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Reena Das

Showing results (171-180 of 279) with videos related to

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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 infantManu Jamwal, Anu Aggarwal, Anirban Das, et al.
Journal of Gastroenterology and Hepatology|June 17, 2008
Cervical esophageal web and celiac diseaseSaroj Kant Sinha, Chander Kamal Nain, Harsh Prasad Udawat, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|June 23, 2026
<i>BCOR::RARA</i>-Positive Acute Promyelocytic Leukemia with Crystalline Cytoplasmic Inclusions: A Rare Fusion with a Rare MorphologySatyender Dharamdasani, Venus Thakur, Paras Gupta, et al.
Journal of Clinical Pathology|January 19, 2022
Ultra-rare Hb Regina (<i>HBB</i>:c.289C>G) with coinherited β-thalassaemia trait: solving the puzzle for extreme erythrocytosisNabhajit Mallik, Manu Jamwal, Ritika Sharma, et al.
Gene|November 11, 2023
Genomics of iron refractory iron deficiency anemia phenotype reveals a spectrum of novel pathogenic biallelic and monoallelic TMPRSS6 variants and rare overlapping disordersPankaj Sharma, Prateek Bhatia, Minu Singh, et al.
Rheumatology International|April 24, 2013
Osseous sarcoid with lytic lesions in skullV Suri, Abhijai Singh, Reena Das, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 25, 2016
Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three casesManu Jamwal, Anu Aggarwal, Verinder Kumar, et al.
The Journal of Molecular Diagnostics : JMD|February 10, 2020
Next-Generation Sequencing-Based Diagnosis of Unexplained Inherited Hemolytic Anemias Reveals Wide Genetic and Phenotypic HeterogeneityManu Jamwal, Anu Aggarwal, Arindam Palodhi, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 27, 2022
Prenatal diagnosis for hemophilia A (intron 22 inversion) reveals a rare association with Klinefelter syndrome with diagnostic difficulties in molecular interpretationRitika Sharma, Manu Jamwal, Harikishan Senee, et al.
Leukemia & Lymphoma|April 17, 2019
A novel germline <i>RUNX1</i> mutation with co-occurrence of somatic alterations in a case of myeloid neoplasm with familial thrombocytopenia: first report from IndiaSweta Rajpal, Arihant Jain, Manu Jamwal, et al.
Pageof 28

Showing results (171-180 of 279) with videos related to

Sort By:
Pageof 28
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 infantManu Jamwal, Anu Aggarwal, Anirban Das, et al.
Journal of Gastroenterology and Hepatology|June 17, 2008
Cervical esophageal web and celiac diseaseSaroj Kant Sinha, Chander Kamal Nain, Harsh Prasad Udawat, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|June 23, 2026
<i>BCOR::RARA</i>-Positive Acute Promyelocytic Leukemia with Crystalline Cytoplasmic Inclusions: A Rare Fusion with a Rare MorphologySatyender Dharamdasani, Venus Thakur, Paras Gupta, et al.
Journal of Clinical Pathology|January 19, 2022
Ultra-rare Hb Regina (<i>HBB</i>:c.289C>G) with coinherited β-thalassaemia trait: solving the puzzle for extreme erythrocytosisNabhajit Mallik, Manu Jamwal, Ritika Sharma, et al.
Gene|November 11, 2023
Genomics of iron refractory iron deficiency anemia phenotype reveals a spectrum of novel pathogenic biallelic and monoallelic TMPRSS6 variants and rare overlapping disordersPankaj Sharma, Prateek Bhatia, Minu Singh, et al.
Rheumatology International|April 24, 2013
Osseous sarcoid with lytic lesions in skullV Suri, Abhijai Singh, Reena Das, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 25, 2016
Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three casesManu Jamwal, Anu Aggarwal, Verinder Kumar, et al.
The Journal of Molecular Diagnostics : JMD|February 10, 2020
Next-Generation Sequencing-Based Diagnosis of Unexplained Inherited Hemolytic Anemias Reveals Wide Genetic and Phenotypic HeterogeneityManu Jamwal, Anu Aggarwal, Arindam Palodhi, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 27, 2022
Prenatal diagnosis for hemophilia A (intron 22 inversion) reveals a rare association with Klinefelter syndrome with diagnostic difficulties in molecular interpretationRitika Sharma, Manu Jamwal, Harikishan Senee, et al.
Leukemia & Lymphoma|April 17, 2019
A novel germline <i>RUNX1</i> mutation with co-occurrence of somatic alterations in a case of myeloid neoplasm with familial thrombocytopenia: first report from IndiaSweta Rajpal, Arihant Jain, Manu Jamwal, et al.
Pageof 28