Commentary

por Gowda, Vykuntaraju K., Srinivas, Sahana
Publicado 2014

Neurological Manifestations of Congenital Cytomegalovirus Infection at a Tertiary Care Centre from Southern India

por Gowda, Vykuntaraju K., Kulhalli, Preeti, Vamyanmane, Dhananjaya K.
Publicado 2021

Ohtahara syndrome associated with hemimegalencephaly and intracranial lipoma

por Gowda, Vykuntaraju K., Bhat, Ashwini, Bhat, Maya, Ramaswamy, Premalatha
Publicado 2015

Etiological Profile of Afebrile Seizures in Infants in a Tertiary Care Center from southern India

por Gowda, Vykuntaraju K., Kulhalli, Preeti, Benakappa, Naveen, Benakappa, Asha
Publicado 2019

Childhood Myocerebrohepatopathy Spectrum Disorder due to Polymerase Gamma Pathogenic Variant

por Gowda, Vykuntaraju K., Srinivasan, Varunvenkat M., Shivappa, Sanjay K.
Publicado 2021

Childhood movement disorders: Clinicoetiological pattern and long-term follow-up at tertiary care center from South India

por Parameshwarappa, Navya N., Gowda, Vykuntaraju K., Shivappa, Sanjay K.
Publicado 2023

Paralytic rabies following cat scratch and intra-dermal anti-rabies vaccination

por Gowda, Vykuntaraju K., Basavaraja, G. V., Reddy, Hamsa, Ramaswamy, Premalatha
Publicado 2014

Giant melanocytic nevi with neurocutaneous melanosis masquerading as neurofibromas

por Gowda, Vykuntaraju K., Basude, Anita, Srinivas, Sahana M., Bhat, Maya
Publicado 2016

Mucolipidosis Type II Secondary to GNPTAB Gene Deletion from India

por Gowda, Vykuntaraju K., Raghavan, Varun V., Bhat, Meenakshi, Benakappa, Asha
Publicado 2017

Sandhoff Disease without Hepatosplenomegaly Due to Hexosaminidase B Gene Mutation

por Gowda, Vykuntaraju K., Amoghimath, Raghavendraswami, Srinivasan, Varun M., Bhat, Maya
Publicado 2017

Homocystinuria with Cerebral Venous Sinus Thrombosis: Excellent Recovery with Intravenous Recombinant Tissue Plasminogen Activator

por Gowda, Vykuntaraju K, Nanjundappa, Raghunath C, Pendharkar, Hima, Benakappa, Naveen
Publicado 2017

Case of Childhood Ataxia with Central Nervous System Hypomyelination with a Novel Mutation in EIF2B3 gene

por Gowda, Vykuntaraju K., Srinivasan, Varun M., Bhat, Maya, Benakappa, Asha
Publicado 2017

Spectrum of Nonepileptic Paroxysmal Events in Children from Southern India

por Gowda, Vykuntaraju K, Amoghimath, Raghavendraswami, Benakappa, Naveen, Shivappa, Sanjay K
Publicado 2019

Osteoporosis Pseudoglioma Syndrome

por Gowda, Vykuntaraju K, Vegda, Hemadri, Shivappa, Sanjay K, Benakappa, Naveen
Publicado 2020

Macrophagic Myofasciitis: A Report of Two South Indian Infants

por Gowda, Vykuntaraju K, Srinivasan, Varunvenkat M, Muthane, Yasha, Narayanappa, Gayathri
Publicado 2020

Rare Cause of West syndrome secondary to Tubulinopathy due to Congenital Symmetric Circumferential Skin Creases (CSCSC) Kunze Type due to a Novel Variant in MAPRE2 Gene

por Gowda, Vykuntaraju K., Srinivasan, Varunvenkat M., Reddy, Varsha, Bhat, Maya
Publicado 2022

Anti-NMDAR Encephalitis Presenting as Stroke-like Episodes in Children: A Case Series from a Tertiary Care Referral Centre from Southern India

por Gowda, Vykuntaraju K, Vignesh, Sukanya, Natarajan, Balamurugan, Shivappa, Sanjay K
Publicado 2021

Krabbe Disease with Normal Enzyme Assay with a Pathogenic Variant in GALC Gene—A Report of Two Indian Cases

por Gowda, Vykuntaraju K., Srinivasan, Varunvenkat M., Bhat, Maya, Shivappa, Sanjay K.
Publicado 2021

Familial Global Developmental Delay Secondary to β-Mannosidosis

por Gowda, Vykuntaraju K., Nagarajan, Balamurugan, Suryanarayana, Srividya G., Srinivasan, Varunvenkat M.
Publicado 2021

Treatable Neurodegenerative Disorder: Cerebral Folate Transport Deficiency––Two Children from Southern India

por Gowda, Vykuntaraju K, Natarajan, Balamurugan, Srinivasan, Varunvenkat M, Shivappa, Sanjay K
Publicado 2021