Vykuntaraju K Gowda
95PUBLICATIONS
114CO-AUTHORS

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Publications (95)
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|Jan 22, 2026
Unusual association: Sturge-Weber syndrome with Klippel-Trenaunay syndrome.Vykuntaraju K Gowda, Muskan P Verma, Deepthi Krishna
|Jan 19, 2026
CTC1 mutation causing cerebro-retinal microangiopathy with calcifications and cysts type 1, masquerading as TORCH Infection.Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Himani Reddy Pandey
|Jan 09, 2026
Hypoglycorrhachia: From Glucose Transporter Type 1 Deficiency Syndrome (GLUT1DS) to Pyridox(am)ine-5'-Phosphate Oxidase (PNPO) Deficiency: A Fifteen-Year Diagnostic Journey Redefined by Genomic Insights.Vykuntaraju K Gowda, Archana Varghese, Prem Kumar
|Dec 23, 2025
Biotinidase deficiency deterioration in the second decade, presenting as treatable cerebellar ataxia and encephalopathy masquerading as demyelination.Vykuntaraju K Gowda, Anagha C Badrinath, Varunvenkat M Srinivasan
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Frequent Collaborators
6 joint publications
Henry Houlden
5 joint publications
Mariasavina Severino
4 joint publications
Stephanie Efthymiou
4 joint publications
Reza Maroofian
2 joint publications
Kshitij Mankad
2 joint publications
Susan Blaser
2 joint publications
Varunvenkat M Srinivasan
2 joint publications
Rauan Kaiyrzhanov
2 joint publications
Pasquale Striano
2 joint publications
Sniya Sudhakar