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Leukemia Research
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February 7, 2018
High frequency of intermediate and poor risk copy number abnormalities in pediatric cohort of B-ALL correlate with high MRD post induction
Minu Singh, Prateek Bhatia, Amita Trehan, et al.
Pediatric Hematology and Oncology
|
July 18, 2022
Early mortality continues to be a barrier to excellent survival in childhood acute promyelocytic leukemia: a retrospective study of 62 patients spanning 17 years
Pritam Singha Roy, Vinay Munikoty, Amita Trehan, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine
|
August 5, 2016
Proteomic analysis of differentially expressed proteins in vitreous humor of patients with retinoblastoma using iTRAQ-coupled ESI-MS/MS approach
Jasmine Naru, Ritu Aggarwal, Usha Singh, et al.
Blood Cells, Molecules & Diseases
|
April 30, 2021
A case series highlighting structured hematological, biochemical and molecular approach to clinical oral iron refractoriness in children: A pressing need for a 3-tier system for classification of variants in TMPRSS6 gene
Pankaj Sharma, Prateek Bhatia, Minu Singh, et al.
International Journal of Laboratory Hematology
|
June 30, 2022
A rare occurrence of haemophilia A in a female due to compound heterozygosity of a de novo missense variant (presenting as pseudohomozygous) in F8 gene with Xq28 deletion inherited from mother
Ritika Sharma, Manu Jamwal, Hari Kishan Senee, et al.
Mediterranean Journal of Hematology and Infectious Diseases
|
June 19, 2012
A Study on the Expression of BCR-ABL Transcript in Mixed Phenotype Acute Leukemia (MPAL) Cases Using the Reverse Transcriptase Polymerase Reaction Assay (RT-PCR) and its Correlation with Hematological Remission Status Post Initial Induction Therapy
Prateek Bhatia, Jogeshwar Binota, Neelam Varma, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|
February 7, 2022
Impact of HFE-2 and HAMP Gene Variations on Iron Overload in Pediatric Patients with Non-Transfusion Dependent Thalassemia: A Pilot Study
Niteesh Bharadwaj, Srinivasan Peyam, Prateek Bhatia, et al.
Leukemia & Lymphoma
|
April 7, 2010
Methylenetetrahydrofolate reductase gene polymorphisms: association with risk for pediatric acute lymphoblastic leukemia in north Indians
Swati Sood, Reena Das, Amita Trehan, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 23, 2017
Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infant
Manu Jamwal, Anu Aggarwal, Anirban Das, et al.
Indian Journal of Pediatrics
|
November 28, 2025
Association Between Maternal Cervical Human Papillomavirus Infection and Non-familial Retinoblastoma in Children: A Case-Control Study
Arti Yadav, Manjit Kaur, Tanvi Bhatia, et al.
Page
of 33
Search research articles
Search
Showing results (231-240 of 324) with videos related to
Sort By:
Page
of 33
Leukemia Research
|
February 7, 2018
High frequency of intermediate and poor risk copy number abnormalities in pediatric cohort of B-ALL correlate with high MRD post induction
Minu Singh, Prateek Bhatia, Amita Trehan, et al.
Pediatric Hematology and Oncology
|
July 18, 2022
Early mortality continues to be a barrier to excellent survival in childhood acute promyelocytic leukemia: a retrospective study of 62 patients spanning 17 years
Pritam Singha Roy, Vinay Munikoty, Amita Trehan, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine
|
August 5, 2016
Proteomic analysis of differentially expressed proteins in vitreous humor of patients with retinoblastoma using iTRAQ-coupled ESI-MS/MS approach
Jasmine Naru, Ritu Aggarwal, Usha Singh, et al.
Blood Cells, Molecules & Diseases
|
April 30, 2021
A case series highlighting structured hematological, biochemical and molecular approach to clinical oral iron refractoriness in children: A pressing need for a 3-tier system for classification of variants in TMPRSS6 gene
Pankaj Sharma, Prateek Bhatia, Minu Singh, et al.
International Journal of Laboratory Hematology
|
June 30, 2022
A rare occurrence of haemophilia A in a female due to compound heterozygosity of a de novo missense variant (presenting as pseudohomozygous) in F8 gene with Xq28 deletion inherited from mother
Ritika Sharma, Manu Jamwal, Hari Kishan Senee, et al.
Mediterranean Journal of Hematology and Infectious Diseases
|
June 19, 2012
A Study on the Expression of BCR-ABL Transcript in Mixed Phenotype Acute Leukemia (MPAL) Cases Using the Reverse Transcriptase Polymerase Reaction Assay (RT-PCR) and its Correlation with Hematological Remission Status Post Initial Induction Therapy
Prateek Bhatia, Jogeshwar Binota, Neelam Varma, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|
February 7, 2022
Impact of HFE-2 and HAMP Gene Variations on Iron Overload in Pediatric Patients with Non-Transfusion Dependent Thalassemia: A Pilot Study
Niteesh Bharadwaj, Srinivasan Peyam, Prateek Bhatia, et al.
Leukemia & Lymphoma
|
April 7, 2010
Methylenetetrahydrofolate reductase gene polymorphisms: association with risk for pediatric acute lymphoblastic leukemia in north Indians
Swati Sood, Reena Das, Amita Trehan, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 23, 2017
Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infant
Manu Jamwal, Anu Aggarwal, Anirban Das, et al.
Indian Journal of Pediatrics
|
November 28, 2025
Association Between Maternal Cervical Human Papillomavirus Infection and Non-familial Retinoblastoma in Children: A Case-Control Study
Arti Yadav, Manjit Kaur, Tanvi Bhatia, et al.
Page
of 33