Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 82

1.

Effect of Factor XIII-A G185T Polymorphism on Visual Prognosis after Photodynamic Therapy for Neovascular Macular Degeneration.

Parmeggiani F, Costagliola C, Semeraro F, Romano MR, Rinaldi M, Gallenga CE, Serino ML, Incorvaia C, D'Angelo S, De Nadai K, Dell'Omo R, Russo A, Gemmati D, Perri P.

Int J Mol Sci. 2015 Aug 20;16(8):19796-19811.

2.

The carboxyl-terminal region is NOT essential for secreted and functional levels of coagulation factor X.

Branchini A, Baroni M, Burini F, Puzzo F, Nicolosi F, Mari R, Gemmati D, Bernardi F, Pinotti M.

J Thromb Haemost. 2015 Aug;13(8):1468-74. doi: 10.1111/jth.13034. Epub 2015 Jul 14.

PMID:
26083275
3.

Factor XIII-A dynamics in acute myocardial infarction: a novel prognostic biomarker?

Gemmati D, Zeri G, Orioli E, Mari R, Moratelli S, Vigliano M, Marchesini J, Grossi ME, Pecoraro A, Cuneo A, Ferrari R, Pinotti M, Serino ML, Ansani L.

Thromb Haemost. 2015 Jun 30;114(1):123-32. doi: 10.1160/TH14-11-0952. Epub 2015 May 7.

PMID:
25947356
4.

Sudden sensorineural hearing loss and polymorphisms in iron homeostasis genes: new insights from a case-control study.

Castiglione A, Ciorba A, Aimoni C, Orioli E, Zeri G, Vigliano M, Gemmati D.

Biomed Res Int. 2015;2015:834736. doi: 10.1155/2015/834736. Epub 2015 Feb 18.

5.

Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis.

Paraboschi EM, Rimoldi V, Soldà G, Tabaglio T, Dall'Osso C, Saba E, Vigliano M, Salviati A, Leone M, Benedetti MD, Fornasari D, Saarela J, De Jager PL, Patsopoulos NA, D'Alfonso S, Gemmati D, Duga S, Asselta R.

Hum Mol Genet. 2014 Dec 20;23(25):6746-61. doi: 10.1093/hmg/ddu392. Epub 2014 Jul 30.

PMID:
25080502
6.

Karyotype-phenotype correlation in partial trisomies of the short arm of chromosome 6: a family case report and review of the literature.

Castiglione A, Guaran V, Astolfi L, Orioli E, Zeri G, Gemmati D, Bovo R, Montaldi A, Alghisi A, Martini A.

Cytogenet Genome Res. 2013;141(4):243-59. doi: 10.1159/000353846. Epub 2013 Aug 7. Review.

7.

Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls.

Simone B, De Stefano V, Leoncini E, Zacho J, Martinelli I, Emmerich J, Rossi E, Folsom AR, Almawi WY, Scarabin PY, den Heijer M, Cushman M, Penco S, Vaya A, Angchaisuksiri P, Okumus G, Gemmati D, Cima S, Akar N, Oguzulgen KI, Ducros V, Lichy C, Fernandez-Miranda C, Szczeklik A, Nieto JA, Torres JD, Le Cam-Duchez V, Ivanov P, Cantu-Brito C, Shmeleva VM, Stegnar M, Ogunyemi D, Eid SS, Nicolotti N, De Feo E, Ricciardi W, Boccia S.

Eur J Epidemiol. 2013 Aug;28(8):621-47. doi: 10.1007/s10654-013-9825-8. Epub 2013 Jul 31.

8.

The role of the MTHFR 677C>T polymorphism in methotrexate-induced liver toxicity: a meta-analysis in patients with cancer.

Hagleitner MM, Coenen MJ, Aplenc R, Patiño-Garcia A, Chiusolo P, Gemmati D, De Mattei M, Ongaro A, Krajinovic M, Hoogerbrugge PM, Vermeulen SH, te Loo DM.

Pharmacogenomics J. 2014 Apr;14(2):115-9. doi: 10.1038/tpj.2013.19. Epub 2013 May 7.

PMID:
23648444
9.

Investigation of in vitro cytotoxicity of the redox state of ionic iron in neuroblastoma cells.

Singh AV, Vyas V, Montani E, Cartelli D, Parazzoli D, Oldani A, Zeri G, Orioli E, Gemmati D, Zamboni P.

J Neurosci Rural Pract. 2012 Sep;3(3):301-10. doi: 10.4103/0976-3147.102611. Erratum in: J Neurosci Rural Pract. 2013 Jan-Mar;4(1):98. Maontani, Erica [corrected to Montani, Erica].

10.

Polymorphisms in the genes coding for iron binding and transporting proteins are associated with disability, severity, and early progression in multiple sclerosis.

Gemmati D, Zeri G, Orioli E, De Gaetano FE, Salvi F, Bartolomei I, D'Alfonso S, Dall'osso C, Leone MA, Singh AV, Asselta R, Zamboni P.

BMC Med Genet. 2012 Aug 10;13:70. doi: 10.1186/1471-2350-13-70.

11.

Genetic association and altered gene expression of mir-155 in multiple sclerosis patients.

Paraboschi EM, Soldà G, Gemmati D, Orioli E, Zeri G, Benedetti MD, Salviati A, Barizzone N, Leone M, Duga S, Asselta R.

Int J Mol Sci. 2011;12(12):8695-712. doi: 10.3390/ijms12128695. Epub 2011 Dec 1.

12.

Genetic predictors of response to photodynamictherapy.

Parmeggiani F, Gemmati D, Costagliola C, Semeraro F, Perri P, D'Angelo S, Romano MR, De Nadai K, Sebastiani A, Incorvaia C.

Mol Diagn Ther. 2011 Aug 1;15(4):195-210. doi: 10.2165/11592270-000000000-00000. Review.

PMID:
21913742
13.

Thrombophilia in the occurrence of retinal vascular infarction after photodynamic therapy with verteporfin using the standard protocol.

Parmeggiani F, Gemmati D, Costagliola C.

Arch Ophthalmol. 2010 Dec;128(12):1632; author reply 1632-3. doi: 10.1001/archophthalmol.2010.285. No abstract available.

PMID:
21149800
14.

Interplay of iron metallobiology, metalloproteinases, and FXIII, and role of their gene variants in venous leg ulcer.

Singh AV, Subhashree L, Milani P, Gemmati D, Zamboni P.

Int J Low Extrem Wounds. 2010 Dec;9(4):166-79. doi: 10.1177/1534734610384653. Epub 2010 Nov 30. Review.

PMID:
21118859
15.

Pharmacogenetic aspects in therapeutic management of subfoveal choroidal neovascularisation: role of factor XIII-A 185 T-allele.

Parmeggiani F, Costagliola C, Incorvaia C, Sebastiani A, Gemmati D.

Curr Drug Targets. 2011 Feb;12(2):138-48. Review.

PMID:
20887247
16.

Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis.

Ferlini A, Bovolenta M, Neri M, Gualandi F, Balboni A, Yuryev A, Salvi F, Gemmati D, Liboni A, Zamboni P.

BMC Med Genet. 2010 Apr 28;11:64. doi: 10.1186/1471-2350-11-64.

17.

Impact of coagulation-balance gene predictors on efficacy of photodynamic therapy for choroidal neovascularization in pathologic myopia.

Parmeggiani F, Gemmati D, Costagliola C, Semeraro F, D'Angelo S, Perri P, Sebastiani A, Incorvaia C.

Ophthalmology. 2010 Mar;117(3):517-23. doi: 10.1016/j.ophtha.2009.08.028. Epub 2009 Dec 30.

PMID:
20044141
18.

DNA-array of gene variants in venous leg ulcers: detection of prognostic indicators.

Gemmati D, Federici F, Catozzi L, Gianesini S, Tacconi G, Scapoli GL, Zamboni P.

J Vasc Surg. 2009 Dec;50(6):1444-51. doi: 10.1016/j.jvs.2009.07.103.

19.

Gene polymorphisms in folate metabolizing enzymes in adult acute lymphoblastic leukemia: effects on methotrexate-related toxicity and survival.

Ongaro A, De Mattei M, Della Porta MG, Rigolin G, Ambrosio C, Di Raimondo F, Pellati A, Masieri FF, Caruso A, Catozzi L, Gemmati D.

Haematologica. 2009 Oct;94(10):1391-8. doi: 10.3324/haematol.2009.008326. Epub 2009 Jul 31.

20.

DHFR 19-bp insertion/deletion polymorphism and MTHFR C677T in adult acute lymphoblastic leukaemia: is the risk reduction due to intracellular folate unbalancing?

Gemmati D, De Mattei M, Catozzi L, Della Porta M, Serino ML, Ambrosio C, Cuneo A, Friso S, Krampera M, Orioli E, Zeri G, Ongaro A.

Am J Hematol. 2009 Aug;84(8):526-9. doi: 10.1002/ajh.21451. No abstract available.

PMID:
19536847
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk