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Hemoglobin
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May 26, 2020
Missing Hb Q-India Peak in a Triple-Heterozygous Patient with Hb D-Punjab/Hb Q-India/β-Thalassemia Trait
Praveen Sharma, Aditya Jandial, Sangamitra Rajasekaran, et al.
Hematological Oncology
|
November 20, 2014
Primary bone marrow lymphoma is a rare neoplasm with poor outcome: case series from single tertiary care centre and review of literature
Priyanka Bhagat, Man Updesh Singh Sachdeva, Prashant Sharma, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|
January 9, 2023
A Phase 2 Randomized Controlled Trial of Single-Agent Hydroxyurea Versus Thalidomide Among Adult Transfusion Dependent β Thalassemia Patients
Urmimala Bhattacharjee, Alka Khadwal, Nusrat Shafiq, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 12, 2024
Unearthing the genotype-inhibitor phenotype association in severe haemophilia A: A north Indian cohort study
Debadrita Ray, Ritika Sharma, Narender Kumar, et al.
Japanese Journal of Clinical Oncology
|
September 24, 2011
Diagnostic difficulties of pure intrasinusoidal bone marrow infiltration of non-Hodgkin's lymphoma: a report of eight cases from India
Reena Das, Man Updesh Singh Sachdeva, Pankaj Malhotra, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|
November 8, 2021
Extreme Genotype/Phenotype Heterogeneity of Double Heterozygous Sickle β-Thalassemia in a Family: Implications in Antenatal Diagnosis
Diksha Dev Yadav, Namrata Singh, Sreejesh Sreedharanunni, et al.
Pediatric Blood & Cancer
|
June 12, 2021
Familial genotypic and phenotypic heterogeneity and its implications on genetic counseling exemplified in two cases of hereditary pyropoikilocytosis/erythrocytic spectrin-linked hemolytic anemia masquerading as congenital dyserythropoietic anemia
Manu Jamwal, Anu Aggarwal, Prashant Sharma, et al.
Journal of Clinical Pathology
|
December 20, 2023
Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfall
Manu Jamwal, Sreejesh Sreedharanunni, Ravina Taak, et al.
Rheumatology International
|
January 12, 2011
Macrophage activation syndrome in children with systemic onset juvenile idiopathic arthritis: clinical experience from northwest India
Surjit Singh, Shanmuganathan Chandrakasan, Jasmina Ahluwalia, et al.
Cardiology in the Young
|
July 28, 2025
Detecting early markers of sepsis in paediatric patient with prolonged cardiopulmonary bypass time
Anand Kumar Mishra, Nitish Kumar, Javid Raja, et al.
Page
of 28
Search research articles
Search
Showing results (191-200 of 279) with videos related to
Sort By:
Page
of 28
Hemoglobin
|
May 26, 2020
Missing Hb Q-India Peak in a Triple-Heterozygous Patient with Hb D-Punjab/Hb Q-India/β-Thalassemia Trait
Praveen Sharma, Aditya Jandial, Sangamitra Rajasekaran, et al.
Hematological Oncology
|
November 20, 2014
Primary bone marrow lymphoma is a rare neoplasm with poor outcome: case series from single tertiary care centre and review of literature
Priyanka Bhagat, Man Updesh Singh Sachdeva, Prashant Sharma, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|
January 9, 2023
A Phase 2 Randomized Controlled Trial of Single-Agent Hydroxyurea Versus Thalidomide Among Adult Transfusion Dependent β Thalassemia Patients
Urmimala Bhattacharjee, Alka Khadwal, Nusrat Shafiq, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
February 12, 2024
Unearthing the genotype-inhibitor phenotype association in severe haemophilia A: A north Indian cohort study
Debadrita Ray, Ritika Sharma, Narender Kumar, et al.
Japanese Journal of Clinical Oncology
|
September 24, 2011
Diagnostic difficulties of pure intrasinusoidal bone marrow infiltration of non-Hodgkin's lymphoma: a report of eight cases from India
Reena Das, Man Updesh Singh Sachdeva, Pankaj Malhotra, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|
November 8, 2021
Extreme Genotype/Phenotype Heterogeneity of Double Heterozygous Sickle β-Thalassemia in a Family: Implications in Antenatal Diagnosis
Diksha Dev Yadav, Namrata Singh, Sreejesh Sreedharanunni, et al.
Pediatric Blood & Cancer
|
June 12, 2021
Familial genotypic and phenotypic heterogeneity and its implications on genetic counseling exemplified in two cases of hereditary pyropoikilocytosis/erythrocytic spectrin-linked hemolytic anemia masquerading as congenital dyserythropoietic anemia
Manu Jamwal, Anu Aggarwal, Prashant Sharma, et al.
Journal of Clinical Pathology
|
December 20, 2023
Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfall
Manu Jamwal, Sreejesh Sreedharanunni, Ravina Taak, et al.
Rheumatology International
|
January 12, 2011
Macrophage activation syndrome in children with systemic onset juvenile idiopathic arthritis: clinical experience from northwest India
Surjit Singh, Shanmuganathan Chandrakasan, Jasmina Ahluwalia, et al.
Cardiology in the Young
|
July 28, 2025
Detecting early markers of sepsis in paediatric patient with prolonged cardiopulmonary bypass time
Anand Kumar Mishra, Nitish Kumar, Javid Raja, et al.
Page
of 28