Vykuntaraju K Gowda

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

Vykuntaraju K Gowda, Preeti Kulhalli, N. Benakappa, 2019, Journal of pediatric neurosciences.

Idiopathic intracranial hypertension following measles vaccine

Vykuntaraju K Gowda, Bharathi V. Reddy, Hamsa Reddy, 2014, Journal of Pediatric Neurology.

Neuronal Ceroid Lipofuscinosis: Clinical and Laboratory Profile in Children from Tertiary Care Centre in South India

Hemadri Vegda, Vykuntaraju K Gowda, S. Balu, 2020, Journal of Pediatric Genetics.

Caregiver-reported health-related quality of life of children with cerebral palsy and their families and its association with gross motor function: A South Indian study

Vykuntaraju K Gowda, N. Benakappa, A. Benakappa, 2016, Journal of neurosciences in rural practice.

A Randomized Control Trial of Botulinum Toxin A Administration under Ultrasound Guidance against Manual Palpation in Spastic Cerebral Palsy

Vykuntaraju K Gowda, Sanjay K. Shivappa, Prakruthi Kaushik, 2018, Journal of pediatric neurosciences.

Kearns-Sayre syndrome presenting as epilepsia partialis continua in a child

Vykuntaraju K Gowda, Bharathi V. Reddy, P. Ramaswamy, 2015 .

Biallelic ADAM22 pathogenic variants cause progressive encephalopathy and infantile-onset refractory epilepsy

H. Mefford, A. Paetau, P. Striano, 2022, Brain : a journal of neurology.

Lamellar ichthyosis with severe vitamin D deficiency rickets and myopathy in siblings

Vykuntaraju K Gowda, Sanjay K. Shivappa, P. Ramaswamy, 2014, Journal of Pediatric Neurology.

Recurrent Bilateral Lower Motor Neuron Type of Facial Palsy with Hearing Impairment: Hyperphosphatemic Familial Tumoral Calcinosis

Vykuntaraju K Gowda, S. Srinivas, Gurudatta B. Vishwanathan, 2022, Journal of Pediatric Genetics.

Epileptic Spasms-West syndrome secondary to Dravet syndrome due to SCN gene mutation from India

Hemadri Vegda, Vykuntaraju K Gowda, N. Benakappa, 2021 .

A Treatable Cause of Global Developmental Delay with Epileptic Spasm and Delayed Myelination Due to Cobalamin-Related Remethylation Disorder

Jitendra Saini, Vykuntaraju K Gowda, Varunvenkat M Srinivasan, 2021, Indian Journal of Pediatrics.

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

Vykuntaraju K Gowda, Preeti Kulhalli, Dhananjaya K. Vamyanmane, 2021, Journal of Neurosciences in Rural Practice.

Cohort of Phenotype, Genotype, and Outcome of SCN Developmental and Epileptic Encephalopathies from Southern Part of India

S. Chikara, Hemadri Vegda, Vykuntaraju K Gowda, 2021, Journal of Pediatric Genetics.

Recurrent Stroke Like Episodes Secondary to Ornithine Transcarbamylase Deficiency

Vykuntaraju K Gowda, N. Benakappa, Priyansh Gupta, 2020, The Indian Journal of Pediatrics.

H. Otsubo, L. Lingappa, T. Hershkovitz, 2020, Epilepsia.

Acute flaccid myelitis-Clustering of polio-like illness in the tertiary care centre in Southern India.

J. Saini, Vykuntaraju K Gowda, A. Benakappa, 2018, Journal of tropical pediatrics.

Infantile Systemic Hyalinosis Presenting as Pseudo-Paralysis in Infancy: Study of Six Cases

Vykuntaraju K Gowda, P. Gupta, Sanjay K. Shivappa, 2021, Journal of Pediatric Genetics.

Vitamin B12 deficiency presenting as infantile meningoencephalitis

Vykuntaraju K Gowda, Varunvenkat M Srinivasan, K. Ashwini, 2022, Karnataka Paediatric Journal.

Nutritional Vitamin-B12 deficiency masquerading as a mitochondrial disorder

Vykuntaraju K Gowda, Varunvenkat M Srinivasan, S. Chauhan, 2022, Karnataka Paediatric Journal.

Biotin Thiamin Responsive Basal Ganglia Disease in Siblings

Vykuntaraju K Gowda, N. Benakappa, Varunvenkat M Srinivasan, 2018, The Indian Journal of Pediatrics.

Bilateral Striatal Necrosis with Polyneuropathy with a Novel SLC25A19 (Mitochondrial Thiamine Pyrophosphate Carrier OMIMI*606521) Mutation: Treatable Thiamine Metabolic Disorder—A Report of Two Indian Cases

Vykuntaraju K Gowda, Varunvenkat M Srinivasan, M. Bhat, 2019, Neuropediatrics.

A Treatable Cause of Myelopathy: Biotinidase Deficiency Presenting as Acute Flaccid Paralysis.

Vykuntaraju K Gowda, Sanjay K. Shivappa, Dhananjaya K. Vamyanmane, 2020, Journal of pediatric genetics.

Corticotrophin-ACTH in Comparison to Prednisolone in West Syndrome – A Randomized Study

Vindhya Narayanaswamy, Vykuntaraju K Gowda, N. Benakappa, 2018, The Indian Journal of Pediatrics.

Mucolipidosis Type II Secondary to GNPTAB Gene Deletion from India

Vykuntaraju K Gowda, A. Benakappa, M. Bhat, 2017, Journal of pediatric neurosciences.

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

Vykuntaraju K Gowda, G. Basavaraja, Hamsa Reddy, 2014, Journal of pediatric neurosciences.

Brown−Vialetto−Van Laere and Fazio−Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritance

P. Varalakshmi, S. Efthymiou, H. Houlden, 2020, European journal of neurology.

Fazio-Londe syndrome in siblings from India with different phenotypes

P. Varalakshmi, B. Ashokkumar, Tamilarasan Udhayabanu, 2018, Brain and Development.

SLC52A2 [p.P141T] and SLC52A3 [p.N21S] causing Brown-Vialetto-Van Laere Syndrome in an Indian patient: First genetically proven case with mutations in two riboflavin transporters.

P. Varalakshmi, B. Ashokkumar, H. Said, 2016, Clinica chimica acta; international journal of clinical chemistry.

Tay-Sachs Disease Presenting as Refractory Epilepsy with Autistic Regression Secondary to a Novel Mutation in HEXA Gene

Vykuntaraju K Gowda, A. Benakappa, Varunvenkat M Srinivasan, 2018, The Indian Journal of Pediatrics.

Mineralizing Angiopathy with Basal Ganglia Stroke after Minor Trauma: Case Series Including Two Familial Cases

Vykuntaraju K Gowda, A. Benakappa, S. Sajjan, 2018, Journal of pediatric neurosciences.

A Rare Association of Sturge Weber Syndrome with Neurofibromatosis Type-1

Vykuntaraju K Gowda, Varunvenkat M Srinivasan, H. Chadaga, 2018, The Indian Journal of Pediatrics.

Association of Anti N-methyl-D-aspartate (NMDA) Receptor Encephalitis with Chediak-Higashi Syndrome

Vykuntaraju K Gowda, N. Bhardwaj, S. Srinivas, 2019, Indian Pediatrics.

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

Vykuntaraju K Gowda, Sanjay K. Shivappa, Varunvenkat M Srinivasan, 2021, Journal of Pediatric Neurosciences.

Midface toddler excoriation syndrome (MiTES) can be caused by autosomal recessive biallelic mutations in a gene for congenital insensitivity to pain, PRDM12

M. Nahorski, Vykuntaraju K Gowda, C. Moss, 2018, The British journal of dermatology.

Basal Ganglia Autoimmune Encephalitis Following Leptospirosis.

Vykuntaraju K Gowda, Sanjay K. Shivappa, M. Bhat, 2022, Neurology India.

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

Vykuntaraju K Gowda, Varunvenkat M Srinivasan, M. Bhat, 2021, Annals of Indian Academy of Neurology.

Case Series of Infantile Tremor Syndrome in Tertiary Care Paediatric Centre from Southern India

Vykuntaraju K Gowda, N. Benakappa, A. Benakappa, 2017, Journal of tropical pediatrics.

Infantile Tremor Syndrome (ITS) Presenting as Diabetic Ketoacidosis (DKA)

Vykuntaraju K Gowda, Sanjay K. Shivappa, Kiruthiga Sugumar, 2019, The Indian Journal of Pediatrics.

Mid‐face toddler excoriation syndrome (MiTES): a new paediatric diagnosis

C. Owen, Vykuntaraju K Gowda, R. Hiremagalore, 2017, Clinical and experimental dermatology.

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

H. Pendharkar, Vykuntaraju K Gowda, N. Benakappa, 2017, Iranian journal of child neurology.

Correspondence

Debopam Samanta, D. Dayal, I. Sharawat, 2020 .

Mitochondrial Membrane Protein Associated Neurodegeneration (MPAN) with a Novel C19orf12 Mutation in the First Decade of Life

Vykuntaraju K Gowda, Varunvenkat M Srinivasan, N. Kathrani, 2019, The Indian Journal of Pediatrics.

Profile of Indian Children with Childhood Ataxia and Central Nervous System Hypomyelination/Vanishing White Matter Disease: A Single Center Experience from Southern India

Vykuntaraju K Gowda, N. Benakappa, Sanjay K. Shivappa, 2020, Journal of Pediatric Genetics.

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

Vykuntaraju K Gowda, A. Benakappa, Varunvenkat M Srinivasan, 2017, Journal of Pediatric Neurosciences.

Epidemiology of Congenital Rubella Syndrome (CRS) in India, 2016-18, based on data from sentinel surveillance

R. K. Sachdeva, A. Bavdekar, M. Murhekar, 2020, PLoS neglected tropical diseases.

Siblings with Glutaric Aciduria Type 1 with Atypical Phenotype with Novel Pathogenic Variant in GCDH Gene

Vykuntaraju K Gowda, Varunvenkat M Srinivasan, M. Bhat, 2021, Journal of pediatric neurosciences.

Clinical, Demographic, and Electroencephalographic Profile of Hot-Water Epilepsy in Children

Vykuntaraju K Gowda, A. Benakappa, Sanjay K. Shivappa, 2021, Indian Journal of Pediatrics.

Novel ALDH3A2 mutations in structural and functional domains of FALDH causing diverse clinical phenotypes in Sjögren–Larsson syndrome patients

M. Keller, P. Varalakshmi, S. Efthymiou, 2021, Human mutation.

Oromandibular and Laryngeal Dystonia Secondary to Dystonia 6 Due to THAP1 Variant in a Child

Vykuntaraju K Gowda, Sanjay K. Shivappa, Varunvenkat M Srinivasan, 2021, Indian Journal of Pediatrics.

Clinical Profile and Outcome of Indian Children with Aromatic L-Amino Acid Decarboxylase Deficiency: A primary CSF Neurotransmitter Disorder Mimicking as Dyskinetic Cerebral Palsy

Hemadri Vegda, Vykuntaraju K Gowda, Sanjay K. Shivappa, 2020, Journal of Pediatric Genetics.

Clinical and Radiological Profiles, Treatment, and Outcome of Pediatric Acquired Demyelinating Disorders of Central Nervous System

Vykuntaraju K Gowda, N. Benakappa, A. Benakappa, 2019, Journal of pediatric neurosciences.

Multiple exostoses presenting with high cervical myelopathy in the first decade of life.

Vykuntaraju K Gowda, Praveen-kumar Srikanteswara, Rudra Prasad, 2014, Pediatric neurology.

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

Vykuntaraju K Gowda, Sanjay K. Shivappa, Navya N. Parameshwarappa, 2022, Journal of Neurosciences in Rural Practice.

Etiological Pattern of Movement Disorders in Children

Vykuntaraju K Gowda, Sanjay K. Shivappa, Navya N. Parameshwarappa, 2021, Indian Journal of Pediatrics.

Giant melanocytic nevi with neurocutaneous melanosis masquerading as neurofibromas

Vykuntaraju K Gowda, M. Bhat, S. Srinivas, 2016, Journal of pediatric neurosciences.

Case Series of Ethylmalonic Encephalopathy from Southern India

R. Christopher, Vykuntaraju K Gowda, M. Bhat, 2021, Journal of Pediatric Genetics.

Study of etiological profile of infantile and childhood focal seizures at a tertiary care centre in South India

Shivananda, Vykuntaraju K Gowda, Ramaswamy, 2013, Journal of Pediatric Neurology.

Predictors of non-traumatic coma in a pediatric cohort from a South Indian tertiary care center: Results of a multivariate analysis

Shivananda, Vykuntaraju K Gowda, P. Ramaswamy, 2014, Journal of Pediatric Neurology.

Alternating hemiplegia of childhood during acute episode of gastroenteritis

Vykuntaraju K Gowda, P. Ramaswamy, Sarala H.S. Gowda, 2013, Journal of Pediatric Neurology.

Clinicoradiological description of two children with hemiconvulsion-hemiplegia-epilepsy syndrome

Vykuntaraju K Gowda, P. Ramaswamy, Bhaskar V. Madivala, 2014, Journal of Pediatric Neurology.

Re-emergence of Tetanus: Epidemiological Features, Clinical Profile and Outcome from South India

Vykuntaraju K Gowda, A. Benakappa, Anusha Handral, 2016, The Indian Journal of Pediatrics.

Spectrum of Nonepileptic Paroxysmal Events in Children from Southern India

Vykuntaraju K Gowda, N. Benakappa, Sanjay K. Shivappa, 2019, Journal of Neurosciences in Rural Practice.

Macrophagic Myofasciitis: A Report of Two South Indian Infants

Vykuntaraju K Gowda, G. Narayanappa, Varunvenkat M Srinivasan, 2020, Journal of pediatric neurosciences.

Acute flaccid myelitis: cause, diagnosis, and management

Eliza M. Gordon-Lipkin, Elizabeth M. Wells, R. Scheuermann, 2020, The Lancet.

Sialidosis Type 1 with a Novel Mutation in the Neuraminidase-1 (NEU1) Gene

Vykuntaraju K Gowda, N. Benakappa, A. Benakappa, 2017, The Indian Journal of Pediatrics.

CASPR2-Mediated Autoimmune Encephalitis in a Toddler

A. Mahadevan, Vykuntaraju K Gowda, Sanjay K. Shivappa, 2020, Indian Pediatrics.

Clinical profile, predisposing factors, and associated co-morbidities of children with cerebral palsy in South India

Shivananda, Vykuntaraju K Gowda, Anil Kumar, 2015, Journal of pediatric neurosciences.

Atypical vanishing white matter disease with microcephaly and hepatosplenomegaly provoked after diphtheria pertussis tetanus vaccination

Mamatha, Vykuntaraju K Gowda, Prahalad Kumar, 2014, Journal of Pediatric Neurology online.

A case of Canavan disease with microcephaly

M. Faruq, Vykuntaraju K Gowda, C. Prasad, 2016, Brain and Development.

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

Vykuntaraju K Gowda, Sanjay K. Shivappa, S. Vignesh, 2021, Journal of pediatric neurosciences.

A Case of Juvenile Alexander Disease Presenting as Microcephaly

Vykuntaraju K Gowda, Varunvenkat M Srinivasan, M. Bhat, 2019, Indian Journal of Pediatrics.

Report of Two Siblings with Andermann Syndrome

Vykuntaraju K Gowda, Sanjay K. Shivappa, Varunvenkat M Srinivasan, 2020, The Indian Journal of Pediatrics.

Recent advances in cerebral palsy

Vykuntaraju K Gowda, 2020, Karnataka Pediatric Journal.

A Randomized Controlled Trial on the Study of Effectiveness and Safety of Hormonal (ACTH) Treatment Alone versus Hormonal (ACTH) with Levetiracetam for Epileptic Spasms

Vykuntaraju K Gowda, N. Benakappa, A. Benakappa, 2022, Journal of neurosciences in rural practice.

CERT1 mutations perturb human development by disrupting sphingolipid homeostasis

B. V. van Bon, R. Pfundt, L. Armengol, 2023, The Journal of clinical investigation.

Aicardi syndrome with type 2b interhemispheric cyst

Vykuntaraju K Gowda, Bharathi V. Reddy, P. Ramaswamy, 2013, Journal of Pediatric Epilepsy.

A Novel GCH1 Mutation in An Indian Child with GTP Cyclohydrolase Deficiency

Vykuntaraju K Gowda, A. Benakappa, Varunvenkat M Srinivasan, 2019, Indian Journal of Pediatrics.

Levetiracetam versus Phenobarbitone in Neonatal Seizures — A Randomized Controlled Trial

Vykuntaraju K Gowda, N. Benakappa, A. Benakappa, 2019, Indian Pediatrics.

Clinical and Laboratory Profile of Gangliosidosis from Southern Part of India

Vykuntaraju K Gowda, N. Benakappa, Priyansh Gupta, 2020, Journal of Pediatric Genetics.

Sandhoff Disease without Hepatosplenomegaly Due to Hexosaminidase B Gene Mutation

Vykuntaraju K Gowda, Varunvenkat M Srinivasan, M. Bhat, 2017, Journal of pediatric neurosciences.

Recessive VAMP1 mutations associated with severe congenital myasthenic syndromes - A recognizable clinical phenotype.

H. Lochmüller, A. Nalini, Vykuntaraju K Gowda, 2021, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Acquired immunodeficiency syndrome with subacute sclerosing panencephalitis.

Shivananda, Vykuntaraju K Gowda, V. Sukanya, 2012, Pediatric neurology.

Waardenburg Syndrome Type I

Vykuntaraju K Gowda, Varunvenkat M Srinivasan, S. Srinivas, 2020, The Indian Journal of Pediatrics.

Alternating Hemiplegia of Childhood: A Series of Genetically Confirmed Four Cases from Southern India with Review of Published Literature

Vykuntaraju K Gowda, N. Bhardwaj, A. Sardesai, 2020, Journal of Pediatric Genetics.

Sotos Syndrome Presenting without Gigantism

Vykuntaraju K Gowda, N. Benakappa, Sanjay K. Shivappa, 2020, Indian Journal of Pediatrics.

Canavan Disease: Clinical and Laboratory Profile from Southern Part of India

Vykuntaraju K Gowda, Sanjay K. Shivappa, M. Bhat, 2020, Annals of Indian Academy of Neurology.

Comorbidities and their relationship to subtype of cerebral palsy in a tertiary care hospital in South India

Vykuntaraju K Gowda, A. Benakappa, R. Amoghimath, 2016 .

Association of Scrub Typhus in Children with Acute Encephalitis Syndrome and Meningoencephalitis, Southern India

K. Thennarasu, T. Solomon, V. Ravi, 2023, Emerging infectious diseases.

Clinical Profile and Outcome in Children with Post Diphtheritic Paralysis in a Tertiary Care Hospital in Southern India

Vykuntaraju K Gowda, N. Benakappa, A. Benakappa, 2022, Iranian journal of child neurology.

A Randomized Control Trial of Botulinum Toxin A Administration under Ultrasound Guidance against Manual Palpation in Spastic Cerebral Palsy

Vykuntaraju K Gowda, Sanjay K. Shivappa, Rajeshwari Mannapur, 2018, Journal of pediatric neurosciences.

Intermittent Ataxia with Early Onset Absence Epilepsy in Glucose Transporter Type 1 Deficiency Syndrome.

Vykuntaraju K Gowda, Sukrita Sheshu, 2015, Indian pediatrics.