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Items: 41

1.

Next-generation sequencing and recombinant expression characterized aberrant splicing mechanisms and provided correction strategies in factor VII deficiency.

Ferraresi P, Balestra D, Guittard C, Buthiau D, Pan-Petesh B, Maestri I, Farah R, Pinotti M, Giansily-Blaizot M.

Haematologica. 2019 Jul 4. pii: haematol.2019.217539. doi: 10.3324/haematol.2019.217539. [Epub ahead of print]

2.

Factor XI rs2036914 gene polymorphism and occurrence of adverse events after percutaneous coronary intervention. A prospective evaluation.

Campo G, Lunghi B, Pavasini R, Ferraresi P, Punzetti S, Malag├╣ M, Biscaglia S, Ferrari R, Bernardi F.

Int J Cardiol. 2014 Dec 15;177(2):711-3. No abstract available.

PMID:
25456690
3.

Management of kidney transplantation in a factor VII-deficient patient: case report.

Lapecorella M, Napolitano M, Lucchesi A, Pisani F, Clemente K, Rizza V, Famulari A, Aloisio L, Bernardi F, Pinotti M, Ferraresi P, Di Cocco P.

Transplant Proc. 2012 Sep;44(7):2033-5. doi: 10.1016/j.transproceed.2012.07.001.

PMID:
22974900
4.

Factor IX propeptide mutation and life threatening bleeding.

Vaccarino A, Bazzan M, Giachino O, Colagrande P, Ferraresi P, Stella S, Roccatello D, Bernardi F.

Thromb Res. 2011 Nov;128(5):503-4. doi: 10.1016/j.thromres.2011.06.017. Epub 2011 Aug 5. No abstract available.

PMID:
21820698
5.

Relationship between paraoxonase Q192R gene polymorphism and on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention.

Campo G, Ferraresi P, Marchesini J, Bernardi F, Valgimigli M.

J Thromb Haemost. 2011 Oct;9(10):2106-8. doi: 10.1111/j.1538-7836.2011.04457.x. No abstract available.

6.

Prospective evaluation of on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention relationship with gene polymorphisms and clinical outcome.

Campo G, Parrinello G, Ferraresi P, Lunghi B, Tebaldi M, Miccoli M, Marchesini J, Bernardi F, Ferrari R, Valgimigli M.

J Am Coll Cardiol. 2011 Jun 21;57(25):2474-83. doi: 10.1016/j.jacc.2010.12.047.

7.

Individual differences in the elevated plus-maze and the forced swim test.

Estanislau C, Ramos AC, Ferraresi PD, Costa NF, de Carvalho HM, Batistela S.

Behav Processes. 2011 Jan;86(1):46-51. doi: 10.1016/j.beproc.2010.08.008. Epub 2010 Sep 8.

PMID:
20804831
8.

Temporal and genotype-driven variation of factor VII levels in patients with acute myocardial infarction.

Ferraresi P, Campo G, Marchetti G, Pinotti M, Valgimigli M, Gemmati D, Ferrari R, Bernardi F.

Clin Appl Thromb Hemost. 2009 Feb;15(1):119-22. doi: 10.1177/1076029607308875. No abstract available.

PMID:
19150996
9.

Factor XIIIA-V34L and factor XIIIB-H95R gene variants: effects on survival in myocardial infarction patients.

Gemmati D, Federici F, Campo G, Tognazzo S, Serino ML, De Mattei M, Valgimigli M, Malagutti P, Guardigli G, Ferraresi P, Bernardi F, Ferrari R, Scapoli GL, Catozzi L.

Mol Med. 2007 Jan-Feb;13(1-2):112-20.

10.

Antimicrobial activity of garlic against oral streptococci.

Groppo FC, Ramacciato JC, Motta RH, Ferraresi PM, Sartoratto A.

Int J Dent Hyg. 2007 May;5(2):109-15.

PMID:
17461963
11.

Increased factor VIII coagulant activity levels in male carriers of the factor V R2 polymorphism.

Martinelli N, Girelli D, Ferraresi P, Olivieri O, Lunghi B, Manzato F, Corrocher R, Bernardi F.

Blood Coagul Fibrinolysis. 2007 Mar;18(2):125-9.

PMID:
17287628
12.

Tissue factor and coagulation factor VII levels during acute myocardial infarction: association with genotype and adverse events.

Campo G, Valgimigli M, Ferraresi P, Malagutti P, Baroni M, Arcozzi C, Gemmati D, Percoco G, Parrinello G, Ferrari R, Bernardi F.

Arterioscler Thromb Vasc Biol. 2006 Dec;26(12):2800-6. Epub 2006 Sep 28.

PMID:
17008590
13.

Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII.

Pinotti M, Rizzotto L, Pinton P, Ferraresi P, Chuansumrit A, Charoenkwan P, Marchetti G, Rizzuto R, Mariani G, Bernardi F; International Factor VII Deficiency Study Group.

J Thromb Haemost. 2006 Jun;4(6):1308-14.

14.

In vitro study of fracture resistance of bovine roots using different intraradicular post systems.

Mitsui FH, Marchi GM, Pimenta LA, Ferraresi PM.

Quintessence Int. 2004 Sep;35(8):612-6.

PMID:
15366523
15.

Influence of polymorphisms in the factor VII gene promoter on activated factor VII levels and on the risk of myocardial infarction in advanced coronary atherosclerosis.

Bozzini C, Girelli D, Bernardi F, Ferraresi P, Olivieri O, Pinotti M, Martinelli N, Manzato F, Friso S, Villa G, Pizzolo F, Beltrame F, Corrocher R.

Thromb Haemost. 2004 Sep;92(3):541-9.

PMID:
15351850
16.

Angiotensin-converting enzyme insertion/deletion polymorphism and risk of restenosis after directional coronary atherectomy followed by stent implantation.

Canosi U, Angelica Merlini P, Bernardi F, Repetto A, Bramucci E, Ferrario M, Angoli L, Gnecchi M, Ferraresi P, Marchetti G, Tavazzi L, Ardissino D.

Thromb Haemost. 2004 Apr;91(4):795-800.

PMID:
15045142
17.

Variation of factor VII 140s and 170s loops in fishes: evolutionary aspects and comparison with mutations found in FVII deficiency.

Furlan Freguia C, Toso R, Ferraresi P, Pinotti M, Bernardi F.

Thromb Haemost. 2003 Dec;90(6):1220-2. No abstract available.

PMID:
14652663
18.

Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster.

Marchetti G, Ferraresi P, Legnani C, Pinotti M, Lunghi B, Scapoli C, Gemmati D, Coccheri S, Palareti G, Bernardi F.

Br J Haematol. 2003 May;121(4):632-8.

PMID:
12752105
19.

Gamma knife radiosurgery in meningiomas of the posterior fossa. Experience with 62 treated lesions.

Nicolato A, Foroni R, Pellegrino M, Ferraresi P, Alessandrini F, Gerosa M, Bricolo A.

Minim Invasive Neurosurg. 2001 Dec;44(4):211-7.

PMID:
11830780
20.

The heterozygous 20210 G/A genotype prevalence in patients affected by central and branch retinal vein occlusion: a pilot study.

Incorvaia C, Parmeggiani F, Costagliola C, Lamberti G, Ferraresi P, Bernardi F, Sebastiani A.

Graefes Arch Clin Exp Ophthalmol. 2001 Apr;239(4):251-6.

PMID:
11450488
21.

Multiple brain metastases from "lymphoepithelioma-like" thymic carcinoma: a combined stereotactic-radiosurgical approach.

Nicolato A, Ferraresi P, Bontempini L, Tomazzoli L, Magarotto R, Gerosa M.

Surg Neurol. 2001 Apr;55(4):232-4. No abstract available.

PMID:
11358599
22.

New dosimetric approach for multidimensional dose evaluation in gamma knife radiosurgery. Technical note.

Foroni R, Gambraini G, Danesi U, Mauri M, Pompilio E, Pirola L, Nicolato A, Ferraresi P, Gerosa M.

J Neurosurg. 2000 Dec;93 Suppl 3:239-42.

PMID:
11143257
23.

Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease.

Girelli D, Russo C, Ferraresi P, Olivieri O, Pinotti M, Friso S, Manzato F, Mazzucco A, Bernardi F, Corrocher R.

N Engl J Med. 2000 Sep 14;343(11):774-80.

24.

Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studies.

Pinotti M, Toso R, Girelli D, Bindini D, Ferraresi P, Papa ML, Corrocher R, Marchetti G, Bernardi F.

Blood. 2000 Jun 1;95(11):3423-8.

25.

Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma.

Castoldi E, Rosing J, Girelli D, Hoekema L, Lunghi B, Mingozzi F, Ferraresi P, Friso S, Corrocher R, Tans G, Bernardi F.

Thromb Haemost. 2000 Mar;83(3):362-5.

PMID:
10744138
26.

Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype.

Incorvaia C, Lamberti G, Parmeggiani F, Ferraresi P, Calzolari E, Bernardi F, Sebastiani A.

Am J Ophthalmol. 1999 Aug;128(2):247-8.

PMID:
10458191
27.

Stereotactic radiosurgery for the treatment of arteriovenous malformations in childhood.

Nicolato A, Gerosa M, Ferraresi P, Piovan E, Pasoli A, Perini S, Mazza C.

J Neurosurg Sci. 1997 Dec;41(4):359-71.

PMID:
9555644
28.

Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala223Val MTHFR) in patients with inherited thrombophilic coagulation defects.

Legnani C, Palareti G, Grauso F, Sassi S, Grossi G, Piazzi S, Bernardi F, Marchetti G, Ferraresi P, Coccheri S.

Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):2924-9.

PMID:
9409277
29.

The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease.

Ferraresi P, Marchetti G, Legnani C, Cavallari E, Castoldi E, Mascoli F, Ardissino D, Palareti G, Bernardi F.

Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):2418-22.

PMID:
9409210
30.

Visual control of hand-reaching movement: activity in parietal area 7m.

Ferraina S, Garasto MR, Battaglia-Mayer A, Ferraresi P, Johnson PB, Lacquaniti F, Caminiti R.

Eur J Neurosci. 1997 May;9(5):1090-5.

PMID:
9182962
31.

A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects.

Bernardi F, Legnani C, Micheletti F, Lunghi B, Ferraresi P, Palareti G, Biagi R, Marchetti G.

Thromb Haemost. 1996 Oct;76(4):505-9.

PMID:
8902986
32.

Gamma Knife radiosurgery for intracranial metastases: from local tumor control to increased survival.

Gerosa M, Nicolato A, Severi F, Ferraresi P, Masotto B, Barone G, Foroni R, Piovan E, Pasoli A, Bricolo A.

Stereotact Funct Neurosurg. 1996;66 Suppl 1:184-92.

PMID:
9032860
33.

Gamma Knife radiosurgery in skull base meningiomas. Preliminary experience with 50 cases.

Nicolato A, Ferraresi P, Foroni R, Pasqualin A, Piovan E, Severi F, Masotto B, Gerosa M.

Stereotact Funct Neurosurg. 1996;66 Suppl 1:112-20.

PMID:
9032851
34.

Mutation pattern in clinically asymptomatic coagulation factor VII deficiency.

Bernardi F, Castaman G, Pinotti M, Ferraresi P, Di Iasio MG, Lunghi B, Rodeghiero F, Marchetti G.

Hum Mutat. 1996;8(2):108-15.

PMID:
8844208
36.

[Acute lymphoblastic leukemia L3 in Hodgkin's disease in remission: primary or secondary leukosis?].

Musto P, Lucchi T, Barbieri D, Ferraresi P, Lanza F.

Recenti Prog Med. 1985 Apr;76(4):194-8. Italian. No abstract available.

PMID:
3862191
37.

A case of chronic myelogenous leukemia with 11q- in blast crisis with monoblastic differentiation.

Cuneo A, Barbieri D, Ferraresi P, Castoldi GL.

Nouv Rev Fr Hematol. 1985;27(6):389-91.

PMID:
3867853
38.

Further cytogenetic evidence for a multistep pathogenesis of Ph-positive chronic myelogenous leukemia.

Barbieri D, Ferraresi P, Castoldi G.

Cancer Genet Cytogenet. 1985 Jan 1;14(1-2):111-7.

PMID:
3855271
39.

Comment related to the cytologic demonstration of Reed-Sternberg cells in the sputum from a patient with Hodgkin's disease.

Barbieri D, Ferraresi P, Tomasi P.

Haematologica. 1984 May-Jun;69(3):378. No abstract available.

PMID:
6432650
40.

Normal bone marrow karyotype in paroxysmal nocturnal hemoglobinuria--a cooperative European study.

Zaccaria A, Barbieri D, Castoldi GL, Ferraresi P, Finelli C, Hossfeld DK, Mitelman F, Rosti G, Testoni N, Van den Berghe H.

Cancer Genet Cytogenet. 1983 Jul;9(3):211-5.

PMID:
6861113
41.

[Exposure to asbestos and lymphoid neoplasms].

Spanedda R, La Corte R, Minisci S, Ferraresi P, Burini D, Romanini D.

Med Lav. 1983 Jul-Aug;74(4):295-301. Italian. No abstract available.

PMID:
6664324

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