Anita G. Cairns
South Brisbane, QLD, Australia
Last Updated: 09/26/2026
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Found 29 publications
Strategic consensus on the clinical translation of advanced therapies in paediatric rare neurological disorders.
Journal: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
Published: February 05, 2026
Monoallelic POLR3A Variants Cause Early-Onset Peripheral Neuropathy.
Journal: Annals of neurology
Published: August 25, 2025
Confirmatory long-term efficacy and safety results of ataluren in patients with nmDMD from Study 041, an international, randomized, double-blind, placebo-controlled, Phase III trial.
Journal: Journal of comparative effectiveness research
Published: August 22, 2025
Gestational Age at Birth and Clinical Manifestations of Spinal Muscular Atrophy.
Journal: Neurology
Published: June 27, 2025
Neurodevelopmental screening in children with early-onset spinal muscular atrophy in the treatment era: a strengths-based cohort study.
Journal: Brain communications
Published: February 07, 2025
Effect of creatine monohydrate on motor function in children with facioscapulohumeral muscular dystrophy: A multicenter, randomized, double-blind placebo-controlled crossover trial.
Journal: Pharmacotherapy
Published: November 02, 2024
Heterozygous loss-of-function variants in SPTAN1 cause an early childhood onset distal myopathy.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 15, 2024
Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features.
Journal: medRxiv : the preprint server for health sciences
Published: October 07, 2024
Transition of patients with Duchenne muscular dystrophy from paediatric to adult care: An international Delphi consensus study.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: July 05, 2024
Three novel missense variants in two families with JAG2-associated limb-girdle muscular dystrophy.
Journal: Neuromuscular disorders : NMD
Published: May 15, 2024
A contemporary analysis of the Australian clinical and genetic landscape of spinal muscular atrophy: a registry based study.
Journal: The Lancet regional health. Western Pacific
Published: April 07, 2024
An Evaluation of an Australian Pediatric Neuromuscular Transition Model.
Journal: Pediatric neurology
Published: March 19, 2024
Last Updated: 09/26/2026