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Journal Articles

New CMC Algorithm for Evaluation of Lupus Anticoagulant

Sreya Punjadath Baby, Rutvi Dave, Tulasi Geevar, Ashok Samuel, Jansi Rani, Sukesh C Nair

Blood (2022) 140 (Supplement 1): 8534–8535.

https://doi.org/10.1182/blood-2022-166335

Published: 2022

Journal Articles

Evaluation of Global Hemostasis Assays in Von Willebrand Disease Type 3 in Comparison with Mild to Moderate Hemophilia a

Sreya Punjadath Baby, Rutvi Dave, Tulasi Geevar, Ashok Samuel, Jansi Rani, Sukesh C. Nair

Blood (2022) 140 (Supplement 1): 11315–11316.

https://doi.org/10.1182/blood-2022-167439

Published: 2022

Journal Articles

Intracranial Bleeding in Acute Promyelocytic Leukemia Treated with Arsenic Trioxide-Based Regimens: Impact on Relapse and Survival

Uday Prakash Kulkarni, Sushil Selvarajan, Fouzia NA, Sharon Lionel, Sukesh C Nair, Poonkuzhali Balasubramanian, Thenmozhi Mani, Aby Abraham, Biju George, Vikram Mathews

Blood (2022) 140 (Supplement 1): 8917–8918.

https://doi.org/10.1182/blood-2022-168649

Published: 2022

Journal Articles

Community Based Evaluation of Prevalence of Inhibitors in Patients with Severe Hemophilia A in India and Their Correlation with Environmental and Genetic Factors

Sachin David, MSc, Vikram Mathews, Shashikant Apte, MD, Giridhara R Jayandharan, Ph.D, Sukesh C Nair, MD, Dolly Daniel, MD, Suresh Kumar, MSc, Ansu Abu Alex, MSc, Saravanan Ganesan, MSc, Kannan Subramanian, MD, Rayaz Ahmed, MD, Aby Abraham, MD, Auro Viswabandya, MD, Biju George, MD, Alok Srivastava, MD

Blood (2012) 120 (21): 3380.

https://doi.org/10.1182/blood.V120.21.3380.3380

Published: 2012

Journal Articles

Clinical, Cellular and Molecular Differences Between Newly Diagnosed and Relapsed Patients with Acute Promyelocytic Leukemia: Insights Into Mechanisms of Resistance

Ezhilarasi Chendamarai, Ansu Abu Alex, MSc, Saravanan Ganesan, MSc, Vandana Kamath, MD, Sukesh C Nair, MD, Nancy Beryl Janet, MSc, Vivi M Srivastava, MD, Kavitha M Lakshmi, MSc, Poonkuzhali Balasubramanian, Ph.D, Rayaz Ahmed, MD, Aby Abraham, MD, Auro Viswabandya, MD, Biju George, MD, Alok Srivastava, MD, Vikram Mathews

Blood (2012) 120 (21): 1390.

https://doi.org/10.1182/blood.V120.21.1390.1390

Published: 2012

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

Identifying Myelodysplastic Syndrome Among Patients with Anemia: Neutrophil Characteristics Computed by a Cell Counter (Beckman Coulter LH750), An Effective Screening Tool

Arpana Palle, MD, Josephine Thomas, DMLT, Usha Sitaram, MBBS, Vandana Kamath, MD, Joy J Mammen, MD, Sukesh C Nair, MD

Blood (2011) 118 (21): 5027.

https://doi.org/10.1182/blood.V118.21.5027.5027

Published: 2011

Journal Articles

A Polymorphism In Interferon Gamma Gene Impacts the Extent of Joint Damage In Patients with Severe Hemophilia

Giridhara Rao Jayandharan, Aaron Chapla, Sukesh C Nair, Kavitha Lakshmi, Auro Viswabandya, Vikram Mathews, Alok Srivastava, MD

Blood (2010) 116 (21): 546.

https://doi.org/10.1182/blood.V116.21.546.546

Published: 2010

Journal Articles

Polymorphisms in Coagulant and Inflammatory Genes Modify the Phenotype of Severe Hemophilia A and B.

G. Jayandharan, Mercy Devadharshini, Auro Viswabandya, Sukesh C. Nair, R.V. Shaji, Vikram Mathews, Mammen Chandy, Alok Srivastava

Blood (2006) 108 (11): 1009.

https://doi.org/10.1182/blood.V108.11.1009.1009

Published: 2006

Journal Articles

Two Mutations (1717 T〉C, GP IX;124del145, GPIb beta) Occur Frequently among Patients with Bernard Soulier Syndrome in India.

Rintu Rebecca Jacob, G. Jayandharan, Auro Viswabandya, Shoma Baidya, Sukesh C. Nair, Biju George, Vikram Mathews, Mammen Chandy, Alok Srivastava

Blood (2006) 108 (11): 1096.

https://doi.org/10.1182/blood.V108.11.1096.1096

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

Six Novel Mutations Including Triple Heterozygosity for Phe31Ser, 514delT and 516T→G Mutations in Factor X Gene Is Responsible for Congenital Factor X Deficiency in Patients of Indian and Nepali Origin.

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

Blood (2004) 104 (11): 1042.

https://doi.org/10.1182/blood.V104.11.1042.1042

Published: 2004

NARROW

New CMC Algorithm for Evaluation of Lupus Anticoagulant

Evaluation of Global Hemostasis Assays in Von Willebrand Disease Type 3 in Comparison with Mild to Moderate Hemophilia a

Intracranial Bleeding in Acute Promyelocytic Leukemia Treated with Arsenic Trioxide-Based Regimens: Impact on Relapse and Survival

Community Based Evaluation of Prevalence of Inhibitors in Patients with Severe Hemophilia A in India and Their Correlation with Environmental and Genetic Factors

Clinical, Cellular and Molecular Differences Between Newly Diagnosed and Relapsed Patients with Acute Promyelocytic Leukemia: Insights Into Mechanisms of Resistance

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

Identifying Myelodysplastic Syndrome Among Patients with Anemia: Neutrophil Characteristics Computed by a Cell Counter (Beckman Coulter LH750), An Effective Screening Tool

A Polymorphism In Interferon Gamma Gene Impacts the Extent of Joint Damage In Patients with Severe Hemophilia

Polymorphisms in Coagulant and Inflammatory Genes Modify the Phenotype of Severe Hemophilia A and B.

Two Mutations (1717 T〉C, GP IX;124del145, GPIb beta) Occur Frequently among Patients with Bernard Soulier Syndrome in India.

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

Six Novel Mutations Including Triple Heterozygosity for Phe31Ser, 514delT and 516T→G Mutations in Factor X Gene Is Responsible for Congenital Factor X Deficiency in Patients of Indian and Nepali Origin.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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