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Indian Journal of Pediatrics
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June 8, 2023
PHACE Syndrome (Posterior Fossa Malformations, Hemangioma, Arterial Anomalies, Coarctation of the Aorta/ Cardiac Defects, and Eye Abnormalities) /Cutaneous Hemangioma-Vascular Complex Syndrome/Pascual-Castroviejo Type II Syndrome
Vykuntaraju K Gowda, Varunvenkat M Srinivasan
Indian Journal of Pediatrics
|
March 16, 2023
Ohtahara and West Syndrome due to Pyridox(am)ine-5-Phosphate Oxidase (PNPO) Deficiency with Novel Phenotype and Good Outcome without Pyridoxal-5'-Phosphate
Vykuntaraju K Gowda, Varunvenkat M Srinivasan
Indian Journal of Pediatrics
|
April 24, 2023
Recurrent Familial Acute Necrotizing Encephalopathy of Childhood (ANEC)
Vykuntaraju K Gowda, Varunvenkat M Srinivasan
Indian Journal of Pediatrics
|
May 23, 2022
A Treatable Cause of Global Developmental Delay with Autism Spectrum Disorder Due to Cobalamin Related Remethylation Disorder
Vykuntaraju K Gowda, Varunvenkat M Srinivasan
Indian Journal of Pediatrics
|
May 19, 2023
A Rare Genetic-Metabolic Cause of Epileptic Spasms: Dihydropyrimidine Dehydrogenase Deficiency
Vykuntaraju K Gowda, Varunvenkat M Srinivasan
Indian Journal of Pediatrics
|
December 7, 2025
Metronidazole-Induced Hepatotoxicity in Children with Cockayne Syndrome
Ankit Agrawal, Upasana Ghosh, Varunvenkat M Srinivasan
Neurology India
|
May 6, 2026
Primary Coenzyme Q10 Deficiency Type 7: A Potentially Treatable Cause of Developmental Delay
Varunvenkat M Srinivasan, Mayank Nilay, Rani Manisha
Clinical Dysmorphology
|
May 28, 2026
Integrating Face2Gene analysis in the diagnosis of Van den Ende-Gupta syndrome caused by a novel SCARF2 mutation with expanded skeletal and cardiac features
Varunvenkat M Srinivasan, Mayank Nilay, Rani Manisha
Indian Journal of Pediatrics
|
January 29, 2020
Waardenburg Syndrome Type I
Vykuntaraju K Gowda, Sahana Srinivas, Varunvenkat M Srinivasan
Indian Journal of Pediatrics
|
April 21, 2023
Lathosterolosis - A Rare Treatable Cause for Global Developmental Delay, Cataract, and Liver Dysfunction Masquerading as Galactosemia
Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Uddhav Kinhal
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Search research articles
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Showing results (1-10 of 120) with videos related to
Sort By:
Page
of 12
Indian Journal of Pediatrics
|
June 8, 2023
PHACE Syndrome (Posterior Fossa Malformations, Hemangioma, Arterial Anomalies, Coarctation of the Aorta/ Cardiac Defects, and Eye Abnormalities) /Cutaneous Hemangioma-Vascular Complex Syndrome/Pascual-Castroviejo Type II Syndrome
Vykuntaraju K Gowda, Varunvenkat M Srinivasan
Indian Journal of Pediatrics
|
March 16, 2023
Ohtahara and West Syndrome due to Pyridox(am)ine-5-Phosphate Oxidase (PNPO) Deficiency with Novel Phenotype and Good Outcome without Pyridoxal-5'-Phosphate
Vykuntaraju K Gowda, Varunvenkat M Srinivasan
Indian Journal of Pediatrics
|
April 24, 2023
Recurrent Familial Acute Necrotizing Encephalopathy of Childhood (ANEC)
Vykuntaraju K Gowda, Varunvenkat M Srinivasan
Indian Journal of Pediatrics
|
May 23, 2022
A Treatable Cause of Global Developmental Delay with Autism Spectrum Disorder Due to Cobalamin Related Remethylation Disorder
Vykuntaraju K Gowda, Varunvenkat M Srinivasan
Indian Journal of Pediatrics
|
May 19, 2023
A Rare Genetic-Metabolic Cause of Epileptic Spasms: Dihydropyrimidine Dehydrogenase Deficiency
Vykuntaraju K Gowda, Varunvenkat M Srinivasan
Indian Journal of Pediatrics
|
December 7, 2025
Metronidazole-Induced Hepatotoxicity in Children with Cockayne Syndrome
Ankit Agrawal, Upasana Ghosh, Varunvenkat M Srinivasan
Neurology India
|
May 6, 2026
Primary Coenzyme Q10 Deficiency Type 7: A Potentially Treatable Cause of Developmental Delay
Varunvenkat M Srinivasan, Mayank Nilay, Rani Manisha
Clinical Dysmorphology
|
May 28, 2026
Integrating Face2Gene analysis in the diagnosis of Van den Ende-Gupta syndrome caused by a novel SCARF2 mutation with expanded skeletal and cardiac features
Varunvenkat M Srinivasan, Mayank Nilay, Rani Manisha
Indian Journal of Pediatrics
|
January 29, 2020
Waardenburg Syndrome Type I
Vykuntaraju K Gowda, Sahana Srinivas, Varunvenkat M Srinivasan
Indian Journal of Pediatrics
|
April 21, 2023
Lathosterolosis - A Rare Treatable Cause for Global Developmental Delay, Cataract, and Liver Dysfunction Masquerading as Galactosemia
Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Uddhav Kinhal
Page
of 12