Meganathan Kannan, PhD
Meganathan Kannan, PhD
Assistant Professor, Department of Life Sciences, Central University of Tamil Nadu
Verified email at - Homepage
Cited by
Cited by
Inherited prothrombotic defects in Budd-Chiari syndrome and portal vein thrombosis
M Bhattacharyya, G Makharia, M Kannan, RPH Ahmed, PK Gupta, ...
American journal of clinical pathology 121 (6), 844-847, 2004
Membrane array–based differential profiling of platelets during storage for 52 miRNAs associated with apoptosis
M Kannan, KVK Mohan, S Kulkarni, C Atreya
Transfusion 49 (7), 1443-1450, 2009
Differential profiling of human red blood cells during storage for 52 selected microRNAs
M Kannan, C Atreya
Transfusion 50 (7), 1581-1588, 2010
Gene conversions are a common cause of von Willebrand disease
PK Gupta, E Adamtziki, U Budde, M Jaiprakash, H Kumar, A Harbeck‐Seu, ...
British journal of haematology 130 (5), 752-758, 2005
Disseminated intravascular coagulation in acute leukemia at presentation and during induction therapy
A Dixit, T Chatterjee, P Mishra, M Kannan, DR Choudhry, M Mahapatra, ...
Clinical and Applied Thrombosis/Hemostasis 13 (3), 292-298, 2007
Molecular defects in ITGA2B and ITGB3 genes in patients with Glanzmann thrombasthenia
M Kannan, F Ahmad, BK Yadav, R Kumar, VP Choudhry, R Saxena
Journal of Thrombosis and Haemostasis 7 (11), 1878-1885, 2009
Glanzmann's thrombasthenia: an overview
M Kannan, R Saxena
Clinical and Applied Thrombosis/Hemostasis 15 (2), 152-165, 2009
Roles of protein C, protein S, and antithrombin III in acute leukemia
A Dixit, M Kannan, M Mahapatra, VP Choudhry, R Saxena
American journal of hematology 81 (3), 171-174, 2006
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: a communication from the Platelet Physiology SSC
P Gresele, S Orsini, P Noris, E Falcinelli, MC Alessi, L Bury, M Borhany, ...
Journal of Thrombosis and Haemostasis 18 (3), 732-739, 2020
Mutation reports: intron 1 and 22 inversions in Indian haemophilics
R Ahmed, M Kannan, VP Choudhry, R Saxena
Annals of hematology 82 (9), 546-547, 2003
Inherited platelet function disorders versus other inherited bleeding disorders: An Indian overview
F Ahmad, M Kannan, R Ranjan, J Bajaj, VP Choudhary, R Saxena
Thrombosis research 121 (6), 835-841, 2008
Identification of 32 novel mutations in the factor VIII gene in Indian patients with hemophilia A
RP Ahmed, V Ivaskevicius, M Kannan, E Seifried, J Oldenburg, R Saxena
haematologica 90 (2), 283-284, 2005
Factor V Leiden—the commonest molecular defect in arterial and venous thrombophilia in India
SR RPH Ahmed, PK Gupta, M Kannan, VP Chhoudhry
Thrombosis Research 110 (1), 19-21, 2003
Neonatal thrombosis
R Saxena, M Kannan, VP Choudhry
The Indian Journal of Pediatrics 70 (11), 903-907, 2003
Hypercoagulable state in five thalassemia intermedia patients
M Bhattacharyya, M Kannan, VP Chaudhry, M Mahapatra, H Pati, ...
Clinical and Applied Thrombosis/Hemostasis 13 (4), 422-427, 2007
Venous thrombosis: prevalence of prothrombotic defects in north Indian population.
M Bhattacharyya, M Kannan, VP Chaudhry, R Saxena
Indian journal of pathology & microbiology 46 (4), 621-624, 2003
Characterisation of mutations and molecular studies of type 2 von Willebrand disease
F Ahmad, R Jan, M Kannan, T Obser, MI Hassan, F Oyen, U Budde, ...
Thrombosis and haemostasis 109 (01), 39-46, 2013
Does the MTHFR 677T allele alter the clinical phenotype in severe haemophilia A?
R Ahmed, M Kannan, VP Choudhry, R Saxena
Thrombosis research 109 (1), 71-72, 2003
Protein C system defects in Indian children with thrombosis
PK Gupta, RPH Ahmed, M Bhattacharyya, M Kannan, A Biswas, V Kalra, ...
Annals of hematology 84 (2), 85-88, 2005
Viral persistence and chronicity in hepatitis C virus infection: role of T-cell apoptosis, senescence and exhaustion
M Barathan, R Mohamed, YK Yong, M Kannan, J Vadivelu, A Saeidi, ...
Cells 7 (10), 165, 2018
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