S. Rose

发表

Mitochondrial DNA Damage in Autism

Sarah Wong, C. Giulivi, S. Rose, 2016 .

Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene.

A. Wilde, S. Kääb, B. Beckmann, 2017, Forensic science international.

Levels of phosphorylated axonal neurofilament subunit H (pNfH) are increased in acute ischemic stroke

P. Mccombe, R. Henderson, S. Read, 2011, Journal of the Neurological Sciences.