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Get Amyotrophic Lateral Sclerosis and the Frontotemporal PDF

By Michael J. Strong

ISBN-10: 0199590672

ISBN-13: 9780199590674

Over the last ten years, there was an expanding acceptance that syndromes of frontotemporal disorder (FTD) are a standard prevalence in sufferers with amyotrophic lateral sclerosis (ALS). Such syndromes should be found in as many as 60% of sufferers with ALS. Conversely, the incidence of motor neuron disorder in sufferers with clinically natural frontotemporal dementia is more and more well-known. this implies that to a point there are overlapping syndromes during which either ALS and FTD happen in the similar person.

This quantity summarizes the advances in our knowing of those issues, in addition to the capability courting among the 2. Key themes contain advances in our skill to clinically describe the frontotemporal syndromes, preclinical detection, neuroimaging, and genetics. The exploding box of latest markers in neuropathology is tested, as is the position of recent genetic mutations in DNA/RNA shipping platforms. This ebook is the fundamental reference textual content for this subject, and may be of curiosity to neurologists and neurological trainees with a medical or examine curiosity within the FTDs or ALS, neuropsychologists, neuropathologists, and researchers.

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Extra info for Amyotrophic Lateral Sclerosis and the Frontotemporal Dementias

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Changes in the incidence of amyotrophic lateral sclerosis in Wakayama, Japan. Amyo Lat Scler, 6, 155–163. 24. Yoshida S, Uebayashi Y, Kihira T, et al. (1998). Epidemiology of motor neuron disease in the Kii Peninsula of Japan, 1989–1993: active or disappearing focus? J Neurol Sci, 155, 146–155. 25. Kuzuhara S, Kokubo Y, Narita Y, Ryogen S. (1998). Continuing high incidence rates and frequent familial occurrence of Amyotropic Lateral Sclerosis and Parkinsonism-Dementia complex of the Kii Peninsula of Japan.

Rosenfeld J. (2000). Fasciculations without fibrillations: the dilemma of early diagnosis. Amyotroph Lateral Scler Other Motor Neuron Disord, S53–S56. 29. Brooks BR, Thisted RA, Appel SH, et al. (2004). Treatment of pseudobulbar affect in ALS with dextromethorphan/quinidine: a randomized trial. Neurology, 63, 1364–1370. 30. Visser J, de Jong JMBV, de Visser M. (2008). The history of progressive muscular atrophy: syndrome or disease? Neurology, 70, 723–727. 31. Maragakis NJ. (2010). Motor neuron disease: progressive muscular atrophy in the ALS spectrum.

33. Jackson CE, Rosenfeld J. (2001). Motor neuron disease. Phys Med Rehabil Clin N Am, 12, 335–33x. 34. Ludolph AC, Knirsch U. (1999). Problems and pitfalls in the diagnosis of ALS. J Neurol Sci, 165 (Suppl 1), S14–S20. 35. Traynor BJ, Codd MB, Corr B, et al. (2000). Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic criteria. Arch Neurol, 57, 1171–1176. 36. Mortara P, Chio A, Rosso MG, et al. (1984). Motor neuron disease in the province of Turin, Italy, 1966–1980.

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Amyotrophic Lateral Sclerosis and the Frontotemporal Dementias by Michael J. Strong


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