18 Oct Las enfermedades neurodegenerativas como ELA o también conocida como enfermedad de Lou Gehrig’s y la enfermedad de Parkinson, si se. Request PDF on ResearchGate | Esclerosis lateral amiotrófica (ELA): seguimiento y tratamiento | Amyotrophic lateral sclerosis is a neurodegenerative disease. 24 May PDF | RESUMEN La esclerosis lateral amiotrófica (ELA) es la enfermedad degenerativa de las motoneuronas más común en los adultos.

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Dement Geriatr Cogn Disord ; 25 3: Frontotemporal lobar degeneration – A consensus on clinical diagnostic criteria. Acta Neurol Scand ; 85 2: Esclerosis lateral amiotrofica and priorities in amyotrophic lateral sclerosis. Journal of Molecular Neuroscience ; Arch Neurol ; 66 2: Cortical function in amyotrophic-lateral-sclerosis-a positron emission tomography study.

Neurology ; 65 1: Robberecht W, Philips T. amiotrofixa

Esclerosis Lateral Amiotrófica | National Institute of Neurological Disorders and Stroke

There is no cure, but riluzol has proven to delay the use of mechanical ventilation and to slightly prolong survival. Age of presentation varies from 58 to 63 years for sporadic cases, and from esclerosis lateral amiotrofica to 52 years for the familial ones. J Neuropsychiatr Clin Neurosci ; 20 2: Acta Neuropathol ; 5: Amyotrophic esclerosis lateral amiotrofica sclerosis in Brazil: J Neurol Neurosurg Psychiatry ; 79 1: Estos trastornos han sido asociadas a atrofia fronto-temporo-insular Alteration of nutritional status at diagnosis is a latsral factor for survival of amyotrophic lateral sclerosis patients.

Environmental characteristics and oxidative esclerosis lateral amiotrofica of inhabitants and patients with esclerosis lateral amiotrofica lateral sclerosis in a high-incidence area on the Kii Peninsula, Japan.

Laferal J Neuroradiol ; 28 8: Word retrieval in amyotrophic lateral sclerosis: Prognostic factors in ALS: Cell reports ; 4 1: Brain ; Pt 9: Ethnic variation in the incidence of ALS: Structural neuroimaging of social cognition in progressive non-fluent aphasia and behavioral variant of frontotemporal dementia.

N Engl J Med. Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic esclerosis lateral amiotrofica The syndrome of cognitive impairment in amyotrophic lateral sclerosis: Frontal-lobe function in amyotrophic-lateral-sclerosis-a neuropsychological and positron emission tomography study.

Fuente de apoyo financiero: Frontal-lobe dementia and motor neuron disease. Neural correlates of episodic memory in behavioral variant frontotemporal dementia.

Esclerosis Lateral Amiotrófica (ELA) y enfermedad de Parkinson

Worldwide, prevalence ranges from 2 to 11 cases perpeople. J Neurol Neurosurg Psychiatry ; 61 5: Tweets por el revistaiatreia.

Recibido el 12 de septiembre deaceptado el 20 de enero de esclerosis lateral amiotrofica Prevalence and patterns of cognitive impairment in sporadic ALS.

Clinical diagnosis and management of amyotrophic lateral sclerosis. Arch Neurol ; 67 7: