Damian R. Clark
North Adelaide, SA, Australia
Last Updated: 09/26/2026
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Found 13 publications
Detailed immune cell profiling of paediatric patient with limb girdle muscular dystrophy R3.
Journal: Journal of the neurological sciences
Published: March 16, 2025
Cost-Effectiveness of Newborn Screening for Spinal Muscular Atrophy in Australian Hospitals.
Journal: Neurology and therapy
Published: February 21, 2025
Developmental regression with early feeding difficulties and characteristic neuroimaging features of H-ABC in an infant from a TUBB4A genetic variant.
Journal: Journal of paediatrics and child health
Published: August 31, 2023
Screening for Carpal Tunnel Syndrome in Patients With Mucopolysaccharidosis.
Journal: Journal of child neurology
Published: March 12, 2020
Benefits of powered standing wheelchair devices for adolescents with Duchenne muscular dystrophy in the first year of use.
Journal: Journal of paediatrics and child health
Published: November 29, 2019
Tarsal tunnel syndrome in the mucopolysaccharidoses: A case series and literature review.
Journal: JIMD reports
Published: June 27, 2019
SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures.
Journal: Neurology
Published: December 16, 2014
A population-based post mortem study of sudden unexpected death in epilepsy.
Journal: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
Published: November 22, 2014
Phenotypic variation of TTC19-deficient mitochondrial complex III deficiency: a case report and literature review.
Journal: American journal of medical genetics. Part A
Published: August 20, 2014
High resolution chromosomal microarray in undiagnosed neurological disorders.
Journal: Journal of paediatrics and child health
Published: May 03, 2013
Mutations in TPM2 and congenital fibre type disproportion.
Journal: Neuromuscular disorders : NMD
Published: March 17, 2012
Last Updated: 09/26/2026