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Journal Articles

Prothrombin "Carmel": Identification of a Novel Homozygous Mutation in the Prothrombin Gene Causing Coagulation Factor II Deficiency and Inherited Bleeding Disorder in an Israeli Arab Family

Emad Muhammad, PhD, Aliza Cassel, PhD, Miriam Berl, Meir Preis, MD PhD, Ayala Rozano Gorelick, MD

Blood (2017) 130 (Supplement 1): 4872.

https://doi.org/10.1182/blood.V130.Suppl_1.4872.4872

Published: 2017

Journal Articles

Thromboelastography in the Characterization of Coagulation Status in Antiphospholipid Syndrome

Natalie H Wallace, MD MPH, Anne Dumont, BS, Adrienne Burns, PA, Tormey A Christopher, MD, Henry M Rinder, MD, Martin A Kriegel, MD PhD, Lenore M Buckley, MD MPH, Doruk Erkan, MD MPH, Alfred I Lee, MD PhD

Blood (2016) 128 (22): 4983.

https://doi.org/10.1182/blood.V128.22.4983.4983

Published: 2016

Journal Articles

Asymptomatic Dysprothrombinemia (Prothtombin Himi) with p.M380T and p.R431H Shows Severely Reduced Clotting Activity, Moderate Antithrombin Resistance and Severe Thrombomodulin Binding Defect

Eriko Morishita, MD PhD, Mao Takata, BSc, Fumina Taniguchi, BSc, Masashi Akiyama, PhD, Akiko Sekiya, PhD, Akira Takagi, PhD, Toshiyuki Miyata, PhD, Tetsuhito Kojima, MD PhD

Blood (2016) 128 (22): 2574.

https://doi.org/10.1182/blood.V128.22.2574.2574

Published: 2016

Journal Articles

Early Detection of Lupus Anticoagulant-Hypoprothrombinemia Syndrome By Rotational Thromboelastometry

Soumya Reddy, MD, Sarah Friend, MD, Dulcinea Quintana, MD, Evelyn L. Lockhart, MD

Blood (2015) 126 (23): 4699.

https://doi.org/10.1182/blood.V126.23.4699.4699

Published: 2015

Journal Articles

Rare Inherited Clotting Factor Deficiencies in Paediatric Population Single Tertiary Centre Experience in Saudi Arabia

Mahasen al Saleh, Tarek Owaidah, MD FRCPA, Abdulrahman Al Musa, Hazzaa Al-Zahrani, MBBS,MRCP, Suleman Al-Sweedan, Nicy Joseph, Rubina Malik, Khawar Siddiqui, MSc, Sohaib Zulfiqar, Rafat Jafri

Blood (2014) 124 (21): 5064.

https://doi.org/10.1182/blood.V124.21.5064.5064

Published: 2014

Journal Articles

Genetic Diagnosis of Inherited Bleeding Disorders in 1250 Probands From India: A Single Centre Experience

Giridhara R Jayandharan, Ph.D, Govindanattar Sankari Devi, S RajKumar, Everette Nelson, Ramachandran V Shaji, Neeraj Arora, P Shenbagaapriya, Sukesh C Nair, MD, Auro Viswabandya, MD, Biju George, MD, Vikram Mathews, Alok Srivastava, MD

Blood (2012) 120 (21): 1127.

https://doi.org/10.1182/blood.V120.21.1127.1127

Published: 2012

Journal Articles

Rare Congenital Bleeding Disorders from a Tertiary Haematology Referral Center in Western India

Anjali Jaydeep Kelkar, MD, MNAMS, MBBS, Shashikant Apte, MD, FRCPA, Varsha Melinkeri, Samir Melinkeri, Ashay Karpe, Saurabh Bhave, Bhavna Sayaji

Blood (2008) 112 (11): 4519.

https://doi.org/10.1182/blood.V112.11.4519.4519

Published: 2008

Journal Articles

High Incidence of Venous Thromboembolism (VTE) in Patients with Cancer Hospitalized at a University Hospital in Chile. Efficacy of Pharmacological Thromboprophylaxis.

Guillermo F. Conte, MD, Gaston L. Figueroa, MD, Arie D. Altmann, Luisa A. Donaire

Blood (2006) 108 (11): 4119.

https://doi.org/10.1182/blood.V108.11.4119.4119

Published: 2006

Journal Articles

Liver Transplantation for Prothrombin Deficiency Causing Life-Threatening Bleeds.

Nancy A. Dower, MD, PhD, Wilma McClure, John J. Akabutu, MD

Blood (2006) 108 (11): 4069.

https://doi.org/10.1182/blood.V108.11.4069.4069

Published: 2006

Journal Articles

A Fatal Bleeding Disorder Due to Antibody Mediated Acquired Factor X and Prothrombin Deficiency.

Leanne Rochanda, BA, Donald I. Feinstein, MD, Gregory J. del Zoppo, MD, Howard A. Liebman, MD

Blood (2006) 108 (11): 4072.

https://doi.org/10.1182/blood.V108.11.4072.4072

Published: 2006

Journal Articles

Molecular Genetics of Hereditary Prothrombin Deficiency in Indian Patients: Identification of a Novel Ala362→Thr (Prothrombin Vellore 1) Mutation by Conformation Sensitive Gel Electrophoresis.

G Jayandharan, R.V. Shaji, Auro Viswabandhya, Sukesh C. Nair, Joy Mammen, Biju George, Vikram Mathews, Mammen Chandy, Alok Srivastava

Blood (2004) 104 (11): 1037.

https://doi.org/10.1182/blood.V104.11.1037.1037

Published: 2004

Journal Articles

Properties of Recombinant Human Thromboplastin that Determine Sensitivity to Vitamin K-Dependent Coagulation Factors.

Stephanie A. Smith, James H. Morrissey

Blood (2004) 104 (11): 533.

https://doi.org/10.1182/blood.V104.11.533.533

Published: 2004

Journal Articles

Combined deficiency of protease-activated receptor-4 and fibrinogen recapitulates the hemostatic defect but not the embryonic lethality of prothrombin deficiency

Eric Camerer, Daniel N. Duong, Justin R. Hamilton, Shaun R. Coughlin

Blood (2004) 103 (1): 152–154.

https://doi.org/10.1182/blood-2003-08-2707

Published: 2004

Journal Articles

The Nature of the Hemorrhagic Disorder Accompanying Hemolytic Transfusion Reactions in Man

JULIUS R. KREVANS, DUDLEY P. JACKSON, C. LOCKARD CONLEY, ROBERT C. HARTMANN

Blood (1957) 12 (9): 834–843.

https://doi.org/10.1182/blood.V12.9.834.834

Published: 1957

NARROW

Prothrombin "Carmel": Identification of a Novel Homozygous Mutation in the Prothrombin Gene Causing Coagulation Factor II Deficiency and Inherited Bleeding Disorder in an Israeli Arab Family

Thromboelastography in the Characterization of Coagulation Status in Antiphospholipid Syndrome

Asymptomatic Dysprothrombinemia (Prothtombin Himi) with p.M380T and p.R431H Shows Severely Reduced Clotting Activity, Moderate Antithrombin Resistance and Severe Thrombomodulin Binding Defect

Early Detection of Lupus Anticoagulant-Hypoprothrombinemia Syndrome By Rotational Thromboelastometry

Rare Inherited Clotting Factor Deficiencies in Paediatric Population Single Tertiary Centre Experience in Saudi Arabia

Genetic Diagnosis of Inherited Bleeding Disorders in 1250 Probands From India: A Single Centre Experience

Rare Congenital Bleeding Disorders from a Tertiary Haematology Referral Center in Western India

High Incidence of Venous Thromboembolism (VTE) in Patients with Cancer Hospitalized at a University Hospital in Chile. Efficacy of Pharmacological Thromboprophylaxis.

Liver Transplantation for Prothrombin Deficiency Causing Life-Threatening Bleeds.

A Fatal Bleeding Disorder Due to Antibody Mediated Acquired Factor X and Prothrombin Deficiency.

Molecular Genetics of Hereditary Prothrombin Deficiency in Indian Patients: Identification of a Novel Ala362→Thr (Prothrombin Vellore 1) Mutation by Conformation Sensitive Gel Electrophoresis.

Properties of Recombinant Human Thromboplastin that Determine Sensitivity to Vitamin K-Dependent Coagulation Factors.

Combined deficiency of protease-activated receptor-4 and fibrinogen recapitulates the hemostatic defect but not the embryonic lethality of prothrombin deficiency

The Nature of the Hemorrhagic Disorder Accompanying Hemolytic Transfusion Reactions in Man

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American Society of Hematology

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American Society of Hematology

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