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Profil bibliographique

Achanya Palayullakandi

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

19Publications signalées
84Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Autism Spectrum Disorder ResearchChild Nutrition and Feeding IssuesLymphoma Diagnosis and TreatmentLung Cancer Diagnosis and TreatmentFolate and B Vitamins Research

Les publications récentes

Accès ouvert 2026 article OpenAlex

Biochemical Trends During Chelation Therapy in Children with Neuro-Wilson Disease: A Prospective Observational Case Series

Pradeep Kumar Gunasekaran, Achanya Palayullakandi, Arushi Gahlot Saini, Renu Suthar et autres

A bstract Monitoring copper metabolism during chelation therapy in children with neuro-Wilson disease (NWD) remains challenging, particularly given inter-individual variability and heterogeneous treatment strategies. In this prospective observational case series conducted over 18 months, serial biochemical parameters were evaluated in ten children …

us, in (code pays fourni par la source)

0 citations Journal of Pediatric Neurosciences
Accès ouvert 2026 article OpenAlex

Development and Validation of a Comprehensive Acute Encephalitis Syndrome Severity Score in Children with Acute Encephalitis Syndrome

Indar Kumar Sharawat, Prateek K Panda, Vyas Kumar Rathaur, Achanya Palayullakandi et autres

Background and aims: No comprehensive scoring system is currently available to predict functional neurological outcomes in children with acute encephalitis syndrome (AES).We therefore developed and validated a score specifically tailored for these children.Patients and methods: We developed the comprehensive acute encephalitis syndrome …

in (code pays fourni par la source)

0 citations Indian Journal of Critical Care Medicine
Accès ouvert 2025 article OpenAlex

Biallelic Mutations in ADAM22 Presenting as Ohtahara Syndrome in an Indian Family: Expanding the Electroclinical Phenotype of ADAM22-Related Neurologic Disorder

Prateek Kumar Panda, Achanya Palayullakandi, Diksha Gupta, Suthiraj Sopanam et autres

Dear Editor, Epilepsy is frequently associated with ion channel gene mutations, but other genetic defects, including those in the Leucine-rich glioma inactivated-1-A disintegrin and metalloproteinase (LGI1-ADAM22/ADAM23) complex, also contribute to complex developmental epileptic encephalopathies.This complex, involving catalytically inactive ADAM22 and ADAM23, regulates …

in (code pays fourni par la source)

1 citation Annals of Indian Academy of Neurology
Accès ouvert 2025 article OpenAlex

Opsoclonus Myoclonus Ataxia Syndrome: An Atypical Presentation of Tuberculous Meningitis

Diksha Gupta, Achanya Palayullakandi, Suthiraj Sopanam, Prateek Kumar Panda et autres

Opsoclonus myoclonus ataxia syndrome (OMAS) is a rare neuroinflammatory disorder that is typically associated with paraneoplastic and postinfectious processes. Opsoclonus myoclonus ataxia syndrome has not been previously reported in association with tuberculous meningitis (TBM). This report presents a unique case in which …

in (code pays fourni par la source)

1 citation American Journal of Tropical Medicine and Hygiene

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