C Carcassi
Overview
Explore the profile of C Carcassi including associated specialties, affiliations and a list of published articles.
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78
Citations
466
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0
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Recent Articles
1.
Gialluisi A, Menabo S, Baldazzi L, Casula L, Meloni A, Farci M, et al.
Clin Genet
. 2017 Jun;
93(2):223-227.
PMID: 28644547
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21OHD-CAH) is an autosomal recessive disorder affecting steroidogenesis, due to mutations in CYP21A2 (6p21.3). 21OHD-CAH neonatal screening is based on 17-hydroxyprogesterone (17OHP) serum...
2.
Caocci G, Greco M, Fanni D, Senes G, Littera R, Lai S, et al.
Eur J Histochem
. 2016 Jun;
60(2):2606.
PMID: 27349312
Non-classical human leucocyte antigen (HLA)-G class I molecules have an important role in tumor immune escape mechanisms. We investigated HLA-G expression in lymphonode biopsies taken from 8 controls and 20...
3.
Fasano M, Rendine S, Pasi A, Bontadini A, Cosentini E, Carcassi C, et al.
Tissue Antigens
. 2014 Feb;
83(3):168-73.
PMID: 24571475
The killer cell immunoglobulin-like receptor (KIR)-human leukocyte antigen (HLA) interaction represents an example of genetic epistasis, where the concomitant presence of specific genes or alleles encoding receptor-ligand units is necessary...
4.
Piga M, Paladini F, Lai S, Erre G, Passiu G, Carcassi C, et al.
Clin Exp Rheumatol
. 2012 Oct;
30(3 Suppl 72):S51-6.
PMID: 23021043
Objectives: To define the contribution of HLA genes and extended HLA haplotypes to the susceptibility to Behçet's disease (BD) in Sardinia. Methods: Forty-five unrelated Sardinian patients with BD, diagnosed according...
5.
Cauli A, Dessole G, Vacca A, Porru G, Cappai L, Piga M, et al.
Scand J Rheumatol
. 2012 Feb;
41(3):214-8.
PMID: 22360441
Objective: Previous reports have highlighted the relevance of HLA-B27 expression in the pathogenesis of ankylosing spondylitis (AS). The aim of the current study was to estimate the level of HLA-B27...
6.
Capalbo A, Sagnella F, Apa R, Fulghesu A, Lanzone A, Morciano A, et al.
Clin Endocrinol (Oxf)
. 2012 Feb;
77(1):113-9.
PMID: 22356187
Objective: Polycystic ovary syndrome (PCOS) is a frequent condition, affecting about 15% of women of reproductive age. Because of its familial occurrence, a multifactorial model of susceptibility, including both genetic...
7.
Orru S, Manolakos E, Orru N, Kokotas H, Mascia V, Carcassi C, et al.
Clin Genet
. 2011 Mar;
81(2):172-8.
PMID: 21418058
Recently, rare mutations in the TARDBP gene have been identified in familial and sporadic amyotrophic lateral sclerosis (ALS) patients. The purpose of this study was to characterize the genetic variability...
8.
Testi M, Lai S, Orru S, Alba F, Cappai L, Firdous N, et al.
Tissue Antigens
. 2011 Feb;
77(3):235-8.
PMID: 21299529
The study of human leukocyte antigen (HLA), allele and haplotype frequencies within populations provides an important source of information for anthropological investigation, organ and hematopoietic stem-cell transplantation purposes as well...
9.
Pasi A, Crocchiolo R, Bontempelli M, Carcassi C, Carella G, Crespiatico L, et al.
Bone Marrow Transplant
. 2010 Oct;
46(7):916-22.
PMID: 20972469
Uncertainty still exists on the role of polymorphisms outside the HLA-DRB1 binding site or inside the HLA-DRB3 binding groove in unrelated hematopoietic SCT (HSCT). The ideal model to solve the...
10.
Angiolucci M, Murru R, Melis G, Carcassi C, Mais V
Ultrasound Obstet Gynecol
. 2010 May;
37(2):219-25.
PMID: 20503243
Objectives: To identify the abnormal transvaginal ultrasound (TVS) findings typical of aneuploidic pregnancies that end with early pregnancy loss (EPL). Methods: This was a prospective clinical trial over a 2½-year...