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Items: 34

1.

Exome-Based Rare-Variant Analyses in CKD.

Cameron-Christie S, Wolock CJ, Groopman E, Petrovski S, Kamalakaran S, Povysil G, Vitsios D, Zhang M, Fleckner J, March RE, Gelfman S, Marasa M, Li Y, Sanna-Cherchi S, Kiryluk K, Allen AS, Fellström BC, Haefliger C, Platt A, Goldstein DB, Gharavi AG.

J Am Soc Nephrol. 2019 Jun;30(6):1109-1122. doi: 10.1681/ASN.2018090909. Epub 2019 May 13.

PMID:
31085678
2.

Correction: Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study.

Rasouly HM, Wynn J, Marasa M, Reingold R, Chatterjee D, Kapoor S, Piva S, Kil BH, Mu X, Alvarez M, Nestor J, Mehl K, Revah-Politi A, Lippa N, Ernst ME, Bier L, Espinal A, Haser B, Sinha A, Halim I, Fasel D, Cuneo N, Thompson JJ, Verbitsky M, Cohn EG, Goldman J, Marder K, Klitzman RL, Orjuela MA, So YS, Fedotov A, Crew KD, Kiryluk K, Appelbaum PS, Weng C, Siegel K, Gharavi AG, Chung WK.

Genet Med. 2019 May 1. doi: 10.1038/s41436-019-0528-8. [Epub ahead of print]

PMID:
31040387
3.

Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study.

Milo Rasouly H, Wynn J, Marasa M, Reingold R, Chatterjee D, Kapoor S, Piva S, Kil BH, Mu X, Alvarez M, Nestor J, Mehl K, Revah-Politi A, Lippa N, Ernst ME, Bier L, Espinal A, Haser B, Sinha A, Halim I, Fasel D, Cuneo N, Thompson JJ, Verbitsky M, Cohn EG, Goldman J, Marder K, Klitzman RL, Orjuela MA, So YS, Fedotov A, Crew KD, Kiryluk K, Appelbaum PS, Weng C, Siegel K, Gharavi AG, Chung WK.

Genet Med. 2019 Apr 1. doi: 10.1038/s41436-019-0497-y. [Epub ahead of print] Erratum in: Genet Med. 2019 May 1;:.

PMID:
30930462
4.

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

Verbitsky M, Westland R, Perez A, Kiryluk K, Liu Q, Krithivasan P, Mitrotti A, Fasel DA, Batourina E, Sampson MG, Bodria M, Werth M, Kao C, Martino J, Capone VP, Vivante A, Shril S, Kil BH, Marasa M, Zhang JY, Na YJ, Lim TY, Ahram D, Weng PL, Heinzen EL, Carrea A, Piaggio G, Gesualdo L, Manca V, Masnata G, Gigante M, Cusi D, Izzi C, Scolari F, van Wijk JAE, Saraga M, Santoro D, Conti G, Zamboli P, White H, Drozdz D, Zachwieja K, Miklaszewska M, Tkaczyk M, Tomczyk D, Krakowska A, Sikora P, Jarmoliński T, Borszewska-Kornacka MK, Pawluch R, Szczepanska M, Adamczyk P, Mizerska-Wasiak M, Krzemien G, Szmigielska A, Zaniew M, Dobson MG, Darlow JM, Puri P, Barton DE, Furth SL, Warady BA, Gucev Z, Lozanovski VJ, Tasic V, Pisani I, Allegri L, Rodas LM, Campistol JM, Jeanpierre C, Alam S, Casale P, Wong CS, Lin F, Miranda DM, Oliveira EA, Simoes-E-Silva AC, Barasch JM, Levy B, Wu N, Hildebrandt F, Ghiggeri GM, Latos-Bielenska A, Materna-Kiryluk A, Zhang F, Hakonarson H, Papaioannou VE, Mendelsohn CL, Gharavi AG, Sanna-Cherchi S.

Nat Genet. 2019 Apr;51(4):764. doi: 10.1038/s41588-019-0376-0.

PMID:
30816350
5.

Diagnostic Utility of Exome Sequencing for Kidney Disease.

Groopman EE, Marasa M, Cameron-Christie S, Petrovski S, Aggarwal VS, Milo-Rasouly H, Li Y, Zhang J, Nestor J, Krithivasan P, Lam WY, Mitrotti A, Piva S, Kil BH, Chatterjee D, Reingold R, Bradbury D, DiVecchia M, Snyder H, Mu X, Mehl K, Balderes O, Fasel DA, Weng C, Radhakrishnan J, Canetta P, Appel GB, Bomback AS, Ahn W, Uy NS, Alam S, Cohen DJ, Crew RJ, Dube GK, Rao MK, Kamalakaran S, Copeland B, Ren Z, Bridgers J, Malone CD, Mebane CM, Dagaonkar N, Fellström BC, Haefliger C, Mohan S, Sanna-Cherchi S, Kiryluk K, Fleckner J, March R, Platt A, Goldstein DB, Gharavi AG.

N Engl J Med. 2019 Jan 10;380(2):142-151. doi: 10.1056/NEJMoa1806891. Epub 2018 Dec 26.

PMID:
30586318
6.

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.

Verbitsky M, Westland R, Perez A, Kiryluk K, Liu Q, Krithivasan P, Mitrotti A, Fasel DA, Batourina E, Sampson MG, Bodria M, Werth M, Kao C, Martino J, Capone VP, Vivante A, Shril S, Kil BH, Marasà M, Zhang JY, Na YJ, Lim TY, Ahram D, Weng PL, Heinzen EL, Carrea A, Piaggio G, Gesualdo L, Manca V, Masnata G, Gigante M, Cusi D, Izzi C, Scolari F, van Wijk JAE, Saraga M, Santoro D, Conti G, Zamboli P, White H, Drozdz D, Zachwieja K, Miklaszewska M, Tkaczyk M, Tomczyk D, Krakowska A, Sikora P, Jarmoliński T, Borszewska-Kornacka MK, Pawluch R, Szczepanska M, Adamczyk P, Mizerska-Wasiak M, Krzemien G, Szmigielska A, Zaniew M, Dobson MG, Darlow JM, Puri P, Barton DE, Furth SL, Warady BA, Gucev Z, Lozanovski VJ, Tasic V, Pisani I, Allegri L, Rodas LM, Campistol JM, Jeanpierre C, Alam S, Casale P, Wong CS, Lin F, Miranda DM, Oliveira EA, Simões-E-Silva AC, Barasch JM, Levy B, Wu N, Hildebrandt F, Ghiggeri GM, Latos-Bielenska A, Materna-Kiryluk A, Zhang F, Hakonarson H, Papaioannou VE, Mendelsohn CL, Gharavi AG, Sanna-Cherchi S.

Nat Genet. 2019 Jan;51(1):117-127. doi: 10.1038/s41588-018-0281-y. Epub 2018 Dec 21. Erratum in: Nat Genet. 2019 Apr;51(4):764.

PMID:
30578417
7.

Pitfalls and Challenges of Consenting to Genetic Research Studies.

Milo Rasouly H, Marasa M.

Kidney Int Rep. 2018 Aug 22;3(6):1245-1248. doi: 10.1016/j.ekir.2018.08.004. eCollection 2018 Nov. No abstract available.

8.

CureGN Study Rationale, Design, and Methods: Establishing a Large Prospective Observational Study of Glomerular Disease.

Mariani LH, Bomback AS, Canetta PA, Flessner MF, Helmuth M, Hladunewich MA, Hogan JJ, Kiryluk K, Nachman PH, Nast CC, Rheault MN, Rizk DV, Trachtman H, Wenderfer SE, Bowers C, Hill-Callahan P, Marasa M, Poulton CJ, Revell A, Vento S, Barisoni L, Cattran D, D'Agati V, Jennette JC, Klein JB, Laurin LP, Twombley K, Falk RJ, Gharavi AG, Gillespie BW, Gipson DS, Greenbaum LA, Holzman LB, Kretzler M, Robinson B, Smoyer WE, Guay-Woodford LM; CureGN Consortium.

Am J Kidney Dis. 2019 Feb;73(2):218-229. doi: 10.1053/j.ajkd.2018.07.020. Epub 2018 Nov 9.

PMID:
30420158
9.

Superior Mesenteric Artery Syndrome: Clinical, Endoscopic, and Radiological Findings.

Sinagra E, Raimondo D, Albano D, Guarnotta V, Blasco M, Testai S, Marasà M, Mastrella V, Alaimo V, Bova V, Albano G, Sorrentino D, Tomasello G, Cappello F, Leone A, Rossi F, Galia M, Lagalla R, Midiri F, Morreale GC, Amvrosiadis G, Martorana G, Spampinato MG, Virgilio V, Midiri M.

Gastroenterol Res Pract. 2018 Aug 27;2018:1937416. doi: 10.1155/2018/1937416. eCollection 2018.

10.

Deep Phenotyping on Electronic Health Records Facilitates Genetic Diagnosis by Clinical Exomes.

Son JH, Xie G, Yuan C, Ena L, Li Z, Goldstein A, Huang L, Wang L, Shen F, Liu H, Mehl K, Groopman EE, Marasa M, Kiryluk K, Gharavi AG, Chung WK, Hripcsak G, Friedman C, Weng C, Wang K.

Am J Hum Genet. 2018 Jul 5;103(1):58-73. doi: 10.1016/j.ajhg.2018.05.010. Epub 2018 Jun 28.

11.

Mycophenolate Mofetil in Combination with Steroids for Treatment of C3 Glomerulopathy: A Case Series.

Avasare RS, Canetta PA, Bomback AS, Marasa M, Caliskan Y, Ozluk Y, Li Y, Gharavi AG, Appel GB.

Clin J Am Soc Nephrol. 2018 Mar 7;13(3):406-413. doi: 10.2215/CJN.09080817. Epub 2018 Jan 11.

12.

C3 glomerulonephritis and dense deposit disease share a similar disease course in a large United States cohort of patients with C3 glomerulopathy.

Bomback AS, Santoriello D, Avasare RS, Regunathan-Shenk R, Canetta PA, Ahn W, Radhakrishnan J, Marasa M, Rosenstiel PE, Herlitz LC, Markowitz GS, D'Agati VD, Appel GB.

Kidney Int. 2018 Apr;93(4):977-985. doi: 10.1016/j.kint.2017.10.022. Epub 2018 Jan 6.

PMID:
29310824
13.

Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.

Lata S, Marasa M, Li Y, Fasel DA, Groopman E, Jobanputra V, Rasouly H, Mitrotti A, Westland R, Verbitsky M, Nestor J, Slater LM, D'Agati V, Zaniew M, Materna-Kiryluk A, Lugani F, Caridi G, Rampoldi L, Mattoo A, Newton CA, Rao MK, Radhakrishnan J, Ahn W, Canetta PA, Bomback AS, Appel GB, Antignac C, Markowitz GS, Garcia CK, Kiryluk K, Sanna-Cherchi S, Gharavi AG.

Ann Intern Med. 2018 Jan 16;168(2):100-109. doi: 10.7326/M17-1319. Epub 2017 Dec 5. Erratum in: Ann Intern Med. 2018 Feb 20;168(4):308.

14.

CD55 Deficiency and Protein-Losing Enteropathy.

Angeletti A, Marasà M, Cravedi P.

N Engl J Med. 2017 Oct 12;377(15):1499. doi: 10.1056/NEJMc1710011. No abstract available.

PMID:
29022673
15.

Integrated non-invasive approach to atherosclerosis with cardiac CT and carotid ultrasound in patients with suspected coronary artery disease.

La Grutta L, Marasà M, Toia P, Ajello D, Albano D, Maffei E, Grassedonio E, Novo G, Galia M, Caruso G, Novo S, Cademartiri F, Midiri M.

Radiol Med. 2017 Jan;122(1):16-21. doi: 10.1007/s11547-016-0692-8. Epub 2016 Oct 13.

PMID:
27738787
16.

A compact very wideband amplifying filter based on RTD loaded composite right/left-handed transmission lines.

Abu-Marasa MO, El-Khozondar HJ.

Springerplus. 2015 Nov 25;4:733. doi: 10.1186/s40064-015-1529-y. eCollection 2015.

17.

Refractory focal segmental glomerulosclerosis in the adult: complete and sustained remissions of two episodes of nephrotic syndrome after a single dose of rituximab.

Marasà M, Cravedi P, Ruggiero B, Ruggenenti P.

BMJ Case Rep. 2014 Aug 25;2014. pii: bcr2014205507. doi: 10.1136/bcr-2014-205507.

18.

Rituximab in steroid-dependent or frequently relapsing idiopathic nephrotic syndrome.

Ruggenenti P, Ruggiero B, Cravedi P, Vivarelli M, Massella L, Marasà M, Chianca A, Rubis N, Ene-Iordache B, Rudnicki M, Pollastro RM, Capasso G, Pisani A, Pennesi M, Emma F, Remuzzi G; Rituximab in Nephrotic Syndrome of Steroid-Dependent or Frequently Relapsing Minimal Change Disease Or Focal Segmental Glomerulosclerosis (NEMO) Study Group.

J Am Soc Nephrol. 2014 Apr;25(4):850-63. doi: 10.1681/ASN.2013030251. Epub 2014 Jan 30.

19.

Rituximab in idiopathic membranous nephropathy.

Ruggenenti P, Cravedi P, Chianca A, Perna A, Ruggiero B, Gaspari F, Rambaldi A, Marasà M, Remuzzi G.

J Am Soc Nephrol. 2012 Aug;23(8):1416-25. doi: 10.1681/ASN.2012020181. Epub 2012 Jul 19.

20.

Perioperative Minimal Induction Therapy: A Further Step toward More Effective Immunosuppression in Transplantation.

Gennarini A, Cravedi P, Marasà M, Perna A, Rota G, Bontempelli M, Sandrini S, Remuzzi G, Ruggenenti P.

J Transplant. 2012;2012:426042. doi: 10.1155/2012/426042. Epub 2012 May 20.

21.

Delayed-onset superior mesenteric artery syndrome presenting as oesophageal peptic stricture.

Sinagra E, Montalbano LM, Linea C, Giunta M, Tesè L, La Seta F, Malizia G, Orlando A, Marasà M, D'Amico G.

Case Rep Gastroenterol. 2012 Jan;6(1):94-102. doi: 10.1159/000336278. Epub 2012 Feb 10.

22.

Prevention of low back pain in sedentary healthy workers: a pilot study.

Moore C, Holland J, Shaib F, Ceridan E, Schonard C, Marasa M.

Am J Med Sci. 2012 Aug;344(2):90-5. doi: 10.1097/MAJ.0b013e3182364942.

PMID:
22173041
23.

Hypertension after kidney transplantation: an important, but still neglected issue.

Marasà M, Remuzzi G, Cravedi P.

J Hypertens. 2011 Dec;29(12):2310-1. doi: 10.1097/HJH.0b013e32834d7815. No abstract available.

PMID:
22075952
24.

Membranous nephropathy associated with IgG4-related disease.

Cravedi P, Abbate M, Gagliardini E, Galbusera M, Buelli S, Sabadini E, Marasà M, Beck LH Jr, Salant DJ, Benigni A, D'Agati V, Remuzzi G.

Am J Kidney Dis. 2011 Aug;58(2):272-5. doi: 10.1053/j.ajkd.2011.05.002. Epub 2011 Jun 12.

PMID:
21658826
25.

Efficacy and safety of rituximab second-line therapy for membranous nephropathy: a prospective, matched-cohort study.

Cravedi P, Sghirlanzoni MC, Marasà M, Salerno A, Remuzzi G, Ruggenenti P.

Am J Nephrol. 2011;33(5):461-8. doi: 10.1159/000327611. Epub 2011 Apr 21.

PMID:
21508634
26.

IL-6 -174G/C polymorphism and IL-6 serum levels in patients with liver cirrhosis and hepatocellular carcinoma.

Giannitrapani L, Soresi M, Giacalone A, Campagna ME, Marasà M, Cervello M, Marasà S, Montalto G.

OMICS. 2011 Mar;15(3):183-6. doi: 10.1089/omi.2010.0093. Epub 2011 Feb 17.

PMID:
21329460
27.

Autologous mesenchymal stromal cells and kidney transplantation: a pilot study of safety and clinical feasibility.

Perico N, Casiraghi F, Introna M, Gotti E, Todeschini M, Cavinato RA, Capelli C, Rambaldi A, Cassis P, Rizzo P, Cortinovis M, Marasà M, Golay J, Noris M, Remuzzi G.

Clin J Am Soc Nephrol. 2011 Feb;6(2):412-22. doi: 10.2215/CJN.04950610. Epub 2010 Oct 7.

28.

Monoclonal antibodies for podocytopathies: rationale and clinical responses.

Marasà M, Kopp JB.

Nat Rev Nephrol. 2009 Jun;5(6):337-48. doi: 10.1038/nrneph.2009.70. Review.

PMID:
19474828
29.

Upon oxidative stress, the antiapoptotic Hsp60/procaspase-3 complex persists in mucoepidermoid carcinoma cells.

Campanella C, Bucchieri F, Ardizzone NM, Marino Gammazza A, Montalbano A, Ribbene A, Di Felice V, Bellafiore M, David S, Rappa F, Marasà M, Peri G, Farina F, Czarnecka AM, Conway de Macario E, Macario AJ, Zummo G, Cappello F.

Eur J Histochem. 2008 Oct-Dec;52(4):221-8.

PMID:
19109096
30.

Activation of PPARgamma enhances in vitro the immunosuppressive effect of cyclosporine on T lymphocytes.

Rampino T, Ranghino A, Guidetti C, Gregorini M, Soccio G, Marasà M, Libetta C, Guida G, De Amici M, Dal Canton A.

Transpl Immunol. 2007 Jul;18(1):32-6. Epub 2007 Apr 12.

PMID:
17584600
31.

Neutralization of macrophage-stimulating protein ameliorates renal injury in anti-thy 1 glomerulonephritis.

Rampino T, Soccio G, Gregorini M, Guidetti C, Marasà M, Maggio M, Panichi V, Migliori M, Libetta C, Dal Canton A.

J Am Soc Nephrol. 2007 May;18(5):1486-96. Epub 2007 Apr 4.

32.

Platelet-Independent defect in hemostasis associated with sirolimus use.

Rampino T, Marasà M, Malvezzi PM, Soccio G, Roscini E, Gamba G, Noris P, Alessiani M, Dal Canton A.

Transplant Proc. 2004 Apr;36(3):700-2.

PMID:
15110636
33.

Comparison of the quality of life between HIV-positive haemophilia patients and HIV-negative haemophilia patients.

Djulbegovic B, Goldsmith G, Vaughn D, Birkimer J, Marasa M, Joseph G, Huang A, Hadley T.

Haemophilia. 1996 Jul;2(3):166-72. doi: 10.1111/j.1365-2516.1996.tb00161.x.

PMID:
27214111
34.

Safety and efficacy of purified factor IX concentrate and antifibrinolytic agents for dental extractions in hemophilia B.

Djulbegovic B, Marasa M, Pesto A, Kushner GM, Hadley T, Joseph G, Goldsmith G.

Am J Hematol. 1996 Feb;51(2):168-70.

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