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MeSH Review

Paraparesis, Spastic

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Disease relevance of Paraparesis, Spastic


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Biological context of Paraparesis, Spastic


Anatomical context of Paraparesis, Spastic


Gene context of Paraparesis, Spastic


Analytical, diagnostic and therapeutic context of Paraparesis, Spastic


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  13. A pathogenic presenilin-1 deletion causes abberrant Abeta 42 production in the absence of congophilic amyloid plaques. Steiner, H., Revesz, T., Neumann, M., Romig, H., Grim, M.G., Pesold, B., Kretzschmar, H.A., Hardy, J., Holton, J.L., Baumeister, R., Houlden, H., Haass, C. J. Biol. Chem. (2001) [Pubmed]
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  16. Apoptosis induced by beta-N-oxalylamino-L-alanine on a motoneuron hybrid cell line. La Bella, V., Alexianu, M.E., Colom, L.V., Ionescu, A., Mohamed, A.H., Appel, S.H. Neuroscience (1996) [Pubmed]
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  20. Adrenoleukodystrophy: clinical and biochemical manifestations in carriers. O'Neill, B.P., Moser, H.W., Saxena, K.M., Marmion, L.C. Neurology (1984) [Pubmed]
  21. Intrafamilial phenotypic variability in Friedreich ataxia associated with a G130V mutation in the FRDA gene. McCabe, D.J., Wood, N.W., Ryan, F., Hanna, M.G., Connolly, S., Moore, D.P., Redmond, J., Barton, D.E., Murphy, R.P. Arch. Neurol. (2002) [Pubmed]
  22. Expression analysis of 21 transcripts physically anchored within the chromosomal region 10q24. Nobile, C., Pitzalis, S. Genomics (1999) [Pubmed]
  23. Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus. Sztriha, L., Frossard, P., Hofstra, R.M., Verlind, E., Nork, M. J. Child Neurol. (2000) [Pubmed]
  24. Unusual clinical and magnetic resonance imaging findings in a family with proteolipid protein gene mutation. Battini, R., Bianchi, M.C., Boespflug-Tanguy, O., Tosetti, M., Bonanni, P., Canapicchi, R., Cioni, G. Arch. Neurol. (2003) [Pubmed]
  25. Friedreich's ataxia presenting as adult-onset spastic paraparesis. Gates, P.C., Paris, D., Forrest, S.M., Williamson, R., Gardner, R.J. Neurogenetics (1998) [Pubmed]
  26. Natural killer (NK) cells in HTLV-I-associated myelopathy/tropical spastic paraparesis-decrease in NK cell subset populations and activity in HTLV-I seropositive individuals. Yu, F., Itoyama, Y., Fujihara, K., Goto, I. J. Neuroimmunol. (1991) [Pubmed]
  27. Myelopathy in seronegative Sjögren syndrome and/or primary progressive multiple sclerosis. Pericot, I., Brieva, L., Tintoré, M., Río, J., Sastre-Garriga, J., Nos, C., Montalban, X. Mult. Scler. (2003) [Pubmed]
  28. Segmental demyelination induced by cerebrospinal fluid of progressive spastic paraparesis: correlation with altered proteolytic parameters. Schmidt, J., Nien, J.K., Scherson, A., Campos, E.O., Cartier, L., Alvarez, J. Neurosci. Lett. (1996) [Pubmed]
  29. Expression of matrix metalloproteinases and tissue inhibitors of metalloproteinases in HTLV-I-associated myelopathy. Umehara, F., Okada, Y., Fujimoto, N., Abe, M., Izumo, S., Osame, M. J. Neuropathol. Exp. Neurol. (1998) [Pubmed]
  30. Cotton wool plaques in non-familial late-onset Alzheimer disease. Le, T.V., Crook, R., Hardy, J., Dickson, D.W. J. Neuropathol. Exp. Neurol. (2001) [Pubmed]
  31. BSCL2 mutations in two Dutch families with overlapping Silver syndrome-distal hereditary motor neuropathy. van de Warrenburg, B.P., Scheffer, H., van Eijk, J.J., Versteeg, M.H., Kremer, H., Zwarts, M.J., Schelhaas, H.J., van Engelen, B.G. Neuromuscul. Disord. (2006) [Pubmed]
  32. Investigation of mitochondrial function in hereditary spastic paraparesis. McDermott, C.J., Taylor, R.W., Hayes, C., Johnson, M., Bushby, K.M., Turnbull, D.M., Shaw, P.J. Neuroreport (2003) [Pubmed]
  33. Antibody reactivities to tumor-suppressor protein p53 and HTLV-I Tof, Rex and Tax in HTLV-I-infected people with differing clinical status. Chen, Y.M., Chen, S.H., Fu, C.Y., Chen, J.Y., Osame, M. Int. J. Cancer (1997) [Pubmed]
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