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Medical Journal, Armed Forces India
|
December 25, 2023
Diagnosis of 22q11.2 deletion syndrome in children with congenital heart diseases and facial dysmorphisms
Manisha Agarwal, Vivek Kumar, Aradhana Dwivedi
Journal of Pediatric Genetics
|
December 1, 2021
Partial Trisomy 16q21-q24.3 with Novel Cardiac Manifestation of Left Ventricular Noncompaction Cardiomyopathy: A Case Report
Aradhana Dwivedi, Vivek Kumar, H Ravi Ramamurthy
Medical Journal, Armed Forces India
|
December 30, 2024
NEDRIHF syndrome or PURA syndrome : A rare cause of central hypotonia
Swati Richa, Aradhana Dwivedi, Subhash Chandra Shaw, et al.
BMJ Case Reports
|
September 21, 2024
Early presentation of urological abnormalities in a case of Wolfram syndrome
Shilika Lalwani, Vikram Singh Shekhawat, Amit Nachankar, et al.
BMJ Case Reports
|
March 20, 2020
Type B lactic acidosis due to Warburg effect in a child presenting with T cell acute lymphoblastic leukaemia: a milder phenotype
Sanjeev Khera, Suman Kumar Pramanik, Suprita Kalra, et al.
Journal of Genetics
|
January 22, 2026
Copy number variation: an important genetic mechanism in <i>SMARCAL1</i>-related immunoosseous dysplasia (Schimke type) in Indian patients
Aradhana Dwivedi, Suprita Kalra, Puneet Singh, et al.
Medical Journal, Armed Forces India
|
December 25, 2023
Correlation of renal length with anthropometric and demographic data in healthy children: A prospective cross sectional study
Aradhana Dwivedi, Madhuri Kanitkar, Daljit Singh, et al.
International Journal of Applied & Basic Medical Research
|
September 23, 2024
Screening for Fabry disease in patients on Hemodialysis
Gaurav Batta, R Vishnuprasad, Anshita Batta, et al.
Journal of Genetics
|
December 23, 2022
Novel combination of <i>FLNC</i> (c.5707G>A; p. Glu1903Lys) and <i>BAG3</i> (c.610G>A; p.Gly204Arg) genetic variant expressing restrictive cardiomyopathy phenotype in an adolescent girl
Vivek Kumar, Pramod Kumar, Lakshita Chauhan, et al.
Molecular and Cellular Pediatrics
|
May 10, 2025
Novel WAC gene variant identified in the first documented case of DeSanto-Shinawi Syndrome in India
Aradhana Dwivedi, Lakshita Chauhan, Pramod Kumar, et al.
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Search research articles
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Showing results (1-10 of 18) with videos related to
Sort By:
Page
of 2
Medical Journal, Armed Forces India
|
December 25, 2023
Diagnosis of 22q11.2 deletion syndrome in children with congenital heart diseases and facial dysmorphisms
Manisha Agarwal, Vivek Kumar, Aradhana Dwivedi
Journal of Pediatric Genetics
|
December 1, 2021
Partial Trisomy 16q21-q24.3 with Novel Cardiac Manifestation of Left Ventricular Noncompaction Cardiomyopathy: A Case Report
Aradhana Dwivedi, Vivek Kumar, H Ravi Ramamurthy
Medical Journal, Armed Forces India
|
December 30, 2024
NEDRIHF syndrome or PURA syndrome : A rare cause of central hypotonia
Swati Richa, Aradhana Dwivedi, Subhash Chandra Shaw, et al.
BMJ Case Reports
|
September 21, 2024
Early presentation of urological abnormalities in a case of Wolfram syndrome
Shilika Lalwani, Vikram Singh Shekhawat, Amit Nachankar, et al.
BMJ Case Reports
|
March 20, 2020
Type B lactic acidosis due to Warburg effect in a child presenting with T cell acute lymphoblastic leukaemia: a milder phenotype
Sanjeev Khera, Suman Kumar Pramanik, Suprita Kalra, et al.
Journal of Genetics
|
January 22, 2026
Copy number variation: an important genetic mechanism in <i>SMARCAL1</i>-related immunoosseous dysplasia (Schimke type) in Indian patients
Aradhana Dwivedi, Suprita Kalra, Puneet Singh, et al.
Medical Journal, Armed Forces India
|
December 25, 2023
Correlation of renal length with anthropometric and demographic data in healthy children: A prospective cross sectional study
Aradhana Dwivedi, Madhuri Kanitkar, Daljit Singh, et al.
International Journal of Applied & Basic Medical Research
|
September 23, 2024
Screening for Fabry disease in patients on Hemodialysis
Gaurav Batta, R Vishnuprasad, Anshita Batta, et al.
Journal of Genetics
|
December 23, 2022
Novel combination of <i>FLNC</i> (c.5707G>A; p. Glu1903Lys) and <i>BAG3</i> (c.610G>A; p.Gly204Arg) genetic variant expressing restrictive cardiomyopathy phenotype in an adolescent girl
Vivek Kumar, Pramod Kumar, Lakshita Chauhan, et al.
Molecular and Cellular Pediatrics
|
May 10, 2025
Novel WAC gene variant identified in the first documented case of DeSanto-Shinawi Syndrome in India
Aradhana Dwivedi, Lakshita Chauhan, Pramod Kumar, et al.
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