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A novel OPA1 mutation causing variable age of onset autosomal dominant optic atrophy plus in an Australian family.

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Cortical excitability changes distinguish the motor neuron disease phenotypes from hereditary spastic paraplegia.

European journal of neurology·2015

Overexpression of miR-210 is associated with SDH-related pheochromocytomas, paragangliomas, and gastrointestinal stromal tumours.

Endocrine-related cancer·2014

SPAST mutations in Australian patients with hereditary spastic paraplegia.

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Phase 2a Randomized Controlled Trial of TPN-101, A Nucleoside Reverse Transcriptase Inhibitor, in Progressive Supranuclear Palsy.

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Evolution of Epidemiological Studies in Movement Disorders.

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Apathy in Lewy Body Disorders: A Position Paper.

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Movement disorders : official journal of the Movement Disorder Society·2026

Joint Risk Factor Combinations with Additive Interaction Increase the Risk of Parkinson's Disease.

Movement disorders : official journal of the Movement Disorder Society·2026

Discovery of Signature Metabolites as Potential Biomarkers for Anguillid Herpesvirus 1 (AngHV-1) During Outbreak in Anguilla bicolor Glass Eel.

Journal of fish diseases·2026

Outcomes of Recombinant Zoster Vaccination in Herpes Zoster Ophthalmicus: A Secondary Analysis of the Zoster Eye Disease Study.

Cornea·2026

Acetaminophen Overdose and Self-Induced Ethanol Enema.

Cureus·2026

Multifocal Epithelioid Hemangioma With FOSB Overexpression.

Journal of cutaneous pathology·2026

High-salt microenvironment worsens the progression of atopic dermatitis via activating the SGK-1-mTOR pathway in keratinocytes.

Genes & diseases·2026

Real-World Clinical Efficacy of Food and Drug Administration-Approved Budesonide Oral Suspension Across Histologic, Endoscopic, and Symptomatic Outcomes.

Gastro hep advances·2026

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