Teresa Sofia Seara Sevivas

Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC.

Sevivas, Teresa, Journal of thrombosis and haemostasis : JTH. 2019. https://doi.org/10.1111/jth.14683 . 10.1111/jth.14683 . Journal of thrombosis and haemostasis : JTH

Phenotype description and response to thrombopoietin receptor agonist in DIAPH1-related disorder.

Sevivas, Teresa, Blood advances. 2018. https://europepmc.org/articles/PMC6156883 . 10.1182/bloodadvances.2018020370 . Blood advances

Cerebral Venous Sinus Thrombosis in a Child with Idiopathic Nephrotic Syndrome: a case report.

Sevivas, Teresa, Jornal brasileiro de nefrologia : 'orgao oficial de Sociedades Brasileira e Latino-Americana de Nefrologia. 2018. https://europepmc.org/articles/PMC6534000 . 10.1590/2175-8239-jbn-2018-0009 . Jornal brasileiro de nefrologia : 'orgao oficial de Sociedades Brasileira e Latino-Americana de Nefrologia

Anaphylaxis after treatment with recombinant factor VIII: investigation and therapeutic challenge.

Sevivas, Teresa, BMJ case reports. 2018. https://doi.org/10.1136/bcr-2018-227426 . 10.1136/bcr-2018-227426 . BMJ case reports

Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders.

Sevivas, Teresa, Haematologica. 2017. https://europepmc.org/articles/PMC5777202 . 10.3324/haematol.2017.171132 . Haematologica

Varicella complicated by cellulitis and deep vein thrombosis.

Sevivas, Teresa, BMJ case reports. 2017. https://europepmc.org/articles/PMC5589027 . 10.1136/bcr-2017-221499 . BMJ case reports

Identification of two novel mutations in RASGRP2 affecting platelet CalDAG-GEFI expression and function in patients with bleeding diathesis.

Sevivas, Teresa, Platelets. 2017. https://europepmc.org/articles/PMC5942149 . 10.1080/09537104.2017.1336214 . Platelets

Defects of splicing in antithrombin deficiency.

Sevivas, Teresa, Research and practice in thrombosis and haemostasis. 2017. https://europepmc.org/articles/PMC6058262 . 10.1002/rth2.12025 . Research and practice in thrombosis and haemostasis

VWF collagen (types III and VI)-binding defects in a cohort of type 2M VWD patients - a strategy for improvement of a challenging diagnosis.

Sevivas, Teresa, Haemophilia : the official journal of the World Federation of Hemophilia. 2017. https://doi.org/10.1111/hae.13156 . 10.1111/hae.13156 . Haemophilia : the official journal of the World Federation of Hemophilia

Hypoglycosylation is a common finding in antithrombin deficiency in the absence of a SERPINC1 gene defect.

Sevivas, Teresa, Journal of thrombosis and haemostasis : JTH. 2016. https://doi.org/10.1111/jth.13372 . 10.1111/jth.13372 . Journal of thrombosis and haemostasis : JTH

Genotype-phenotype correlation in a cohort of Portuguese patients comprising the entire spectrum of VWD types: impact of NGS.

Sevivas, Teresa, Thrombosis and haemostasis. 2016. https://doi.org/10.1160/TH15-07-0604 . 10.1160/th15-07-0604 . Thrombosis and haemostasis

Antithrombin Dublin (p.Val30Glu): a relatively common variant with moderate thrombosis risk of causing transient antithrombin deficiency.

Sevivas, Teresa, Thrombosis and haemostasis. 2016. https://doi.org/10.1160/TH15-11-0871 . 10.1160/th15-11-0871 . Thrombosis and haemostasis

Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese Study.

Sevivas, Teresa, European journal of haematology. 2015. https://doi.org/10.1111/ejh.12488 . 10.1111/ejh.12488 . European journal of haematology

Functional and molecular characterization of inherited platelet disorders in the Iberian Peninsula: results from a collaborative study.

Sevivas, Teresa, Orphanet journal of rare diseases. 2014. https://europepmc.org/articles/PMC4302577 . 10.1186/s13023-014-0213-6 . Orphanet journal of rare diseases

Proteomic analysis of platelet N-glycoproteins in PMM2-CDG patients.

Sevivas, Teresa, Thrombosis research. 2013. https://doi.org/10.1016/j.thromres.2013.12.024 . 10.1016/j.thromres.2013.12.024 . Thrombosis research

JAK2V617F allele burden is associated with thrombotic mechanisms activation in polycythemia vera and essential thrombocythemia patients.

Sevivas, Teresa, International journal of hematology. 2013. https://doi.org/10.1007/s12185-013-1475-9 . 10.1007/s12185-013-1475-9 . International journal of hematology

GPI-anchor and GPI-anchored protein expression in PMM2-CDG patients.

Sevivas, Teresa, Orphanet journal of rare diseases. 2013. https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24139637/?tool=EBI . 10.1186/1750-1172-8-170 . Orphanet journal of rare diseases

Congenital disorder of glycosylation (PMM2-CDG) in a patient with antithrombin deficiency and severe thrombophilia.

Sevivas, Teresa, Journal of thrombosis and haemostasis : JTH. 2012. https://doi.org/10.1111/jth.12031 . 10.1111/jth.12031 . Journal of thrombosis and haemostasis : JTH

The international factor IX treatment network survey.

Sevivas, Teresa, Haemophilia : the official journal of the World Federation of Hemophilia. 2012. https://doi.org/10.1111/j.1365-2516.2012.02767.x . 10.1111/j.1365-2516.2012.02767.x . Haemophilia : the official journal of the World Federation of Hemophilia

Severe intracranial haemorrhage in neonatal alloimmune thrombocytopenia.

Sevivas, Teresa, BMJ case reports. 2011. https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22679192/?tool=EBI . 10.1136/bcr.07.2011.4563 . BMJ case reports