User profiles for Elena Chinni
Elena ChinniIRCCS Casa Sollievo della Sofferenza Verified email at operapadrepio.it Cited by 429 |
Haplotype M2 in the annexin A5 (ANXA5) gene and the occurrence of obstetric complications
G Tiscia, D Colaizzo, E Chinni… - Thrombosis and …, 2009 - thieme-connect.com
Inherited or acquired thrombophilias have been largely explored as a cause of pregnancy
complications. However, pathogenesis of obstetric complications, as fetal loss and …
complications. However, pathogenesis of obstetric complications, as fetal loss and …
Reduction of ADAMTS13 levels predicts mortality in SARS-CoV-2 patients
…, L di Mauro, G Miscio, A Mirijello, E Chinni… - TH Open, 2020 - thieme-connect.com
In SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) infected patients, hemostasis
shows an uncontrolled activation, with a high D-dimer concentration. 1, 2 It has been …
shows an uncontrolled activation, with a high D-dimer concentration. 1, 2 It has been …
[HTML][HTML] Annexin V expression in human placenta is influenced by the carriership of the common haplotype M2
In a group of placentas from patients with preeclampsia or fetal growth restriction, reduced
annexin V gene expression in those carrying the M2 haplotype was observed. This is the first “…
annexin V gene expression in those carrying the M2 haplotype was observed. This is the first “…
[HTML][HTML] The prognostic value of ADAMTS-13 and von Willebrand factor in COVID-19 patients: prospective evaluation by care setting
…, F Cappucci, L Fischetti, D Colaizzo, E Chinni… - Diagnostics, 2021 - mdpi.com
Background: Endothelial dysfunction, coupled with inflammation, induces thrombo-inflammation.
In COVID-19, this process is believed to be associated with clinical severity. Von …
In COVID-19, this process is believed to be associated with clinical severity. Von …
Role of the M2 haplotype within the annexin A5 gene in the occurrence of pregnancy-related venous thromboembolism
OBJECTIVE: Knowledge about risk factors for venous thromboembolism (VTE) is still limited.
A recently found haplotype within the natural anticoagulant protein annexin A5 (ANXA5) …
A recently found haplotype within the natural anticoagulant protein annexin A5 (ANXA5) …
Venous thromboembolism in assisted reproductive technologies: comparison between unsuccessful versus successful cycles in an Italian cohort
M Villani, G Favuzzi, P Totaro, E Chinni… - Journal of thrombosis …, 2018 - Springer
Pregnancies after assisted reproductive technologies (ART) have been associated with an
increased risk of venous thromboembolism (VTE). On the contrary, the magnitude of this risk …
increased risk of venous thromboembolism (VTE). On the contrary, the magnitude of this risk …
[HTML][HTML] Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype–phenotype relationship
…, V Mirabelli, G D'Andrea, E Chinni… - Human Genome …, 2017 - nature.com
Congenital Factor XI (FXI) deficiency shows a high variability in clinical phenotype. To date,
many allele variants have been shown to cause this bleeding disorder. However, the …
many allele variants have been shown to cause this bleeding disorder. However, the …
Correlation between factors involved in the local haemostasis and angiogenesis in full term human placenta
INTRODUCTION: Few studies have been carried out to investigate whether distinct areas of
full term placenta express different amounts of markers involved in the placental …
full term placenta express different amounts of markers involved in the placental …
Markers of haemostasis and angiogenesis in placentae from gestational vascular complications: impairment of mechanisms involved in maintaining intervillous blood …
E Chinni, D Colaizzo, GL Tiscia, P Martinelli… - Thrombosis research, 2010 - Elsevier
INTRODUCTION: Preeclampsia (PE) and fetal growth restriction (FGR) are multifactorial
diseases, whose pathogenesis is largely unknown. A significant relationship between …
diseases, whose pathogenesis is largely unknown. A significant relationship between …
[HTML][HTML] Identification of novel mutations in patients with fibrinogen disorders and genotype/phenotype correlations
E Chinni, G Tiscia, G Favuzzi, F Cappucci… - Blood …, 2019 - ncbi.nlm.nih.gov
Background Congenital fibrinogen disorders are caused by variants occurring within the
fibrinogen gene cluster. We describe ten subjects with disease-causative variants, adding …
fibrinogen gene cluster. We describe ten subjects with disease-causative variants, adding …