Salvatore Contini
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    Explore the profile of Salvatore Contini including associated specialties, affiliations and a list of published articles.
          
  Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
  
  
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          Snapshot
              Articles
              19
            
            
              Citations
              121
            
            
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  Recent Articles
          1.
        
    
    Shen J, Senes F, Wen X, Monti P, Lin S, Pinna C, et al.
  
  
    Immunol Res
    . 2024 Sep;
          72(6):1470-1478.
    
    PMID: 39316338
  
  
          Background: Pomalidomide, a third-generation oral immunomodulatory drug, exhibits efficacy in patients with relapsed multiple myeloma or those refractory to bortezomib and lenalidomide (RRMM). Methods: In this clinical context, we employed...
      
2.
        
    
    Cabiddu A, Carrillo S, Contini S, Spada S, Acciaro M, Giovanetti V, et al.
  
  
    Animals (Basel)
    . 2022 Oct;
          12(19).
    
    PMID: 36230416
  
  
          The fatty acid profile, vitamins A and E, cholesterol, antioxidant power colour and the phenols profile of Sarda sheep milk from 11 commercial sheep flocks managed under permanent grassland were...
      
3.
        
    
    Fozza C, Barraqueddu F, Corda G, Contini S, Virdis P, Dore F, et al.
  
  
    J Immunol Methods
    . 2016 Nov;
          440:1-11.
    
    PMID: 27823906
  
  
          The T-cell receptor (TCR) is the key player within the so called immunological synapse and the analysis of its repertoire offers a picture of both versatility and wideness of the...
      
4.
        
    
    Danjou F, Fozza C, Zoledziewska M, Mulas A, Corda G, Contini S, et al.
  
  
    Exp Hematol
    . 2016 Jul;
          44(11):1034-1038.
    
    PMID: 27449989
  
  
          Because different findings suggest that an immune dysregulation plays a role in the pathogenesis of myelodysplastic syndrome (MDS), we analyzed a large cohort of patients from a homogeneous Sardinian population...
      
5.
        
    
    Fozza C, Corda G, Barraqueddu F, Virdis P, Contini S, Isoni A, et al.
  
  
    Hematol Oncol
    . 2016 Feb;
          36(2):492-494.
    
    PMID: 26857096
  
  
          No abstract available.
      
6.
        
    
    Fozza C, Corda G, Barraqueddu F, Virdis P, Contini S, Galleu A, et al.
  
  
    Leuk Res
    . 2015 Jul;
          39(9):957-63.
    
    PMID: 26209197
  
  
          Patients with myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML) with multilineage dysplasia show several immunological abnormalities. In this clinical setting, by combining flow cytometry and CDR3 spectratyping we monitored...
      
7.
        
    
    Fozza C, Corda G, Virdis P, Contini S, Barraqueddu F, Galleu A, et al.
  
  
    Eur J Haematol
    . 2014 Jul;
          94(4):298-309.
    
    PMID: 25040028
  
  
          Although a number of studies suggest that different immune pathways may play a role in the pathogenesis of non-Hodgkin's lymphomas (NHL), the shape of the T-cell compartment has been only...
      
8.
        
    
    Fozza C, Dore F, Isoni M, Longu F, Dessi L, Coppola L, et al.
  
  
    Am J Case Rep
    . 2014 Jul;
          15:288-90.
    
    PMID: 25006360
  
  
          Patient: Male, 64 FINAL DIAGNOSIS: Acute myeloid leukemia (AML) Symptoms: - Medication: - Clinical Procedure: - Specialty: - Objective: Unusual clinical course. Background: Central nervous system (CNS) involvement is a...
      
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    Fozza C, Pardini S, Marras T, Longu F, Isoni A, Contini S, et al.
  
  
    Ann Hematol
    . 2013 Oct;
          93(5):899-900.
    
    PMID: 24081576
  
  
          No abstract available.
      
10.
        
    
    Fozza C, Poddie F, Contini S, Galleu A, Cottoni F, Longinotti M, et al.
  
  
    Case Rep Hematol
    . 2012 Sep;
          2011:848461.
    
    PMID: 22937313
  
  
          Keratitis-ichthyosis-deafness (KID) syndrome is a rare congenital disorder characterized by skin lesions, neurosensorial hypoacusia, and keratitis, usually due to the c.148G → A mutation involving the connexin 26 gene. We...