Dr Teresa Fidalgo
Health Care Professional, Medicine And Medical Sciences
My co-authors include
Unraveling the effect of silent, intronic and missense mutations on VWF splicing: contr...
(SNPs) in genes ABO, F11 and FGG associated to VTE
Blood Coagulation & Fibrinolysis
Atypical adult-onset methylmalonic acidemia and homocystinuria presenting as hemolytic ...
CEN Case Reports
Combined study of ADAMTS13 and complement genes in the diagnosis of TMA's using NGS
Research and Practice in Thrombosis and Haemostasis
Acquired von Willebrand– how the clinical-laboratory correlation improves a challenging...
VWF collagen (types III and VI)-binding defects in a cohort of type 2M VWD patients
In this report, we discuss the case of aHUS with a C3 mutation and an uncommon presenta...
Open Access Journal of Urology & Nephrology
Detection of new pathogenic mutations in patients with congenital haemolytic anaemia us...
International Journal of Laboratory Hematology
Genotype–phenotype correlation in a cohort of Portuguese patients comprising the entire...
Thrombosis and Haemostasis
New combinedCFH/MCPmutations and a rare clinical course in atypical haemolytic uraemic ...
Clinical Kidney Journal
Familial thrombotic risk based on the genetic background of Protein C Deficiency
European Journal Of Haematology
JAK2V617F allele burden is associated with thrombotic mechanisms activation in polycyth...
International Journal of Hematology
Molecular diagnosis of haemophilia A at C.Hospitalar de Coimbra in Portugal: study of 1...