ISTH 2020 Congress

Venous Thromboembolism and Cardioembolism » Thrombophilia

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ISTH 2020 Congress
- 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