Victoria Casero-Rodriguez
VIC, Australia
Last Updated: 09/26/2026
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Found 10 publications
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory services.
Journal: European journal of medical genetics
Published: January 23, 2022
Anti-voltage-Gated Potassium Channel (VGKC) Antibodies and Acquired Neuromyotonia in Patients with Immune Dysregulation, Polyendocrinopathy, Enteropathy X-Lined (IPEX) Syndrome.
Journal: Journal of clinical immunology
Published: June 09, 2021
Aberrant splicing and transcriptional activity of TPP1 result in CLN2-like disorder.
Journal: European journal of medical genetics
Published: January 25, 2021
The severe epilepsy syndromes of infancy: A population-based study.
Journal: Epilepsia
Published: November 05, 2020
Neuronal ceroid lipofuscinosis type 2: an Australian case series.
Journal: Journal of paediatrics and child health
Published: October 15, 2019
Cerebral hypomyelination associated with biallelic variants of FIG4.
Journal: Human mutation
Published: August 21, 2018
Acute spinal cord syndrome secondary to venous congestion.
Journal: Neurology
Published: September 21, 2016
SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures.
Journal: Neurology
Published: December 16, 2014
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
Journal: Nature genetics
Published: December 28, 2012
Guillain-Barré syndrome following pandemic (H1N1) 2009 influenza A immunisation in Victoria: a self-controlled case series.
Journal: The Medical journal of Australia
Published: November 21, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026