People

Demographic and Clinical Predictors of Trait Impulsivity in Parkinson’s Disease Patients. Maddeson Riley, Megan Bakeberg, Michelle Byrnes, Alexa Jefferson, Soumya Ghosh, Rick Stell, Frank L. Mastaglia, Dana Hince, and Ryan S. Anderton. Parkinson’s Disease. DOI:10.1155/2018/9472120

Extended “Timed Up and Go” assessment as a clinical indicator of cognitive state in Parkinson’s disease. Evans T, Jefferson A, Byrnes M, Walters S, Ghosh S, Mastaglia FL, Anderton RS J Neurological Sciences 375, 86-91, 2017 [Scimago – Quartile, Q2; Rank, 8,561]

C/Prof Soumya Ghosh received funding from MSWA in 2016 to conduct a pilot study of balance treatment and non-invasive brain stimulation for people with secondary progressive MS and primary progressive MS.

Lakshmi Nagarajan , Ashleigh Murch, Reimar Junckerstorff, Peter Shipman, Rex Henderson, Soumya Ghosh (2015) Child with a heterozygous deletion of 2 Mb that includes the DAG 1 gene, presenting as developmental delay. Journal of Pediatric Neurology.

Lakshmi Nagarajan, Michael Lee, Linda Palumbo, Sharon Lee, Snehal Shah, Peter Walsh, Patricia Cannell, Soumya Ghosh (2015) Seizure outcomes in children with epilepsy after resective brain surgery. European Journal of Paediatric Neurology 19: 577-583 doi: 10.1016/j.ejpn.2015.05.006

Gulati P, Cannell P, Ghia T, Bint, L, Walsh P, Ghosh S, Nagarajan L. (2015) Lacosamide as adjunctive therapy in Treatment Resistant Epilepsy in Childhood. Journal of Paediatrics and Child health. doi: 10.1111/jpc.12850.

Lakshmi Nagarajan , Ashleigh Murch, Reimar Junckerstorff, Peter Shipman, Rex Henderson, Soumya Ghosh (2015) Child with a heterozygous deletion of 2 Mb that includes the DAG 1 gene, presenting as developmental delay. Journal of Pediatric Neurology. DOI http://dx.doi.org/10.1055/s-0035-1556829

Ghosh GN, Wycoco V, Ghosh S (2015) Transient visual hallucinations due to posterior callosal stroke. J Stroke & Cerebrovasc Dis 24: e147

Ghosh GN, Wycoco V, Ghosh S (2015) Transient visual hallucinations due to posterior callosal stroke. J Stroke & Cerebrovasc Dis 24: e147

Lakshmi Nagarajan , Ashleigh Murch, Reimar Junckerstorff, Peter Shipman, Rex Henderson, Soumya Ghosh (2015) Child with a heterozygous deletion of 2 Mb that includes the DAG 1 gene, presenting as developmental delay. Journal of Pediatric Neurology.