Chi-ren Tsai
1650, Taiwan Boulevard Sec. 4, Taichung 407220
Taitung, TNQ 40722, Taiwan
Taitung, TNQ 40722, Taiwan
Last Updated: 09/26/2026
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Found 30 publications
Neurodevelopmental SHQ1 variants navigate the control of apoptosis, endoplasmic reticulum stress, and oxidative stress in neuroblastoma cells.
Journal: Neuroscience
Published: April 08, 2025
Refining the Phenotypic and Genotypic Spectrum of WDR73-Related Galloway-Mowat Syndrome: A Case Series and Systematic Review.
Journal: Neurology. Genetics
Published: February 04, 2025
Genotype-phenotype variations in PURA syndrome: Asian and non-Asian perspectives from a systematic review.
Journal: Orphanet journal of rare diseases
Published: December 27, 2024
Cerebellar atrophy in genetic epileptic encephalopathies: A cohort study and a systematic review.
Journal: Seizure
Published: May 07, 2024
Resolving unsolved whole-genome sequencing data in paediatric neurological disorders: a cohort study.
Journal: Archives of disease in childhood
Published: February 10, 2024
Long-Term Outcome of Pediatric Patients with Anti-NMDA Receptor Encephalitis in a Single Center.
Journal: Children (Basel, Switzerland)
Published: December 04, 2022
Clinico-Radiological Phenotype of UBTF c.628G>A Pathogenic Variant-Related Neurodegeneration in Childhood: A Case Report and Literature Review
Journal: Brain sciences
Published: July 10, 2022
Intrafamilial phenotypic variability in TBC1D24-TLDc homozygous pathogenic variant-related developmental and epileptic encephalopathy.
Journal: Clinical neurology and neurosurgery
Published: September 04, 2021
Frasier Syndrome: A Rare Cause of Refractory Steroid-Resistant Nephrotic Syndrome.
Journal: Children (Basel, Switzerland)
Published: July 02, 2021
Diagnostic yield and treatment impact of whole-genome sequencing in paediatric neurological disorders.
Journal: Developmental medicine and child neurology
Published: September 23, 2020
Last Updated: 09/26/2026