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Vinod Gupta

Showing results (11-20 of 26) with videos related to

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Human Mutation|January 4, 2020
Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemiaVinod Gupta, Anuja Kulkarni, Prashant Warang, et al.
Annals of Hematology|September 8, 2017
Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutationsPrabhakar Kedar, Vaishali Parmar, Rati Devendra, et al.
Cureus|May 22, 2023
Giant Cell Arteritis in an Elderly Female With Pulmonary TuberculosisAshwin Parchani, Ashish Baweja, Harnoor Singh, et al.
Journal of Clinical Pathology|October 20, 2018
Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patientsPrabhakar S Kedar, Vinod Gupta, Rashmi Dongerdiye, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 20, 2025
Elastographic evaluation for fatty liver disease in north Indian children and adolescents with type 1 diabetesVinod Gupta, Devi Dayal, Anmol Bhatia, et al.
Blood Cells, Molecules & Diseases|July 31, 2017
Does novel P5'N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?Prashant Warang, Rati Devendra, Ashish Chiddarwar, et al.
Indian Journal of Clinical Biochemistry : IJCB|July 5, 2021
Interpreting HbA1c in Presence of Deficiency AnemiasSeema Bhargava, Khageshwar Mahato, Anjali Manocha, et al.
Annals of Human Biology|December 14, 2019
G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, IndiaRati Devendra, Vinod Gupta, Somashekhar S Biradar, et al.
Indian Journal of Pediatrics|April 29, 2019
Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological DysfunctionPrabhakar S Kedar, Rashmi Dongerdiye, Pooja Chilwirwar, et al.
JCO Global Oncology|July 17, 2025
Comprehensive Genomic Profiling of Anaplastic Thyroid Cancer Identifies Alterations in <i>THRA</i>, a Potential Modifier of Cellular PlasticityVaishakhi Trivedi, Vanita Noronha, Munita Bal, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Human Mutation|January 4, 2020
Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemiaVinod Gupta, Anuja Kulkarni, Prashant Warang, et al.
Annals of Hematology|September 8, 2017
Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutationsPrabhakar Kedar, Vaishali Parmar, Rati Devendra, et al.
Cureus|May 22, 2023
Giant Cell Arteritis in an Elderly Female With Pulmonary TuberculosisAshwin Parchani, Ashish Baweja, Harnoor Singh, et al.
Journal of Clinical Pathology|October 20, 2018
Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patientsPrabhakar S Kedar, Vinod Gupta, Rashmi Dongerdiye, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 20, 2025
Elastographic evaluation for fatty liver disease in north Indian children and adolescents with type 1 diabetesVinod Gupta, Devi Dayal, Anmol Bhatia, et al.
Blood Cells, Molecules & Diseases|July 31, 2017
Does novel P5'N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?Prashant Warang, Rati Devendra, Ashish Chiddarwar, et al.
Indian Journal of Clinical Biochemistry : IJCB|July 5, 2021
Interpreting HbA1c in Presence of Deficiency AnemiasSeema Bhargava, Khageshwar Mahato, Anjali Manocha, et al.
Annals of Human Biology|December 14, 2019
G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, IndiaRati Devendra, Vinod Gupta, Somashekhar S Biradar, et al.
Indian Journal of Pediatrics|April 29, 2019
Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological DysfunctionPrabhakar S Kedar, Rashmi Dongerdiye, Pooja Chilwirwar, et al.
JCO Global Oncology|July 17, 2025
Comprehensive Genomic Profiling of Anaplastic Thyroid Cancer Identifies Alterations in <i>THRA</i>, a Potential Modifier of Cellular PlasticityVaishakhi Trivedi, Vanita Noronha, Munita Bal, et al.
Pageof 3