Padraic J. Smith-Grattan
Westmead, NSW, Australia
Last Updated: 09/26/2026
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Found 10 publications
Paroxysmal dyskinesias with drowsiness and thalamic lesions in GABA transaminase deficiency.
Journal: Neurology
Published: June 03, 2018
GNAO1-related movement disorder with life-threatening exacerbations: movement phenomenology and response to DBS.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: January 16, 2017
Genetic epilepsy with febrile seizures plus: Refining the spectrum.
Journal: Neurology
Published: November 13, 2016
Pediatric functional neurologic symptoms.
Journal: Handbook of clinical neurology
Published: October 11, 2016
Phenotypic insights into ADCY5-associated disease.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 19, 2015
Intravenous immunoglobulin in acute Sydenham's chorea: A systematic review.
Journal: Journal of paediatrics and child health
Published: March 27, 2015
Movement disorders in children with anti-NMDAR encephalitis and other autoimmune encephalopathies.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: May 16, 2014
Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study.
Journal: Developmental medicine and child neurology
Published: April 21, 2012
Mitochondrial dysfunction in a novel form of autosomal recessive ataxia.
Journal: Mitochondrion
Published: March 02, 2012
Response to Zhang et al.
Journal: Journal of paediatrics and child health
Published: December 17, 2011
Showing 1-10 of 10
Last Updated: 09/26/2026