Dian K. Nurputra

Yogyakarta, YO, Indonesia

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 31 publications

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.

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.

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.

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

Journal: Indian journal of pediatrics

Published: March 08, 2025

Identification of volatile organic compound as a novel modality for cervical cancer detection.

Identification of volatile organic compound as a novel modality for cervical cancer detection.

Journal: Obstetrics & gynecology science

Published: January 16, 2025

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

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

Journal: Annals of Indian Academy of Neurology

Published: October 29, 2024

Performance of cellulose-based card for direct genetic testing of spinal muscular atrophy.

Performance of cellulose-based card for direct genetic testing of spinal muscular atrophy.

Journal: BMC biotechnology

Published: September 22, 2024

Developmental outcome in infancy after epilepsy surgery and its associated factors: A systematic review and meta-analysis.

Developmental outcome in infancy after epilepsy surgery and its associated factors: A systematic review and meta-analysis.

Journal: Epilepsy & behavior : E&B

Published: August 23, 2024

Development of a Mobile-Based Personal Health Record for Pediatric Attention-Deficit/Hyperactivity Disorder Management: Protocol for a Study Based on Action Research Design.

Development of a Mobile-Based Personal Health Record for Pediatric Attention-Deficit/Hyperactivity Disorder Management: Protocol for a Study Based on Action Research Design.

Journal: JMIR research protocols

Published: May 04, 2024

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.

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

Published: February 09, 2024

Association between glaucoma susceptibility with combined defects in mitochondrial oxidative phosphorylation and fatty acid beta oxidation.

Association between glaucoma susceptibility with combined defects in mitochondrial oxidative phosphorylation and fatty acid beta oxidation.

Journal: Molecular aspects of medicine

Published: June 28, 2023

A Brief Analysis on Clinical Severity of Mandibulofacial Dysostosis Guion-Almeida Type.

A Brief Analysis on Clinical Severity of Mandibulofacial Dysostosis Guion-Almeida Type.

Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association

Published: November 01, 2022

A systematic review on Treacher Collins syndrome: Correlation between molecular genetic findings and clinical severity.

A systematic review on Treacher Collins syndrome: Correlation between molecular genetic findings and clinical severity.

Journal: Clinical genetics

Published: August 17, 2022

Showing 1-12 of 31

Last Updated: 09/26/2026