Progression in primary lateral sclerosis: A prospective analysis

References

• Rowland LP. Primary lateral sclerosis, hereditary spastic paraplegia, and mutations in the alsin gene: historical background for the first International Conference. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005; 6: 67–76
   PubMed Web of Science ®Google Scholar
• Swash M, Desai J, Misra VP. What is primary lateral sclerosis?. J Neurol Sci. 1999; 170: 5–10
   PubMed Web of Science ®Google Scholar
• Pringle CE, Hudson AJ, Munoz DG, Kiernan JA, Brown WF, Ebers GC. Primary lateral sclerosis. Clinical features, neuropathology and diagnostic criteria. Brain. 1992; 115: 495–520
   PubMed Web of Science ®Google Scholar
• Gordon PH, Cheng B, Katz IB, Pinto M, Hays AP, Mitsumoto H, et al. The natural history of primary lateral sclerosis. Neurology. 2006; 66: 647–53
   PubMed Web of Science ®Google Scholar
• Tartaglia MC, Rowe A, Findlater K, Orange JB, Grace G, Strong MJ. Differentiation between primary lateral sclerosis and amyotrophic lateral sclerosis: examination of symptoms and signs at disease onset and during follow-up. Arch Neurol. 2007; 64: 232–6
   PubMedGoogle Scholar
• Tomik B, Zur KA, Szczudlik A. Pure primary lateral sclerosis: case reports. Clin Neurol Neurosurg. 2008; 110: 387–91
   PubMed Web of Science ®Google Scholar
• Singer MA, Kojan S, Barohn RJ, Herbelin L, Nations SP, Trivedi JR, et al. Primary lateral sclerosis: clinical and laboratory features in 25 patients. J Clin Neuromuscul Dis. 2005; 7: 1–9
   PubMedGoogle Scholar
• Zhai P, Pagan F, Statland J, Butman JA, Floeter MK. Primary lateral sclerosis: a heterogeneous disorder composed of different subtypes?. Neurology. 2003; 60: 1258–65
   PubMed Web of Science ®Google Scholar
• Le Forestier N, Maisonobe T, Piquard A, Rivaud S, Crevier-Buchman L, Salachas F, et al. Does primary lateral sclerosis exist? A study of 20 patients and a review of the literature. Brain. 2001; 124: 1989–99
   PubMed Web of Science ®Google Scholar
• de Carvalho M, Swash M. Can selection of rapidly progressing patients shorten clinical trials in amyotrophic lateral sclerosis?. Arch Neurol. 2006; 63: 557–60
   PubMedGoogle Scholar
• Talman P, Forbes A, Mathers S. Clinical phenotypes and natural progression for motor neuron disease: analysis from an Australian database. Amyotroph Lateral Scler. 2009; 10: 79–84
   PubMed Web of Science ®Google Scholar
• Chio, A, Logroscino, G, Hardiman, O, Swingler, R, Mitchell, D, Beghi, E, , et al. Prognostic factors in ALS: a critical review. Amyotroph Lateral Scler 2008; 1–14, [Epub ahead of print].
   PubMedGoogle Scholar
• Czaplinski A, Yen AA, Simpson EP, Appel SH. Predictability of disease progression in amyotrophic lateral sclerosis. Muscle Nerve. 2006; 34: 702–8
   PubMed Web of Science ®Google Scholar
• Haverkamp LJ, Appel V, Appel SH. Natural history of amyotrophic lateral sclerosis in a database population. Validation of a scoring system and a model for survival prediction. Brain. 1995; 118(Pt 3)707–19
   PubMed Web of Science ®Google Scholar
• Wijesekera LC, Mathers S, Talman P, Galtrey C, Parkinson MH, Ganesalingam J, et al. Natural history and clinical features of the flail arm and flail leg ALS variants. Neurology. 2009; 72: 1087–94
   PubMed Web of Science ®Google Scholar
• Gouveia LO, de Carvalho M. Young-onset sporadic amyotrophic lateral sclerosis: a distinct nosological entity?. Amyotroph Lateral Scler. 2007; 8: 323–7
   PubMed Web of Science ®Google Scholar
• Appel V, Stewart SS, Smith G, Appel SH. A rating scale for amyotrophic lateral sclerosis: description and preliminary experience. Ann Neurol. 1987; 22: 328–33
   PubMed Web of Science ®Google Scholar
• Bohannon RW, Smith MB. Interrater reliability of a modified Ashworth scale of muscle spasticity. Phys Ther. 1987; 67: 206–7
   PubMed Web of Science ®Google Scholar
• Litvan I, Mangone CA, Werden W, Bueri JA, Estol CJ, Garcea DO, et al. Reliability of the NINDS Myotatic Reflex Scale. Neurology. 1996; 47: 969–72
   PubMed Web of Science ®Google Scholar
• Liniger C, Albeanu A, Bloise D, Assal JP. The tuning fork revisited. Diabet Med. 1990; 7: 859–64
   PubMed Web of Science ®Google Scholar
• Fink JK. Sporadically occurring neurologic disease: HSP genes and apparently sporadic spastic paraplegia. Neurology. 2008; 71: 1468–9
   PubMed Web of Science ®Google Scholar
• Gastaut JL, Bartolomei F. Mills' syndrome: ascending (or descending) progressive hemiplegia: a hemiplegic form of primary lateral sclerosis?. J Neurol Neurosurg Psychiatry. 1994; 57: 1280–1
   PubMed Web of Science ®Google Scholar
• Turner MR, Gerhard A, Al-Chalabi A, Shaw CE, Hughes RA, Banati RB, et al. Mills' and other isolated upper motor neuron syndromes: in vivo study with 11C-(R)-PK11195 PET. J Neurol Neurosurg Psychiatry. 2005; 76: 871–4
   PubMed Web of Science ®Google Scholar
• Ravits J, Paul P, Jorg C. Focality of upper and lower motor neuron degeneration at the clinical onset of ALS. Neurology. 2007; 68: 1571–5
   PubMed Web of Science ®Google Scholar
• de Carvalho M, Swash M. The onset of amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry. 2006; 77: 388–9
   PubMed Web of Science ®Google Scholar
• Mitsumoto H, Ulug AM, Pullman SL, Gooch CL, Chan S, Tang MX, et al. Quantitative objective markers for upper and lower motor neuron dysfunction in ALS. Neurology. 2007; 68: 1402–10
   PubMed Web of Science ®Google Scholar
• Butman JA, Floeter MK. Decreased thickness of primary motor cortex in primary lateral sclerosis. AJNR Am J Neuroradiol. 2007; 28: 87–91
   PubMed Web of Science ®Google Scholar
• Tartaglia MC, Laluz V, Rowe A, Findlater K, Lee DH, Kennedy K, et al. Brain atrophy in primary lateral sclerosis. Neurology. 2009; 72: 1236–41
   PubMed Web of Science ®Google Scholar
• Rothstein JD. Current hypotheses for the underlying biology of amyotrophic lateral sclerosis. Ann Neurol. 2009; 65(Suppl 1)S3–9
   PubMed Web of Science ®Google Scholar
• Boillee S, Yamanaka K, Lobsiger CS, Copeland NG, Jenkins NA, Kassiotis G, et al. Onset and progression in inherited ALS determined by motor neurons and microglia. Science. 2006; 312: 1389–92
   PubMed Web of Science ®Google Scholar
• Steinacker P, Hendrich C, Sperfeld AD, Jesse S, von Arnim CA, Lehnert S, et al. TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Arch Neurol. 2008; 65: 1481–7
   PubMed Web of Science ®Google Scholar
• Hand CK, Devon RS, Gros-Louis F, Rochefort D, Khoris J, Meininger V, et al. Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis. Arch Neurol. 2003; 60: 1768–71
   PubMedGoogle Scholar
• Hand CK, Rouleau GA. Familial amyotrophic lateral sclerosis. Muscle Nerve. 2002; 25: 135–59
   PubMed Web of Science ®Google Scholar
• Brugman F, Wokke JH, Vianney de Jong JM, Franssen H, Faber CG, van den Berg LH. Primary lateral sclerosis as a phenotypic manifestation of familial ALS. Neurology. 2005; 64: 1778–9
   PubMed Web of Science ®Google Scholar
• Praline, J, Guennoc, AM, Vourc'h, P, de Toffol, B, Corcia, P . Primary lateral sclerosis may occur within familial amyotrophic lateral sclerosis pedigrees. Amyotroph Lateral Scler. 2008:1–3. [Epub ahead of print].
   PubMedGoogle Scholar
• Yang Y, Hentati A, Deng HX, Dabbagh O, Sasaki T, Hirano M, et al. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nat Genet. 2001; 29: 160–5
   PubMed Web of Science ®Google Scholar
• Fink JK. Hereditary spastic paraplegia. Curr Neurol Neurosci Rep. 2006; 6: 65–76
   PubMed Web of Science ®Google Scholar
• Brugman F, Eymard-Pierre E, van den Berg LH, Wokke JH, Gauthier-Barichard F, Boespflug-Tanguy O. Adult-onset primary lateral sclerosis is not associated with mutations in the ALS2 gene. Neurology. 2007; 69: 702–4
   PubMed Web of Science ®Google Scholar
• Brugman F, Veldink JH, Franssen H, de Visser M, de Jong JM, Faber CG, et al. Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes. Arch Neurol 2009; 66: 509–14
   PubMedGoogle Scholar
• Craciun, L, Floeter, MK. Motor Unit Number Estimation in Primary Lateral Sclerosis. Submitted.
   Google Scholar