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Orphanet Journal of Rare Diseases
|
March 28, 2026
Burden and severity of inherited monoamine neurotransmitter rare genetic disorders in India
Runa Hamid, Vykuntaraju K Gowda, Lloyd Tauro, et al.
Indian Journal of Dermatology
|
May 11, 2026
The Therapeutic Challenge in a Rare Case of Immunoglobulin A Type of Epidermolysis Bullosa Acquisita
Shreya K Gowda, Biswanath Behera, Madhusmita Sethy, et al.
Indian Pediatrics
|
July 23, 2022
Rhizomelic Chondro-Dysplasia Punctate (RCDP)
Vykuntaraju K Gowda, Varunvenkat M Srinivasa, Dhananjaya K Vamyanmane
Indian Journal of Pediatrics
|
March 30, 2018
Dihydropteridine Reductase Deficiency: A Treatable Neurotransmitter Movement Disorder Masquerading as Refractory Epilepsy Due to Novel Mutation
Vykuntaraju K Gowda, Hemadriben Vegda, Naveen Benakappa, et al.
Journal of Pediatric Neurosciences
|
September 14, 2019
Etiological Profile of Afebrile Seizures in Infants in a Tertiary Care Center from southern India
Vykuntaraju K Gowda, Preeti Kulhalli, Naveen Benakappa, et al.
BMJ Case Reports
|
April 29, 2014
Lead aVR: beyond 'No man's land'
Bhupinder Singh, Amjad Ali, Vivek Singla, et al.
Indian Journal of Pediatrics
|
June 25, 2021
Etiological Pattern of Movement Disorders in Children
Navya N Parameshwarappa, Vykuntaraju K Gowda, Sanjay K Shivappa
Annals of Indian Academy of Neurology
|
April 1, 2022
Childhood Myocerebrohepatopathy Spectrum Disorder due to Polymerase Gamma Pathogenic Variant
Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Sanjay K Shivappa
Indian Dermatology Online Journal
|
July 25, 2025
A Brief Review of Scalp Biopsy and its Interpretation
Shreya K Gowda, Biswanath Behera, Madhusmita Sethy, et al.
Clinical and Experimental Dermatology
|
July 29, 2025
Intertriginous and periorificial vegetating paradigm
Shreya K Gowda, Rhea Ahuja, Sudheer Arava, et al.
Page
of 35
Search research articles
Search
Showing results (61-70 of 343) with videos related to
Sort By:
Page
of 35
Orphanet Journal of Rare Diseases
|
March 28, 2026
Burden and severity of inherited monoamine neurotransmitter rare genetic disorders in India
Runa Hamid, Vykuntaraju K Gowda, Lloyd Tauro, et al.
Indian Journal of Dermatology
|
May 11, 2026
The Therapeutic Challenge in a Rare Case of Immunoglobulin A Type of Epidermolysis Bullosa Acquisita
Shreya K Gowda, Biswanath Behera, Madhusmita Sethy, et al.
Indian Pediatrics
|
July 23, 2022
Rhizomelic Chondro-Dysplasia Punctate (RCDP)
Vykuntaraju K Gowda, Varunvenkat M Srinivasa, Dhananjaya K Vamyanmane
Indian Journal of Pediatrics
|
March 30, 2018
Dihydropteridine Reductase Deficiency: A Treatable Neurotransmitter Movement Disorder Masquerading as Refractory Epilepsy Due to Novel Mutation
Vykuntaraju K Gowda, Hemadriben Vegda, Naveen Benakappa, et al.
Journal of Pediatric Neurosciences
|
September 14, 2019
Etiological Profile of Afebrile Seizures in Infants in a Tertiary Care Center from southern India
Vykuntaraju K Gowda, Preeti Kulhalli, Naveen Benakappa, et al.
BMJ Case Reports
|
April 29, 2014
Lead aVR: beyond 'No man's land'
Bhupinder Singh, Amjad Ali, Vivek Singla, et al.
Indian Journal of Pediatrics
|
June 25, 2021
Etiological Pattern of Movement Disorders in Children
Navya N Parameshwarappa, Vykuntaraju K Gowda, Sanjay K Shivappa
Annals of Indian Academy of Neurology
|
April 1, 2022
Childhood Myocerebrohepatopathy Spectrum Disorder due to Polymerase Gamma Pathogenic Variant
Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Sanjay K Shivappa
Indian Dermatology Online Journal
|
July 25, 2025
A Brief Review of Scalp Biopsy and its Interpretation
Shreya K Gowda, Biswanath Behera, Madhusmita Sethy, et al.
Clinical and Experimental Dermatology
|
July 29, 2025
Intertriginous and periorificial vegetating paradigm
Shreya K Gowda, Rhea Ahuja, Sudheer Arava, et al.
Page
of 35