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Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1997
The neurological syndrome of infantile cobalamin deficiency: developmental regression and involuntary movementsP J Grattan-Smith, B Wilcken, P G Procopis, et al.The Medical Journal of Australia|November 17, 1986
Wilson's disease in childhood. A plea for increased awarenessS F Dorney, K R Kamath, P G Procopis, et al.Pediatric Neurology|October 6, 2000
Anterior horn cell disease and olivopontocerebellar hypoplasiaM M Ryan, C M Cooke-Yarborough, P G Procopis, et al.The Medical Journal of Australia|October 28, 1985
Serious neurological complications of measles--a continuing preventable problemP J Grattan-Smith, P G Procopis, G A Wise, et al.Neuromuscular Disorders : NMD|July 19, 2000
Childhood chronic inflammatory demyelinating polyneuropathy: clinical course and long-term outcomeM M Ryan, P J Grattan-Smith, P G Procopis, et al.Brain & Development|March 1, 1992
ACTH treatment in intractable seizures of childhoodA Charuvanij, R A Ouvrier, P G Procopis, et al.Medical and Pediatric Oncology|January 1, 1991
Bulbar and pseudobulbar palsy complicating therapy with high-dose cytosine arabinoside in children with leukemiaP J Shaw, P G Procopis, M A Menser, et al.Clinical and Experimental Neurology|January 1, 1981
Bilateral optic nerve hypoplasiaR A Ouvrier, D Lewis, P G Procopis, et al.Journal of the Royal College of Physicians of London|January 1, 1980
Chemotherapy of the myeloid leukaemiasJ StuartThe Medical Journal of Australia|March 25, 1978
The development of serum immunoglobulins G, A and M in Australian Aboriginal infantsJ StuartPageof 182