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ISTH 2020 Congress

Venous Thromboembolism and Cardioembolism » Thrombophilia

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    • Venous Thromboembolism and Cardioembolism
      • Thrombophilia

Abstract Number: PB2229

A New Global Assay for Detection of Protein C Pathway-Associated Thrombophilia Using Thrombomodulin-Mediated Clot Waveform Analysis

N. Hashimoto, K. Ogiwara, K. Nogami, M. Shima

Abstract Number: PB2220

Are We Choosing Wisely? Heritable Thrombophilia (HT) Testing in a District General Hospital in the UK

L. Khalil

Abstract Number: PB2240

Characterisation of Antithrombin p.Thr147Ala, the First Common Founder Variant from African Origin Responsible for Inherited Antithrombin Deficiency

B. de la Morena-Barrio1, J. Padilla2, I. Pareyn3, C. Bravo-Pérez2, K. Vanhoorelbeke3, I. Martínez-Martínez2, V. Vicente2, J. Corral2, K. Jochmans4, M.E. de la Morena-Barrio2, C. Orlando4

Abstract Number: PB2238

Deep Vein Thrombosis Associated with Protein S Deficiency

P. Romadhon, M. Savitri, P. Niken, U. Bintoro, M. Sedana, A. Ashariati

Abstract Number: PB2247

Efficacy and Safety Profile of Direct Oral Anticoagulants in Consecutive Patients with Severe Hereditary Thrombophilia: A Single-centre Cohort Study

E. Campello1, C. Simion1, L. Spiezia1, D. Tormene1, G. Camporese2, G. Saggiorato1, F. Dalla Valle1, P. Simioni1

Abstract Number: PB2221

Evaluation of Platelet Indices in Patients with Splanchnic Vein Thrombosis

N. Kumar1, S. Sharma1, I. Bihana1, V. Uppal1, J. Ahluwalia1, N. Varma1, S. Naseem1, S.K. Sinha2

Abstract Number: PB2223

High Prevalence of the Hereditary Anticoagulant Deficiency in Chronic Thromboembolic Pulmonary Hypertension (CTEPH)

T.-Y. Lian1, Y.-J. Zhu1, Y.-P. Zhou1, X.-X. Yan2, T. Wu1, X. Jiang2, X.-Q. Xu2, K. Sun2, L. Hua2, Z.-C. Jing1

Abstract Number: PB2235

Homozygous Antithrombin Budapest 3 Deficiency Causes Inferior Vena Cava System Agenesis

C. Bravo-Perez1, R. Gindele2, M.E. de la Morena-Barrio1, P. Ilonczai3, I. Zuazu1, M. Speker2, Z. Olah4, J. Rodriguez-Sevilla5, L. Entrena6, M. Infante7, J. Garcia7, B. de la Morena-Barrio1, A. Miñano1, V. Vicente1, J. Corral1, Z. Bereczky8

Abstract Number: PB2246

Hypoplasminogenemia – A Forgotten Diagnosis: A Case Series of Genotype and Phenotype Correlation

R.S. Alesci1, C. Hecking1, T. Alef2

Abstract Number: PB2226

Increased Levels of Procoagulant Factors and the Risk of Venous Thromboembolism

L. Spiezia, E. Vedovetto, M. Marobin, E. Borella, G. Turatti, P. Simioni

Abstract Number: PB2236

Inherited Deficiency of Antithrombin, Protein C or Protein S Is Associated with an Increased Risk of Cancer at a Younger Age

D. Tormene1, S. Gavasso2, G. Turatti2, C. Simion2, M. Marobin2, E. Campello2, P. Simioni2

Abstract Number: PB2233

Is May-Thurner Syndrome a Forgotten Cause of Deep Vein Thrombosis?

S. Lopes, R. Pombal, L. Vieira, D. Ferreira, H. Cruz Gomes, M. Figueiredo

Abstract Number: PB2237

Mandor´s Disease: A Manifestation of Rare Conditions

Y. Cherif, M. Mrouki, S. Derbel, T. Ben Achour, F. Ben Dahmen, M. Abdallah

Abstract Number: PB2225

Positive Thrombophilia Study in the Context of Starting Hormonal Treatment in the Gender Dysphory: Experience in a Single Center

B. Díaz Roldán, J.F. Domínguez Rodríguez, A.R. Carranco Falcón

Abstract Number: PB2227

Primary Aortic Thrombus with Multiple Visceral Embolisation: A Presenting Manifestation of Chronic Myelomonocytic Leukemia

V. Chadachan, N. Pandit

Abstract Number: PB2239

Relation between the von Willebrand Factor and ADAMTS13 with Venous Thrombosis Risk. Results from the Retrove Project

D. Llobet1, C. Vallvé1, A. Oliver2, M. Carrasco1, N. Vilalta1, J. Mateo1, J.C. Souto1

Abstract Number: PB2234

Relevance of Thrombophilia Screening in Adult Renal Transplant Recipients

D. Bahri1, H. Baccouche1, L. Ben Fatma2, S. Hadded2, A. Chakroun1, S. Mahjoub1, M.K. Zouaghi2, N. Ben Romdhane1

Abstract Number: PB2244

Risk of Recurrence after a First-lifetime Venous Thrombosis: Impact of Inherited Thrombophilia

M. Belhadj1,2, H. Baccouche1,2, F. Said1,2, M.H. Houman1,2, N. Ben Romdhane1,2

Abstract Number: PB2243

The Presence of Paraproteinaemia in Patients with Antiphospholipid Syndrome – A Single Centre Case Series

A. Doyle, K.A. Breen, B.J. Hunt

Abstract Number: PB2232

The Prothrombin Belgrade Mutation Causing Antithrombin Resistance Does Not Affect Fibrin Clot Formation

S. Dunjic1, M. Cumbo1, I. Pruner2, M. Gvozdenov1, A. Taxiarchis2, B. Tomic1, J. Antovic2,3, V. Djordjevic1

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