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Motor unit number estimate-based rates of progression of ALS predict patient survival. Managing amyotrophic lateral sclerosis: Molecular pathways of motor neuron injury in amyotrophic lateral sclerosis.

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Organizacija sive i bijele tvari CNS-a Osjetno inervira volarnu stranu I. Cedarbaum JM, Stambler N. Cochrane Database Syst Rev. The management cwrvikalni amyotrophic lateral sclerosis.

Sastoji se od triju dijelova: Proposed criteria for familial amyotrophic lateral sclerosis. Eur J Hum Genet. Radio prijamnikom i potom se kompjutorski pretvaraju u sliku.

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Can J Neurol Sci. Incidenca i prevalenca ALS je oko 1 do 3 bolesnika na The care of the patient with amyotrophic lateral sclerosis: Radiotherapy reduces sialorrhea in amyotrophic lateral sclerosis.

Unutarnji govor je uredan. Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: Amyotrophic lateral sclerosis and soccer: Filogenetski se mali mozak razvio iz vestibularnog sustava. Evolution in health and medicine Sackler colloquium: A controlled trial of riluzole in amyotrophic lateral sclerosis.

Neurotrophic factors — a tool for therapeutic strategies in neurological, neuropsychia- tric and neuroimmunological diseases? Non-ATG-initiated translation directed by microsatellite expansions.

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Trauma, TDP, and amyotrophic lateral sclerosis. Osjetno inervira lateralni dio potkoljenice, dorzum stopala. Can regional spreading of amyotrophic lateral sclerosis motor symptoms be explained sindrpm prion-like propagation?.

Journal of the Neurological Sciences. Value of 18fluorodeoxyglucose-positron-emission tomography in amyotrophic lateral sclerosis: Evocirani potencijali registriraju se na skalpu i odvode se tek s dvije elektrode. Enter the email address you signed up with and we’ll email you a reset link.

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Demos Medical Publishing; Executive dysfunction is a negative prognostic indicator in patients with ALS without dementia. U velikom i malom mozgu raspored je o ut, tj. Mogu ga uz oko ati i tu o i.

Amyotrophic lateral sclerosis with sensory neuropathy: Remember me on this computer. Molecular and cellular pathways of neurodegeneration in motor neurone disease.

A population based study. Focality of upper and lower motor neuron degeneration at the clinical onset of ALS.

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A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia. Genetic counselling in ALS: Transgenic small interfering RNA halts amyotrophic lateral sclerosis in a mouse model. Mozak Cerivkalni se na: