Crosti F, Redaelli S, Fossati C, Piras R, Biondi A, Dalprà L, Selicorni A.

Am J Med Genet B Neuropsychiatr Genet. 2013 Jul;162B(5):485-6. doi: 10.1002/ajmg.b.32173. Epub 2013 Jun 6. No abstract available.

PMID:
23740672
27.

Two patients with history of STEC-HUS, posttransplant recurrence and complement gene mutations.

Alberti M, Valoti E, Piras R, Bresin E, Galbusera M, Tripodo C, Thaiss F, Remuzzi G, Noris M.

Am J Transplant. 2013 Aug;13(8):2201-6. doi: 10.1111/ajt.12297. Epub 2013 Jun 3.

28.

Atypical hemolytic uremic syndrome with MCP mutations preceded by respiratory infection.

Yasuda K, Sasaki K, Yamato M, Rakugi H, Isaka Y, Hayashi T, Piras R, Bresin E.

CEN Case Rep. 2013 May;2(1):34-37. doi: 10.1007/s13730-012-0034-1. Epub 2012 Oct 5.

29.

A case of familial glomerulopathy with fibronectin deposits caused by the Y973C mutation in fibronectin.

Ertoy Baydar D, Kutlugun AA, Bresin E, Piras R.

Am J Kidney Dis. 2013 Mar;61(3):514-8. doi: 10.1053/j.ajkd.2012.08.050. Epub 2012 Dec 6.

PMID:
23219110
30.

Cardiac involvement in patients with lamin A/C gene mutations: a cohort observation.

Carboni N, Sardu C, Cocco E, Marrosu G, Manzi RC, Nissardi V, Isola F, Mateddu A, Solla E, Maioli MA, Oppo V, Piras R, Coghe G, Lai C, Marrosu MG.

Muscle Nerve. 2012 Aug;46(2):187-92. doi: 10.1002/mus.23294.

PMID:
22806367
31.

Absence of histological myopathy in chronic myeloid leukemia patients complaining of muscle spasms and myalgia during treatment with nilotinib.

Caocci G, Maioli MA, Atzeni S, Piras R, Carboni N, La Nasa G.

Leuk Res. 2012 Sep;36(9):e206-8. doi: 10.1016/j.leukres.2012.06.006. Epub 2012 Jun 26. No abstract available.

PMID:
22742815
32.

Fibronectin glomerulopathy: an unusual cause of adult-onset nephrotic syndrome.

Nadamuni M, Piras R, Mazbar S, Higgins JP, Kambham N.

Am J Kidney Dis. 2012 Nov;60(5):839-42. doi: 10.1053/j.ajkd.2012.04.029. Epub 2012 Jun 20.

PMID:
22721928
33.

Haplotype affinities resolve a major component of goat (Capra hircus) MtDNA D-loop diversity and reveal specific features of the Sardinian stock.

Piras D, Doro MG, Casu G, Melis PM, Vaccargiu S, Piras I, Parracciani D, Stradoni R, Frongia B, Lai G, Sale S, Cattari W, Piras R, Querci O, Demuro P, Cui S, Atzori F, Mancosu M, Marchiori F, Cammelli R, Spiga A, Loddo PP, Pili G, Boi R, Argiolas G, Mereu P, Leoni GG, Naitana S, Pirastu M, Novelletto A.

PLoS One. 2012;7(2):e30785. doi: 10.1371/journal.pone.0030785. Epub 2012 Feb 17.

34.

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.

35.

Dilated cardiomyopathy with conduction defects in a patient with partial merosin deficiency due to mutations in the laminin-α2-chain gene: a chance association or a novel phenotype?

Carboni N, Marrosu G, Porcu M, Mateddu A, Solla E, Cocco E, Maioli MA, Oppo V, Piras R, Marrosu MG.

Muscle Nerve. 2011 Nov;44(5):826-8. doi: 10.1002/mus.22228.

PMID:
22006699
36.

Cardiac and muscle imaging findings in a family with X-linked Emery-Dreifuss muscular dystrophy.

Carboni N, Mura M, Mercuri E, Marrosu G, Manzi RC, Cocco E, Nissardi V, Isola F, Mateddu A, Solla E, Maioli MA, Oppo V, Piras R, Marini S, Lai C, Politano L, Marrosu MG.

Neuromuscul Disord. 2012 Feb;22(2):152-8. doi: 10.1016/j.nmd.2011.09.001. Epub 2011 Oct 10.

PMID:
21993399
37.

MYO1E mutations and childhood familial focal segmental glomerulosclerosis.

Mele C, Iatropoulos P, Donadelli R, Calabria A, Maranta R, Cassis P, Buelli S, Tomasoni S, Piras R, Krendel M, Bettoni S, Morigi M, Delledonne M, Pecoraro C, Abbate I, Capobianchi MR, Hildebrandt F, Otto E, Schaefer F, Macciardi F, Ozaltin F, Emre S, Ibsirlioglu T, Benigni A, Remuzzi G, Noris M; PodoNet Consortium.

N Engl J Med. 2011 Jul 28;365(4):295-306. doi: 10.1056/NEJMoa1101273. Epub 2011 Jul 14.

38.

Aberrant splicing in the LMNA gene caused by a novel mutation on the polypyrimidine tract of intron 5.

Carboni N, Floris M, Mateddu A, Porcu M, Marrosu G, Solla E, Cocco E, Mura M, Marini S, Maioli MA, Piras R, Aste R, Marrosu MG.

Muscle Nerve. 2011 May;43(5):688-93. doi: 10.1002/mus.21937. Epub 2011 Apr 1.

PMID:
21462202
39.

The cohort of the multiple sclerosis center of Cagliari.

Marrosu MG, Lorefice L, Frau J, Coghe G, Fenu G, Piras R, Melis M, Cocco E.

Neurol Sci. 2011 Jan;31 Suppl 3:309-12. doi: 10.1007/s10072-010-0470-7.

PMID:
21267619
40.

Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype.

Noris M, Caprioli J, Bresin E, Mossali C, Pianetti G, Gamba S, Daina E, Fenili C, Castelletti F, Sorosina A, Piras R, Donadelli R, Maranta R, van der Meer I, Conway EM, Zipfel PF, Goodship TH, Remuzzi G.

Clin J Am Soc Nephrol. 2010 Oct;5(10):1844-59. doi: 10.2215/CJN.02210310. Epub 2010 Jul 1.

41.

Muscle imaging analogies in a cohort of patients with different clinical phenotypes caused by LMNA gene mutations.

Carboni N, Mura M, Marrosu G, Cocco E, Marini S, Solla E, Mateddu A, Maioli MA, Piras R, Mallarini G, Mercuro G, Porcu M, Marrosu MG.

Muscle Nerve. 2010 Apr;41(4):458-63. doi: 10.1002/mus.21514.

PMID:
19882644
42.

Insights on blastomere nuclearity.

Gil M, D'Ommar G, Póo ME, Sosa A, Piras M, Piras R, Rísquez F.

J Assist Reprod Genet. 2007 Jan;24(1):17-22. Epub 2006 Dec 16.

43.

PEN-2 gene mutation in a familial Alzheimer's disease case.

Sala Frigerio C, Piscopo P, Calabrese E, Crestini A, Malvezzi Campeggi L, Civita di Fava R, Fogliarino S, Albani D, Marcon G, Cherchi R, Piras R, Forloni G, Confaloni A.

J Neurol. 2005 Sep;252(9):1033-6. Epub 2005 Mar 16.

PMID:
16170650
44.

Extrinsic autonomic neuropathy in a case of transition from diffuse esophageal spasm to achalasia.

Usai Satta P, Oppia F, Piras R, Loriga F.

Clin Auton Res. 2004 Aug;14(4):270-2. No abstract available.

PMID:
15316846
45.

Synthesis and antitumor evaluation of 6-thioxo-, 6-oxo- and 2,4-dioxopyrimidine derivatives.

Cocco MT, Congiu C, Onnis V, Piras R.

Farmaco. 2001 Oct;56(10):741-8.

PMID:
11718266
46.

Sterol composition and biosynthesis in Trypanosoma cruzi amastigotes.

Liendo A, Visbal G, Piras MM, Piras R, Urbina JA.

Mol Biochem Parasitol. 1999 Oct 25;104(1):81-91.

PMID:
10589983
47.

Antiproliferative effects and mechanism of action of SCH 56592 against Trypanosoma (Schizotrypanum) cruzi: in vitro and in vivo studies.

Urbina JA, Payares G, Contreras LM, Liendo A, Sanoja C, Molina J, Piras M, Piras R, Perez N, Wincker P, Loebenberg D.

Antimicrob Agents Chemother. 1998 Jul;42(7):1771-7.

48.

Cure of short- and long-term experimental Chagas' disease using D0870.

Urbina JA, Payares G, Molina J, Sanoja C, Liendo A, Lazardi K, Piras MM, Piras R, Perez N, Wincker P, Ryley JF.

Science. 1996 Aug 16;273(5277):969-71.

PMID:
8688084
49.

Antiproliferative effects of delta 24(25) sterol methyl transferase inhibitors on Trypanosoma (Schizotrypanum) cruzi: in vitro and in vivo studies.

Urbina JA, Vivas J, Lazardi K, Molina J, Payares G, Piras MM, Piras R.

Chemotherapy. 1996 Jul-Aug;42(4):294-307.

PMID:
8804798
50.

Trypanosoma cruzi: immunity-induced in mice and rats by trypomastigote excretory-secretory antigens and identification of a peptide sequence containing a T cell epitope with protective activity.

Taibi A, Plumas-Marty B, Guevara-Espinoza A, Schöneck R, Pessoa H, Loyens M, Piras R, Aguirre T, Gras-Masse H, Bossus M, et al.

J Immunol. 1993 Sep 1;151(5):2676-89.

PMID:
7689612

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