Kristy Iskandar

8PUBLICATIONS
17CO-AUTHORS
Epidemiology not elsewhere classifiedInfant and child healthVirologyNeurology and neuromuscular diseasesDigital forensics
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Publications (8)

|Jan 16, 2026
ADK deficiency without hypermethioninemia presenting as intractable epilepsy: a rare neurometabolic case and literature review.

Agung Triono, Kristy Iskandar, Neti Nurani

|Sep 19, 2025
Bridging the gap: pyridoxine-dependent epilepsy (PDE-ALDH7A1) diagnosis and management in a low-resource setting.

Andika Priamas Nugrahanto, Agung Triono, Neti Nurani

|Apr 29, 2025
Diagnostic Challenges in Detecting Rubella Viral RNA in Cases of Congenital Rubella Syndrome Using RT-PCR in the Era of Elimination.

Elisabeth Siti Herini, Agung Triono, Kristy Iskandar

|May 25, 2023
De novo mutation of the TSC2 gene in patient with Tuberous Sclerosis Complex-Associated Neuropsychiatric Disorders (TAND) Phenotype: a case report.

Agung Triono, Elisabeth S Herini, Kristy Iskandar

|Oct 31, 2022
Dp71 and intellectual disability in Indonesian patients with Duchenne muscular dystrophy.

Kristy Iskandar, Agung Triono, Sunartini

|Oct 17, 2022
Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report.

Kristy Iskandar, Sunartini, Farida Niken Astari

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Frequent Collaborators

5 joint publications

Agung Triono

3 joint publications

Elisabeth Siti Herini

2 joint publications

Dian Kesumapramudya Nurputra

2 joint publications

Irma Sri Hidayati