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BMJ Case Reports|December 12, 2025
Acute leukoencephalopathy with restricted diffusion (ALERD) in a toddler: A diagnostic challenge unmasking hereditary sensory autonomic neuropathy type 4Vykuntaraju K Gowda, Archana Varghese, Uddhava V Kinhal, et al.
Annals of Indian Academy of Neurology|March 22, 2025
Unmasking Osmotic Demyelination Syndrome/Extrapontine Myelinolysis in Acute Intermittent Porphyria: Preventable Complications-Challenges in Diagnosis and ManagementVykuntaraju K Gowda, Priyanka A Nayak, Uddhava V Kinhal, et al.
Brain & Development|August 21, 2025
Treatable and preventable causes of inborn errors of metabolism: Cohort of neurotransmitter disorders in children from IndiaVykuntaraju K Gowda, Annsmol P Markose, Varunvenkat M Srinivasan, et al.
American Journal of Medical Genetics. Part A|October 18, 2024
Expanding the Phenotype of NRROS -Related SENEBAC SyndromeVarunvenkat M Srinivasan, Vykuntaraju K Gowda, Annsmol P Markose, et al.
Indian Pediatrics|April 22, 2025
Cannabidiol in Drug-Resistant Epilepsy (DRE) in Children: A Retrospective StudyVykuntaraju K Gowda, Halima Simin, Uddhava V Kinhal, et al.
Clinical Dysmorphology|November 6, 2025
USP18 gene mutation associated with recurrent encephalopathy, intracranial calcification, and microcephaly: case report, long-term follow-up, and literature reviewVykuntaraju K Gowda, Varunvenkat M Srinivasan, Archana Varghese, et al.
BMJ Case Reports|September 26, 2025
Hypomagnesaemia with secondary hypocalcaemia due to a novel TRPM6 mutationVykuntaraju K Gowda, Rajesh R N, Uddhava V Kinhal, et al.
American Journal of Medical Genetics. Part A|March 25, 2025
Expanding the Phenotypic Spectrum of DPH2-Related DisorderVykuntaraju K Gowda, Varunvenkat M Srinivasan, Uddhava V Kinhal, et al.
Emerging Infectious Diseases|March 23, 2023
Association of Scrub Typhus in Children with Acute Encephalitis Syndrome and Meningoencephalitis, Southern IndiaTina Damodar, Bhagteshwar Singh, Namratha Prabhu, et al.
Annals of Clinical and Translational Neurology|August 9, 2023
Pure cerebellar ataxia due to bi-allelic PRDX3 variants including recurring p.Asp202AsnStephanie Efthymiou, Luiz E Novis, Georgios Koutsis, et al.
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