PROF DR VIDOSAVA RAKOČEVIĆ STOJANOVIĆ dr sci.med.
Title: Professor of Neurology Institution: Institute of Neurology, School of Medicine, Belgrade, Serbia, Belgrade, Dr Subotica 6 Phone : +381 113064247 Fax: +381 11 2682988 E-mail:
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Short CV:
Female, born June 29th, 1957, Peć, Serbia; PhD - School of Medicine, University of Belgrade, M.D., 1976-1982.Post graduate studies in Neurology at School of Medicine, University of Belgrade,Period 1982-1984, 1989-1994, Ph.D. Training: Internship 1986-1990, Belgrade, Yugoslavia Neurology Specialist Trainee, Institute of Neurology, University Clinical Center, Belgrade, 1989 Psychiatric Specialist Trainee, Institute of Psychiatry, University Clinical Center, Belgrade, Research fellow: Department of Cardiomyology, Institute for cardiomyology, Napoli, Italy, 1991, /International School for Advanced Studies/ and “Life” Center, New Castle, UK, 2010. Current positions: The supervisor and coordinator of diagnosing and managing of all DM1 and DM2 patients and other myopathies in adult population from Serbia. Member of the team from Department of Neuromuscular disorders , Institute of Neurology Clinical Centre Serbia, School of Medicine Belgrade, Serbia. Memberships and scientific activities: European DM Consortium, EFNS, WNS, Serbian neurological society, TREAT-NMD society. In the period from 1992 to 2010. I have been invloved in the five projects of the Ministry of Science and Technology of Serbia which covered the scientific research in the field of hereditary neuromuscular disorders. In this moment I am a head of the project about investigation in the field of neuromuscular disorders, in the period from 2011. to 2014.
Academic appointments:
Professor of Neurology from 2010, Institute of Neurology, University Clinical Center, School of Medicine, University of Belgrade, Belgrade, Serbia
References:
Total: 260 publications to presently 65 published as a whole in distinguished international medical journals.
Scientific research and occupation: Neurological diseases, neuromuscular disorders, muscular dystrophies and hereditary neuropathies as well as congenital myasthenic syndromes, myasthenia gravis, secondary myopathies and neuropathies, cardiac disorders in patients with myotonic dystrophy and others muscular dystrophies, cardiac abnormalities in patients with myasthenia gravis and other neuromuscular disorders.
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