Showing 221 - 240 results of 3,105 for search '"amyotrophic lateral sclerosis"', query time: 0.13s Refine Results
  1. 221

    Expression of HLA-DR in pheripheral nerve of amyotrophic lateral sclerosis by A.S.B. Oliveira, E. Isozaki, D. Younger, A.A. Gabbai, A.P. Hays

    Published 1994-12-01
    “…To investigate the possibility of local antigen presentation within the peripheral nerve in amyotrophic lateral sclerosis (ALS), cryostat sections of 83 peripheral nerve biopsies were stained for the demonstration of HLA-DR using a monoclonal antibody. …”
    Get full text
    Article
  2. 222
  3. 223
  4. 224
  5. 225
  6. 226
  7. 227
  8. 228
  9. 229

    Smoking and risk for amyotrophic lateral sclerosis: analysis of the EPIC cohort. by Gallo, V, Bueno-De-Mesquita, H, Vermeulen, R, Andersen, P, Kyrozis, A, Linseisen, J, Kaaks, R, Allen, N, Roddam, A, Boshuizen, H, Peeters, P, Palli, D, Mattiello, A, Sieri, S, Tumino, R, Jiménez-Martín, J, Díaz, M, Suarez, L, Trichopoulou, A, Agudo, A, Arriola, L, Barricante-Gurrea, A, Bingham, S, Khaw, K, Manjer, J

    Published 2009
    “…OBJECTIVE: Cigarette smoking has been reported as "probable" risk factor for Amyotrophic Lateral Sclerosis (ALS), a poorly understood disease in terms of aetiology. …”
    Journal article
  10. 230

    Human cerebral evolution and the clinical syndrome of amyotrophic lateral sclerosis by Henderson, R, Garton, F, Kiernan, M, Turner, M, Eisen, A

    Published 2018
    “…<p>The adult neurodegenerative disorder amyotrophic lateral sclerosis (ALS) is unmistakeable from clinical descriptions now more than a century old.1 Neither the site of symptom onset in ALS2 nor pattern of symptom spread3–5 is truly random. …”
    Journal article
  11. 231

    The diagnostic pathway and prognosis in bulbar-onset amyotrophic lateral sclerosis. by Turner, M, Scaber, J, Goodfellow, J, Lord, M, Marsden, R, Talbot, K

    Published 2010
    “…BACKGROUND: Despite the inevitability of disease progression in amyotrophic lateral sclerosis, there is a high degree of prognostic heterogeneity in all subtypes. …”
    Journal article
  12. 232

    Advancing mechanistic understanding and biomarker development in amyotrophic lateral sclerosis by Thompson, AG, Oeckl, P, Feneberg, E, Bowser, R, Otto, M, Fischer, R, Kessler, B, Turner, MR

    Published 2021
    “…<br><strong>Introduction<br></strong> Proteomic analysis has contributed significantly to the study of the neurodegenerative disease amyotrophic lateral sclerosis (ALS). It has helped to define the pathological change common to nearly all cases, namely intracellular aggregates of phosphorylated TDP-43, shifting the focus of pathogenesis in ALS toward RNA biology. …”
    Journal article
  13. 233

    A case of celiac disease mimicking amyotrophic lateral sclerosis. by Turner, M, Chohan, G, Quaghebeur, G, Greenhall, R, Hadjivassiliou, M, Talbot, K

    Published 2007
    “…DIAGNOSIS: Celiac disease with neurological involvement, mimicking amyotrophic lateral sclerosis. MANAGEMENT: Strict gluten-free diet.…”
    Journal article
  14. 234
  15. 235

    Oculomotor dysfunction in amyotrophic lateral sclerosis: a comprehensive review. by Sharma, R, Hicks, S, Berna, C, Kennard, C, Talbot, K, Turner, M

    Published 2011
    “…Although traditionally regarded as spared, a range of oculomotor dysfunction has been recorded in patients with amyotrophic lateral sclerosis (ALS). Most frequent is ophthalmoparesis, particularly in patients with prolonged survival; however, pursuit, nystagmus, and saccadic impairments have also been reported. …”
    Journal article
  16. 236
  17. 237
  18. 238

    Autoimmune disease preceding amyotrophic lateral sclerosis: an epidemiologic study. by Turner, M, Goldacre, R, Ramagopalan, S, Talbot, K, Goldacre, M

    Published 2013
    “…OBJECTIVE: To study whether the risk of amyotrophic lateral sclerosis (ALS) is increased in people with prior autoimmune disease. …”
    Journal article
  19. 239
  20. 240

    Does interneuronal dysfunction contribute to neurodegeneration in amyotrophic lateral sclerosis? by Turner, M, Kiernan, M

    Published 2012
    “…Amyotrophic lateral sclerosis (ALS) is typically regarded as a sporadic neurodegenerative disorder that results in a catastrophic failure of the motor system, with characteristically variable involvement of upper and lower motor neuronal populations. …”
    Journal article