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Items: 1 to 50 of 71

1.

Alazami syndrome: the first case of papillary thyroid carcinoma.

Ivanovski I, Caraffi SG, Magnani E, Rosato S, Pollazzon M, Matalonga L, Piana S, Nicoli D, Baldo C, Bernasconi S, Frasoldati A, Zuffardi O, Garavelli L.

J Hum Genet. 2020 Jan;65(2):133-141. doi: 10.1038/s10038-019-0682-5. Epub 2019 Oct 28.

PMID:
31656314
2.

Concurrent heterozygous Von-Hippel-Lindau and transmembrane-protein-127 gene mutation causing an erythropoietin-secreting pheochromocytoma in a normotensive patient with severe erythrocytosis.

Negro A, Graiani G, Nicoli D, Farnetti E, Casali B, Verzicco I, Tedeschi S, Ghirarduzzi A, Cannone V, Marco LDE, Filice A, Gemelli G, Giunta A, Cabassi A.

J Hypertens. 2020 Feb;38(2):340-346. doi: 10.1097/HJH.0000000000002253.

PMID:
31568062
3.

The clinical relevance of multiple DPYD polymorphisms on patients candidate for fluoropyrimidine based-chemotherapy. An Italian case-control study.

Iachetta F, Bonelli C, Romagnani A, Zamponi R, Tofani L, Farnetti E, Nicoli D, Damato A, Banzi M, Casali B, Pinto C.

Br J Cancer. 2019 Apr;120(8):834-839. doi: 10.1038/s41416-019-0423-8. Epub 2019 Mar 12.

4.

Computational development of a molecular-based approach to improve risk stratification of endometrial cancer patients.

Torricelli F, Nicoli D, Bellazzi R, Ciarrocchi A, Farnetti E, Mastrofilippo V, Zamponi R, La Sala GB, Casali B, Mandato VD.

Oncotarget. 2018 May 22;9(39):25517-25528. doi: 10.18632/oncotarget.25354. eCollection 2018 May 22.

5.

Prognostic Impact of ABO Blood Group on Type I Endometrial Cancer Patients- Results from Our Own and Other Studies.

Mandato VD, Torricelli F, Mastrofilippo V, Ciarlini G, Pirillo D, Farnetti E, Fornaciari L, Casali B, Gelli MC, Abrate M, Aguzzoli L, La Sala GB, Nicoli D.

J Cancer. 2017 Aug 23;8(14):2828-2835. doi: 10.7150/jca.19524. eCollection 2017.

6.

Subcutaneous pigmented clear cell sarcoma as a challenging simulator of melanoma.

Bombonato C, Moscarella E, Longo C, Castagnetti F, Nicoli D, Piana S.

Australas J Dermatol. 2018 May;59(2):e156-e159. doi: 10.1111/ajd.12706. Epub 2017 Aug 17. No abstract available.

PMID:
28815555
7.

Peptide Receptor Radionuclide Therapy-Induced Gitelman-like Syndrome.

Negro A, Rossi GM, Nicoli D, Versari A, Farnetti E, Santi R, De Pietri S.

Am J Kidney Dis. 2017 Nov;70(5):725-728. doi: 10.1053/j.ajkd.2017.05.024. Epub 2017 Jul 21.

PMID:
28739329
8.

Inflammatory mediators and signalling pathways controlling intervertebral disc degeneration.

Navone SE, Marfia G, Giannoni A, Beretta M, Guarnaccia L, Gualtierotti R, Nicoli D, Rampini P, Campanella R.

Histol Histopathol. 2017 Jun;32(6):523-542. doi: 10.14670/HH-11-846. Epub 2016 Nov 16. Review.

PMID:
27848245
9.

Critical Pitfalls in the use of BRAF Mutation as a Diagnostic Tool in Thyroid Nodules: a Case Report.

Kuhn E, Ragazzi M, Zini M, Giordano D, Nicoli D, Piana S.

Endocr Pathol. 2016 Sep;27(3):220-3. doi: 10.1007/s12022-016-9414-y.

PMID:
26782803
10.

Diamond: immunohistochemistry versus sequencing in EGFR analysis of lung adenocarcinomas.

Ragazzi M, Tamagnini I, Bisagni A, Cavazza A, Pagano M, Baldi L, Boni C, Cantile F, Barbieri F, Nicoli D, Sartori G, de Biase D, Gardini G, Rossi G.

J Clin Pathol. 2016 May;69(5):440-7. doi: 10.1136/jclinpath-2015-203348. Epub 2015 Nov 9.

PMID:
26553934
11.

MicroRNA markers of inflammation and remodelling in temporal arteries from patients with giant cell arteritis.

Croci S, Zerbini A, Boiardi L, Muratore F, Bisagni A, Nicoli D, Farnetti E, Pazzola G, Cimino L, Moramarco A, Cavazza A, Casali B, Parmeggiani M, Salvarani C.

Ann Rheum Dis. 2016 Aug;75(8):1527-33. doi: 10.1136/annrheumdis-2015-207846. Epub 2015 Sep 4.

PMID:
26342092
12.

Polymorphisms in cyclooxygenase-2 gene in endometrial cancer patients.

Torricelli F, Mandato VD, Farnetti E, Abrate M, Casali B, Ciarlini G, Pirillo D, Gelli MC, Costagliola L, Nicoli D, Palomba S, La Sala GB.

Tumour Biol. 2015 Sep;36(10):7423-30. doi: 10.1007/s13277-015-3424-0. Epub 2015 Apr 22.

PMID:
25900875
13.

HNF1B polymorphism influences the prognosis of endometrial cancer patients: a cohort study.

Mandato VD, Farnetti E, Torricelli F, Abrate M, Casali B, Ciarlini G, Pirillo D, Gelli MC, Nicoli D, Grassi M, LA Sala GB, Palomba S.

BMC Cancer. 2015 Apr 7;15:229. doi: 10.1186/s12885-015-1246-5.

14.

Prognostic value of MGMT promoter status in non-resectable glioblastoma after adjuvant therapy.

Iaccarino C, Orlandi E, Ruggeri F, Nicoli D, Torricelli F, Maggi M, Cerasti D, Pisanello A, Pedrazzi G, Froio E, Crafa P, D'Abbiero N, Michiara M, Ghadirpour R, Servadei F.

Clin Neurol Neurosurg. 2015 May;132:1-8. doi: 10.1016/j.clineuro.2015.01.029. Epub 2015 Feb 7.

PMID:
25723791
15.

A novel BRAF mutation in association with primary amelanotic melanoma with oral metastases.

Zalaudek I, Ciarrocchi A, Piana S, Argenziano G, Torricelli F, Sancisi V, Gandolfi G, Longo C, Moscarella E, Banzi C, Nicoli D.

J Eur Acad Dermatol Venereol. 2015 Feb;29(2):387-90. doi: 10.1111/jdv.12358. Epub 2014 Jan 7.

PMID:
24393566
16.

Large cell carcinoma of the lung: clinically oriented classification integrating immunohistochemistry and molecular biology.

Rossi G, Mengoli MC, Cavazza A, Nicoli D, Barbareschi M, Cantaloni C, Papotti M, Tironi A, Graziano P, Paci M, Stefani A, Migaldi M, Sartori G, Pelosi G.

Virchows Arch. 2014 Jan;464(1):61-8. doi: 10.1007/s00428-013-1501-6. Epub 2013 Nov 13.

PMID:
24221342
17.

Cadherin 6 is a new RUNX2 target in TGF-β signalling pathway.

Sancisi V, Gandolfi G, Ragazzi M, Nicoli D, Tamagnini I, Piana S, Ciarrocchi A.

PLoS One. 2013 Sep 12;8(9):e75489. doi: 10.1371/journal.pone.0075489. eCollection 2013.

18.

TLR-4 and VEGF polymorphisms in chronic periaortitis.

Atzeni F, Boiardi L, Vaglio A, Nicoli D, Farnetti E, Palmisano A, Pipitone N, Martorana D, Moroni G, Longhi S, Bonatti F, Buzio C, Salvarani C.

PLoS One. 2013 May 14;8(5):e62330. doi: 10.1371/journal.pone.0062330. Print 2013.

19.

Fluoropyrimidine toxicity in patients with dihydropyrimidine dehydrogenase splice site variant: the need for further revision of dose and schedule.

Magnani E, Farnetti E, Nicoli D, Casali B, Savoldi L, Focaccetti C, Boni C, Albini A, Banzi M.

Intern Emerg Med. 2013 Aug;8(5):417-23. doi: 10.1007/s11739-013-0936-8. Epub 2013 Apr 13.

PMID:
23585145
20.

Elevation of angiotensin-II type-1-receptor autoantibodies titer in primary aldosteronism as a result of aldosterone-producing adenoma.

Rossitto G, Regolisti G, Rossi E, Negro A, Nicoli D, Casali B, Toniato A, Caroccia B, Seccia TM, Walther T, Rossi GP.

Hypertension. 2013 Feb;61(2):526-33. doi: 10.1161/HYPERTENSIONAHA.112.202945. Epub 2012 Dec 17.

PMID:
23248149
21.

Haptoglobin phenotype and epithelial ovarian cancer.

Mandato VD, Magnani E, Abrate M, Casali B, Nicoli D, Farnetti E, Formisano D, Pirillo D, Ciarlini G, De Iaco P, Strada I, Zamagni C, La Sala GB.

Anticancer Res. 2012 Oct;32(10):4353-8.

PMID:
23060558
22.

CC chemokine receptor 5 polymorphism in Italian patients with giant cell arteritis.

Pazzola G, Boiardi L, Casali B, Farnetti E, Nicoli D, Pipitone N, Padovano I, Caruso A, Catanoso M, Salvarani C.

Mod Rheumatol. 2013 Sep;23(5):851-5. doi: 10.1007/s10165-012-0751-5. Epub 2012 Sep 23.

PMID:
23001713
23.

CC chemokine receptor 5 polymorphism in Italian patients with Behcet's disease.

Atzeni F, Boiardi L, Casali B, Farnetti E, Nicoli D, Sarzi-Puttini P, Pipitone N, Olivieri I, Cantini F, Salvi F, La Corte R, Triolo G, Filippini D, Paolazzi G, Salvarani C.

Rheumatology (Oxford). 2012 Dec;51(12):2141-5. doi: 10.1093/rheumatology/kes238. Epub 2012 Sep 9.

24.

IL-23A, IL-23R, IL-17A and IL-17R polymorphisms in different psoriatic arthritis clinical manifestations in the northern Italian population.

Catanoso MG, Boiardi L, Macchioni P, Garagnani P, Sazzini M, De Fanti S, Farnetti E, Casali B, Chiarolanza I, Nicoli D, Luiselli D, Salvarani C.

Rheumatol Int. 2013 May;33(5):1165-76. doi: 10.1007/s00296-012-2501-6. Epub 2012 Sep 7.

PMID:
22955875
25.

Runx2 isoform I controls a panel of proinvasive genes driving aggressiveness of papillary thyroid carcinomas.

Sancisi V, Borettini G, Maramotti S, Ragazzi M, Tamagnini I, Nicoli D, Piana S, Ciarrocchi A.

J Clin Endocrinol Metab. 2012 Oct;97(10):E2006-15. doi: 10.1210/jc.2012-1903. Epub 2012 Jul 20.

26.

BRAFV600E mutation does not mean distant metastasis in thyroid papillary carcinomas.

Sancisi V, Nicoli D, Ragazzi M, Piana S, Ciarrocchi A.

J Clin Endocrinol Metab. 2012 Sep;97(9):E1745-9. doi: 10.1210/jc.2012-1526. Epub 2012 Jun 27.

PMID:
22740704
27.

Very early onset and severe complicated phenotype caused by a new spastic paraplegia 3A gene mutation.

Fusco C, Frattini D, Farnetti E, Nicoli D, Casali B, Della Giustina E.

J Child Neurol. 2012 Oct;27(10):1348-50. Epub 2012 Feb 28.

PMID:
22378671
28.

Activating c-KIT mutations in a subset of thymic carcinoma and response to different c-KIT inhibitors.

Schirosi L, Nannini N, Nicoli D, Cavazza A, Valli R, Buti S, Garagnani L, Sartori G, Calabrese F, Marchetti A, Buttitta F, Felicioni L, Migaldi M, Rea F, Di Chiara F, Mengoli MC, Rossi G.

Ann Oncol. 2012 Sep;23(9):2409-14. doi: 10.1093/annonc/mdr626. Epub 2012 Feb 21.

29.

PLA1/A2 polymorphism of the platelet glycoprotein receptors IIIA in Behçet's disease.

Atzeni F, Boiardi L, Nicoli D, Farnetti E, Casali B, Sarzi-Puttini P, Pipitone N, Olivieri I, Cantini F, Salvi F, La Corte R, Triolo G, Filippini D, Paolazzi G, Salvarani C.

Clin Exp Rheumatol. 2011 Jul-Aug;29(4 Suppl 67):S38-43. Epub 2011 Sep 27.

PMID:
21813062
30.

Detection of IDH1 mutations and the status of MGMT promoter on intraoperative fresh tissue section from frameless neuronavigation needle biopsy. Analysis on 17 patients with brain glial tumor ineligible for craniotomy and tumor resection.

Iaccarino I, Nicoli D, Serra S, Froio E, Pisanello A, De Berti G, Ghadirpour R, Marcello N, Servadei F, Carinci F.

Int J Immunopathol Pharmacol. 2011 Apr-Jun;24(2 Suppl):45-50.

PMID:
21781445
31.

Analysis of MGMT promoter methylation status on intraoperative fresh tissue section from frameless neuronavigation needle biopsy of 25 patients with brain tumor.

Iaccarino C, Nicoli D, Serra S, Froio E, Pisanello A, De Berti G, Ghadirpour R, Marcello N, Servadei F, Carinci F.

Int J Immunopathol Pharmacol. 2011 Apr-Jun;24(2 Suppl):37-43.

PMID:
21781444
32.

A clinical phenotype mimicking essential hypertension in a newly discovered family with Liddle's syndrome.

Rossi E, Farnetti E, Nicoli D, Sazzini M, Perazzoli F, Regolisti G, Grasselli C, Santi R, Negro A, Mazzeo V, Mantero F, Luiselli D, Casali B.

Am J Hypertens. 2011 Aug;24(8):930-5. doi: 10.1038/ajh.2011.76. Epub 2011 Apr 28.

PMID:
21525970
33.

CC chemokine receptor 5 polymorphism in chronic periaortitis.

Boiardi L, Vaglio A, Nicoli D, Farnetti E, Palmisano A, Pipitone N, Maritati F, Casali B, Martorana D, Moroni G, Gallelli B, Buzio C, Salvarani C.

Rheumatology (Oxford). 2011 Jun;50(6):1025-32. doi: 10.1093/rheumatology/keq416. Epub 2011 Jan 21.

PMID:
21258050
34.

Increase in clusterin forms part of the stress response in Hodgkin's lymphoma.

Frazzi R, Casali B, Iori M, Nicoli D, Mammi C, Merli F.

Int J Oncol. 2011 Mar;38(3):677-84. doi: 10.3892/ijo.2011.907. Epub 2011 Jan 14.

PMID:
21240462
35.

G/R 241 polymorphism of intercellular adhesion molecule 1 (ICAM-1) is associated with Fuchs uveitis.

Cimino L, Boiardi L, Aldigeri R, Casali B, Nicoli D, Farnetti E, Salvarani C, Cirone D, De Martino L, Pupino A, Cappuccini L.

Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4447-50. doi: 10.1167/iovs.09-4669. Epub 2010 May 5.

PMID:
20445114
36.

Analysis of MGMT promoter methylation status on intraoperative fresh tissue section from frameless neuronavigation needle biopsy: a preliminary study of ten patients.

Iaccarino C, Nicoli D, Gallo C, Nasi D, Pisanello A, De Berti G, Ghadirpour R, Marcello N, Servadei F.

Acta Neurochir (Wien). 2010 Jul;152(7):1189-96. doi: 10.1007/s00701-010-0639-0. Epub 2010 Mar 31.

PMID:
20354736
37.

Toll-like receptor 4 (TLR4) gene polymorphisms in giant cell arteritis.

Boiardi L, Casali B, Farnetti E, Pipitone N, Nicoli D, Macchioni P, Cimino L, Bajocchi GL, Catanoso MG, Pattacini L, Ghinoi A, Restuccia G, Salvarani C.

Clin Exp Rheumatol. 2009 Jan-Feb;27(1 Suppl 52):S40-4.

PMID:
19646345
38.

Toll-like receptor 4 (TLR4) gene polymorphisms in Italian patients with Behçet's disease.

Boiardi L, Atzeni F, Casali B, Farnetti E, Nicoli D, Pipitone N, Catanoso MG, Olivieri I, Cantini F, Salvi F, La Corte R, Triolo G, Filippini D, Paolazzi G, Salvarani C.

Clin Exp Rheumatol. 2009 Mar-Apr;27(2 Suppl 53):S43-7.

PMID:
19796532
39.

Protein Z G79A and A-13G gene polymorphisms in Italian patients with Behçet's disease.

Ghinoi A, Boiardi L, Atzeni F, Casali B, Farnetti E, Nicoli D, Pipitone N, Olivieri I, Cantini F, Salvi F, La Corte R, Triolo G, Filippini D, Paolazzi G, Salvarani C.

Clin Exp Rheumatol. 2009 Mar-Apr;27(2 Suppl 53):S23-8.

PMID:
19796528
40.

Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation.

Fusco C, Frattini D, Farnetti E, Nicoli D, Casali B, Fiorentino F, Nuccitelli A, Giustina ED.

Brain Dev. 2010 Aug;32(7):592-4. doi: 10.1016/j.braindev.2009.08.003. Epub 2009 Sep 6.

PMID:
19735987
41.

Liddle's syndrome caused by a novel missense mutation (P617L) of the epithelial sodium channel beta subunit.

Rossi E, Farnetti E, Debonneville A, Nicoli D, Grasselli C, Regolisti G, Negro A, Perazzoli F, Casali B, Mantero F, Staub O.

J Hypertens. 2008 May;26(5):921-7. doi: 10.1097/HJH.0b013e3282f85dfe.

PMID:
18398334
42.

PlA1/A2 polymorphism of the platelet glycoprotein receptor IIIA and risk of cranial ischemic complications in giant cell arteritis.

Salvarani C, Casali B, Farnetti E, Pipitone N, Formisano D, Nicoli D, Macchioni P, Cimino L, Bajocchi G, Grazia Catanoso M, Restuccia G, Ghinoi A, Boiardi L.

Arthritis Rheum. 2007 Oct;56(10):3502-8.

43.

-463 G/A myeloperoxidase promoter polymorphism in giant cell arteritis.

Salvarani C, Casali B, Farnetti E, Pipitone N, Nicoli D, Macchioni PL, Cimino L, Bajocchi GL, Catanoso MG, Pattacini L, Ghinoi A, Restuccia G, Boiardi L.

Ann Rheum Dis. 2008 Apr;67(4):485-8. Epub 2007 Aug 17.

PMID:
17704068
44.

The codon 72 polymorphic variants of p53 in Italian rheumatoid arthritis patients.

Macchioni P, Nicoli D, Casali B, Catanoso M, Farnetti E, Boiardi L, Salvarani C.

Clin Exp Rheumatol. 2007 May-Jun;25(3):416-21.

PMID:
17631738
45.

Interleukin-10 promoter polymorphisms in giant cell arteritis.

Boiardi L, Casali B, Farnetti E, Pipitone N, Nicoli D, Macchioni P, Cimino L, Bajocchi G, Catanoso MG, Pattacini L, Salvarani C.

Arthritis Rheum. 2006 Dec;54(12):4011-7.

46.

Relationship between interleukin 6 promoter polymorphism at position -174, IL-6 serum levels, and the risk of relapse/recurrence in polymyalgia rheumatica.

Boiardi L, Casali B, Farnetti E, Pipitone N, Nicoli D, Cantini F, Macchioni P, Bajocchi G, Catanoso MG, Pulsatelli L, Consonni D, Salvarani C.

J Rheumatol. 2006 Apr;33(4):703-8.

PMID:
16583473
47.

High risk of cutaneous melanoma amongst carriers of the intercellular adhesion molecule-1 R241 allele.

Vinceti M, Pellacani G, Casali B, Malagoli C, Nicoli D, Farnetti E, Bassissi S, Bergomi M, Seidenari S.

Melanoma Res. 2006 Feb;16(1):93-6.

PMID:
16432463
48.

Interleukin-6 promoter polymorphism at position -174 in giant cell arteritis.

Salvarani C, Casali B, Farnetti E, Pipitone N, Nicoli D, Macchioni P, Cimino L, Bajocchi G, Catanoso MG, Boiardi L.

J Rheumatol. 2005 Nov;32(11):2173-7.

PMID:
16265697
49.

Vascular endothelial growth factor gene polymorphisms in Behçet's disease.

Salvarani C, Boiardi L, Casali B, Olivieri I, Cantini F, Salvi F, Malatesta R, La Corte R, Triolo G, Ferrante A, Filippini D, Paolazzi G, Sarzi-Puttini P, Nicoli D, Farnetti E, Chen Q, Pulsatelli L.

J Rheumatol. 2004 Sep;31(9):1785-9.

PMID:
15338501
50.

An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene.

Guidetti D, Casali B, Mazzei RL, Cenacchi G, De Berti G, Zuccoli G, Nicoli D, Conforti FL, Sprovieri T, Pasquinelli G, Brini M.

Neurol Sci. 2004 Feb;24(6):401-6.

PMID:
14767686

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