Massimo Milani

Dr. Massimo Milani

orcid

Research Focus & Metrics

Academic Career Length

40Years (1987-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 1990 in Genomics
Verified
Journal Article
Closed access
WKWilliam J. Kimberling
William J. Kimberling
MWMichael D. Weston
Michael D. Weston
CMClaes Möller
Claes Möller
SDSandra L.H. Davenport
Sandra L.H. Davenport
YSYin Y. Shugart
Yin Y. Shugart
RSRichard J. H. Smith
Richard J. H. Smith

16 October 2006 in Journal of the European Academy of Dermatology and Venereology
Verified
Journal Article
Closed access
PDF file
Antonella TostiAntonella Tosti
Antonella Tosti
MIMatilde Iorizzo
Matilde Iorizzo
GBGian Luca Botta
Gian Luca Botta
MMMassimo Milani
Massimo Milani

1 April 2009 in Blood Coagulation & Fibrinolysis
Verified
Journal Article
Closed access
GAGuido Arpaia
Guido Arpaia
MCMonica Carpenedo
Monica Carpenedo
MVMagda Verga
Magda Verga
OMOrnella Mastrogiacomo
Ornella Mastrogiacomo
DFDaniele Fagnani
Daniele Fagnani
CCClaudio Cimminiello
Claudio Cimminiello
To see whether D-Dimer levels can identifying patients at high risk of venous thrombotic events and establish the best benefit/risk-of-bleeding ratio. Current guidelines do not recommend routine prophylaxis against venous thromboembolism (VTE) in cancer patients receiving chemotherapy, but the risk increases about 6.5-fold because of this treatment. D-dimer was measured at baseline in 124 cancer patients scheduled for their first chemotherapy. VTE events, including symptomatic episodes of deep vein thrombosis or pulmonary embolism or both, were recorded during the first 6 months of therapy, and asymptomatic deep vein thrombosis was revealed by compression ultrasonography at baseline and after 90 and 180 days. During follow-up, there were 11 episodes of VTE (8.9%). Mean D-dimer values were higher in patients with VTE (2195 ± 1382 vs. 695 ± 1039 ng/ml, (P < 0.001). On grouping D-dimer values in tertiles, only 2.4% (confidence interval, 0.9–5.7%) in the first (650 ng/dl) (P = 0.003). The VTE-free interval was significantly shorter in the third tertile than in the first (P = 0.0218, log–rank test; relative risk for third vs. first tertile, 11.0; 95% confidence interval, 1.4–81.3; P = 0.0033). Multivariate analysis found that only baseline D-dimer concentrations were correlated with the subsequent development of VTE. Baseline D-dimer values in cancer patients scheduled for chemotherapy might be used to select those at low risk of VTE, most likely to be safe without prophylaxis.

3 July 2003 in International Journal of Dermatology
Verified
Journal Article
Closed access
PDF file
GMGiuseppe Mancuso
Giuseppe Mancuso
ABAntonella Balducci
Antonella Balducci
CCChiara Casadio
Chiara Casadio
PFPaolo Farina
Paolo Farina
MSMauro Staffa
Mauro Staffa
MMMassimo Milani
Massimo Milani

1 January 2003 in British Journal of Dermatology
Verified
Journal Article
Closed access
PDF file
LAL. Andreassi
L. Andreassi
AGA. Giannetti
A. Giannetti
MMMassimo Milani
Massimo Milani
OGOn Behalf of The Scale Investigators Group
On Behalf of The Scale Investigators Group

13 August 2007 in Current Medical Research and Opinion
Verified
Journal Article
Closed access
GCGianni Cadario
Gianni Cadario
AGAntonia G. Galluccio
Antonia G. Galluccio
MPMichele Pezza
Michele Pezza
AAAntonella Appino
Antonella Appino
MMMassimo Milani
Massimo Milani
FMFulvio Mastrandrea
Fulvio Mastrandrea
Background: Specific subcutaneous immunotherapy (SCIT) with house dust mite (HDM) preparation has recently been shown to improve eczema in patients with atopic dermatitis (AD). So far, there is less data regarding efficacy and safety of specific sublingual immunotherapy (SLIT) in patients with AD.Study aim: To evaluate in an open non-controlled, non-randomized pilot trial the effect of SLIT with HDM allergen extracts preparation (SLITone, ALK Abellò Italy) on SCORAD in adult patients with mild–moderate AD.Patients and methods: 86 Subjects (53 females and 33 males) between 3 and 60 years of age with AD and IgE-proved (Class > 2) HDM sensitization were enrolled after their informed consent in the trial. Exclusion criteria were severe asthma and treatment with systemic or high potent topical corticosteroids or immunosuppressant agents. Patients were treated with SLIT (Dermatophagoides pteronyssinus and Dermatophagoides farinae extracts: SLITone, ALK-Abellò) for at least 12 months. SCORAD was evaluate...