References
- Desai J, Swash M. IgM paraproteinaemia in a patient with primary lateral sclerosis. Neuromuscul Disord. 1999; 9:38–40.
- Shy ME, Rowland LP, Smith T, Trojaborg W, Latov N, Sherman W, . Motor neuron disease and plasma cell dyscrasia. Neurology. 1986;36:1429–36.
- Younger DS, Rowland LP, Latov N, Sherman W, Pesce M, Lange DJ, . Motor neuron disease and amyotrophic lateral sclerosis: relation of high CSF protein content to paraproteinaemia and clinical syndromes. Neurology. 1990;40:595–9.
- Sadiq SA, Latov N. Monoclonal gammopathy and motor neuron disease. Advances in Neurology. 1991;56:413–20.
- Nobile-Orazio E, Carpo M, Meucci N. Are there immunologically treatable motor neuron diseases? Amyotroph Lateral Scler Other Motor Neuron Disord. 2001;2 (Suppl 1):S23–30.
- Gordon PH, Rowland LP, Younger DS, Sherman WH, Hays AP, Louis ED, . Lymphoproliferative disorders and motor neuron disease: an update. Neurology. 1997; 48:1671–8.
- Brooks BR, Miller RG, Swash M, Munsat TL. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000;1:293–9.
- Cedarbaum JM, Stambler N, Malta E, Fuller C, Hilt D, Thurmond B, . The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III). J Neurol Sci. 1999;169:13–21.
- Andersen PM. Amyotrophic lateral sclerosis associated with mutations in the Cu/Zn superoxide dismutase gene. Curr Neurol Neurosci Rep. 2006;6:37–46.
- Luigetti M, Conte A, Madia F, Marangi G, Zollino M, Mancuso I, . Heterozygous SOD1-D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. Neurol Sci. 2009; 30:517–20.
- Robberecht W, Aguirre T, van den Bosch L, Tilkin P, Cassiman JJ, Matthijs G. D90A heterozygosity in the SOD1 gene is associated with familial and apparently sporadic amyotrophic lateral sclerosis. Neurology. 1996; 47:1336–9.
- Axelsson U, Bachmann R, Hallen J. Frequency of pathological proteins (M-components) from 6995 sera from an adult population. Acta Medica Scandinavica. 1966;179: 235–47.
- DeJesus-Hernandez M, Mackenzie IR, Boeve BF, Boxer AL, Baker M, Rutherford NJ, . Expanded GGGGCC hexanucleotide repeat in non-coding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron. 2011;72:245–56.