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SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis outcome measures and the role of albumin and creatinine:

Amyotrophic lateral sclerosis onset after prolonged treatment with a VEGF receptors inhibitor.

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Influence of cigarette smoking on ALS outcome: Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: Neurobiol Aging ; ALS clinical trials: Amyotroph Lateral Scler.

J Neurol Sci. Influence of arterial hypertension, type 2 diabetes and cardiovascular risk factors on ALS outcome: Non-self-sufficiency as a primary outcome measure in ALS trials.

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No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. The epidemiology and treatment of ALS: Neuroepidemiology ; The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease.

Projected increase in amyotrophic lateral sclerosis from to Neurol Sci. J Neurol Neurosurg Psychiatry ; A motor neuron disease-mimic syndrome?

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Am J Epidemiol. Identifying potential risk factors for developing amyotrophic lateral sclerosis.

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NBA A de novo nonsense mutation of the FUS gene in an apparently familial amyotrophic lateral sclerosis case. Genetic architecture of ALS in Sardinia. Is there a place for physical activity? A curriculum vitae adriano ferrari scale for prognostication in Parkinson disease: Lancet Neurol.

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The last months of life of people with amyotrophic lateral sclerosis in mechanical invasive ventilation: Resting state functional connectivity alterations in primary lateral sclerosis. S 17 Eur J Neurol. Amyotrophic lateral sclerosis outcome measures and the role of albumin and creatinine: JAMA Neurol. Of animals and men.

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Amyotrophic lateral sclerosis-frontotemporal lobar dementia in 3 families bph evolve case study quizlet p. Front Mol Neurosci Homozygosity analysis in amyotrophic lateral sclerosis. Front Mol Neurosci.

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Ann Neurol. Common polymorphisms of chemokine C-X3-C motif receptor 1 gene modify amyotrophic lateral sclerosis outcome: A familial ALS case carrying a novel p.

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The implications of different definitions of illness when treating patients suffering from amyotrophic lateral sclerosis. Too soon, too much.

Physical fitness and amyotrophic lateral sclerosis: Cytotherapy C9orf72 expansion differentially affects males with spinal onset amyotrophic lateral sclerosis. Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials.

FUS mutations in sporadic amyotrophic lateral sclerosis.

Genetics of multiple system atrophy: J Neurol Nov; The role of pre-morbid diabetes on developing Amyotrophic Lateral Sclerosis. PLoS One. Dis Model Mech. CHCHD10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients.

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Alzheimers Dement. Amyotroph Lateral Scler ; A Therapeutic Opportunity?


Persistent idiopathic hypoglossal nerve palsy: Biochim Biophys Acta. C9ORF72 intermediate repeat expansion in patients affected by atypical parkinsonian syndromes or Parkinson's disease complicated by psychosis or dementia in a Sardinian population. NADPH oxidases as drug targets and biomarkers in neurodegenerative diseases: S 15 Consistent bone marrow-derived cell mobilization following repeated short courses of granulocyte-colony-stimulating factor in patients with amyotrophic lateral sclerosis: A Bayesian spatial analysis of the incident cases.

SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. The quest for exogenous risk factors in ALS: Hum Mol Genet.

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Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Physical Activity and ALS.

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C9ORF72 and parkinsonism: Cognitive correlates in amyotrophic lateral sclerosis: Repeated courses of granulocyte colony-stimulating factor in amyotrophic lateral sclerosis: The changing picture of amyotrophic lateral sclerosis: Chromosome 9p21 in descriptive essay short story amyotrophic lateral sclerosis in the UK and seven other countries: Eur J Hum Genet.

Apparent anticipation in SOD1 familial amyotrophic lateral sclerosis. Eur J Phys Rehabil Med.

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Weak link, innocent bystander, or central player in neurodegeneration? Amyotrophic lateral sclerosis, physical exercise, trauma and sports: Extensive genetics of ALS: Age-related penetrance of the C9orf72 repeat expansion.

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