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British Journal of Haematology
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May 24, 2019
A nonsense variant in the Hexokinase 1 gene (HK1) causing severe non-spherocytic haemolytic anaemia: genetic analysis exemplifies ambiguity due to multiple Isoforms
Manu Jamwal, Anu Aggarwal, Arindam Palodi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
July 17, 2025
P2RY12-Related Platelet Dysfunction in an Indian Child: Unravelling the Diagnostic Enigma of Suspected Platelet Storage Pool Disorder
Vasant Kumar, Manu Jamwal, Chander Hans, et al.
Annals of Hematology
|
October 9, 2020
Hemolytic erythrocytosis: an amalgamated phenotype from coinherited Chuvash polycythemia and G6PD Kerala-Kalyan with acquired transient stomatocytosis
Manu Jamwal, Nabhajit Mallik, Arun Vijayalakshmi Aravindan, et al.
Pathology
|
July 1, 2023
Dehydrated hereditary stomatocytosis masquerading as primary haemochromatosis: a diagnostic challenge
Manu Jamwal, Namrata Singh, Prashant Sharma, et al.
Acta Cardiologica
|
October 6, 2017
Coagulation F13A1 V34L, fibrinogen and homocysteine versus conventional risk factors in the pathogenesis of MI in young persons
Vikarn Vishwajeet, Manu Jamwal, Prashant Sharma, et al.
Blood Cells, Molecules & Diseases
|
July 8, 2018
Homozygous KLF1 mutation c.901C>T (p.Arg301Cys) resulting in mild thalassemia intermedia in an Indian: A next-generation sequencing diagnosis
Neetu Rani, Manu Jamwal, Jasbir Kaur, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|
June 23, 2026
First Report of <i>MYH9</i> E1841K Variant in an Indian Family: A Case of Familial Macrothrombocytopenia and Review of Literature
Ritika Sharma, Manu Jamwal, Reena Das, et al.
British Journal of Haematology
|
October 12, 2019
Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing: First South Asian study
Anu Aggarwal, Manu Jamwal, Prashant Sharma, et al.
International Journal of Laboratory Hematology
|
March 10, 2022
Hemoglobin Andrew-Minneapolis-Bijnor HBB:c.[413T>C;435G>C] in a complex genotype with β-thalassemia trait: A diagnostic and management conundrum
Niranjan Shiwaji Khaire, Manu Jamwal, Prashant Sharma, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
March 12, 2026
Severe Congenital Factor X Deficiency in an Indian Child With a Concomitant Novel ITGA2 Variant
Vasant Kumar, Debadrita Ray, Manu Jamwal, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 63) with videos related to
Sort By:
Page
of 7
British Journal of Haematology
|
May 24, 2019
A nonsense variant in the Hexokinase 1 gene (HK1) causing severe non-spherocytic haemolytic anaemia: genetic analysis exemplifies ambiguity due to multiple Isoforms
Manu Jamwal, Anu Aggarwal, Arindam Palodi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
July 17, 2025
P2RY12-Related Platelet Dysfunction in an Indian Child: Unravelling the Diagnostic Enigma of Suspected Platelet Storage Pool Disorder
Vasant Kumar, Manu Jamwal, Chander Hans, et al.
Annals of Hematology
|
October 9, 2020
Hemolytic erythrocytosis: an amalgamated phenotype from coinherited Chuvash polycythemia and G6PD Kerala-Kalyan with acquired transient stomatocytosis
Manu Jamwal, Nabhajit Mallik, Arun Vijayalakshmi Aravindan, et al.
Pathology
|
July 1, 2023
Dehydrated hereditary stomatocytosis masquerading as primary haemochromatosis: a diagnostic challenge
Manu Jamwal, Namrata Singh, Prashant Sharma, et al.
Acta Cardiologica
|
October 6, 2017
Coagulation F13A1 V34L, fibrinogen and homocysteine versus conventional risk factors in the pathogenesis of MI in young persons
Vikarn Vishwajeet, Manu Jamwal, Prashant Sharma, et al.
Blood Cells, Molecules & Diseases
|
July 8, 2018
Homozygous KLF1 mutation c.901C>T (p.Arg301Cys) resulting in mild thalassemia intermedia in an Indian: A next-generation sequencing diagnosis
Neetu Rani, Manu Jamwal, Jasbir Kaur, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|
June 23, 2026
First Report of <i>MYH9</i> E1841K Variant in an Indian Family: A Case of Familial Macrothrombocytopenia and Review of Literature
Ritika Sharma, Manu Jamwal, Reena Das, et al.
British Journal of Haematology
|
October 12, 2019
Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing: First South Asian study
Anu Aggarwal, Manu Jamwal, Prashant Sharma, et al.
International Journal of Laboratory Hematology
|
March 10, 2022
Hemoglobin Andrew-Minneapolis-Bijnor HBB:c.[413T>C;435G>C] in a complex genotype with β-thalassemia trait: A diagnostic and management conundrum
Niranjan Shiwaji Khaire, Manu Jamwal, Prashant Sharma, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
March 12, 2026
Severe Congenital Factor X Deficiency in an Indian Child With a Concomitant Novel ITGA2 Variant
Vasant Kumar, Debadrita Ray, Manu Jamwal, et al.
Page
of 7