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Amyotrophic Lateral Sclerosis Volume 6, 2005 - Issue 2
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Review article

Primary lateral sclerosis, hereditary spastic paraplegia, and mutations in the alsin gene: Historical background for the first International Conference

Lewis P. Rowland Eleanor and Lou Gehrig MDA/ALS Center, Neurological Institute, Columbia University Medical Center, New York, USACorrespondence[email protected]
Pages 67-76 | Accepted 07 Mar 2005, Published online: 10 Jul 2009

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Mary Kay Floeter & Reversa Mills. (2009) Progression in primary lateral sclerosis: A prospective analysis. Amyotrophic Lateral Sclerosis 10:5-6, pages 339-346.
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Lewis P. Rowland. (2009) T.L. Bunina, Asao Hirano, and the post mortem cellular diagnosis of amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis 10:2, pages 74-78.
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Articles from other publishers (23)

W.B.V.R. Pinto, R. Debona, P.P. Nunes, A.C.D. Assis, C.G. Lopes, T. Bortholin, R.B. Dias, F.G.M. Naylor, M.A.T. Chieia, P.V.S. Souza & A.S.B. Oliveira. (2019) Atypical Motor Neuron Disease variants: Still a diagnostic challenge in Neurology. Revue Neurologique 175:4, pages 221-232.
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Ramnath Santosh Ramanathan & Sandeep Rana. (2018) Demographics and clinical characteristics of primary lateral sclerosis: case series and a review of literature. Neurodegenerative Disease Management 8:1, pages 17-23.
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Kevin B. Boylan, Mark A. Ross & Eric J. Sorenson. 2017. Neurodegeneration. Neurodegeneration 137 160 .
Thomas Musacchio, Ann-Kathrin Zaum, Nurcan Üçeyler, Claudia Sommer, Nora Pfeifroth, Karlheinz Reiners, Erdmute Kunstmann, Jens Volkmann, Simone Rost & Stephan Klebe. (2016) ALS and MMN mimics in patients with BSCL2 mutations: the expanding clinical spectrum of SPG17 hereditary spastic paraplegia. Journal of Neurology 264:1, pages 11-20.
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Jeffrey M. Statland, Richard J. Barohn, Mazen M. Dimachkie, Mary Kay Floeter & Hiroshi Mitsumoto. (2015) Primary Lateral Sclerosis. Neurologic Clinics 33:4, pages 749-760.
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S. Klebe, G. Stevanin & C. Depienne. (2015) Clinical and genetic heterogeneity in hereditary spastic paraplegias: From SPG1 to SPG72 and still counting. Revue Neurologique 171:6-7, pages 505-530.
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Alessia De Felice, Annamaria Confaloni, Alessio Crestini, Roberta De Simone, Fiorella Malchiodi-Albedi, Alberto Martire, Andrea Matteucci, Luisa Minghetti, Patrizia Popoli, Aldina Venerosi & Gemma Calamandrei. 2015. Branched Chain Amino Acids in Clinical Nutrition. Branched Chain Amino Acids in Clinical Nutrition 229 241 .
Tracy M. Deangelis & Aaron Miller. 2014. Multiple Sclerosis and Related Disorders. Multiple Sclerosis and Related Disorders 317 342 .
Kathrin N Karle, Rebecca Schüle, Stephan Klebe, Susanne Otto, Christian Frischholz, Inga Liepelt-Scarfone & Ludger Schöls. (2013) Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP). Orphanet Journal of Rare Diseases 8:1.
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John K. Fink. 2013. Emery and Rimoin's Principles and Practice of Medical Genetics. Emery and Rimoin's Principles and Practice of Medical Genetics 1 54 .
Takayuki Kosaka, Yong‐Juan Fu, Atsushi Shiga, Haruka Ishidaira, Chun‐Feng Tan, Takashi Tani, Ryoko Koike, Osamu Onodera, Masatoyo Nishizawa, Akiyoshi Kakita & Hitoshi Takahashi. (2011) Primary lateral sclerosis: Upper‐motor‐predominant amyotrophic lateral sclerosis with frontotemporal lobar degeneration – immunohistochemical and biochemical analyses of TDP‐43. Neuropathology 32:4, pages 373-384.
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P. Piscopo, A. Crestini, A. Adduci, A. Ferrante, M. Massari, P. Popoli, N. Vanacore & A. Confaloni. (2011) Altered oxidative stress profile in the cortex of mice fed an enriched branched-chain amino acids diet: Possible link with amyotrophic lateral sclerosis?. Journal of Neuroscience Research 89:8, pages 1276-1283.
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P. H. GordonB. ChengI. B. KatzH. MitsumotoL. P. Rowland. (2009) Clinical features that distinguish PLS, upper motor neuron–dominant ALS, and typical ALS. Neurology 72:22, pages 1948-1952.
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Maria F. Pazyra-Murphy, Aymeric Hans, Stephanie L. Courchesne, Christoph Karch, Katharina E. Cosker, Heather M. Heerssen, Fiona L. Watson, Taekyung Kim, Michael E. Greenberg & Rosalind A. Segal. (2009) A Retrograde Neuronal Survival Response: Target-Derived Neurotrophins Regulate MEF2D and bcl-w. The Journal of Neuroscience 29:20, pages 6700-6709.
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N. Le Forestier & V. Meininger. (2009) La sclérose latérale primitive : l’avènement de critères consensuels internationaux. Revue Neurologique 165:5, pages 415-429.
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P. Couratier & J.-M. Vallat. (2008) Sclerosi laterale primitiva. EMC - Neurologia 8:4, pages 1-5.
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P. Couratier & J.-M. Vallat. (2008) Sclérose latérale primitive. EMC - Neurologie 5:2, pages 1-5.
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T. Prez Concha. (2007) Enfermedades de las motoneuronas. Medicine - Programa de Formaci?n M?dica Continuada Acreditado 9:78, pages 4989-4996.
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Mike A. Singer, Jeffrey M. Statland, Gil I. Wolfe & Richard J. Barohn. (2007) Primary lateral sclerosis. Muscle & Nerve 35:3, pages 291-302.
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P.Nigel Leigh. 2007. Motor neuron disorders and related diseases. Motor neuron disorders and related diseases 249 278 .
Lewis P. Rowland. (2006) Frontotemporal dementia, chromosome 17, and progranulin. Annals of Neurology 60:3, pages 275-277.
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Ou Bai, Sherry Vorbach, Mark Hallett & Mary Kay Floeter. (2006) Movement‐related cortical potentials in primary lateral sclerosis. Annals of Neurology 59:4, pages 682-690.
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P. H. GordonB. ChengI. B. KatzM. PintoA. P. HaysH. MitsumotoL. P. Rowland. (2006) The natural history of primary lateral sclerosis. Neurology 66:5, pages 647-653.
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