Get Amyotrophic Lateral Sclerosis PDF

By Hiroshi Mitsumoto MD

ISBN-10: 0803602693

ISBN-13: 9780803602694

ISBN-10: 1423763467

ISBN-13: 9781423763468

Amyotrophic Lateral Sclerosis provides the main complete, clinically-focused info on ALS (Lou Gehrig's affliction) in print. the 3 authors, well known for his or her paintings during this region, offer cohesive and balanced insurance of this syndrome, together with the heritage, scientific positive aspects, pathology and pathogenesis, remedy and administration of ALS. To facilitate figuring out, each one bankruptcy is more advantageous by means of finished tables and figures, in addition to certain bankruptcy summaries.

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Extra resources for Amyotrophic Lateral Sclerosis

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In Hudson, A (ed): Amyotrophic Lateral Sclerosis. University of Toronto Press, Toronto, 1990, pp 108-143. 37. Koerner, DR: Amyotrophic lateral sclerosis on Guam: A clinical study and review of the literature. Ann Intern Med 37:1204-1220, 1952. 38. Kurland, LT and Muldeer, DW: Epidemiologic investigations of amyotrophic lateral sclerosis. Preliminary report on geographic distribution, with special reference to the Mariana Islands, including clinical and pathological observations. Neurology 4:355-378 (part 1), 438-448 (part 2), 1954.

Bell, C: The nervous system of the human body. Longman, London, 1830, pp 132-136, pp 160-161. 6. Ben Hamida, M, Hentati, F, and Ben Hamida, C: Hereditary motor system diseases. (Chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy. Brain 113:347-363, 1990. 15 7. Brain, WR: Diseases of the Nervous System. Oxford University Press, London, 1933. 8. Brain, WR and Walton, JN: Brain's Disease of the Nervous System. Oxford University Press, London, 1969, pp 595-606.

He also included deuteropathic cases secondary to other conditions such as tumors and syringomyelia. Furthermore, Charcot maintained that PBP was a syndrome distinct from ALS. Nosologic Controversy In the mid-19th century, the distinction between bulbar palsy and pseudobulbar palsy was not known. In fact, Charcot considered PBP to be a spastic syndrome because degeneration of motor neurons occurred in the medulla. On the other hand, Leyden,41 a prominent German neurologist, thought that PBP was an atonic syndrome because of lesions in the corticospinal tracts.

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Amyotrophic Lateral Sclerosis by Hiroshi Mitsumoto MD

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