A form of multiple sclerosis characterized by a progressive deterioration in neurologic function which is in contrast to the more typical relapsing remitting form. If the clinical course is free of distinct remissions, it is referred to as primary progressive multiple sclerosis. When the progressive decline is punctuated by acute exacerbations, it is referred to as progressive relapsing multiple sclerosis. The term secondary progressive multiple sclerosis is used when relapsing remitting multiple sclerosis evolves into the chronic progressive form. (From Ann Neurol 1994;36 Suppl:S73-S79; Adams et al., Principles of Neurology, 6th ed, pp903-914)
A form of multiple sclerosis characterized by a progressive deterioration in neurologic function which is in contrast to the more typical relapsing remitting form. If the clinical course is free of distinct remissions, it is referred to as primary progressive multiple sclerosis. When the progressive decline is punctuated by acute exacerbations, it is referred to as progressive relapsing multiple sclerosis. The term secondary progressive multiple sclerosis is used when relapsing remitting multiple sclerosis evolves into the chronic progressive form. (From Ann Neurol 1994;36 Suppl:S73-S79; Adams et al., Principles of Neurology, 6th ed, pp903-914)
A form of multiple sclerosis characterized by a progressive deterioration in neurologic function which is in contrast to the more typical relapsing remitting form. If the clinical course is free of distinct remissions, it is referred to as primary progressive multiple sclerosis. When the progressive decline is punctuated by acute exacerbations, it is referred to as progressive relapsing multiple sclerosis. The term secondary progressive multiple sclerosis is used when relapsing remitting multiple sclerosis evolves into the chronic progressive form. (From Ann Neurol 1994;36 Suppl:S73-S79; Adams et al., Principles of Neurology, 6th ed, pp903-914)
Multiple sclerosis -- Research -- Planning -- Congresses : Summary of a workshop on Research in Multiple Sclerosis, April 5-6, 2001 : based on the Institute of Medicine report on Multiple sclerosis : current status and strategies for the future / prepared by Miram Davis and Janet E. Joy
A form of multiple sclerosis characterized by a progressive deterioration in neurologic function which is in contrast to the more typical relapsing remitting form. If the clinical course is free of distinct remissions, it is referred to as primary progressive multiple sclerosis. When the progressive decline is punctuated by acute exacerbations, it is referred to as progressive relapsing multiple sclerosis. The term secondary progressive multiple sclerosis is used when relapsing remitting multiple sclerosis evolves into the chronic progressive form. (From Ann Neurol 1994;36 Suppl:S73-S79; Adams et al., Principles of Neurology, 6th ed, pp903-914)
Multiple sclerosis -- Treatment -- Case studies : Navigating life with multiple sclerosis / Kathleen Costello, MS, ANP-BC, MSCN (Associate Vice-President, National Multiple Sclerosis Society Nurse Practitioner, the Johns Hopkins Multiple Sclerosis Center, Baltimore, MD), Ben W. Thrower, MD (Medical Director, Andrew C. Carlos Multiple Sclerosis Institute at Shepherd Center, Atlanta, GA), Barbara S. Giesser, MD (Clinical Director, UCLA Multiple Sclerosis Program, David Geffen UCLA School of Medicine, Los Angeles, CA)
Multiple Signal Classification. : Signals, systems, and transforms / Charles L. Phillips, emeritus, Auburn University, Auburn, Alabama, John M. Parr, University of Evansville, Evansville, Indiana, Eve A. Riskin, University of Washington, Seattle, Washington ; Global Edition contributions by T. Prabhakar
Multiple stars -- Congresses : Multiple stars across the H-R diagram : proceedings of the ESO Workshop held in Garching, Germany, 12-15 July 2005 / S. Hubrig, M. Petr-Gotzens, A. Tokovinin (eds.)
A syndrome complex composed of three conditions which represent clinical variants of the same disease process: STRIATONIGRAL DEGENERATION; SHY-DRAGER SYNDROME; and the sporadic form of OLIVOPONTOCEREBELLAR ATROPHIES. Clinical features include autonomic, cerebellar, and basal ganglia dysfunction. Pathologic examination reveals atrophy of the basal ganglia, cerebellum, pons, and medulla, with prominent loss of autonomic neurons in the brain stem and spinal cord. (From Adams et al., Principles of Neurology, 6th ed, p1076; Baillieres Clin Neurol 1997 Apr;6(1):187-204; Med Clin North Am 1999 Mar;83(2):381-92)
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Multiple System Atrophy : Multiple system atrophy / Gregor Wenning, Alessandra Fanciulli, editors
A syndrome complex composed of three conditions which represent clinical variants of the same disease process: STRIATONIGRAL DEGENERATION; SHY-DRAGER SYNDROME; and the sporadic form of OLIVOPONTOCEREBELLAR ATROPHIES. Clinical features include autonomic, cerebellar, and basal ganglia dysfunction. Pathologic examination reveals atrophy of the basal ganglia, cerebellum, pons, and medulla, with prominent loss of autonomic neurons in the brain stem and spinal cord. (From Adams et al., Principles of Neurology, 6th ed, p1076; Baillieres Clin Neurol 1997 Apr;6(1):187-204; Med Clin North Am 1999 Mar;83(2):381-92)
The most common clinical form of FRONTOTEMPORAL LOBAR DEGENERATION, this dementia presents with personality and behavioral changes often associated with disinhibition, apathy, and lack of insight
Multiple Trauma -- therapy : Damage control management in the polytrauma patient / Hans-Christoph Pape, Andrew Peitzman, Michael Rotondo, Peter Giannoudis
