Agung Triono

Whole-exome sequencing in pediatric drug-resistant epilepsy: diagnostic yield and clinical impact in a resource-limited setting.

Journal: Neurogenetics

Published: May 22, 2026

Association between phenotypes and genotype of developmental and epileptic encephalopathy in next-generation sequencing methods in infants: A scoping review.

Journal: The Medical journal of Malaysia

Published: July 31, 2025

ADK deficiency without hypermethioninemia presenting as intractable epilepsy: a rare neurometabolic case and literature review.

Journal: Neurogenetics

Published: July 28, 2025

Diagnostic Challenges in Detecting Rubella Viral RNA in Cases of Congenital Rubella Syndrome Using RT-PCR in the Era of Elimination.

Journal: The Pediatric infectious disease journal

Published: April 29, 2025

Bridging the gap: pyridoxine-dependent epilepsy (PDE-ALDH7A1) diagnosis and management in a low-resource setting.

Journal: Neurogenetics

Published: April 22, 2025

Diagnostic Value of the Cerebrospinal Fluid Heparin-binding Protein for Pediatric Bacterial Intracranial Infections.

Journal: Indian journal of pediatrics

Published: March 08, 2025

Expression of Human Myxovirus Resistance Protein 1 (MxA) in Shunt Infections.

Journal: Annals of Indian Academy of Neurology

Published: October 29, 2024

Exome sequencing facilitates personalized treatment in developmental and epileptic encephalopathy patients: transforming current clinical practice in Indonesia.

Journal: The Lancet regional health. Southeast Asia

Published: October 11, 2024

Longitudinal management in Duchenne muscular dystrophy with exon 63 duplication.

Journal: BMJ case reports

Published: October 01, 2024

Diagnostic Value of Serum Procalcitonin, CSF Neutrophil-to-lymphocyte Ratio, and CSF Lactate in Pediatric Bacterial Meningoencephalitis.

Journal: Annals of Indian Academy of Neurology

Published: May 12, 2024

Multidisciplinary approach on divergent outcomes in spinal muscular atrophies: comparing DYNC1H1 and SMN1 gene mutations.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Whole-exome sequencing in pediatric drug-resistant epilepsy: diagnostic yield and clinical impact in a resource-limited setting.

Whole-exome sequencing in pediatric drug-resistant epilepsy: diagnostic yield and clinical impact in a resource-limited setting.

Association between phenotypes and genotype of developmental and epileptic encephalopathy in next-generation sequencing methods in infants: A scoping review.

Association between phenotypes and genotype of developmental and epileptic encephalopathy in next-generation sequencing methods in infants: A scoping review.

ADK deficiency without hypermethioninemia presenting as intractable epilepsy: a rare neurometabolic case and literature review.

ADK deficiency without hypermethioninemia presenting as intractable epilepsy: a rare neurometabolic case and literature review.

Diagnostic Challenges in Detecting Rubella Viral RNA in Cases of Congenital Rubella Syndrome Using RT-PCR in the Era of Elimination.

Diagnostic Challenges in Detecting Rubella Viral RNA in Cases of Congenital Rubella Syndrome Using RT-PCR in the Era of Elimination.

Bridging the gap: pyridoxine-dependent epilepsy (PDE-ALDH7A1) diagnosis and management in a low-resource setting.

Bridging the gap: pyridoxine-dependent epilepsy (PDE-ALDH7A1) diagnosis and management in a low-resource setting.

Diagnostic Value of the Cerebrospinal Fluid Heparin-binding Protein for Pediatric Bacterial Intracranial Infections.

Diagnostic Value of the Cerebrospinal Fluid Heparin-binding Protein for Pediatric Bacterial Intracranial Infections.

Expression of Human Myxovirus Resistance Protein 1 (MxA) in Shunt Infections.

Expression of Human Myxovirus Resistance Protein 1 (MxA) in Shunt Infections.

Exome sequencing facilitates personalized treatment in developmental and epileptic encephalopathy patients: transforming current clinical practice in Indonesia.

Exome sequencing facilitates personalized treatment in developmental and epileptic encephalopathy patients: transforming current clinical practice in Indonesia.

Longitudinal management in Duchenne muscular dystrophy with exon 63 duplication.

Longitudinal management in Duchenne muscular dystrophy with exon 63 duplication.

Diagnostic Value of Serum Procalcitonin, CSF Neutrophil-to-lymphocyte Ratio, and CSF Lactate in Pediatric Bacterial Meningoencephalitis.

Diagnostic Value of Serum Procalcitonin, CSF Neutrophil-to-lymphocyte Ratio, and CSF Lactate in Pediatric Bacterial Meningoencephalitis.

Multidisciplinary approach on divergent outcomes in spinal muscular atrophies: comparing DYNC1H1 and SMN1 gene mutations.

Multidisciplinary approach on divergent outcomes in spinal muscular atrophies: comparing DYNC1H1 and SMN1 gene mutations.

Genetic exploration of Dravet syndrome: two case report.

Genetic exploration of Dravet syndrome: two case report.