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Items: 1 to 20 of 43

1.

" Endovascular Treatment of Poplital Artery Aneurysms: A Word of Caution after Long-Term Follow-Up".

Maraglino C, Canu G, Ambrosi R, Briolini F, Gotti R, Cefalì P, Calliari F, Ferrero P, Terraneo F.

Ann Vasc Surg. 2016 Nov 26. pii: S0890-5096(16)31260-2. doi: 10.1016/j.avsg.2016.08.023. [Epub ahead of print]

PMID:
27903472
2.

Early functional results using the nitibond prosthesis in stapes surgery.

Canu G, Lauretani F, Russo FY, Ferrary E, Lamas G, Sterkers O, De Seta D, Bernardeschi D.

Acta Otolaryngol. 2016 Nov 4:1-6. [Epub ahead of print]

PMID:
27809651
3.

Red blood cell PK deficiency: An update of PK-LR gene mutation database.

Canu G, De Bonis M, Minucci A, Capoluongo E.

Blood Cells Mol Dis. 2016 Mar;57:100-9. doi: 10.1016/j.bcmd.2015.12.009. Review.

PMID:
26832193
4.

Crater-Like Ulceration of Aortic Arch.

Simon C, Calabrese A, Canu G, Merlo M, Galletti L.

Aorta (Stamford). 2014 Dec 1;2(6):289-92. doi: 10.12945/j.aorta.2014.14-029.

5.

Management of epi- and mesotympanic cholesteatomas by one-stage trans-canal atticotomy in adults.

Bernardeschi D, Russo FY, Nguyen Y, Canu G, Mosnier I, De Seta D, Ferrary E, Sterkers O.

Eur Arch Otorhinolaryngol. 2016 Oct;273(10):2941-6. doi: 10.1007/s00405-015-3875-3.

PMID:
26728485
6.

Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review.

Minucci A, Scambia G, Santonocito C, Concolino P, Canu G, Mignone F, Saggese I, Guarino D, Costella A, Molinario R, De Bonis M, Ferrandina G, Petrillo M, Scaglione GL, Capoluongo E.

Expert Rev Mol Diagn. 2015;15(10):1383-403. doi: 10.1586/14737159.2015.1081059. Review.

PMID:
26306726
7.

A rare case of juvenile hypertension: coexistence of type 2 multiple endocrine neoplasia -related bilateral pheochromocytoma and reninoma in a young patient with ACE gene polymorphism.

Paragliola RM, Capoluongo E, Torino F, Minucci A, Canu G, Prete A, Pontecorvi A, Corsello SM.

BMC Endocr Disord. 2015 Jun 18;15:30. doi: 10.1186/s12902-015-0022-5.

8.

Radiation Therapy-Induced Cardiovascular Disease Treated by a Percutaneous Approach.

Fiocca L, Coccato M, Sirbu V, Vassileva A, Guagliumi G, Musumeci G, Terzi A, Canu G, Cerchierini E, Cugola D, Valsecchi O.

Case Rep Cardiol. 2015;2015:851624. doi: 10.1155/2015/851624.

9.

Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome.

Minucci A, Ruggiero A, Canu G, Maurizi P, De Bonis M, Concolino P, De Luca D, Capoluongo E.

Pediatr Blood Cancer. 2015 Sep;62(9):1680-1. doi: 10.1002/pbc.25500. No abstract available.

PMID:
25822733
10.

Calcitonin measurement in fine-needle aspirate washouts vs. cytologic examination for diagnosis of primary or metastatic medullary thyroid carcinoma.

de Crea C, Raffaelli M, Maccora D, Carrozza C, Canu G, Fadda G, Bellantone R, Lombardi CP.

Acta Otorhinolaryngol Ital. 2014 Dec;34(6):399-405. Review.

11.

[Acute coronary syndrome following a 100 µg carbetocin injection during an emergency Cesarean delivery].

Jacquenod P, Cattenoz M, Canu G, Bois E, Lieutaud T.

Can J Anaesth. 2015 May;62(5):513-7. doi: 10.1007/s12630-015-0344-9. French.

PMID:
25715846
12.

Transcriptional diversity during lineage commitment of human blood progenitors.

Chen L, Kostadima M, Martens JH, Canu G, Garcia SP, Turro E, Downes K, Macaulay IC, Bielczyk-Maczynska E, Coe S, Farrow S, Poudel P, Burden F, Jansen SB, Astle WJ, Attwood A, Bariana T, de Bono B, Breschi A, Chambers JC; BRIDGE Consortium., Choudry FA, Clarke L, Coupland P, van der Ent M, Erber WN, Jansen JH, Favier R, Fenech ME, Foad N, Freson K, van Geet C, Gomez K, Guigo R, Hampshire D, Kelly AM, Kerstens HH, Kooner JS, Laffan M, Lentaigne C, Labalette C, Martin T, Meacham S, Mumford A, Nürnberg S, Palumbo E, van der Reijden BA, Richardson D, Sammut SJ, Slodkowicz G, Tamuri AU, Vasquez L, Voss K, Watt S, Westbury S, Flicek P, Loos R, Goldman N, Bertone P, Read RJ, Richardson S, Cvejic A, Soranzo N, Ouwehand WH, Stunnenberg HG, Frontini M, Rendon A.

Science. 2014 Sep 26;345(6204):1251033. doi: 10.1126/science.1251033.

13.

ST-segment-elevation myocardial infarction patients randomized to a pharmaco-invasive strategy or primary percutaneous coronary intervention: Strategic Reperfusion Early After Myocardial Infarction (STREAM) 1-year mortality follow-up.

Sinnaeve PR, Armstrong PW, Gershlick AH, Goldstein P, Wilcox R, Lambert Y, Danays T, Soulat L, Halvorsen S, Ortiz FR, Vandenberghe K, Regelin A, Bluhmki E, Bogaerts K, Van de Werf F; STREAM investigators..

Circulation. 2014 Sep 30;130(14):1139-45. doi: 10.1161/CIRCULATIONAHA.114.009570.

14.

The cockayne syndrome B protein is essential for neuronal differentiation and neuritogenesis.

Ciaffardini F, Nicolai S, Caputo M, Canu G, Paccosi E, Costantino M, Frontini M, Balajee AS, Proietti-De-Santis L.

Cell Death Dis. 2014 May 29;5:e1268. doi: 10.1038/cddis.2014.228.

15.

Hypotestosteronemia is frequent in ST-elevation myocardial infarction patients and is associated with coronary microvascular obstruction.

Niccoli G, Milardi D, D'Amario D, Fracassi F, Grande G, Panico RA, Roberto M, Mirizzi AM, Canu G, De Marinis L, Carrozza C, Pontecorvi A, Crea F.

Eur J Prev Cardiol. 2015 Jul;22(7):855-63. doi: 10.1177/2047487314533084.

PMID:
24821730
16.

Is capillary electrophoresis on microchip devices able to genotype uridine diphosphate glucuronosyltransferase 1A1 TATA-box polymorphisms?

Minucci A, Canu G, De Bonis M, Delibato E, Capoluongo E.

J Sep Sci. 2014 Jun;37(12):1521-3. doi: 10.1002/jssc.201400235.

PMID:
24687976
17.

DNA from buccal swab is suitable for rapid genotyping of angiotensin-converting enzyme insertion/deletion (I/D) polymorphism.

Minucci A, Canu G, Concolino P, Guarino D, Boccia S, Ficarra S, Zuppi C, Giardina B, Capoluongo E.

Clin Chim Acta. 2014 Apr 20;431:125-30. doi: 10.1016/j.cca.2013.12.041.

PMID:
24406276
18.

Bivalirudin started during emergency transport for primary PCI.

Steg PG, van 't Hof A, Hamm CW, Clemmensen P, Lapostolle F, Coste P, Ten Berg J, Van Grunsven P, Eggink GJ, Nibbe L, Zeymer U, Campo dell' Orto M, Nef H, Steinmetz J, Soulat L, Huber K, Deliargyris EN, Bernstein D, Schuette D, Prats J, Clayton T, Pocock S, Hamon M, Goldstein P; EUROMAX Investigators..

N Engl J Med. 2013 Dec 5;369(23):2207-17. doi: 10.1056/NEJMoa1311096.

19.

Fibrinolysis or primary PCI in ST-segment elevation myocardial infarction.

Armstrong PW, Gershlick AH, Goldstein P, Wilcox R, Danays T, Lambert Y, Sulimov V, Rosell Ortiz F, Ostojic M, Welsh RC, Carvalho AC, Nanas J, Arntz HR, Halvorsen S, Huber K, Grajek S, Fresco C, Bluhmki E, Regelin A, Vandenberghe K, Bogaerts K, Van de Werf F; STREAM Investigative Team..

N Engl J Med. 2013 Apr 11;368(15):1379-87. doi: 10.1056/NEJMoa1301092.

20.

Gilbert and Crigler Najjar syndromes: an update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database.

Canu G, Minucci A, Zuppi C, Capoluongo E.

Blood Cells Mol Dis. 2013 Apr;50(4):273-80. doi: 10.1016/j.bcmd.2013.01.003.

PMID:
23403257
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